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Showing metabocard for PE-NMe(9D3/9D5) (HMDB0113817)
Record Information | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Version | 5.0 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Status | Expected but not Quantified | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Creation Date | 2017-09-09 00:11:33 UTC | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Update Date | 2022-11-30 19:25:16 UTC | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
HMDB ID | HMDB0113817 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Secondary Accession Numbers | None | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Metabolite Identification | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Common Name | PE-NMe(9D3/9D5) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Description | PE-NMe(9D3/9D5) is a monomethylphosphatidylethanolamine. It is a glycerophospholipid, and it is formed by sequential methylation of phosphatidylethanolamine as part of a mechanism for biosynthesis of phosphatidylcholine. Monomethylphosphatidylethanolamines are usually found at trace levels in animal or plant tissues. They can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. PE-NMe(9D3/9D5), in particular, consists of one chain of 9-(3,4-dimethyl-5-propylfuran-2-yl)nonanoic acid at the C-1 position and one chain of 9-(3,4-dimethyl-5-pentylfuran-2-yl)nonanoic acid at the C-2 position. Fatty acids containing 16, 18 and 20 carbons are the most common. Phospholipids are ubiquitous in nature. They are key components of the cell lipid bilayer and are involved in metabolism and signaling. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structure | MOL for HMDB0113817 (PE-NMe(9D3/9D5))Mrv1652309091702112D 57 58 0 0 1 0 999 V2000 -3.6589 -1.6557 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 20.7932 -0.5381 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 18.7397 1.8562 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.9841 1.4830 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.1507 -2.0477 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.6050 -1.6745 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.3978 5.0309 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.8384 -1.7419 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 19.9727 -0.4518 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.3535 -1.0745 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.6531 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9360 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.9386 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.6505 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.3675 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2215 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.2241 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.3649 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5330 -1.1607 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.0820 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5070 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.5096 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.0794 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 19.6371 0.3018 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0481 -0.4933 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.7965 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7926 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.7952 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.7939 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.3978 3.6020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.9853 2.8875 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.6518 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.9373 0.9355 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 18.4041 1.1025 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 17.5972 0.9310 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1849 -1.2940 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9919 -1.1225 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.9373 0.1105 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 18.8166 0.3881 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.2276 -0.5795 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 17.5109 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0781 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.0807 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.5083 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.9853 4.3164 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 11.0807 -1.1270 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 7.5083 0.9355 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.0478 2.1730 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.2228 2.9980 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.3662 0.1105 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 7.3978 2.1730 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.2228 1.3480 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.2228 -0.3020 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 18.2646 -0.2250 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.3244 0.0336 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.2228 2.1730 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0 9.6518 0.5230 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 8 1 1 0 0 0 0 9 2 1 0 0 0 0 10 8 1 0 0 0 0 13 11 1 0 0 0 0 14 12 1 0 0 0 0 15 11 1 0 0 0 0 16 12 1 0 0 0 0 17 13 1 0 0 0 0 18 14 1 0 0 0 0 19 10 1 0 0 0 0 20 15 1 0 0 0 0 21 16 1 0 0 0 0 22 17 1 0 0 0 0 23 18 1 0 0 0 0 24 9 1 0 0 0 0 25 19 1 0 0 0 0 26 20 1 0 0 0 0 27 21 1 0 0 0 0 28 22 1 0 0 0 0 29 23 1 0 0 0 0 31 30 1 0 0 0 0 34 3 1 0 0 0 0 35 4 1 0 0 0 0 35 34 1 0 0 0 0 36 5 1 0 0 0 0 37 6 1 0 0 0 0 37 36 1 0 0 0 0 38 32 1 0 0 0 0 38 33 1 0 0 0 0 39 24 1 0 0 0 0 39 34 2 0 0 0 0 40 25 1 0 0 0 0 40 36 2 0 0 0 0 41 26 1 0 0 0 0 41 35 2 0 0 0 0 42 27 1 0 0 0 0 42 37 2 0 0 0 0 43 28 1 0 0 0 0 44 29 1 0 0 0 0 45 7 1 0 0 0 0 45 30 1 0 0 0 0 46 43 2 0 0 0 0 47 44 2 0 0 0 0 50 32 1 0 0 0 0 50 43 1 0 0 0 0 51 31 1 0 0 0 0 52 33 1 0 0 0 0 38 53 1 6 0 0 0 53 44 1 0 0 0 0 54 39 1 0 0 0 0 54 41 1 0 0 0 0 55 40 1 0 0 0 0 55 42 1 0 0 0 0 56 48 1 0 0 0 0 56 49 2 0 0 0 0 56 51 1 0 0 0 0 56 52 1 0 0 0 0 38 57 1 6 0 0 0 M END 3D MOL for HMDB0113817 (PE-NMe(9D3/9D5))HMDB0113817 RDKit 3D PE-NMe(9D3/9D5) 132133 0 0 0 0 0 0 0 0999 V2000 2.2409 4.5009 4.9695 C 0 0 0 0 0 0 0 0 0 0 0 0 3.6751 4.0956 5.2733 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0431 4.2812 6.6899 C 0 0 0 0 0 0 0 0 0 0 0 0 3.3036 3.6017 7.7468 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2639 2.1568 7.9395 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8026 1.2429 6.9178 C 0 0 0 0 0 0 0 0 0 0 0 0 1.5476 0.8389 6.8193 O 0 0 0 0 0 0 0 0 0 0 0 0 1.3582 0.0204 5.8211 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0137 -0.5626 5.5180 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.6046 0.2378 4.3370 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.9565 -0.3011 4.0380 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.6829 0.3984 2.9696 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.2095 0.4019 1.5929 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9160 0.9744 1.1907 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.7349 2.4281 1.5737 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6300 2.8996 1.0822 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7409 2.8343 -0.3919 C 0 0 0 0 0 0 0 0 0 0 0 0 0.4371 3.8975 -1.0423 O 0 0 0 0 0 0 0 0 0 0 0 0 1.1418 1.7269 -1.1032 O 0 0 0 0 0 0 0 0 0 0 0 0 1.1907 1.8541 -2.5274 C 0 0 2 0 0 0 0 0 0 0 0 0 0.3445 0.7700 -3.1966 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8493 -0.5140 -2.8929 O 0 0 0 0 0 0 0 0 0 0 0 0 0.2375 -1.6503 -3.3686 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.7859 -1.5359 -4.0764 O 0 0 0 0 0 0 0 0 0 0 0 0 0.7426 -3.0225 -3.0753 C 0 0 0 0 0 0 0 0 0 0 0 0 0.2365 -3.5550 -1.7899 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2084 -3.7100 -1.5589 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.0352 -4.6479 -2.3158 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.2403 -4.5475 -3.7737 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.1862 -5.6492 -4.2716 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.5537 -5.6384 -3.7459 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.4754 -4.5246 -4.0808 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.0703 -3.1546 -3.7532 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.7166 -2.1999 -4.6098 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.4188 -1.0893 -4.0093 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9782 0.2027 -4.6575 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.1313 1.1946 -4.6413 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.7409 2.4948 -5.2888 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.5616 -1.2430 -2.6504 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.3353 -0.2847 -1.5391 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.9799 -2.5713 -2.5039 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.2599 -3.1681 -1.1654 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6121 1.5941 -3.0151 C 0 0 0 0 0 0 0 0 0 0 0 0 3.5307 2.4699 -2.4694 O 0 0 0 0 0 0 0 0 0 0 0 0 5.0616 2.0864 -3.0740 P 0 0 0 0 0 5 0 0 0 0 0 0 5.1407 2.2568 -4.5665 O 0 0 0 0 0 0 0 0 0 0 0 0 6.1631 3.1637 -2.3437 O 0 0 0 0 0 0 0 0 0 0 0 0 5.4502 0.4994 -2.6901 O 0 0 0 0 0 0 0 0 0 0 0 0 5.3804 0.3490 -1.3073 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7618 -1.0954 -1.0185 C 0 0 0 0 0 0 0 0 0 0 0 0 5.6944 -1.2821 0.4176 N 0 0 0 0 0 0 0 0 0 0 0 0 6.0478 -2.6329 0.8011 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5552 -0.1493 5.1957 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8168 -1.0082 4.0155 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4678 0.6215 5.8871 C 0 0 0 0 0 0 0 0 0 0 0 0 4.9178 0.6967 5.5645 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0522 4.5919 3.9018 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9355 5.3653 5.5928 H 0 0 0 0 0 0 0 0 0 0 0 0 1.5956 3.6514 5.3478 H 0 0 0 0 0 0 0 0 0 0 0 0 3.9360 3.1658 4.8223 H 0 0 0 0 0 0 0 0 0 0 0 0 4.2889 4.8764 4.6931 H 0 0 0 0 0 0 0 0 0 0 0 0 4.0427 5.3894 6.9380 H 0 0 0 0 0 0 0 0 0 0 0 0 5.1291 4.0061 6.7897 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2251 4.0358 7.8304 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7229 4.0303 8.7368 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6691 1.9898 8.9185 H 0 0 0 0 0 0 0 0 0 0 0 0 4.2860 1.7515 8.2826 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.6957 -0.4181 6.3562 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1073 -1.6213 5.2031 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.6385 1.3149 4.6606 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1066 0.1350 3.5420 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.5880 -0.1997 4.9870 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.8323 -1.4058 3.8312 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.8031 0.0918 2.9871 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.8205 1.5133 3.2593 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0301 0.8884 0.9482 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2674 -0.6783 1.1651 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9272 1.0155 0.0163 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0023 0.4276 1.3725 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8611 2.5785 2.6532 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4744 3.0816 1.0582 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3939 2.2132 1.5400 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7505 3.9458 1.4272 H 0 0 0 0 0 0 0 0 0 0 0 0 0.9009 2.8561 -2.8642 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3814 0.9655 -4.2869 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.7164 0.8766 -2.8530 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5498 -3.6757 -3.9148 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8751 -2.9321 -3.0138 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7218 -2.9049 -0.9825 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7864 -4.5531 -1.6024 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.6417 -2.6320 -1.6216 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3154 -3.9736 -0.4367 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0195 -4.8136 -1.7498 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5546 -5.6944 -2.1154 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.5369 -3.6009 -4.1903 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2619 -4.8429 -4.2812 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1413 -5.5889 -5.3872 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7382 -6.6583 -4.0168 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.1022 -6.6033 -4.0325 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4884 -5.7259 -2.6165 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.5923 -4.5403 -5.2159 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.5248 -4.7345 -3.7038 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1089 0.6385 -4.1713 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.7784 -0.0400 -5.7152 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.0238 0.7964 -5.1784 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.3670 1.4034 -3.5725 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.1915 2.6312 -6.2965 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.6219 2.5311 -5.3736 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.9969 3.3357 -4.6183 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.2474 -0.0911 -0.9679 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.8278 0.6234 -1.9377 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.5842 -0.7149 -0.8123 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.3232 -3.1518 -0.5372 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.0105 -2.5734 -0.5878 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.6819 -4.1823 -1.2578 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6387 1.7882 -4.1276 H 0 0 0 0 0 0 0 0 0 0 0 0 2.9105 0.5501 -2.8788 H 0 0 0 0 0 0 0 0 0 0 0 0 6.1353 3.0837 -1.3574 H 0 0 0 0 0 0 0 0 0 0 0 0 4.3402 0.5481 -0.9587 H 0 0 0 0 0 0 0 0 0 0 0 0 6.1177 1.0375 -0.8732 H 0 0 0 0 0 0 0 0 0 0 0 0 6.8218 -1.2491 -1.3321 H 0 0 0 0 0 0 0 0 0 0 0 0 5.1095 -1.8025 -1.5777 H 0 0 0 0 0 0 0 0 0 0 0 0 6.3092 -0.5533 0.8377 H 0 0 0 0 0 0 0 0 0 0 0 0 6.8985 -2.9634 0.1486 H 0 0 0 0 0 0 0 0 0 0 0 0 5.1922 -3.2912 0.5415 H 0 0 0 0 0 0 0 0 0 0 0 0 6.3394 -2.7013 1.8480 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8976 -1.4118 3.5658 H 0 0 0 0 0 0 0 0 0 0 0 0 3.3627 -0.3714 3.2793 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4847 -1.8411 4.3757 H 0 0 0 0 0 0 0 0 0 0 0 0 5.4206 -0.1813 6.0293 H 0 0 0 0 0 0 0 0 0 0 0 0 5.3656 1.5889 6.0554 H 0 0 0 0 0 0 0 0 0 0 0 0 4.9857 0.7205 4.4621 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 2 3 1 0 3 4 1 0 4 5 1 0 5 6 1 0 6 7 1 0 7 8 1 0 8 9 1 0 9 10 1 0 10 11 1 0 11 12 1 0 12 13 1 0 13 14 1 0 14 15 1 0 15 16 1 0 16 17 1 0 17 18 2 0 17 19 1 0 19 20 1 0 20 21 1 0 21 22 1 0 22 23 1 0 23 24 2 0 23 25 1 0 25 26 1 0 26 27 1 0 27 28 1 0 28 29 1 0 29 30 1 0 30 31 1 0 31 32 1 0 32 33 1 0 33 34 1 0 34 35 1 0 35 36 1 0 36 37 1 0 37 38 1 0 35 39 2 0 39 40 1 0 39 41 1 0 41 42 1 0 20 43 1 0 43 44 1 0 44 45 1 0 45 46 2 0 45 47 1 0 45 48 1 0 48 49 1 0 49 50 1 0 50 51 1 0 51 52 1 0 8 53 2 0 53 54 1 0 53 55 1 0 55 56 1 0 55 6 2 0 41 33 2 0 1 57 1 0 1 58 1 0 1 59 1 0 2 60 1 0 2 61 1 0 3 62 1 0 3 63 1 0 4 64 1 0 4 65 1 0 5 66 1 0 5 67 1 0 9 68 1 0 9 69 1 0 10 70 1 0 10 71 1 0 11 72 1 0 11 73 1 0 12 74 1 0 12 75 1 0 13 76 1 0 13 77 1 0 14 78 1 0 14 79 1 0 15 80 1 0 15 81 1 0 16 82 1 0 16 83 1 0 20 84 1 1 21 85 1 0 21 86 1 0 25 87 1 0 25 88 1 0 26 89 1 0 26 90 1 0 27 91 1 0 27 92 1 0 28 93 1 0 28 94 1 0 29 95 1 0 29 96 1 0 30 97 1 0 30 98 1 0 31 99 1 0 31100 1 0 32101 1 0 32102 1 0 36103 1 0 36104 1 0 37105 1 0 37106 1 0 38107 1 0 38108 1 0 38109 1 0 40110 1 0 40111 1 0 40112 1 0 42113 1 0 42114 1 0 42115 1 0 43116 1 0 43117 1 0 47118 1 0 49119 1 0 49120 1 0 50121 1 0 50122 1 0 51123 1 0 52124 1 0 52125 1 0 52126 1 0 54127 1 0 54128 1 0 54129 1 0 56130 1 0 56131 1 0 56132 1 0 M END 3D SDF for HMDB0113817 (PE-NMe(9D3/9D5))Mrv1652309091702112D 57 58 0 0 1 0 999 V2000 -3.6589 -1.6557 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 20.7932 -0.5381 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 18.7397 1.8562 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.9841 1.4830 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.1507 -2.0477 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.6050 -1.6745 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.3978 5.0309 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.8384 -1.7419 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 19.9727 -0.4518 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.3535 -1.0745 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.6531 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9360 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.9386 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.6505 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.3675 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2215 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.2241 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.3649 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.5330 -1.1607 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.0820 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5070 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.5096 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.0794 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 19.6371 0.3018 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.0481 -0.4933 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.7965 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7926 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.7952 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.7939 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.3978 3.6020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.9853 2.8875 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.6518 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.9373 0.9355 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 18.4041 1.1025 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 17.5972 0.9310 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1849 -1.2940 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.9919 -1.1225 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.9373 0.1105 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 18.8166 0.3881 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.2276 -0.5795 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 17.5109 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0781 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.0807 -0.3020 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.5083 0.1105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.9853 4.3164 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 11.0807 -1.1270 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 7.5083 0.9355 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.0478 2.1730 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.2228 2.9980 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.3662 0.1105 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 7.3978 2.1730 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.2228 1.3480 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.2228 -0.3020 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 18.2646 -0.2250 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.3244 0.0336 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.2228 2.1730 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0 9.6518 0.5230 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 8 1 1 0 0 0 0 9 2 1 0 0 0 0 10 8 1 0 0 0 0 13 11 1 0 0 0 0 14 12 1 0 0 0 0 15 11 1 0 0 0 0 16 12 1 0 0 0 0 17 13 1 0 0 0 0 18 14 1 0 0 0 0 19 10 1 0 0 0 0 20 15 1 0 0 0 0 21 16 1 0 0 0 0 22 17 1 0 0 0 0 23 18 1 0 0 0 0 24 9 1 0 0 0 0 25 19 1 0 0 0 0 26 20 1 0 0 0 0 27 21 1 0 0 0 0 28 22 1 0 0 0 0 29 23 1 0 0 0 0 31 30 1 0 0 0 0 34 3 1 0 0 0 0 35 4 1 0 0 0 0 35 34 1 0 0 0 0 36 5 1 0 0 0 0 37 6 1 0 0 0 0 37 36 1 0 0 0 0 38 32 1 0 0 0 0 38 33 1 0 0 0 0 39 24 1 0 0 0 0 39 34 2 0 0 0 0 40 25 1 0 0 0 0 40 36 2 0 0 0 0 41 26 1 0 0 0 0 41 35 2 0 0 0 0 42 27 1 0 0 0 0 42 37 2 0 0 0 0 43 28 1 0 0 0 0 44 29 1 0 0 0 0 45 7 1 0 0 0 0 45 30 1 0 0 0 0 46 43 2 0 0 0 0 47 44 2 0 0 0 0 50 32 1 0 0 0 0 50 43 1 0 0 0 0 51 31 1 0 0 0 0 52 33 1 0 0 0 0 38 53 1 6 0 0 0 53 44 1 0 0 0 0 54 39 1 0 0 0 0 54 41 1 0 0 0 0 55 40 1 0 0 0 0 55 42 1 0 0 0 0 56 48 1 0 0 0 0 56 49 2 0 0 0 0 56 51 1 0 0 0 0 56 52 1 0 0 0 0 38 57 1 6 0 0 0 M END > <DATABASE_ID> HMDB0113817 > <DATABASE_NAME> hmdb > <SMILES> [H][C@@](COC(=O)CCCCCCCCC1=C(C)C(C)=C(CCC)O1)(COP(O)(=O)OCCNC)OC(=O)CCCCCCCCC1=C(C)C(C)=C(CCCCC)O1 > <INCHI_IDENTIFIER> InChI=1S/C44H76NO10P/c1-8-10-19-25-40-36(5)37(6)42(55-40)27-21-16-12-14-18-23-29-44(47)53-38(33-52-56(48,49)51-31-30-45-7)32-50-43(46)28-22-17-13-11-15-20-26-41-35(4)34(3)39(54-41)24-9-2/h38,45H,8-33H2,1-7H3,(H,48,49)/t38-/m1/s1 > <INCHI_KEY> VGDDWCSEYRXVDP-KXQOOQHDSA-N > <FORMULA> C44H76NO10P > <MOLECULAR_WEIGHT> 810.063 > <EXACT_MASS> 809.520684649 > <JCHEM_ACCEPTOR_COUNT> 5 > <JCHEM_ATOM_COUNT> 132 > <JCHEM_AVERAGE_POLARIZABILITY> 96.835946036727 > <JCHEM_BIOAVAILABILITY> 0 > <JCHEM_DONOR_COUNT> 2 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 0 > <JCHEM_IUPAC> [(2R)-2-{[9-(3,4-dimethyl-5-pentylfuran-2-yl)nonanoyl]oxy}-3-{[9-(3,4-dimethyl-5-propylfuran-2-yl)nonanoyl]oxy}propoxy][2-(methylamino)ethoxy]phosphinic acid > <ALOGPS_LOGP> 7.04 > <JCHEM_LOGP> 10.692187491811355 > <ALOGPS_LOGS> -5.43 > <JCHEM_MDDR_LIKE_RULE> 0 > <JCHEM_NUMBER_OF_RINGS> 2 > <JCHEM_PHYSIOLOGICAL_CHARGE> 0 > <JCHEM_PKA_STRONGEST_ACIDIC> 1.8562099844677986 > <JCHEM_PKA_STRONGEST_BASIC> 10.045225536700087 > <JCHEM_POLAR_SURFACE_AREA> 146.67000000000002 > <JCHEM_REFRACTIVITY> 223.7625000000001 > <JCHEM_ROTATABLE_BOND_COUNT> 36 > <JCHEM_RULE_OF_FIVE> 0 > <ALOGPS_SOLUBILITY> 3.04e-03 g/l > <JCHEM_TRADITIONAL_IUPAC> (2R)-2-{[9-(3,4-dimethyl-5-pentylfuran-2-yl)nonanoyl]oxy}-3-{[9-(3,4-dimethyl-5-propylfuran-2-yl)nonanoyl]oxy}propoxy(2-(methylamino)ethoxy)phosphinic acid > <JCHEM_VEBER_RULE> 0 $$$$ 3D-SDF for HMDB0113817 (PE-NMe(9D3/9D5))HMDB0113817 RDKit 3D PE-NMe(9D3/9D5) 132133 0 0 0 0 0 0 0 0999 V2000 2.2409 4.5009 4.9695 C 0 0 0 0 0 0 0 0 0 0 0 0 3.6751 4.0956 5.2733 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0431 4.2812 6.6899 C 0 0 0 0 0 0 0 0 0 0 0 0 3.3036 3.6017 7.7468 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2639 2.1568 7.9395 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8026 1.2429 6.9178 C 0 0 0 0 0 0 0 0 0 0 0 0 1.5476 0.8389 6.8193 O 0 0 0 0 0 0 0 0 0 0 0 0 1.3582 0.0204 5.8211 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0137 -0.5626 5.5180 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.6046 0.2378 4.3370 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.9565 -0.3011 4.0380 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.6829 0.3984 2.9696 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.2095 0.4019 1.5929 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.9160 0.9744 1.1907 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.7349 2.4281 1.5737 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6300 2.8996 1.0822 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7409 2.8343 -0.3919 C 0 0 0 0 0 0 0 0 0 0 0 0 0.4371 3.8975 -1.0423 O 0 0 0 0 0 0 0 0 0 0 0 0 1.1418 1.7269 -1.1032 O 0 0 0 0 0 0 0 0 0 0 0 0 1.1907 1.8541 -2.5274 C 0 0 2 0 0 0 0 0 0 0 0 0 0.3445 0.7700 -3.1966 C 0 0 0 0 0 0 0 0 0 0 0 0 0.8493 -0.5140 -2.8929 O 0 0 0 0 0 0 0 0 0 0 0 0 0.2375 -1.6503 -3.3686 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.7859 -1.5359 -4.0764 O 0 0 0 0 0 0 0 0 0 0 0 0 0.7426 -3.0225 -3.0753 C 0 0 0 0 0 0 0 0 0 0 0 0 0.2365 -3.5550 -1.7899 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.2084 -3.7100 -1.5589 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.0352 -4.6479 -2.3158 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.2403 -4.5475 -3.7737 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.1862 -5.6492 -4.2716 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.5537 -5.6384 -3.7459 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.4754 -4.5246 -4.0808 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.0703 -3.1546 -3.7532 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.7166 -2.1999 -4.6098 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.4188 -1.0893 -4.0093 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.9782 0.2027 -4.6575 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.1313 1.1946 -4.6413 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.7409 2.4948 -5.2888 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.5616 -1.2430 -2.6504 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.3353 -0.2847 -1.5391 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.9799 -2.5713 -2.5039 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.2599 -3.1681 -1.1654 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6121 1.5941 -3.0151 C 0 0 0 0 0 0 0 0 0 0 0 0 3.5307 2.4699 -2.4694 O 0 0 0 0 0 0 0 0 0 0 0 0 5.0616 2.0864 -3.0740 P 0 0 0 0 0 5 0 0 0 0 0 0 5.1407 2.2568 -4.5665 O 0 0 0 0 0 0 0 0 0 0 0 0 6.1631 3.1637 -2.3437 O 0 0 0 0 0 0 0 0 0 0 0 0 5.4502 0.4994 -2.6901 O 0 0 0 0 0 0 0 0 0 0 0 0 5.3804 0.3490 -1.3073 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7618 -1.0954 -1.0185 C 0 0 0 0 0 0 0 0 0 0 0 0 5.6944 -1.2821 0.4176 N 0 0 0 0 0 0 0 0 0 0 0 0 6.0478 -2.6329 0.8011 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5552 -0.1493 5.1957 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8168 -1.0082 4.0155 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4678 0.6215 5.8871 C 0 0 0 0 0 0 0 0 0 0 0 0 4.9178 0.6967 5.5645 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0522 4.5919 3.9018 H 0 0 0 0 0 0 0 0 0 0 0 0 1.9355 5.3653 5.5928 H 0 0 0 0 0 0 0 0 0 0 0 0 1.5956 3.6514 5.3478 H 0 0 0 0 0 0 0 0 0 0 0 0 3.9360 3.1658 4.8223 H 0 0 0 0 0 0 0 0 0 0 0 0 4.2889 4.8764 4.6931 H 0 0 0 0 0 0 0 0 0 0 0 0 4.0427 5.3894 6.9380 H 0 0 0 0 0 0 0 0 0 0 0 0 5.1291 4.0061 6.7897 H 0 0 0 0 0 0 0 0 0 0 0 0 2.2251 4.0358 7.8304 H 0 0 0 0 0 0 0 0 0 0 0 0 3.7229 4.0303 8.7368 H 0 0 0 0 0 0 0 0 0 0 0 0 2.6691 1.9898 8.9185 H 0 0 0 0 0 0 0 0 0 0 0 0 4.2860 1.7515 8.2826 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.6957 -0.4181 6.3562 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1073 -1.6213 5.2031 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.6385 1.3149 4.6606 H 0 0 0 0 0 0 0 0 0 0 0 0 0.1066 0.1350 3.5420 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.5880 -0.1997 4.9870 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.8323 -1.4058 3.8312 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.8031 0.0918 2.9871 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.8205 1.5133 3.2593 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0301 0.8884 0.9482 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.2674 -0.6783 1.1651 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.9272 1.0155 0.0163 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0023 0.4276 1.3725 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.8611 2.5785 2.6532 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.4744 3.0816 1.0582 H 0 0 0 0 0 0 0 0 0 0 0 0 1.3939 2.2132 1.5400 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7505 3.9458 1.4272 H 0 0 0 0 0 0 0 0 0 0 0 0 0.9009 2.8561 -2.8642 H 0 0 0 0 0 0 0 0 0 0 0 0 0.3814 0.9655 -4.2869 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.7164 0.8766 -2.8530 H 0 0 0 0 0 0 0 0 0 0 0 0 0.5498 -3.6757 -3.9148 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8751 -2.9321 -3.0138 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7218 -2.9049 -0.9825 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7864 -4.5531 -1.6024 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.6417 -2.6320 -1.6216 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.3154 -3.9736 -0.4367 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.0195 -4.8136 -1.7498 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.5546 -5.6944 -2.1154 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.5369 -3.6009 -4.1903 H 0 0 0 0 0 0 0 0 0 0 0 0 -1.2619 -4.8429 -4.2812 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1413 -5.5889 -5.3872 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.7382 -6.6583 -4.0168 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.1022 -6.6033 -4.0325 H 0 0 0 0 0 0 0 0 0 0 0 0 -4.4884 -5.7259 -2.6165 H 0 0 0 0 0 0 0 0 0 0 0 0 -5.5923 -4.5403 -5.2159 H 0 0 0 0 0 0 0 0 0 0 0 0 -6.5248 -4.7345 -3.7038 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.1089 0.6385 -4.1713 H 0 0 0 0 0 0 0 0 0 0 0 0 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0.1486 H 0 0 0 0 0 0 0 0 0 0 0 0 5.1922 -3.2912 0.5415 H 0 0 0 0 0 0 0 0 0 0 0 0 6.3394 -2.7013 1.8480 H 0 0 0 0 0 0 0 0 0 0 0 0 1.8976 -1.4118 3.5658 H 0 0 0 0 0 0 0 0 0 0 0 0 3.3627 -0.3714 3.2793 H 0 0 0 0 0 0 0 0 0 0 0 0 3.4847 -1.8411 4.3757 H 0 0 0 0 0 0 0 0 0 0 0 0 5.4206 -0.1813 6.0293 H 0 0 0 0 0 0 0 0 0 0 0 0 5.3656 1.5889 6.0554 H 0 0 0 0 0 0 0 0 0 0 0 0 4.9857 0.7205 4.4621 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 2 3 1 0 3 4 1 0 4 5 1 0 5 6 1 0 6 7 1 0 7 8 1 0 8 9 1 0 9 10 1 0 10 11 1 0 11 12 1 0 12 13 1 0 13 14 1 0 14 15 1 0 15 16 1 0 16 17 1 0 17 18 2 0 17 19 1 0 19 20 1 0 20 21 1 0 21 22 1 0 22 23 1 0 23 24 2 0 23 25 1 0 25 26 1 0 26 27 1 0 27 28 1 0 28 29 1 0 29 30 1 0 30 31 1 0 31 32 1 0 32 33 1 0 33 34 1 0 34 35 1 0 35 36 1 0 36 37 1 0 37 38 1 0 35 39 2 0 39 40 1 0 39 41 1 0 41 42 1 0 20 43 1 0 43 44 1 0 44 45 1 0 45 46 2 0 45 47 1 0 45 48 1 0 48 49 1 0 49 50 1 0 50 51 1 0 51 52 1 0 8 53 2 0 53 54 1 0 53 55 1 0 55 56 1 0 55 6 2 0 41 33 2 0 1 57 1 0 1 58 1 0 1 59 1 0 2 60 1 0 2 61 1 0 3 62 1 0 3 63 1 0 4 64 1 0 4 65 1 0 5 66 1 0 5 67 1 0 9 68 1 0 9 69 1 0 10 70 1 0 10 71 1 0 11 72 1 0 11 73 1 0 12 74 1 0 12 75 1 0 13 76 1 0 13 77 1 0 14 78 1 0 14 79 1 0 15 80 1 0 15 81 1 0 16 82 1 0 16 83 1 0 20 84 1 1 21 85 1 0 21 86 1 0 25 87 1 0 25 88 1 0 26 89 1 0 26 90 1 0 27 91 1 0 27 92 1 0 28 93 1 0 28 94 1 0 29 95 1 0 29 96 1 0 30 97 1 0 30 98 1 0 31 99 1 0 31100 1 0 32101 1 0 32102 1 0 36103 1 0 36104 1 0 37105 1 0 37106 1 0 38107 1 0 38108 1 0 38109 1 0 40110 1 0 40111 1 0 40112 1 0 42113 1 0 42114 1 0 42115 1 0 43116 1 0 43117 1 0 47118 1 0 49119 1 0 49120 1 0 50121 1 0 50122 1 0 51123 1 0 52124 1 0 52125 1 0 52126 1 0 54127 1 0 54128 1 0 54129 1 0 56130 1 0 56131 1 0 56132 1 0 M END PDB for HMDB0113817 (PE-NMe(9D3/9D5))HEADER PROTEIN 09-SEP-17 NONE TITLE NULL COMPND NULL SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 09-SEP-17 0 HETATM 1 C UNK 0 -6.830 -3.091 0.000 0.00 0.00 C+0 HETATM 2 C UNK 0 38.814 -1.004 0.000 0.00 0.00 C+0 HETATM 3 C UNK 0 34.981 3.465 0.000 0.00 0.00 C+0 HETATM 4 C UNK 0 31.704 2.768 0.000 0.00 0.00 C+0 HETATM 5 C UNK 0 -0.281 -3.822 0.000 0.00 0.00 C+0 HETATM 6 C UNK 0 2.996 -3.126 0.000 0.00 0.00 C+0 HETATM 7 C UNK 0 13.809 9.391 0.000 0.00 0.00 C+0 HETATM 8 C UNK 0 -5.298 -3.252 0.000 0.00 0.00 C+0 HETATM 9 C UNK 0 37.282 -0.843 0.000 0.00 0.00 C+0 HETATM 10 C UNK 0 -4.393 -2.006 0.000 0.00 0.00 C+0 HETATM 11 C UNK 0 27.352 0.206 0.000 0.00 0.00 C+0 HETATM 12 C UNK 0 7.347 -0.564 0.000 0.00 0.00 C+0 HETATM 13 C UNK 0 26.019 -0.564 0.000 0.00 0.00 C+0 HETATM 14 C UNK 0 8.681 0.206 0.000 0.00 0.00 C+0 HETATM 15 C UNK 0 28.686 -0.564 0.000 0.00 0.00 C+0 HETATM 16 C UNK 0 6.013 0.206 0.000 0.00 0.00 C+0 HETATM 17 C UNK 0 24.685 0.206 0.000 0.00 0.00 C+0 HETATM 18 C UNK 0 10.015 -0.564 0.000 0.00 0.00 C+0 HETATM 19 C UNK 0 -2.862 -2.167 0.000 0.00 0.00 C+0 HETATM 20 C UNK 0 30.020 0.206 0.000 0.00 0.00 C+0 HETATM 21 C UNK 0 4.680 -0.564 0.000 0.00 0.00 C+0 HETATM 22 C UNK 0 23.351 -0.564 0.000 0.00 0.00 C+0 HETATM 23 C UNK 0 11.348 0.206 0.000 0.00 0.00 C+0 HETATM 24 C UNK 0 36.656 0.563 0.000 0.00 0.00 C+0 HETATM 25 C UNK 0 -1.956 -0.921 0.000 0.00 0.00 C+0 HETATM 26 C UNK 0 31.353 -0.564 0.000 0.00 0.00 C+0 HETATM 27 C UNK 0 3.346 0.206 0.000 0.00 0.00 C+0 HETATM 28 C UNK 0 22.018 0.206 0.000 0.00 0.00 C+0 HETATM 29 C UNK 0 12.682 -0.564 0.000 0.00 0.00 C+0 HETATM 30 C UNK 0 13.809 6.724 0.000 0.00 0.00 C+0 HETATM 31 C UNK 0 13.039 5.390 0.000 0.00 0.00 C+0 HETATM 32 C UNK 0 18.017 -0.564 0.000 0.00 0.00 C+0 HETATM 33 C UNK 0 16.683 1.746 0.000 0.00 0.00 C+0 HETATM 34 C UNK 0 34.354 2.058 0.000 0.00 0.00 C+0 HETATM 35 C UNK 0 32.848 1.738 0.000 0.00 0.00 C+0 HETATM 36 C UNK 0 0.345 -2.415 0.000 0.00 0.00 C+0 HETATM 37 C UNK 0 1.851 -2.095 0.000 0.00 0.00 C+0 HETATM 38 C UNK 0 16.683 0.206 0.000 0.00 0.00 C+0 HETATM 39 C UNK 0 35.124 0.724 0.000 0.00 0.00 C+0 HETATM 40 C UNK 0 -0.425 -1.082 0.000 0.00 0.00 C+0 HETATM 41 C UNK 0 32.687 0.206 0.000 0.00 0.00 C+0 HETATM 42 C UNK 0 2.012 -0.564 0.000 0.00 0.00 C+0 HETATM 43 C UNK 0 20.684 -0.564 0.000 0.00 0.00 C+0 HETATM 44 C UNK 0 14.016 0.206 0.000 0.00 0.00 C+0 HETATM 45 N UNK 0 13.039 8.057 0.000 0.00 0.00 N+0 HETATM 46 O UNK 0 20.684 -2.104 0.000 0.00 0.00 O+0 HETATM 47 O UNK 0 14.016 1.746 0.000 0.00 0.00 O+0 HETATM 48 O UNK 0 16.889 4.056 0.000 0.00 0.00 O+0 HETATM 49 O UNK 0 15.349 5.596 0.000 0.00 0.00 O+0 HETATM 50 O UNK 0 19.350 0.206 0.000 0.00 0.00 O+0 HETATM 51 O UNK 0 13.809 4.056 0.000 0.00 0.00 O+0 HETATM 52 O UNK 0 15.349 2.516 0.000 0.00 0.00 O+0 HETATM 53 O UNK 0 15.349 -0.564 0.000 0.00 0.00 O+0 HETATM 54 O UNK 0 34.094 -0.420 0.000 0.00 0.00 O+0 HETATM 55 O UNK 0 0.606 0.063 0.000 0.00 0.00 O+0 HETATM 56 P UNK 0 15.349 4.056 0.000 0.00 0.00 P+0 HETATM 57 H UNK 0 18.017 0.976 0.000 0.00 0.00 H+0 CONECT 1 8 CONECT 2 9 CONECT 3 34 CONECT 4 35 CONECT 5 36 CONECT 6 37 CONECT 7 45 CONECT 8 1 10 CONECT 9 2 24 CONECT 10 8 19 CONECT 11 13 15 CONECT 12 14 16 CONECT 13 11 17 CONECT 14 12 18 CONECT 15 11 20 CONECT 16 12 21 CONECT 17 13 22 CONECT 18 14 23 CONECT 19 10 25 CONECT 20 15 26 CONECT 21 16 27 CONECT 22 17 28 CONECT 23 18 29 CONECT 24 9 39 CONECT 25 19 40 CONECT 26 20 41 CONECT 27 21 42 CONECT 28 22 43 CONECT 29 23 44 CONECT 30 31 45 CONECT 31 30 51 CONECT 32 38 50 CONECT 33 38 52 CONECT 34 3 35 39 CONECT 35 4 34 41 CONECT 36 5 37 40 CONECT 37 6 36 42 CONECT 38 32 33 53 57 CONECT 39 24 34 54 CONECT 40 25 36 55 CONECT 41 26 35 54 CONECT 42 27 37 55 CONECT 43 28 46 50 CONECT 44 29 47 53 CONECT 45 7 30 CONECT 46 43 CONECT 47 44 CONECT 48 56 CONECT 49 56 CONECT 50 32 43 CONECT 51 31 56 CONECT 52 33 56 CONECT 53 38 44 CONECT 54 39 41 CONECT 55 40 42 CONECT 56 48 49 51 52 CONECT 57 38 MASTER 0 0 0 0 0 0 0 0 57 0 116 0 END 3D PDB for HMDB0113817 (PE-NMe(9D3/9D5))COMPND HMDB0113817 HETATM 1 C1 UNL 1 2.241 4.501 4.970 1.00 0.00 C HETATM 2 C2 UNL 1 3.675 4.096 5.273 1.00 0.00 C HETATM 3 C3 UNL 1 4.043 4.281 6.690 1.00 0.00 C HETATM 4 C4 UNL 1 3.304 3.602 7.747 1.00 0.00 C HETATM 5 C5 UNL 1 3.264 2.157 7.940 1.00 0.00 C HETATM 6 C6 UNL 1 2.803 1.243 6.918 1.00 0.00 C HETATM 7 O1 UNL 1 1.548 0.839 6.819 1.00 0.00 O HETATM 8 C7 UNL 1 1.358 0.020 5.821 1.00 0.00 C HETATM 9 C8 UNL 1 0.014 -0.563 5.518 1.00 0.00 C HETATM 10 C9 UNL 1 -0.605 0.238 4.337 1.00 0.00 C HETATM 11 C10 UNL 1 -1.957 -0.301 4.038 1.00 0.00 C HETATM 12 C11 UNL 1 -2.683 0.398 2.970 1.00 0.00 C HETATM 13 C12 UNL 1 -2.209 0.402 1.593 1.00 0.00 C HETATM 14 C13 UNL 1 -0.916 0.974 1.191 1.00 0.00 C HETATM 15 C14 UNL 1 -0.735 2.428 1.574 1.00 0.00 C HETATM 16 C15 UNL 1 0.630 2.900 1.082 1.00 0.00 C HETATM 17 C16 UNL 1 0.741 2.834 -0.392 1.00 0.00 C HETATM 18 O2 UNL 1 0.437 3.897 -1.042 1.00 0.00 O HETATM 19 O3 UNL 1 1.142 1.727 -1.103 1.00 0.00 O HETATM 20 C17 UNL 1 1.191 1.854 -2.527 1.00 0.00 C HETATM 21 C18 UNL 1 0.345 0.770 -3.197 1.00 0.00 C HETATM 22 O4 UNL 1 0.849 -0.514 -2.893 1.00 0.00 O HETATM 23 C19 UNL 1 0.238 -1.650 -3.369 1.00 0.00 C HETATM 24 O5 UNL 1 -0.786 -1.536 -4.076 1.00 0.00 O HETATM 25 C20 UNL 1 0.743 -3.022 -3.075 1.00 0.00 C HETATM 26 C21 UNL 1 0.236 -3.555 -1.790 1.00 0.00 C HETATM 27 C22 UNL 1 -1.208 -3.710 -1.559 1.00 0.00 C HETATM 28 C23 UNL 1 -2.035 -4.648 -2.316 1.00 0.00 C HETATM 29 C24 UNL 1 -2.240 -4.548 -3.774 1.00 0.00 C HETATM 30 C25 UNL 1 -3.186 -5.649 -4.272 1.00 0.00 C HETATM 31 C26 UNL 1 -4.554 -5.638 -3.746 1.00 0.00 C HETATM 32 C27 UNL 1 -5.475 -4.525 -4.081 1.00 0.00 C HETATM 33 C28 UNL 1 -5.070 -3.155 -3.753 1.00 0.00 C HETATM 34 O6 UNL 1 -4.717 -2.200 -4.610 1.00 0.00 O HETATM 35 C29 UNL 1 -4.419 -1.089 -4.009 1.00 0.00 C HETATM 36 C30 UNL 1 -3.978 0.203 -4.657 1.00 0.00 C HETATM 37 C31 UNL 1 -5.131 1.195 -4.641 1.00 0.00 C HETATM 38 C32 UNL 1 -4.741 2.495 -5.289 1.00 0.00 C HETATM 39 C33 UNL 1 -4.562 -1.243 -2.650 1.00 0.00 C HETATM 40 C34 UNL 1 -4.335 -0.285 -1.539 1.00 0.00 C HETATM 41 C35 UNL 1 -4.980 -2.571 -2.504 1.00 0.00 C HETATM 42 C36 UNL 1 -5.260 -3.168 -1.165 1.00 0.00 C HETATM 43 C37 UNL 1 2.612 1.594 -3.015 1.00 0.00 C HETATM 44 O7 UNL 1 3.531 2.470 -2.469 1.00 0.00 O HETATM 45 P1 UNL 1 5.062 2.086 -3.074 1.00 0.00 P HETATM 46 O8 UNL 1 5.141 2.257 -4.567 1.00 0.00 O HETATM 47 O9 UNL 1 6.163 3.164 -2.344 1.00 0.00 O HETATM 48 O10 UNL 1 5.450 0.499 -2.690 1.00 0.00 O HETATM 49 C38 UNL 1 5.380 0.349 -1.307 1.00 0.00 C HETATM 50 C39 UNL 1 5.762 -1.095 -1.019 1.00 0.00 C HETATM 51 N1 UNL 1 5.694 -1.282 0.418 1.00 0.00 N HETATM 52 C40 UNL 1 6.048 -2.633 0.801 1.00 0.00 C HETATM 53 C41 UNL 1 2.555 -0.149 5.196 1.00 0.00 C HETATM 54 C42 UNL 1 2.817 -1.008 4.016 1.00 0.00 C HETATM 55 C43 UNL 1 3.468 0.621 5.887 1.00 0.00 C HETATM 56 C44 UNL 1 4.918 0.697 5.565 1.00 0.00 C HETATM 57 H1 UNL 1 2.052 4.592 3.902 1.00 0.00 H HETATM 58 H2 UNL 1 1.936 5.365 5.593 1.00 0.00 H HETATM 59 H3 UNL 1 1.596 3.651 5.348 1.00 0.00 H HETATM 60 H4 UNL 1 3.936 3.166 4.822 1.00 0.00 H HETATM 61 H5 UNL 1 4.289 4.876 4.693 1.00 0.00 H HETATM 62 H6 UNL 1 4.043 5.389 6.938 1.00 0.00 H HETATM 63 H7 UNL 1 5.129 4.006 6.790 1.00 0.00 H HETATM 64 H8 UNL 1 2.225 4.036 7.830 1.00 0.00 H HETATM 65 H9 UNL 1 3.723 4.030 8.737 1.00 0.00 H HETATM 66 H10 UNL 1 2.669 1.990 8.918 1.00 0.00 H HETATM 67 H11 UNL 1 4.286 1.752 8.283 1.00 0.00 H HETATM 68 H12 UNL 1 -0.696 -0.418 6.356 1.00 0.00 H HETATM 69 H13 UNL 1 0.107 -1.621 5.203 1.00 0.00 H HETATM 70 H14 UNL 1 -0.638 1.315 4.661 1.00 0.00 H HETATM 71 H15 UNL 1 0.107 0.135 3.542 1.00 0.00 H HETATM 72 H16 UNL 1 -2.588 -0.200 4.987 1.00 0.00 H HETATM 73 H17 UNL 1 -1.832 -1.406 3.831 1.00 0.00 H HETATM 74 H18 UNL 1 -3.803 0.092 2.987 1.00 0.00 H HETATM 75 H19 UNL 1 -2.821 1.513 3.259 1.00 0.00 H HETATM 76 H20 UNL 1 -3.030 0.888 0.948 1.00 0.00 H HETATM 77 H21 UNL 1 -2.267 -0.678 1.165 1.00 0.00 H HETATM 78 H22 UNL 1 -0.927 1.016 0.016 1.00 0.00 H HETATM 79 H23 UNL 1 -0.002 0.428 1.373 1.00 0.00 H HETATM 80 H24 UNL 1 -0.861 2.579 2.653 1.00 0.00 H HETATM 81 H25 UNL 1 -1.474 3.082 1.058 1.00 0.00 H HETATM 82 H26 UNL 1 1.394 2.213 1.540 1.00 0.00 H HETATM 83 H27 UNL 1 0.751 3.946 1.427 1.00 0.00 H HETATM 84 H28 UNL 1 0.901 2.856 -2.864 1.00 0.00 H HETATM 85 H29 UNL 1 0.381 0.965 -4.287 1.00 0.00 H HETATM 86 H30 UNL 1 -0.716 0.877 -2.853 1.00 0.00 H HETATM 87 H31 UNL 1 0.550 -3.676 -3.915 1.00 0.00 H HETATM 88 H32 UNL 1 1.875 -2.932 -3.014 1.00 0.00 H HETATM 89 H33 UNL 1 0.722 -2.905 -0.982 1.00 0.00 H HETATM 90 H34 UNL 1 0.786 -4.553 -1.602 1.00 0.00 H HETATM 91 H35 UNL 1 -1.642 -2.632 -1.622 1.00 0.00 H HETATM 92 H36 UNL 1 -1.315 -3.974 -0.437 1.00 0.00 H HETATM 93 H37 UNL 1 -3.020 -4.814 -1.750 1.00 0.00 H HETATM 94 H38 UNL 1 -1.555 -5.694 -2.115 1.00 0.00 H HETATM 95 H39 UNL 1 -2.537 -3.601 -4.190 1.00 0.00 H HETATM 96 H40 UNL 1 -1.262 -4.843 -4.281 1.00 0.00 H HETATM 97 H41 UNL 1 -3.141 -5.589 -5.387 1.00 0.00 H HETATM 98 H42 UNL 1 -2.738 -6.658 -4.017 1.00 0.00 H HETATM 99 H43 UNL 1 -5.102 -6.603 -4.033 1.00 0.00 H HETATM 100 H44 UNL 1 -4.488 -5.726 -2.617 1.00 0.00 H HETATM 101 H45 UNL 1 -5.592 -4.540 -5.216 1.00 0.00 H HETATM 102 H46 UNL 1 -6.525 -4.735 -3.704 1.00 0.00 H HETATM 103 H47 UNL 1 -3.109 0.638 -4.171 1.00 0.00 H HETATM 104 H48 UNL 1 -3.778 -0.040 -5.715 1.00 0.00 H HETATM 105 H49 UNL 1 -6.024 0.796 -5.178 1.00 0.00 H HETATM 106 H50 UNL 1 -5.367 1.403 -3.573 1.00 0.00 H HETATM 107 H51 UNL 1 -5.192 2.631 -6.297 1.00 0.00 H HETATM 108 H52 UNL 1 -3.622 2.531 -5.374 1.00 0.00 H HETATM 109 H53 UNL 1 -4.997 3.336 -4.618 1.00 0.00 H HETATM 110 H54 UNL 1 -5.247 -0.091 -0.968 1.00 0.00 H HETATM 111 H55 UNL 1 -3.828 0.623 -1.938 1.00 0.00 H HETATM 112 H56 UNL 1 -3.584 -0.715 -0.812 1.00 0.00 H HETATM 113 H57 UNL 1 -4.323 -3.152 -0.537 1.00 0.00 H HETATM 114 H58 UNL 1 -6.010 -2.573 -0.588 1.00 0.00 H HETATM 115 H59 UNL 1 -5.682 -4.182 -1.258 1.00 0.00 H HETATM 116 H60 UNL 1 2.639 1.788 -4.128 1.00 0.00 H HETATM 117 H61 UNL 1 2.910 0.550 -2.879 1.00 0.00 H HETATM 118 H62 UNL 1 6.135 3.084 -1.357 1.00 0.00 H HETATM 119 H63 UNL 1 4.340 0.548 -0.959 1.00 0.00 H HETATM 120 H64 UNL 1 6.118 1.038 -0.873 1.00 0.00 H HETATM 121 H65 UNL 1 6.822 -1.249 -1.332 1.00 0.00 H HETATM 122 H66 UNL 1 5.110 -1.803 -1.578 1.00 0.00 H HETATM 123 H67 UNL 1 6.309 -0.553 0.838 1.00 0.00 H HETATM 124 H68 UNL 1 6.899 -2.963 0.149 1.00 0.00 H HETATM 125 H69 UNL 1 5.192 -3.291 0.541 1.00 0.00 H HETATM 126 H70 UNL 1 6.339 -2.701 1.848 1.00 0.00 H HETATM 127 H71 UNL 1 1.898 -1.412 3.566 1.00 0.00 H HETATM 128 H72 UNL 1 3.363 -0.371 3.279 1.00 0.00 H HETATM 129 H73 UNL 1 3.485 -1.841 4.376 1.00 0.00 H HETATM 130 H74 UNL 1 5.421 -0.181 6.029 1.00 0.00 H HETATM 131 H75 UNL 1 5.366 1.589 6.055 1.00 0.00 H HETATM 132 H76 UNL 1 4.986 0.720 4.462 1.00 0.00 H CONECT 1 2 57 58 59 CONECT 2 3 60 61 CONECT 3 4 62 63 CONECT 4 5 64 65 CONECT 5 6 66 67 CONECT 6 7 55 55 CONECT 7 8 CONECT 8 9 53 53 CONECT 9 10 68 69 CONECT 10 11 70 71 CONECT 11 12 72 73 CONECT 12 13 74 75 CONECT 13 14 76 77 CONECT 14 15 78 79 CONECT 15 16 80 81 CONECT 16 17 82 83 CONECT 17 18 18 19 CONECT 19 20 CONECT 20 21 43 84 CONECT 21 22 85 86 CONECT 22 23 CONECT 23 24 24 25 CONECT 25 26 87 88 CONECT 26 27 89 90 CONECT 27 28 91 92 CONECT 28 29 93 94 CONECT 29 30 95 96 CONECT 30 31 97 98 CONECT 31 32 99 100 CONECT 32 33 101 102 CONECT 33 34 41 41 CONECT 34 35 CONECT 35 36 39 39 CONECT 36 37 103 104 CONECT 37 38 105 106 CONECT 38 107 108 109 CONECT 39 40 41 CONECT 40 110 111 112 CONECT 41 42 CONECT 42 113 114 115 CONECT 43 44 116 117 CONECT 44 45 CONECT 45 46 46 47 48 CONECT 47 118 CONECT 48 49 CONECT 49 50 119 120 CONECT 50 51 121 122 CONECT 51 52 123 CONECT 52 124 125 126 CONECT 53 54 55 CONECT 54 127 128 129 CONECT 55 56 CONECT 56 130 131 132 END SMILES for HMDB0113817 (PE-NMe(9D3/9D5))[H][C@@](COC(=O)CCCCCCCCC1=C(C)C(C)=C(CCC)O1)(COP(O)(=O)OCCNC)OC(=O)CCCCCCCCC1=C(C)C(C)=C(CCCCC)O1 INCHI for HMDB0113817 (PE-NMe(9D3/9D5))InChI=1S/C44H76NO10P/c1-8-10-19-25-40-36(5)37(6)42(55-40)27-21-16-12-14-18-23-29-44(47)53-38(33-52-56(48,49)51-31-30-45-7)32-50-43(46)28-22-17-13-11-15-20-26-41-35(4)34(3)39(54-41)24-9-2/h38,45H,8-33H2,1-7H3,(H,48,49)/t38-/m1/s1 3D Structure for HMDB0113817 (PE-NMe(9D3/9D5)) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms |
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Chemical Formula | C44H76NO10P | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Average Molecular Weight | 810.063 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Monoisotopic Molecular Weight | 809.520684649 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
IUPAC Name | [(2R)-2-{[9-(3,4-dimethyl-5-pentylfuran-2-yl)nonanoyl]oxy}-3-{[9-(3,4-dimethyl-5-propylfuran-2-yl)nonanoyl]oxy}propoxy][2-(methylamino)ethoxy]phosphinic acid | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Traditional Name | (2R)-2-{[9-(3,4-dimethyl-5-pentylfuran-2-yl)nonanoyl]oxy}-3-{[9-(3,4-dimethyl-5-propylfuran-2-yl)nonanoyl]oxy}propoxy(2-(methylamino)ethoxy)phosphinic acid | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
CAS Registry Number | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SMILES | [H][C@@](COC(=O)CCCCCCCCC1=C(C)C(C)=C(CCC)O1)(COP(O)(=O)OCCNC)OC(=O)CCCCCCCCC1=C(C)C(C)=C(CCCCC)O1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Identifier | InChI=1S/C44H76NO10P/c1-8-10-19-25-40-36(5)37(6)42(55-40)27-21-16-12-14-18-23-29-44(47)53-38(33-52-56(48,49)51-31-30-45-7)32-50-43(46)28-22-17-13-11-15-20-26-41-35(4)34(3)39(54-41)24-9-2/h38,45H,8-33H2,1-7H3,(H,48,49)/t38-/m1/s1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Key | VGDDWCSEYRXVDP-KXQOOQHDSA-N | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical Taxonomy | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Description | This compound belongs to the class of organic compounds known as monomethylphosphatidylethanolamines. These are lipids with a structure containing a glycerol moiety linked at its terminal C3 atom to a N-methylphosphoethanolamine group, and at its C1 and C2 terminal atoms by an acyl group. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Kingdom | Organic compounds | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Super Class | Lipids and lipid-like molecules | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Class | Glycerophospholipids | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sub Class | Glycerophosphoethanolamines | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Direct Parent | Monomethylphosphatidylethanolamines | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Alternative Parents |
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Substituents |
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Molecular Framework | Aromatic heteromonocyclic compounds | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
External Descriptors | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ontology | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Physiological effect | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Disposition | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Process | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Role | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Physical Properties | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
State | Solid | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Experimental Molecular Properties |
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Experimental Chromatographic Properties | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Predicted Molecular Properties |
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Predicted Chromatographic Properties | Predicted Collision Cross Sections
Predicted Kovats Retention IndicesUnderivatized
Derivatized | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Spectra | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
MS/MS Spectra
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Biological Properties | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cellular Locations | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Biospecimen Locations | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Tissue Locations | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Pathways | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Normal Concentrations | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Abnormal Concentrations | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Associated Disorders and Diseases | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Disease References | None | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Associated OMIM IDs | None | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
External Links | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DrugBank ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Phenol Explorer Compound ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
FooDB ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
KNApSAcK ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Chemspider ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
KEGG Compound ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
BioCyc ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
BiGG ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Wikipedia Link | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
METLIN ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
PubChem Compound | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
PDB ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ChEBI ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Food Biomarker Ontology | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
VMH ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
MarkerDB ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Good Scents ID | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
References | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synthesis Reference | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Material Safety Data Sheet (MSDS) | Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
General References | Not Available |