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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 08:44:01 UTC

Update Date

2021-09-26 23:03:21 UTC

HMDB ID

HMDB0251375

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Dimethandrolone

Description

Dimethandrolone belongs to the class of organic compounds known as estrogens and derivatives. These are steroids with a structure containing a 3-hydroxylated estrane. Based on a literature review a significant number of articles have been published on Dimethandrolone. This compound has been identified in human blood as reported by (PMID: 31557052 ). Dimethandrolone is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Dimethandrolone is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

HMDB0251375
     RDKit          3D
Dimethandrolone
 52 55  0  0  0  0  0  0  0  0999 V2000
   -0.0417    1.8215    2.0855 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1418    1.6795    0.6076 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5816    1.6986    0.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2867    0.3981    0.3042 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9906    0.2215    1.6360 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3971    0.3803   -0.7551 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5797   -0.1278   -0.2451 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9287   -0.5092   -1.8527 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5998   -1.0772   -1.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4819   -0.8059   -0.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0530   -0.7501    0.4594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6367   -1.9943   -0.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0990   -3.1947    0.7017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1296   -1.9498    0.1794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6903   -0.6480   -0.2731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6899   -0.6896   -1.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2617    0.5670   -1.5860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8772    0.6636   -2.6845 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0831    1.7516   -0.6873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6407    1.8529   -0.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0690    0.5794    0.2771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5875    0.5111    0.0069 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6770    2.5960    2.4336 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0128    0.8942    2.6561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0562    2.2607    2.3049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3215    2.6040    0.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1127    2.4413    0.8429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6355    2.0867   -0.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9050    0.8581    1.6801 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3407    0.3331    2.4979 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3824   -0.8369    1.6305 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6122    1.4157   -1.1108 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3715    0.3201   -0.6345 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9040    0.0585   -2.8102 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6263   -1.3671   -2.0436 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8307   -0.5875   -2.1083 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5413   -2.1665   -1.7324 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9582   -1.6808    0.5096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0738   -0.8168    1.5532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4708   -2.1156   -1.1391 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6357   -2.9028    1.4821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3987   -3.8975   -0.0268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9078   -3.7497    1.2405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5604   -2.8097   -0.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3112   -2.1282    1.2599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1184   -1.6087   -1.5049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7698    1.6887    0.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3339    2.6611   -1.2372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0768    2.2636   -1.1101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6331    2.6660    0.5455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2175    0.5209    1.3866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4759    0.6207   -1.1115 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
  4  6  1  0
  6  7  1  0
  6  8  1  0
  8  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  2  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  2  1  0
 10  4  1  0
 22 11  1  0
 21 15  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  5 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 16 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 22 52  1  0
M  END


  Mrv1652309112110442D          

 22 25  0  0  0  0            999 V2000
    1.3081   -0.2240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8399    0.4067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520    0.2615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1838    0.8922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9960    0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278    1.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399    1.2325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2475    2.1537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4354    2.2989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9035    1.6682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0914    1.8134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5596    1.1827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7475    1.3279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962    0.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5867    1.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3574    2.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4672    2.1038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9990    2.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8111    2.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3429    3.2200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1073    2.8462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8637    2.7283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 16 22  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0251375

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1CC2=CC(=O)CCC2C2C(C)CC3(C)C(O)CCC3C12

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O2/c1-11-8-13-9-14(21)4-5-15(13)18-12(2)10-20(3)16(19(11)18)6-7-17(20)22/h9,11-12,15-19,22H,4-8,10H2,1-3H3

> <INCHI_KEY>
KVIKZOGGZHCGFH-UHFFFAOYSA-N

> <FORMULA>
C20H30O2

> <MOLECULAR_WEIGHT>
302.458

> <EXACT_MASS>
302.224580206

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
35.819271571191734

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
14-hydroxy-9,15,17-trimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-5-one

> <ALOGPS_LOGP>
2.74

> <JCHEM_LOGP>
3.6394143703333346

> <ALOGPS_LOGS>
-4.09

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.541755828100072

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.37182197858561

> <JCHEM_PKA_STRONGEST_BASIC>
-0.886505736742227

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
89.05189999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.46e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-hydroxy-9,15,17-trimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-5-one

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0251375
     RDKit          3D
Dimethandrolone
 52 55  0  0  0  0  0  0  0  0999 V2000
   -0.0417    1.8215    2.0855 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1418    1.6795    0.6076 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5816    1.6986    0.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2867    0.3981    0.3042 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9906    0.2215    1.6360 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3971    0.3803   -0.7551 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5797   -0.1278   -0.2451 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9287   -0.5092   -1.8527 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5998   -1.0772   -1.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4819   -0.8059   -0.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0530   -0.7501    0.4594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6367   -1.9943   -0.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0990   -3.1947    0.7017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1296   -1.9498    0.1794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6903   -0.6480   -0.2731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6899   -0.6896   -1.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2617    0.5670   -1.5860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8772    0.6636   -2.6845 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0831    1.7516   -0.6873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6407    1.8529   -0.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0690    0.5794    0.2771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5875    0.5111    0.0069 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6770    2.5960    2.4336 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0128    0.8942    2.6561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0562    2.2607    2.3049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3215    2.6040    0.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1127    2.4413    0.8429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6355    2.0867   -0.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9050    0.8581    1.6801 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3407    0.3331    2.4979 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3824   -0.8369    1.6305 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6122    1.4157   -1.1108 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3715    0.3201   -0.6345 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9040    0.0585   -2.8102 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6263   -1.3671   -2.0436 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8307   -0.5875   -2.1083 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5413   -2.1665   -1.7324 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9582   -1.6808    0.5096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0738   -0.8168    1.5532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4708   -2.1156   -1.1391 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6357   -2.9028    1.4821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3987   -3.8975   -0.0268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9078   -3.7497    1.2405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5604   -2.8097   -0.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3112   -2.1282    1.2599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1184   -1.6087   -1.5049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7698    1.6887    0.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3339    2.6611   -1.2372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0768    2.2636   -1.1101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6331    2.6660    0.5455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2175    0.5209    1.3866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4759    0.6207   -1.1115 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
  4  6  1  0
  6  7  1  0
  6  8  1  0
  8  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  2  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  2  1  0
 10  4  1  0
 22 11  1  0
 21 15  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  5 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 16 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 22 52  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0       2.442  -0.418   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.434   0.759   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.950   0.488   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.943   1.666   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.459   1.394   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.452   2.572   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.968   2.301   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.929   4.020   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.413   4.291   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.420   3.114   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.904   3.385   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.911   2.208   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.395   2.479   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.179   1.534   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.095   2.398   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.667   3.877   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.872   3.927   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.865   5.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.381   4.833   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.374   6.011   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.200   5.313   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.612   5.093   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    4   11                                                  
CONECT   11   10   12   19                                                  
CONECT   12   11    2   13                                                  
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   13   18   21                                             
CONECT   18   17   19                                                       
CONECT   19   18   11   20                                                  
CONECT   20   19                                                            
CONECT   21   17                                                            
CONECT   22   16                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   50    0
END

COMPND    HMDB0251375
HETATM    1  C1  UNL     1      -0.042   1.822   2.086  1.00  0.00           C  
HETATM    2  C2  UNL     1       0.142   1.679   0.608  1.00  0.00           C  
HETATM    3  C3  UNL     1       1.582   1.699   0.184  1.00  0.00           C  
HETATM    4  C4  UNL     1       2.287   0.398   0.304  1.00  0.00           C  
HETATM    5  C5  UNL     1       2.991   0.221   1.636  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.397   0.380  -0.755  1.00  0.00           C  
HETATM    7  O1  UNL     1       4.580  -0.128  -0.245  1.00  0.00           O  
HETATM    8  C7  UNL     1       2.929  -0.509  -1.853  1.00  0.00           C  
HETATM    9  C8  UNL     1       1.600  -1.077  -1.485  1.00  0.00           C  
HETATM   10  C9  UNL     1       1.482  -0.806  -0.023  1.00  0.00           C  
HETATM   11  C10 UNL     1       0.053  -0.750   0.459  1.00  0.00           C  
HETATM   12  C11 UNL     1      -0.637  -1.994  -0.049  1.00  0.00           C  
HETATM   13  C12 UNL     1      -0.099  -3.195   0.702  1.00  0.00           C  
HETATM   14  C13 UNL     1      -2.130  -1.950   0.179  1.00  0.00           C  
HETATM   15  C14 UNL     1      -2.690  -0.648  -0.273  1.00  0.00           C  
HETATM   16  C15 UNL     1      -3.690  -0.690  -1.123  1.00  0.00           C  
HETATM   17  C16 UNL     1      -4.262   0.567  -1.586  1.00  0.00           C  
HETATM   18  O2  UNL     1      -4.877   0.664  -2.684  1.00  0.00           O  
HETATM   19  C17 UNL     1      -4.083   1.752  -0.687  1.00  0.00           C  
HETATM   20  C18 UNL     1      -2.641   1.853  -0.239  1.00  0.00           C  
HETATM   21  C19 UNL     1      -2.069   0.579   0.277  1.00  0.00           C  
HETATM   22  C20 UNL     1      -0.587   0.511   0.007  1.00  0.00           C  
HETATM   23  H1  UNL     1       0.677   2.596   2.434  1.00  0.00           H  
HETATM   24  H2  UNL     1       0.013   0.894   2.656  1.00  0.00           H  
HETATM   25  H3  UNL     1      -1.056   2.261   2.305  1.00  0.00           H  
HETATM   26  H4  UNL     1      -0.322   2.604   0.147  1.00  0.00           H  
HETATM   27  H5  UNL     1       2.113   2.441   0.843  1.00  0.00           H  
HETATM   28  H6  UNL     1       1.635   2.087  -0.855  1.00  0.00           H  
HETATM   29  H7  UNL     1       3.905   0.858   1.680  1.00  0.00           H  
HETATM   30  H8  UNL     1       2.341   0.333   2.498  1.00  0.00           H  
HETATM   31  H9  UNL     1       3.382  -0.837   1.630  1.00  0.00           H  
HETATM   32  H10 UNL     1       3.612   1.416  -1.111  1.00  0.00           H  
HETATM   33  H11 UNL     1       5.372   0.320  -0.634  1.00  0.00           H  
HETATM   34  H12 UNL     1       2.904   0.059  -2.810  1.00  0.00           H  
HETATM   35  H13 UNL     1       3.626  -1.367  -2.044  1.00  0.00           H  
HETATM   36  H14 UNL     1       0.831  -0.588  -2.108  1.00  0.00           H  
HETATM   37  H15 UNL     1       1.541  -2.167  -1.732  1.00  0.00           H  
HETATM   38  H16 UNL     1       1.958  -1.681   0.510  1.00  0.00           H  
HETATM   39  H17 UNL     1       0.074  -0.817   1.553  1.00  0.00           H  
HETATM   40  H18 UNL     1      -0.471  -2.116  -1.139  1.00  0.00           H  
HETATM   41  H19 UNL     1       0.636  -2.903   1.482  1.00  0.00           H  
HETATM   42  H20 UNL     1       0.399  -3.897  -0.027  1.00  0.00           H  
HETATM   43  H21 UNL     1      -0.908  -3.750   1.241  1.00  0.00           H  
HETATM   44  H22 UNL     1      -2.560  -2.810  -0.373  1.00  0.00           H  
HETATM   45  H23 UNL     1      -2.311  -2.128   1.260  1.00  0.00           H  
HETATM   46  H24 UNL     1      -4.118  -1.609  -1.505  1.00  0.00           H  
HETATM   47  H25 UNL     1      -4.770   1.689   0.190  1.00  0.00           H  
HETATM   48  H26 UNL     1      -4.334   2.661  -1.237  1.00  0.00           H  
HETATM   49  H27 UNL     1      -2.077   2.264  -1.110  1.00  0.00           H  
HETATM   50  H28 UNL     1      -2.633   2.666   0.545  1.00  0.00           H  
HETATM   51  H29 UNL     1      -2.218   0.521   1.387  1.00  0.00           H  
HETATM   52  H30 UNL     1      -0.476   0.621  -1.112  1.00  0.00           H  
CONECT    1    2   23   24   25
CONECT    2    3   22   26
CONECT    3    4   27   28
CONECT    4    5    6   10
CONECT    5   29   30   31
CONECT    6    7    8   32
CONECT    7   33
CONECT    8    9   34   35
CONECT    9   10   36   37
CONECT   10   11   38
CONECT   11   12   22   39
CONECT   12   13   14   40
CONECT   13   41   42   43
CONECT   14   15   44   45
CONECT   15   16   16   21
CONECT   16   17   46
CONECT   17   18   18   19
CONECT   19   20   47   48
CONECT   20   21   49   50
CONECT   21   22   51
CONECT   22   52
END

HMDB0251375
     RDKit          3D
Dimethandrolone
 52 55  0  0  0  0  0  0  0  0999 V2000
   -0.0417    1.8215    2.0855 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1418    1.6795    0.6076 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5816    1.6986    0.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2867    0.3981    0.3042 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9906    0.2215    1.6360 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3971    0.3803   -0.7551 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5797   -0.1278   -0.2451 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9287   -0.5092   -1.8527 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5998   -1.0772   -1.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4819   -0.8059   -0.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0530   -0.7501    0.4594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6367   -1.9943   -0.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0990   -3.1947    0.7017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1296   -1.9498    0.1794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6903   -0.6480   -0.2731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6899   -0.6896   -1.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2617    0.5670   -1.5860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8772    0.6636   -2.6845 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0831    1.7516   -0.6873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6407    1.8529   -0.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0690    0.5794    0.2771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5875    0.5111    0.0069 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6770    2.5960    2.4336 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0128    0.8942    2.6561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0562    2.2607    2.3049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3215    2.6040    0.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1127    2.4413    0.8429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6355    2.0867   -0.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9050    0.8581    1.6801 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3407    0.3331    2.4979 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3824   -0.8369    1.6305 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6122    1.4157   -1.1108 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3715    0.3201   -0.6345 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9040    0.0585   -2.8102 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6263   -1.3671   -2.0436 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8307   -0.5875   -2.1083 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5413   -2.1665   -1.7324 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9582   -1.6808    0.5096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0738   -0.8168    1.5532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4708   -2.1156   -1.1391 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6357   -2.9028    1.4821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3987   -3.8975   -0.0268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9078   -3.7497    1.2405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5604   -2.8097   -0.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3112   -2.1282    1.2599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1184   -1.6087   -1.5049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7698    1.6887    0.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3339    2.6611   -1.2372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0768    2.2636   -1.1101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6331    2.6660    0.5455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2175    0.5209    1.3866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4759    0.6207   -1.1115 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
  4  6  1  0
  6  7  1  0
  6  8  1  0
  8  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  2  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  2  1  0
 10  4  1  0
 22 11  1  0
 21 15  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  5 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 16 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 22 52  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₂

Average Molecular Weight

302.458

Monoisotopic Molecular Weight

302.224580206

IUPAC Name

14-hydroxy-9,15,17-trimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-5-one

Traditional Name

14-hydroxy-9,15,17-trimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-5-one

CAS Registry Number

Not Available

SMILES

CC1CC2=CC(=O)CCC2C2C(C)CC3(C)C(O)CCC3C12

InChI Identifier

InChI=1S/C20H30O2/c1-11-8-13-9-14(21)4-5-15(13)18-12(2)10-20(3)16(19(11)18)6-7-17(20)22/h9,11-12,15-19,22H,4-8,10H2,1-3H3

InChI Key

KVIKZOGGZHCGFH-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as estrogens and derivatives. These are steroids with a structure containing a 3-hydroxylated estrane.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Estrane steroids

Direct Parent

Estrogens and derivatives

Alternative Parents

Substituents

Estrogen-skeleton
17-hydroxysteroid
Oxosteroid
Hydroxysteroid
3-oxosteroid
3-oxo-delta-4-steroid
Delta-4-steroid
Cyclohexenone
Cyclic alcohol
Cyclic ketone
Secondary alcohol
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	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
logP	2.74	ALOGPS
logP	3.64	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	19.37	ChemAxon
pKa (Strongest Basic)	-0.89	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	89.05 m³·mol⁻¹	ChemAxon
Polarizability	35.82 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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
DeepCCS	[M-2H]-	204.842	30932474
DeepCCS	[M+Na]+	180.233	30932474

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Predicted by Siyang on May 30, 2022	16.7034 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.26 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	2696.7 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	445.2 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	213.0 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	191.2 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	380.6 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	692.8 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	717.3 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	84.2 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1306.3 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	500.6 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1537.9 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	415.1 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	462.0 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	243.6 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	441.8 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	19.7 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Dimethandrolone	CC1CC2=CC(=O)CCC2C2C(C)CC3(C)C(O)CCC3C12	3676.5	Standard polar	33892256
Dimethandrolone	CC1CC2=CC(=O)CCC2C2C(C)CC3(C)C(O)CCC3C12	2767.0	Standard non polar	33892256
Dimethandrolone	CC1CC2=CC(=O)CCC2C2C(C)CC3(C)C(O)CCC3C12	2720.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Dimethandrolone,2TMS,isomer #1	CC1CC2(C)C(O[Si](C)(C)C)CCC2C2C(C)CC3=CC(O[Si](C)(C)C)=CCC3C12	2719.8	Semi standard non polar	33892256
Dimethandrolone,2TMS,isomer #1	CC1CC2(C)C(O[Si](C)(C)C)CCC2C2C(C)CC3=CC(O[Si](C)(C)C)=CCC3C12	2729.2	Standard non polar	33892256
Dimethandrolone,2TMS,isomer #1	CC1CC2(C)C(O[Si](C)(C)C)CCC2C2C(C)CC3=CC(O[Si](C)(C)C)=CCC3C12	2837.6	Standard polar	33892256
Dimethandrolone,2TBDMS,isomer #1	CC1CC2(C)C(O[Si](C)(C)C(C)(C)C)CCC2C2C(C)CC3=CC(O[Si](C)(C)C(C)(C)C)=CCC3C12	3178.7	Semi standard non polar	33892256
Dimethandrolone,2TBDMS,isomer #1	CC1CC2(C)C(O[Si](C)(C)C(C)(C)C)CCC2C2C(C)CC3=CC(O[Si](C)(C)C(C)(C)C)=CCC3C12	3221.4	Standard non polar	33892256
Dimethandrolone,2TBDMS,isomer #1	CC1CC2(C)C(O[Si](C)(C)C(C)(C)C)CCC2C2C(C)CC3=CC(O[Si](C)(C)C(C)(C)C)=CCC3C12	3086.9	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Dimethandrolone GC-MS (Non-derivatized) - 70eV, Positive	splash10-00dl-0190000000-20ab9a5ffea9de30628c	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dimethandrolone GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dimethandrolone GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dimethandrolone GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dimethandrolone GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dimethandrolone GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-04	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 - Dimethandrolone 10V, Positive-QTOF	splash10-0udr-0059000000-a7466c653a5228cc94e6	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dimethandrolone 20V, Positive-QTOF	splash10-029i-0961000000-aa45ef0e4ab7b8628eef	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dimethandrolone 40V, Positive-QTOF	splash10-0005-9840000000-bdd8563444baa34d0c7d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dimethandrolone 10V, Negative-QTOF	splash10-0udi-0009000000-16d58525184e918518fa	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dimethandrolone 20V, Negative-QTOF	splash10-0udi-0009000000-16d58525184e918518fa	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dimethandrolone 40V, Negative-QTOF	splash10-0002-0390000000-156cca8129133d4a347c	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

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

11456026

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Dimethandrolone

METLIN ID

Not Available

PubChem Compound

22559975

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for Dimethandrolone (HMDB0251375)

MOL for HMDB0251375 (Dimethandrolone)

3D MOL for HMDB0251375 (Dimethandrolone)

3D SDF for HMDB0251375 (Dimethandrolone)

3D-SDF for HMDB0251375 (Dimethandrolone)

PDB for HMDB0251375 (Dimethandrolone)

3D PDB for HMDB0251375 (Dimethandrolone)

SMILES for HMDB0251375 (Dimethandrolone)

INCHI for HMDB0251375 (Dimethandrolone)

Structure for HMDB0251375 (Dimethandrolone)

3D Structure for HMDB0251375 (Dimethandrolone)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra