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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 20:37:18 UTC

Update Date

2022-03-07 02:54:34 UTC

HMDB ID

HMDB0035611

Secondary Accession Numbers

HMDB35611

Metabolite Identification

Common Name

Dammaradienol

Description

6-Hydroxy-8-heptacosanone belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. 6-Hydroxy-8-heptacosanone is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv0541 05061308352D          

 31 34  0  0  0  0            999 V2000
    3.0648    1.5833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2691    1.3688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6850    1.9530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8795    1.7811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2954    2.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3019   -1.3193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5888   -1.7316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8740   -1.3193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8740   -0.4946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3019    0.3298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3019   -0.4946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0167   -0.0825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7314   -0.4946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7314   -1.3193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4446   -1.7316    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4446    1.2136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6488    0.9992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4345    0.2034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5888   -0.0825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5888    0.7422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8740    1.1544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1593    0.7422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6239    0.9964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1090    0.3298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6239   -0.3380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1593   -0.0825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0738   -0.9028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5471   -2.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0167   -1.7316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4861   -2.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8804    0.3365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 17  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4 23  1  0  0  0  0
  6  7  1  0  0  0  0
  6 11  1  0  0  0  0
  6 29  1  0  0  0  0
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 16 17  1  0  0  0  0
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 19 20  1  0  0  0  0
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 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

HMDB0035611
     RDKit          3D
Dammaradienol
 81 84  0  0  0  0  0  0  0  0999 V2000
    3.3865   -0.2207   -2.2998 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4340   -0.3855   -1.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.6450   -0.4850    0.9847 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.6836    1.5006    0.0593 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0974   -0.3173    1.2208 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv0541 05061308352D          

 31 34  0  0  0  0            999 V2000
    3.0648    1.5833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035611

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)=CCCC(=C)C1CCC2(C)C1CCC1C3(C)CCC(O)C(C)(C)C3CCC21C

> <INCHI_IDENTIFIER>
InChI=1S/C30H50O/c1-20(2)10-9-11-21(3)22-14-18-29(7)23(22)12-13-25-28(6)17-16-26(31)27(4,5)24(28)15-19-30(25,29)8/h10,22-26,31H,3,9,11-19H2,1-2,4-8H3

> <INCHI_KEY>
WZAMDSBJONFHAO-UHFFFAOYSA-N

> <FORMULA>
C30H50O

> <MOLECULAR_WEIGHT>
426.7174

> <EXACT_MASS>
426.386166222

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
54.63163909394484

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,6,6,10,11-pentamethyl-14-(6-methylhepta-1,5-dien-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-ol

> <ALOGPS_LOGP>
7.51

> <JCHEM_LOGP>
7.808264016000002

> <ALOGPS_LOGS>
-6.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.489433390177716

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8351218351362667

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
133.7388

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.32e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,6,6,10,11-pentamethyl-14-(6-methylhepta-1,5-dien-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0035611
     RDKit          3D
Dammaradienol
 81 84  0  0  0  0  0  0  0  0999 V2000
    3.3865   -0.2207   -2.2998 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4340   -0.3855   -1.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7505   -0.8998   -0.4713 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3516    0.0849    0.5076 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6450   -0.4850    0.9847 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7529    0.1970    0.7667 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6836    1.5006    0.0593 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0974   -0.3173    1.2208 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3903   -0.1429   -0.0785 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0902   -1.3357    0.8349 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5915   -1.5643    0.7961 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2505   -0.9609   -0.5727 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8185   -1.8868   -1.5749 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0629    0.3237   -0.3607 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6265    1.3237   -1.2885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7688    1.8021   -0.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5731    0.6578   -0.2287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0283    0.9755   -0.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3248    2.0441   -1.2331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3156    1.7693    1.1244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7117    2.2771    1.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7552    1.2610    0.8770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7145    1.1781    1.9145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1033   -0.0979    0.8232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7456   -0.6050    2.1639 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1950   -1.0345    0.2706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9818   -0.1512   -0.2133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4374   -1.5219   -0.2160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9913   -1.6724    0.1239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2138   -0.6900   -0.7409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6334   -1.0051   -2.1484 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2341   -0.4325   -2.9764 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5136    0.1347   -2.8016 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5988   -1.8408    0.1058 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4794   -1.0549   -1.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6542    0.1118    1.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4860    1.0483    0.0212 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6969   -1.4399    1.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2425    1.3846   -0.9596 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0522    2.2045    0.6303 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7087    1.9112   -0.1164 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5821    0.5526    1.7209 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8850   -1.0957    1.9790 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6836   -0.6877    0.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8711    0.6220    0.6631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3280   -1.0981    1.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6653   -2.2297    0.5781 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1094   -0.8867    1.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2992   -2.6075    0.8809 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1310   -2.7927   -1.5907 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8559   -1.5626   -2.6116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7822   -2.3661   -1.2476 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7283    0.7185    0.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2731    2.2458   -1.2381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5580    1.0549   -2.3444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2089    2.2644   -1.6976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5944    2.5407    0.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2679    0.5920    0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4396    2.2496   -1.2473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0865    1.7523   -2.2446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9038    3.0225   -0.8950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6495    2.6790    1.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9504    1.2578    2.0118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8847    2.6430    2.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8212    3.2087    0.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3596    1.4733   -0.0382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3332    1.9637    1.8708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9166    0.2226    2.9067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7430   -0.9806    2.3169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4379   -1.4211    2.5309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1340   -1.0901   -0.8291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1799   -0.6987    0.6483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0478   -2.0633    0.6548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5613   -0.0206   -1.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5784   -2.0381   -1.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9859   -2.2134    0.4943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6619   -2.6904   -0.2243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7399   -1.6054    1.1737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6138   -0.5738   -2.4399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9314   -0.6648   -2.9324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8250   -2.1210   -2.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  3
  6  7  1  0
  6  8  1  0
  2  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 24 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 14  9  1  0
 30 17  1  0
 30 12  1  0
 27 18  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  7 39  1  0
  7 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
 10 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 13 50  1  0
 13 51  1  0
 13 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 16 57  1  0
 17 58  1  0
 19 59  1  0
 19 60  1  0
 19 61  1  0
 20 62  1  0
 20 63  1  0
 21 64  1  0
 21 65  1  0
 22 66  1  0
 23 67  1  0
 25 68  1  0
 25 69  1  0
 25 70  1  0
 26 71  1  0
 26 72  1  0
 26 73  1  0
 27 74  1  0
 28 75  1  0
 28 76  1  0
 29 77  1  0
 29 78  1  0
 31 79  1  0
 31 80  1  0
 31 81  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       5.721   2.955   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.236   2.555   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.145   3.646   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.642   3.325   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.551   4.412   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.297  -2.463   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.966  -3.232   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.631  -2.463   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.631  -0.923   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.297   0.616   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.297  -0.923   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.631  -0.154   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.965  -0.923   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -6.965  -2.463   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -8.297  -3.232   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.297   2.265   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.811   1.865   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.411   0.380   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.966  -0.154   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.966   1.385   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.631   2.155   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.297   1.385   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.165   1.860   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.070   0.616   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.165  -0.631   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.297  -0.154   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.138  -1.685   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -6.621  -4.412   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -5.631  -3.232   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -4.641  -4.412   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.643   0.628   0.000  0.00  0.00           C+0
CONECT    1    2   17                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   23                                                  
CONECT    5    4                                                            
CONECT    6    7   11   29                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   19   26   31                                             
CONECT   10   11                                                            
CONECT   11    6   10   12   19                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   29                                                  
CONECT   15   14                                                            
CONECT   16   17                                                            
CONECT   17    1   16   18                                                  
CONECT   18   17                                                            
CONECT   19    9   11   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   26                                                  
CONECT   23    4   22   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26    9   22   25   27                                             
CONECT   27   26                                                            
CONECT   28   29                                                            
CONECT   29    6   14   28   30                                             
CONECT   30   29                                                            
CONECT   31    9                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

COMPND    HMDB0035611
HETATM    1  C1  UNL     1       3.387  -0.221  -2.300  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.434  -0.386  -1.018  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.751  -0.900  -0.471  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.352   0.085   0.508  1.00  0.00           C  
HETATM    5  C5  UNL     1       6.645  -0.485   0.985  1.00  0.00           C  
HETATM    6  C6  UNL     1       7.753   0.197   0.767  1.00  0.00           C  
HETATM    7  C7  UNL     1       7.684   1.501   0.059  1.00  0.00           C  
HETATM    8  C8  UNL     1       9.097  -0.317   1.221  1.00  0.00           C  
HETATM    9  C9  UNL     1       2.390  -0.143  -0.079  1.00  0.00           C  
HETATM   10  C10 UNL     1       2.090  -1.336   0.835  1.00  0.00           C  
HETATM   11  C11 UNL     1       0.592  -1.564   0.796  1.00  0.00           C  
HETATM   12  C12 UNL     1       0.251  -0.961  -0.573  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.818  -1.887  -1.575  1.00  0.00           C  
HETATM   14  C14 UNL     1       1.063   0.324  -0.361  1.00  0.00           C  
HETATM   15  C15 UNL     1       0.627   1.324  -1.288  1.00  0.00           C  
HETATM   16  C16 UNL     1      -0.769   1.802  -0.799  1.00  0.00           C  
HETATM   17  C17 UNL     1      -1.573   0.658  -0.229  1.00  0.00           C  
HETATM   18  C18 UNL     1      -3.028   0.975  -0.169  1.00  0.00           C  
HETATM   19  C19 UNL     1      -3.325   2.044  -1.233  1.00  0.00           C  
HETATM   20  C20 UNL     1      -3.316   1.769   1.124  1.00  0.00           C  
HETATM   21  C21 UNL     1      -4.712   2.277   1.171  1.00  0.00           C  
HETATM   22  C22 UNL     1      -5.755   1.261   0.877  1.00  0.00           C  
HETATM   23  O1  UNL     1      -6.714   1.178   1.915  1.00  0.00           O  
HETATM   24  C23 UNL     1      -5.103  -0.098   0.823  1.00  0.00           C  
HETATM   25  C24 UNL     1      -4.746  -0.605   2.164  1.00  0.00           C  
HETATM   26  C25 UNL     1      -6.195  -1.034   0.271  1.00  0.00           C  
HETATM   27  C26 UNL     1      -3.982  -0.151  -0.213  1.00  0.00           C  
HETATM   28  C27 UNL     1      -3.437  -1.522  -0.216  1.00  0.00           C  
HETATM   29  C28 UNL     1      -1.991  -1.672   0.124  1.00  0.00           C  
HETATM   30  C29 UNL     1      -1.214  -0.690  -0.741  1.00  0.00           C  
HETATM   31  C30 UNL     1      -1.633  -1.005  -2.148  1.00  0.00           C  
HETATM   32  H1  UNL     1       4.234  -0.433  -2.976  1.00  0.00           H  
HETATM   33  H2  UNL     1       2.514   0.135  -2.802  1.00  0.00           H  
HETATM   34  H3  UNL     1       4.599  -1.841   0.106  1.00  0.00           H  
HETATM   35  H4  UNL     1       5.479  -1.055  -1.276  1.00  0.00           H  
HETATM   36  H5  UNL     1       4.654   0.112   1.393  1.00  0.00           H  
HETATM   37  H6  UNL     1       5.486   1.048   0.021  1.00  0.00           H  
HETATM   38  H7  UNL     1       6.697  -1.440   1.503  1.00  0.00           H  
HETATM   39  H8  UNL     1       7.242   1.385  -0.960  1.00  0.00           H  
HETATM   40  H9  UNL     1       7.052   2.204   0.630  1.00  0.00           H  
HETATM   41  H10 UNL     1       8.709   1.911  -0.116  1.00  0.00           H  
HETATM   42  H11 UNL     1       9.582   0.553   1.721  1.00  0.00           H  
HETATM   43  H12 UNL     1       8.885  -1.096   1.979  1.00  0.00           H  
HETATM   44  H13 UNL     1       9.684  -0.688   0.362  1.00  0.00           H  
HETATM   45  H14 UNL     1       2.871   0.622   0.663  1.00  0.00           H  
HETATM   46  H15 UNL     1       2.328  -1.098   1.889  1.00  0.00           H  
HETATM   47  H16 UNL     1       2.665  -2.230   0.578  1.00  0.00           H  
HETATM   48  H17 UNL     1       0.109  -0.887   1.546  1.00  0.00           H  
HETATM   49  H18 UNL     1       0.299  -2.608   0.881  1.00  0.00           H  
HETATM   50  H19 UNL     1       0.131  -2.793  -1.591  1.00  0.00           H  
HETATM   51  H20 UNL     1       0.856  -1.563  -2.612  1.00  0.00           H  
HETATM   52  H21 UNL     1       1.782  -2.366  -1.248  1.00  0.00           H  
HETATM   53  H22 UNL     1       0.728   0.718   0.698  1.00  0.00           H  
HETATM   54  H23 UNL     1       1.273   2.246  -1.238  1.00  0.00           H  
HETATM   55  H24 UNL     1       0.558   1.055  -2.344  1.00  0.00           H  
HETATM   56  H25 UNL     1      -1.209   2.264  -1.698  1.00  0.00           H  
HETATM   57  H26 UNL     1      -0.594   2.541   0.014  1.00  0.00           H  
HETATM   58  H27 UNL     1      -1.268   0.592   0.870  1.00  0.00           H  
HETATM   59  H28 UNL     1      -4.440   2.250  -1.247  1.00  0.00           H  
HETATM   60  H29 UNL     1      -3.087   1.752  -2.245  1.00  0.00           H  
HETATM   61  H30 UNL     1      -2.904   3.022  -0.895  1.00  0.00           H  
HETATM   62  H31 UNL     1      -2.649   2.679   1.013  1.00  0.00           H  
HETATM   63  H32 UNL     1      -2.950   1.258   2.012  1.00  0.00           H  
HETATM   64  H33 UNL     1      -4.885   2.643   2.218  1.00  0.00           H  
HETATM   65  H34 UNL     1      -4.821   3.209   0.542  1.00  0.00           H  
HETATM   66  H35 UNL     1      -6.360   1.473  -0.038  1.00  0.00           H  
HETATM   67  H36 UNL     1      -7.333   1.964   1.871  1.00  0.00           H  
HETATM   68  H37 UNL     1      -4.917   0.223   2.907  1.00  0.00           H  
HETATM   69  H38 UNL     1      -3.743  -0.981   2.317  1.00  0.00           H  
HETATM   70  H39 UNL     1      -5.438  -1.421   2.531  1.00  0.00           H  
HETATM   71  H40 UNL     1      -6.134  -1.090  -0.829  1.00  0.00           H  
HETATM   72  H41 UNL     1      -7.180  -0.699   0.648  1.00  0.00           H  
HETATM   73  H42 UNL     1      -6.048  -2.063   0.655  1.00  0.00           H  
HETATM   74  H43 UNL     1      -4.561  -0.021  -1.184  1.00  0.00           H  
HETATM   75  H44 UNL     1      -3.578  -2.038  -1.215  1.00  0.00           H  
HETATM   76  H45 UNL     1      -3.986  -2.213   0.494  1.00  0.00           H  
HETATM   77  H46 UNL     1      -1.662  -2.690  -0.224  1.00  0.00           H  
HETATM   78  H47 UNL     1      -1.740  -1.605   1.174  1.00  0.00           H  
HETATM   79  H48 UNL     1      -2.614  -0.574  -2.440  1.00  0.00           H  
HETATM   80  H49 UNL     1      -0.931  -0.665  -2.932  1.00  0.00           H  
HETATM   81  H50 UNL     1      -1.825  -2.121  -2.254  1.00  0.00           H  
CONECT    1    2    2   32   33
CONECT    2    3    9
CONECT    3    4   34   35
CONECT    4    5   36   37
CONECT    5    6    6   38
CONECT    6    7    8
CONECT    7   39   40   41
CONECT    8   42   43   44
CONECT    9   10   14   45
CONECT   10   11   46   47
CONECT   11   12   48   49
CONECT   12   13   14   30
CONECT   13   50   51   52
CONECT   14   15   53
CONECT   15   16   54   55
CONECT   16   17   56   57
CONECT   17   18   30   58
CONECT   18   19   20   27
CONECT   19   59   60   61
CONECT   20   21   62   63
CONECT   21   22   64   65
CONECT   22   23   24   66
CONECT   23   67
CONECT   24   25   26   27
CONECT   25   68   69   70
CONECT   26   71   72   73
CONECT   27   28   74
CONECT   28   29   75   76
CONECT   29   30   77   78
CONECT   30   31
CONECT   31   79   80   81
END

HMDB0035611
     RDKit          3D
Dammaradienol
 81 84  0  0  0  0  0  0  0  0999 V2000
    3.3865   -0.2207   -2.2998 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4340   -0.3855   -1.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7505   -0.8998   -0.4713 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3516    0.0849    0.5076 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6450   -0.4850    0.9847 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7529    0.1970    0.7667 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6836    1.5006    0.0593 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0974   -0.3173    1.2208 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3903   -0.1429   -0.0785 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0902   -1.3357    0.8349 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5915   -1.5643    0.7961 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2505   -0.9609   -0.5727 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8185   -1.8868   -1.5749 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0629    0.3237   -0.3607 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6265    1.3237   -1.2885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7688    1.8021   -0.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5731    0.6578   -0.2287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0283    0.9755   -0.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3248    2.0441   -1.2331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3156    1.7693    1.1244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7117    2.2771    1.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7552    1.2610    0.8770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7145    1.1781    1.9145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1033   -0.0979    0.8232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7456   -0.6050    2.1639 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1950   -1.0345    0.2706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9818   -0.1512   -0.2133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4374   -1.5219   -0.2160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9913   -1.6724    0.1239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2138   -0.6900   -0.7409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6334   -1.0051   -2.1484 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2341   -0.4325   -2.9764 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5136    0.1347   -2.8016 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5988   -1.8408    0.1058 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4794   -1.0549   -1.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6542    0.1118    1.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4860    1.0483    0.0212 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6969   -1.4399    1.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2425    1.3846   -0.9596 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0522    2.2045    0.6303 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7087    1.9112   -0.1164 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5821    0.5526    1.7209 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8850   -1.0957    1.9790 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6836   -0.6877    0.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8711    0.6220    0.6631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3280   -1.0981    1.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6653   -2.2297    0.5781 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1094   -0.8867    1.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2992   -2.6075    0.8809 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1310   -2.7927   -1.5907 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8559   -1.5626   -2.6116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7822   -2.3661   -1.2476 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7283    0.7185    0.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2731    2.2458   -1.2381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5580    1.0549   -2.3444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2089    2.2644   -1.6976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5944    2.5407    0.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2679    0.5920    0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4396    2.2496   -1.2473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0865    1.7523   -2.2446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9038    3.0225   -0.8950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6495    2.6790    1.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9504    1.2578    2.0118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8847    2.6430    2.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8212    3.2087    0.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3596    1.4733   -0.0382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3332    1.9637    1.8708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9166    0.2226    2.9067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7430   -0.9806    2.3169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4379   -1.4211    2.5309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1340   -1.0901   -0.8291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1799   -0.6987    0.6483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0478   -2.0633    0.6548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5613   -0.0206   -1.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5784   -2.0381   -1.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9859   -2.2134    0.4943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6619   -2.6904   -0.2243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7399   -1.6054    1.1737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6138   -0.5738   -2.4399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9314   -0.6648   -2.9324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8250   -2.1210   -2.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  3
  6  7  1  0
  6  8  1  0
  2  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 24 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 14  9  1  0
 30 17  1  0
 30 12  1  0
 27 18  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  7 39  1  0
  7 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
 10 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 13 50  1  0
 13 51  1  0
 13 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 16 57  1  0
 17 58  1  0
 19 59  1  0
 19 60  1  0
 19 61  1  0
 20 62  1  0
 20 63  1  0
 21 64  1  0
 21 65  1  0
 22 66  1  0
 23 67  1  0
 25 68  1  0
 25 69  1  0
 25 70  1  0
 26 71  1  0
 26 72  1  0
 26 73  1  0
 27 74  1  0
 28 75  1  0
 28 76  1  0
 29 77  1  0
 29 78  1  0
 31 79  1  0
 31 80  1  0
 31 81  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Dammadienol	HMDB
Dammara-20,24-dien-3 beta-ol	HMDB

Chemical Formula

C₃₀H₅₀O

Average Molecular Weight

426.7174

Monoisotopic Molecular Weight

426.386166222

IUPAC Name

2,6,6,10,11-pentamethyl-14-(6-methylhepta-1,5-dien-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-ol

Traditional Name

2,6,6,10,11-pentamethyl-14-(6-methylhepta-1,5-dien-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-ol

CAS Registry Number

20460-34-8

SMILES

CC(C)=CCCC(=C)C1CCC2(C)C1CCC1C3(C)CCC(O)C(C)(C)C3CCC21C

InChI Identifier

InChI=1S/C30H50O/c1-20(2)10-9-11-21(3)22-14-18-29(7)23(22)12-13-25-28(6)17-16-26(31)27(4,5)24(28)15-19-30(25,29)8/h10,22-26,31H,3,9,11-19H2,1-2,4-8H3

InChI Key

WZAMDSBJONFHAO-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Fatty alcohols

Alternative Parents

Substituents

Fatty alcohol
Beta-hydroxy ketone
Secondary alcohol
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0035611)
Cell membrane (HMDB: HMDB0035611)

Cellular substructure

Extracellular (HMDB: HMDB0035611)
Membrane (HMDB: HMDB0035611)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0035611)

Source

Endogenous

Endogenous (HMDB: HMDB0035611)

Plant

Plant (HMDB: HMDB0035611)
Glycine max (HMDB: HMDB0035611)

Animal

Animal (HMDB: HMDB0035611)

Exogenous

Food

Food (HMDB: HMDB0035611)

Soy

Soy bean (FooDB: FOOD00085)

Tea

Herb and spice

Oilseed crop

Shea tree (FooDB: FOOD00775)

Herbs and Spices (FooDB: FOOD00866)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0035611)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0035611)

Cellular process

Cell signaling (HMDB: HMDB0035611)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0035611)

Role

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	136 - 138 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.00013 g/L	ALOGPS
logP	7.51	ALOGPS
logP	7.81	ChemAxon
logS	-6.5	ALOGPS
pKa (Strongest Acidic)	19.49	ChemAxon
pKa (Strongest Basic)	-0.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	133.74 m³·mol⁻¹	ChemAxon
Polarizability	54.63 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	204.334	31661259
DarkChem	[M-H]-	196.068	31661259
DeepCCS	[M-2H]-	240.58	30932474
DeepCCS	[M+Na]+	215.807	30932474
AllCCS	[M+H]+	215.7	32859911
AllCCS	[M+H-H2O]+	213.9	32859911
AllCCS	[M+NH4]+	217.4	32859911
AllCCS	[M+Na]+	217.9	32859911
AllCCS	[M-H]-	215.5	32859911
AllCCS	[M+Na-2H]-	217.5	32859911
AllCCS	[M+HCOO]-	219.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Dammaradienol	CC(C)=CCCC(=C)C1CCC2(C)C1CCC1C3(C)CCC(O)C(C)(C)C3CCC21C	2650.7	Standard polar	33892256
Dammaradienol	CC(C)=CCCC(=C)C1CCC2(C)C1CCC1C3(C)CCC(O)C(C)(C)C3CCC21C	3215.2	Standard non polar	33892256
Dammaradienol	CC(C)=CCCC(=C)C1CCC2(C)C1CCC1C3(C)CCC(O)C(C)(C)C3CCC21C	3349.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Dammaradienol,1TMS,isomer #1	C=C(CCC=C(C)C)C1CCC2(C)C1CCC1C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3CCC12C	3368.8	Semi standard non polar	33892256
Dammaradienol,1TBDMS,isomer #1	C=C(CCC=C(C)C)C1CCC2(C)C1CCC1C3(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C	3593.8	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Dammaradienol GC-MS (Non-derivatized) - 70eV, Positive	splash10-03dj-2119300000-89fefbc402bd5619973c	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dammaradienol GC-MS (1 TMS) - 70eV, Positive	splash10-001i-3010900000-30bc46f9f1870103fa65	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dammaradienol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dammaradienol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dammaradienol 10V, Positive-QTOF	splash10-0a6r-0002900000-b5e1fdca679d37c5108a	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dammaradienol 20V, Positive-QTOF	splash10-0pdi-3259500000-2de5825f9eee75b6fbd7	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dammaradienol 40V, Positive-QTOF	splash10-0gbi-3469100000-51462e8a328047d6f531	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dammaradienol 10V, Negative-QTOF	splash10-004i-0000900000-100e099c629b0b11fd6b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dammaradienol 20V, Negative-QTOF	splash10-004i-0000900000-fcbdbd6b45fc6218625b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dammaradienol 40V, Negative-QTOF	splash10-0a4l-1009500000-3d0037e69ef0c436e931	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dammaradienol 10V, Positive-QTOF	splash10-004i-1017900000-8b8383c598629e1a750b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dammaradienol 20V, Positive-QTOF	splash10-0a4i-7942000000-ebd8f092fb889b33ae6f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dammaradienol 40V, Positive-QTOF	splash10-0a4i-6910000000-0424b814fbe244a31728	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dammaradienol 10V, Negative-QTOF	splash10-004i-0000900000-590c9e4adfdd12b64d93	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dammaradienol 20V, Negative-QTOF	splash10-004i-0000900000-590c9e4adfdd12b64d93	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dammaradienol 40V, Negative-QTOF	splash10-057i-0006900000-ec1fc45685a8bddbd057	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

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

FDB014322

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

131751814

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

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Dammaradienol (HMDB0035611)

MOL for HMDB0035611 (Dammaradienol)

3D MOL for HMDB0035611 (Dammaradienol)

3D SDF for HMDB0035611 (Dammaradienol)

3D-SDF for HMDB0035611 (Dammaradienol)

PDB for HMDB0035611 (Dammaradienol)

3D PDB for HMDB0035611 (Dammaradienol)

SMILES for HMDB0035611 (Dammaradienol)

INCHI for HMDB0035611 (Dammaradienol)

Structure for HMDB0035611 (Dammaradienol)

3D Structure for HMDB0035611 (Dammaradienol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra