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enzymes (1) Show 1 protein

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2013-05-17 01:20:47 UTC

Update Date

2022-03-07 03:17:44 UTC

HMDB ID

HMDB0060437

Secondary Accession Numbers

HMDB60437

Metabolite Identification

Common Name

Androstan-3alpha,17beta-diol

Description

Androstan-3alpha,17beta-diol, also known as hombreol or (3a,5a,17b)-androstane-3,17-diol, belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. Thus, androstan-3alpha,17beta-diol is considered to be a steroid. Based on a literature review a significant number of articles have been published on Androstan-3alpha,17beta-diol.

Structure

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

HMDB0060437
     RDKit          3D
Androstan-3alpha,17beta-diol
 53 56  0  0  0  0  0  0  0  0999 V2000
    1.6554   -1.0669    1.9135 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5019   -0.6615    0.4822 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2577   -1.6802   -0.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6939   -1.6991    0.0628 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2972   -0.3627    0.3125 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5330   -0.2694   -0.3775 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4748    0.8058   -0.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0074    0.6764    0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4221    1.6985    1.0718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0672    1.7165    0.7857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7047    0.3665    0.9045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0109   -0.7260    0.1668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2952   -0.8258   -1.2794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5622   -0.1176   -1.6964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5968   -0.2515   -0.6347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9773   -1.6850   -0.4066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1488    0.4623    0.6019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6310    1.8832    0.3307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0847    1.5835   -0.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8678    0.4763   -1.0813 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9549   -0.3613   -1.1496 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2493   -0.3587    2.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6589   -1.3426    2.2231 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0314   -2.0032    2.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2023   -1.4757   -1.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8183   -2.6774   -0.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8594   -2.3849    0.9462 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2580   -2.2169   -0.7693 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6045   -0.2217    1.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9360    0.6066   -0.1431 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7653    1.1014   -1.1241 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8046    1.7009    0.5368 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5400    0.9379   -0.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6824    1.5560    2.1122 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8061    2.6959    0.7634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5445    2.3760    1.5436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1702    2.1621   -0.2273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6315    0.0921    2.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3293   -1.6928    0.6486 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5096   -0.4504   -1.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4251   -1.9055   -1.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3499    0.9392   -1.9204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8870   -0.5735   -2.6672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8644   -1.9444   -1.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2602   -1.8159    0.6399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1972   -2.4095   -0.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8131    0.0928    1.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1700    2.3073   -0.5895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5726    2.5302    1.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5377    2.4817   -0.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6334    1.2409    0.8225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7146    0.9294   -2.0955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5894   -0.2390   -0.3949 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
  5  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
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
  8  2  1  0
 17 11  1  0
 12  2  1  0
 20 15  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  1
  6 30  1  0
  7 31  1  0
  7 32  1  0
  8 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 16 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 18 48  1  0
 18 49  1  0
 19 50  1  0
 19 51  1  0
 20 52  1  6
 21 53  1  0
M  END


  Mrv0541 05161318202D          

 21 24  0  0  0  0            999 V2000
    4.5466    1.3336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0307    1.7357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754   -0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195   -0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3367    0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1708    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7345    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3587    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9224    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9193   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4511    0.2673    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4830    0.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6708    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0148    0.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5660    0.9666    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8269    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3905    0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2632    0.1221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0596    1.6179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0  0  0  0
  6  5  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 12  3  1  0  0  0  0
 12 11  1  0  0  0  0
 13  7  1  0  0  0  0
 13 11  1  0  0  0  0
 14  4  1  0  0  0  0
 15  5  1  0  0  0  0
 15 14  1  0  0  0  0
 16  8  1  0  0  0  0
 16 14  1  0  0  0  0
 17  6  1  0  0  0  0
 18  1  1  0  0  0  0
 18  9  1  0  0  0  0
 18 12  1  0  0  0  0
 18 16  1  0  0  0  0
 19  2  1  0  0  0  0
 19 10  1  0  0  0  0
 19 15  1  0  0  0  0
 19 17  1  0  0  0  0
 13 20  1  1  0  0  0
 17 21  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0060437

> <DATABASE_NAME>
hmdb

> <SMILES>
CC12CCC3C(CCC4C[C@H](O)CCC34C)C1CC[C@@H]2O

> <INCHI_IDENTIFIER>
InChI=1S/C19H32O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-17,20-21H,3-11H2,1-2H3/t12?,13-,14?,15?,16?,17+,18?,19?/m1/s1

> <INCHI_KEY>
CBMYJHIOYJEBSB-RLSXWVIDSA-N

> <FORMULA>
C19H32O2

> <MOLECULAR_WEIGHT>
292.4562

> <EXACT_MASS>
292.240230268

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
35.44068001758939

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5R,14S)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol

> <ALOGPS_LOGP>
3.56

> <JCHEM_LOGP>
3.2037568309999997

> <ALOGPS_LOGS>
-4.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.377705356554483

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.2963963211217

> <JCHEM_PKA_STRONGEST_BASIC>
-0.7580100340749988

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
84.63119999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.93e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5R,14S)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0060437
     RDKit          3D
Androstan-3alpha,17beta-diol
 53 56  0  0  0  0  0  0  0  0999 V2000
    1.6554   -1.0669    1.9135 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5019   -0.6615    0.4822 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2577   -1.6802   -0.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6939   -1.6991    0.0628 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2972   -0.3627    0.3125 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5330   -0.2694   -0.3775 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4748    0.8058   -0.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0074    0.6764    0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4221    1.6985    1.0718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0672    1.7165    0.7857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7047    0.3665    0.9045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0109   -0.7260    0.1668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2952   -0.8258   -1.2794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5622   -0.1176   -1.6964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5968   -0.2515   -0.6347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9773   -1.6850   -0.4066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1488    0.4623    0.6019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6310    1.8832    0.3307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0847    1.5835   -0.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8678    0.4763   -1.0813 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9549   -0.3613   -1.1496 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2493   -0.3587    2.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6589   -1.3426    2.2231 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0314   -2.0032    2.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2023   -1.4757   -1.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8183   -2.6774   -0.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8594   -2.3849    0.9462 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2580   -2.2169   -0.7693 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6045   -0.2217    1.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9360    0.6066   -0.1431 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7653    1.1014   -1.1241 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8046    1.7009    0.5368 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5400    0.9379   -0.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6824    1.5560    2.1122 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8061    2.6959    0.7634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5445    2.3760    1.5436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1702    2.1621   -0.2273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6315    0.0921    2.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3293   -1.6928    0.6486 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5096   -0.4504   -1.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4251   -1.9055   -1.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3499    0.9392   -1.9204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8870   -0.5735   -2.6672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8644   -1.9444   -1.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2602   -1.8159    0.6399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1972   -2.4095   -0.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8131    0.0928    1.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1700    2.3073   -0.5895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5726    2.5302    1.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5377    2.4817   -0.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6334    1.2409    0.8225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7146    0.9294   -2.0955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5894   -0.2390   -0.3949 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
  5  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
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
  8  2  1  0
 17 11  1  0
 12  2  1  0
 20 15  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  1
  6 30  1  0
  7 31  1  0
  7 32  1  0
  8 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 16 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 18 48  1  0
 18 49  1  0
 19 50  1  0
 19 51  1  0
 20 52  1  6
 21 53  1  0
M  END

HEADER    PROTEIN                                 16-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-MAY-13         0                                  
HETATM    1  C   UNK     0       8.487   2.489   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.791   3.240   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.541  -1.585   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.025  -1.314   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.770  -0.539   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.495   0.325   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.519   1.947   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.971   2.761   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.003   2.218   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.455   3.032   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.049  -0.678   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.533  -0.407   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.042   0.499   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.502   0.135   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.985   0.406   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.494   1.312   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.923   1.804   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.010   1.041   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.462   1.854   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      13.558   0.228   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       1.978   3.020   0.000  0.00  0.00           O+0
CONECT    1   18                                                            
CONECT    2   19                                                            
CONECT    3    4   12                                                       
CONECT    4    3   14                                                       
CONECT    5    6   15                                                       
CONECT    6    5   17                                                       
CONECT    7    9   13                                                       
CONECT    8   10   16                                                       
CONECT    9    7   18                                                       
CONECT   10    8   19                                                       
CONECT   11   12   13                                                       
CONECT   12    3   11   18                                                  
CONECT   13    7   11   20                                                  
CONECT   14    4   15   16                                                  
CONECT   15    5   14   19                                                  
CONECT   16    8   14   18                                                  
CONECT   17    6   19   21                                                  
CONECT   18    1    9   12   16                                             
CONECT   19    2   10   15   17                                             
CONECT   20   13                                                            
CONECT   21   17                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   48    0
END

COMPND    HMDB0060437
HETATM    1  C1  UNL     1       1.655  -1.067   1.914  1.00  0.00           C  
HETATM    2  C2  UNL     1       1.502  -0.661   0.482  1.00  0.00           C  
HETATM    3  C3  UNL     1       2.258  -1.680  -0.358  1.00  0.00           C  
HETATM    4  C4  UNL     1       3.694  -1.699   0.063  1.00  0.00           C  
HETATM    5  C5  UNL     1       4.297  -0.363   0.313  1.00  0.00           C  
HETATM    6  O1  UNL     1       5.533  -0.269  -0.377  1.00  0.00           O  
HETATM    7  C6  UNL     1       3.475   0.806  -0.071  1.00  0.00           C  
HETATM    8  C7  UNL     1       2.007   0.676   0.119  1.00  0.00           C  
HETATM    9  C8  UNL     1       1.422   1.698   1.072  1.00  0.00           C  
HETATM   10  C9  UNL     1      -0.067   1.716   0.786  1.00  0.00           C  
HETATM   11  C10 UNL     1      -0.705   0.367   0.904  1.00  0.00           C  
HETATM   12  C11 UNL     1       0.011  -0.726   0.167  1.00  0.00           C  
HETATM   13  C12 UNL     1      -0.295  -0.826  -1.279  1.00  0.00           C  
HETATM   14  C13 UNL     1      -1.562  -0.118  -1.696  1.00  0.00           C  
HETATM   15  C14 UNL     1      -2.597  -0.251  -0.635  1.00  0.00           C  
HETATM   16  C15 UNL     1      -2.977  -1.685  -0.407  1.00  0.00           C  
HETATM   17  C16 UNL     1      -2.149   0.462   0.602  1.00  0.00           C  
HETATM   18  C17 UNL     1      -2.631   1.883   0.331  1.00  0.00           C  
HETATM   19  C18 UNL     1      -4.085   1.583  -0.068  1.00  0.00           C  
HETATM   20  C19 UNL     1      -3.868   0.476  -1.081  1.00  0.00           C  
HETATM   21  O2  UNL     1      -4.955  -0.361  -1.150  1.00  0.00           O  
HETATM   22  H1  UNL     1       1.249  -0.359   2.646  1.00  0.00           H  
HETATM   23  H2  UNL     1       2.659  -1.343   2.223  1.00  0.00           H  
HETATM   24  H3  UNL     1       1.031  -2.003   2.039  1.00  0.00           H  
HETATM   25  H4  UNL     1       2.202  -1.476  -1.428  1.00  0.00           H  
HETATM   26  H5  UNL     1       1.818  -2.677  -0.139  1.00  0.00           H  
HETATM   27  H6  UNL     1       3.859  -2.385   0.946  1.00  0.00           H  
HETATM   28  H7  UNL     1       4.258  -2.217  -0.769  1.00  0.00           H  
HETATM   29  H8  UNL     1       4.605  -0.222   1.392  1.00  0.00           H  
HETATM   30  H9  UNL     1       5.936   0.607  -0.143  1.00  0.00           H  
HETATM   31  H10 UNL     1       3.765   1.101  -1.124  1.00  0.00           H  
HETATM   32  H11 UNL     1       3.805   1.701   0.537  1.00  0.00           H  
HETATM   33  H12 UNL     1       1.540   0.938  -0.882  1.00  0.00           H  
HETATM   34  H13 UNL     1       1.682   1.556   2.112  1.00  0.00           H  
HETATM   35  H14 UNL     1       1.806   2.696   0.763  1.00  0.00           H  
HETATM   36  H15 UNL     1      -0.545   2.376   1.544  1.00  0.00           H  
HETATM   37  H16 UNL     1      -0.170   2.162  -0.227  1.00  0.00           H  
HETATM   38  H17 UNL     1      -0.631   0.092   2.002  1.00  0.00           H  
HETATM   39  H18 UNL     1      -0.329  -1.693   0.649  1.00  0.00           H  
HETATM   40  H19 UNL     1       0.510  -0.450  -1.957  1.00  0.00           H  
HETATM   41  H20 UNL     1      -0.425  -1.906  -1.590  1.00  0.00           H  
HETATM   42  H21 UNL     1      -1.350   0.939  -1.920  1.00  0.00           H  
HETATM   43  H22 UNL     1      -1.887  -0.574  -2.667  1.00  0.00           H  
HETATM   44  H23 UNL     1      -3.864  -1.944  -1.055  1.00  0.00           H  
HETATM   45  H24 UNL     1      -3.260  -1.816   0.640  1.00  0.00           H  
HETATM   46  H25 UNL     1      -2.197  -2.410  -0.677  1.00  0.00           H  
HETATM   47  H26 UNL     1      -2.813   0.093   1.439  1.00  0.00           H  
HETATM   48  H27 UNL     1      -2.170   2.307  -0.589  1.00  0.00           H  
HETATM   49  H28 UNL     1      -2.573   2.530   1.205  1.00  0.00           H  
HETATM   50  H29 UNL     1      -4.538   2.482  -0.540  1.00  0.00           H  
HETATM   51  H30 UNL     1      -4.633   1.241   0.822  1.00  0.00           H  
HETATM   52  H31 UNL     1      -3.715   0.929  -2.095  1.00  0.00           H  
HETATM   53  H32 UNL     1      -5.589  -0.239  -0.395  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3    8   12
CONECT    3    4   25   26
CONECT    4    5   27   28
CONECT    5    6    7   29
CONECT    6   30
CONECT    7    8   31   32
CONECT    8    9   33
CONECT    9   10   34   35
CONECT   10   11   36   37
CONECT   11   12   17   38
CONECT   12   13   39
CONECT   13   14   40   41
CONECT   14   15   42   43
CONECT   15   16   17   20
CONECT   16   44   45   46
CONECT   17   18   47
CONECT   18   19   48   49
CONECT   19   20   50   51
CONECT   20   21   52
CONECT   21   53
END

HMDB0060437
     RDKit          3D
Androstan-3alpha,17beta-diol
 53 56  0  0  0  0  0  0  0  0999 V2000
    1.6554   -1.0669    1.9135 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5019   -0.6615    0.4822 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2577   -1.6802   -0.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6939   -1.6991    0.0628 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2972   -0.3627    0.3125 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5330   -0.2694   -0.3775 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4748    0.8058   -0.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0074    0.6764    0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4221    1.6985    1.0718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0672    1.7165    0.7857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7047    0.3665    0.9045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0109   -0.7260    0.1668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2952   -0.8258   -1.2794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5622   -0.1176   -1.6964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5968   -0.2515   -0.6347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9773   -1.6850   -0.4066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1488    0.4623    0.6019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6310    1.8832    0.3307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0847    1.5835   -0.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8678    0.4763   -1.0813 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9549   -0.3613   -1.1496 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2493   -0.3587    2.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6589   -1.3426    2.2231 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0314   -2.0032    2.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2023   -1.4757   -1.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8183   -2.6774   -0.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8594   -2.3849    0.9462 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2580   -2.2169   -0.7693 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6045   -0.2217    1.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9360    0.6066   -0.1431 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7653    1.1014   -1.1241 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8046    1.7009    0.5368 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5400    0.9379   -0.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6824    1.5560    2.1122 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8061    2.6959    0.7634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5445    2.3760    1.5436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1702    2.1621   -0.2273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6315    0.0921    2.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3293   -1.6928    0.6486 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5096   -0.4504   -1.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4251   -1.9055   -1.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3499    0.9392   -1.9204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8870   -0.5735   -2.6672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8644   -1.9444   -1.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2602   -1.8159    0.6399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1972   -2.4095   -0.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8131    0.0928    1.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1700    2.3073   -0.5895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5726    2.5302    1.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5377    2.4817   -0.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6334    1.2409    0.8225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7146    0.9294   -2.0955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5894   -0.2390   -0.3949 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
  5  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
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
  8  2  1  0
 17 11  1  0
 12  2  1  0
 20 15  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  1
  6 30  1  0
  7 31  1  0
  7 32  1  0
  8 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 16 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 18 48  1  0
 18 49  1  0
 19 50  1  0
 19 51  1  0
 20 52  1  6
 21 53  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(3alpha,5alpha,17beta)-Androstane-3,17-diol	ChEBI
3alpha,17beta-Dihydroxy-5alpha-androstane	ChEBI
Hombreol	ChEBI
(3a,5a,17b)-Androstane-3,17-diol	Generator
(3Α,5α,17β)-androstane-3,17-diol	Generator
3a,17b-Dihydroxy-5a-androstane	Generator
3Α,17β-dihydroxy-5α-androstane	Generator
Androstan-3a,17b-diol	Generator
Androstan-3α,17β-diol	Generator
5alpha-Androstan-3alpha,17beta-diol	KEGG
5a-Androstan-3a,17b-diol	Generator
5α-androstan-3α,17β-diol	Generator

Chemical Formula

C₁₉H₃₂O₂

Average Molecular Weight

292.4562

Monoisotopic Molecular Weight

292.240230268

IUPAC Name

(5R,14S)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol

Traditional Name

(5R,14S)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol

CAS Registry Number

Not Available

SMILES

CC12CCC3C(CCC4C[C@H](O)CCC34C)C1CC[C@@H]2O

InChI Identifier

InChI=1S/C19H32O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-17,20-21H,3-11H2,1-2H3/t12?,13-,14?,15?,16?,17+,18?,19?/m1/s1

InChI Key

CBMYJHIOYJEBSB-RLSXWVIDSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Androstane steroids

Direct Parent

Androgens and derivatives

Alternative Parents

Substituents

Androgen-skeleton
17-hydroxysteroid
3-alpha-hydroxysteroid
Hydroxysteroid
3-hydroxysteroid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

androstane-3alpha,17beta-diol (CHEBI:36713 )
C19 steroids (androgens) and derivatives (LMST02020052 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Membrane (HMDB: HMDB0060437)

Process

Not Available

Role

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
Water Solubility	0.019 g/L	ALOGPS
logP	3.56	ALOGPS
logP	3.2	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	18.3	ChemAxon
pKa (Strongest Basic)	-0.76	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	84.63 m³·mol⁻¹	ChemAxon
Polarizability	35.44 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	167.59	31661259
DarkChem	[M-H]-	165.388	31661259
DeepCCS	[M-2H]-	206.99	30932474
DeepCCS	[M+Na]+	182.218	30932474
AllCCS	[M+H]+	177.8	32859911
AllCCS	[M+H-H2O]+	174.8	32859911
AllCCS	[M+NH4]+	180.6	32859911
AllCCS	[M+Na]+	181.5	32859911
AllCCS	[M-H]-	179.1	32859911
AllCCS	[M+Na-2H]-	179.4	32859911
AllCCS	[M+HCOO]-	179.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Androstan-3alpha,17beta-diol	CC12CCC3C(CCC4C[C@H](O)CCC34C)C1CC[C@@H]2O	2344.7	Standard polar	33892256
Androstan-3alpha,17beta-diol	CC12CCC3C(CCC4C[C@H](O)CCC34C)C1CC[C@@H]2O	2442.0	Standard non polar	33892256
Androstan-3alpha,17beta-diol	CC12CCC3C(CCC4C[C@H](O)CCC34C)C1CC[C@@H]2O	2635.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Androstan-3alpha,17beta-diol,1TMS,isomer #1	CC12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2CCC2(C)C1CC[C@@H]2O	2593.1	Semi standard non polar	33892256
Androstan-3alpha,17beta-diol,1TMS,isomer #2	CC12CC[C@@H](O)CC1CCC1C2CCC2(C)C1CC[C@@H]2O[Si](C)(C)C	2591.0	Semi standard non polar	33892256
Androstan-3alpha,17beta-diol,2TMS,isomer #1	CC12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2CCC2(C)C1CC[C@@H]2O[Si](C)(C)C	2586.2	Semi standard non polar	33892256
Androstan-3alpha,17beta-diol,1TBDMS,isomer #1	CC12CC[C@@H](O[Si](C)(C)C(C)(C)C)CC1CCC1C2CCC2(C)C1CC[C@@H]2O	2844.9	Semi standard non polar	33892256
Androstan-3alpha,17beta-diol,1TBDMS,isomer #2	CC12CC[C@@H](O)CC1CCC1C2CCC2(C)C1CC[C@@H]2O[Si](C)(C)C(C)(C)C	2864.8	Semi standard non polar	33892256
Androstan-3alpha,17beta-diol,2TBDMS,isomer #1	CC12CC[C@@H](O[Si](C)(C)C(C)(C)C)CC1CCC1C2CCC2(C)C1CC[C@@H]2O[Si](C)(C)C(C)(C)C	3107.0	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 - Androstan-3alpha,17beta-diol GC-MS (Non-derivatized) - 70eV, Positive	splash10-03gi-0290000000-2102975bd891dd587151	2017-09-20	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Androstan-3alpha,17beta-diol GC-MS (2 TMS) - 70eV, Positive	splash10-05fr-2227900000-87cd967afbbb2453594f	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Androstan-3alpha,17beta-diol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Androstan-3alpha,17beta-diol 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 - Androstan-3alpha,17beta-diol 10V, Positive-QTOF	splash10-004l-0090000000-f273d079c7767f673ac4	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstan-3alpha,17beta-diol 20V, Positive-QTOF	splash10-056r-0290000000-241c15d984d5502957c2	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstan-3alpha,17beta-diol 40V, Positive-QTOF	splash10-00mk-2790000000-1cfe15a3e20555af8c99	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstan-3alpha,17beta-diol 10V, Negative-QTOF	splash10-0006-0090000000-7976b987ec10e61bdb4c	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstan-3alpha,17beta-diol 20V, Negative-QTOF	splash10-006x-0090000000-72251dd83cca96a12d44	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstan-3alpha,17beta-diol 40V, Negative-QTOF	splash10-01r5-0190000000-1da2626be2ffb7cb7813	2017-10-06	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane (predicted from logP)

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

DB01530

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022114

KNApSAcK ID

C00060540

Chemspider ID

15039

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

3%CE%B1-Androstanediol

METLIN ID

5538

PubChem Compound

15818

PDB ID

Not Available

ChEBI ID

36713

Food Biomarker Ontology

Not Available

VMH ID

CE2209

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Magrane M: UniProt Knowledgebase: a hub of integrated protein data. Database (Oxford). 2011 Mar 29;2011:bar009. doi: 10.1093/database/bar009. Print 2011. [PubMed:21447597 ]
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 ]
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Enzymes

Enzyme Details

1. Aldo-keto reductase family 1 member C4

General function:: Involved in oxidoreductase activity
Specific function:: Catalyzes the transformation of the potent androgen dihydrotestosterone (DHT) into the less active form, 5-alpha-androstan-3-alpha,17-beta-diol (3-alpha-diol). Also has some 20-alpha-hydroxysteroid dehydrogenase activity. The biotransformation of the pesticide chlordecone (kepone) to its corresponding alcohol leads to increased biliary excretion of the pesticide and concomitant reduction of its neurotoxicity since bile is the major excretory route.
Gene Name:: AKR1C4
Uniprot ID:: P17516
Molecular weight:: 37094.57

Reactions

Dihydrotestosterone + NADPH + Hydrogen Ion → Androstan-3alpha,17beta-diol + NADP	details

Showing metabocard for Androstan-3alpha,17beta-diol (HMDB0060437)

MOL for HMDB0060437 (Androstan-3alpha,17beta-diol)

3D MOL for HMDB0060437 (Androstan-3alpha,17beta-diol)

3D SDF for HMDB0060437 (Androstan-3alpha,17beta-diol)

3D-SDF for HMDB0060437 (Androstan-3alpha,17beta-diol)

PDB for HMDB0060437 (Androstan-3alpha,17beta-diol)

3D PDB for HMDB0060437 (Androstan-3alpha,17beta-diol)

SMILES for HMDB0060437 (Androstan-3alpha,17beta-diol)

INCHI for HMDB0060437 (Androstan-3alpha,17beta-diol)

Structure for HMDB0060437 (Androstan-3alpha,17beta-diol)

3D Structure for HMDB0060437 (Androstan-3alpha,17beta-diol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes

Reactions