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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2022-09-09 20:08:03 UTC

Update Date

2022-09-22 18:34:45 UTC

HMDB ID

HMDB0341279

Secondary Accession Numbers

None

Metabolite Identification

Common Name

5-Pregnene-3beta,17,20alpha-triol

Description

3,17,20-Trihydroxypregnane, also known as pregnanetriol or 5-beta-pregnane-3,17,20-triol, belongs to the class of organic compounds known as gluco/mineralocorticoids, progestogins and derivatives. These are steroids with a structure based on a hydroxylated prostane moiety. Based on a literature review very few articles have been published on 3,17,20-Trihydroxypregnane.

Structure

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

HMDB0256756
     RDKit          3D
3,17,20-Trihydroxypregnane
 60 63  0  0  0  0  0  0  0  0999 V2000
   -4.4595    1.6529    0.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2493    0.1609    0.6933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9143   -0.0194    1.9323 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8052   -0.1422    0.8157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2744    0.7732    1.7617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5270   -1.4921    1.4491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0191   -1.5995    1.1288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1027   -1.3748   -0.3552 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1465   -1.3584   -1.1235 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0932   -2.4017   -0.5880 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5628   -1.9629   -0.7275 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6306   -0.7586    0.1741 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9927   -0.4353    0.6713 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9380    0.8161    1.4764 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2406    1.3700    1.4584 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0087    1.8628    1.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6413    1.3795    0.5499 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9464    0.3658   -0.5493 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9699    1.1323   -1.4117 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7939   -0.0368   -1.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2317    1.0593   -1.5646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2824    1.1365   -0.5409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0144   -0.1808   -0.4593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8173   -0.3389   -1.7075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6353    2.2574    0.8179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4266    1.7580   -0.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4256    1.9989    0.8182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8262   -0.3905   -0.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8593    0.2559    1.7446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5737    0.4416    2.6634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0096   -2.3031    0.8658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7156   -1.5232    2.5198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8114   -2.6766    1.4025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4273   -0.8795    1.6799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7593   -2.2453   -0.6898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376   -1.7945   -2.1429 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9989   -2.5375    0.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9464   -3.4064   -1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7181   -1.7213   -1.7795 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1592   -2.8197   -0.3631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0054   -0.9582    1.0966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2702   -1.2637    1.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7956   -0.4718   -0.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7590    0.5892    2.5691 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8115    0.9483    0.7961 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7601    2.5067    1.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4428    2.6119    0.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1781    2.2984    0.1395 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1401    0.9465    1.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5265    2.1404   -1.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9619    1.1430   -0.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0036    0.6377   -2.4055 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2279   -0.1157   -2.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7511    0.9417   -2.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3425    2.0234   -1.7007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0412    1.8761   -0.9164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0116    1.4241    0.4649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6951   -1.0061   -1.5945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1708   -0.9021   -2.4508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0380    0.6083   -2.2403 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 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
 23 24  1  0
 23  4  1  0
 23  8  1  0
 20  9  1  0
 18 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  3 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 15 45  1  0
 16 46  1  0
 16 47  1  0
 17 48  1  0
 17 49  1  0
 19 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  0
 21 54  1  0
 21 55  1  0
 22 56  1  0
 22 57  1  0
 24 58  1  0
 24 59  1  0
 24 60  1  0
M  END

  Mrv1533004171503482D          

 24 27  0  0  0  0            999 V2000
    1.7243   -2.0040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2561   -2.6347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9758   -3.4106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1278   -3.3123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390   -1.6970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5218   -1.2340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1731   -1.7404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9853   -1.5952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2655   -0.8192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0777   -0.6740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6095   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4216   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7655   -1.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6731   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8610   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3292   -2.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0489   -2.8566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5171   -2.2259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2368   -3.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4247   -3.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8928   -2.5163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5330   -3.2587    0.0000 C   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  4 23  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0341279

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(O)C1(O)CCC2C3CCC4CC(O)CCC4(C)C3CCC12C

> <INCHI_IDENTIFIER>
InChI=1S/C21H36O3/c1-13(22)21(24)11-8-18-16-5-4-14-12-15(23)6-9-19(14,2)17(16)7-10-20(18,21)3/h13-18,22-24H,4-12H2,1-3H3

> <INCHI_KEY>
SCPADBBISMMJAW-UHFFFAOYSA-N

> <FORMULA>
C21H36O3

> <MOLECULAR_WEIGHT>
336.516

> <EXACT_MASS>
336.266445019

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
40.197126751082244

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
14-(1-hydroxyethyl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol

> <ALOGPS_LOGP>
3.39

> <JCHEM_LOGP>
2.853998557333335

> <ALOGPS_LOGS>
-3.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.109322994199143

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.41738102222639

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3569562491413683

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
95.23189999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.71e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-(1-hydroxyethyl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0256756
     RDKit          3D
3,17,20-Trihydroxypregnane
 60 63  0  0  0  0  0  0  0  0999 V2000
   -4.4595    1.6529    0.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2493    0.1609    0.6933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9143   -0.0194    1.9323 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8052   -0.1422    0.8157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2744    0.7732    1.7617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5270   -1.4921    1.4491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0191   -1.5995    1.1288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1027   -1.3748   -0.3552 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1465   -1.3584   -1.1235 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0932   -2.4017   -0.5880 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5628   -1.9629   -0.7275 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6306   -0.7586    0.1741 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9927   -0.4353    0.6713 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9380    0.8161    1.4764 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2406    1.3700    1.4584 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0087    1.8628    1.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6413    1.3795    0.5499 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9464    0.3658   -0.5493 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9699    1.1323   -1.4117 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7939   -0.0368   -1.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2317    1.0593   -1.5646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2824    1.1365   -0.5409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0144   -0.1808   -0.4593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8173   -0.3389   -1.7075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6353    2.2574    0.8179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4266    1.7580   -0.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4256    1.9989    0.8182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8262   -0.3905   -0.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8593    0.2559    1.7446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5737    0.4416    2.6634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0096   -2.3031    0.8658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7156   -1.5232    2.5198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8114   -2.6766    1.4025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4273   -0.8795    1.6799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7593   -2.2453   -0.6898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376   -1.7945   -2.1429 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9989   -2.5375    0.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9464   -3.4064   -1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7181   -1.7213   -1.7795 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1592   -2.8197   -0.3631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0054   -0.9582    1.0966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2702   -1.2637    1.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7956   -0.4718   -0.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7590    0.5892    2.5691 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8115    0.9483    0.7961 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7601    2.5067    1.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4428    2.6119    0.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1781    2.2984    0.1395 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1401    0.9465    1.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5265    2.1404   -1.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9619    1.1430   -0.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0036    0.6377   -2.4055 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2279   -0.1157   -2.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7511    0.9417   -2.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3425    2.0234   -1.7007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0412    1.8761   -0.9164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0116    1.4241    0.4649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6951   -1.0061   -1.5945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1708   -0.9021   -2.4508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0380    0.6083   -2.2403 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 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
 23 24  1  0
 23  4  1  0
 23  8  1  0
 20  9  1  0
 18 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  3 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 15 45  1  0
 16 46  1  0
 16 47  1  0
 17 48  1  0
 17 49  1  0
 19 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  0
 21 54  1  0
 21 55  1  0
 22 56  1  0
 22 57  1  0
 24 58  1  0
 24 59  1  0
 24 60  1  0
M  END

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       3.219  -3.741   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.211  -4.918   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.688  -6.367   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       5.727  -4.647   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       5.839  -6.183   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.299  -3.168   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.574  -2.304   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.790  -3.249   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.306  -2.978   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.829  -1.529   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.345  -1.258   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.338  -2.436   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.854  -2.164   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.846  -3.342   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      16.362  -3.071   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      14.323  -4.790   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.807  -5.061   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.814  -3.884   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.291  -5.332   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.299  -4.155   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.775  -5.603   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.259  -5.874   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.267  -4.697   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.595  -6.083   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6   23                                             
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   23                                                  
CONECT    9    8   10   20                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   12   19   20                                             
CONECT   19   18                                                            
CONECT   20   18    9   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    4    8   24                                             
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

COMPND    HMDB0256756
HETATM    1  C1  UNL     1      -4.460   1.653   0.392  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.249   0.161   0.693  1.00  0.00           C  
HETATM    3  O1  UNL     1      -4.914  -0.019   1.932  1.00  0.00           O  
HETATM    4  C3  UNL     1      -2.805  -0.142   0.816  1.00  0.00           C  
HETATM    5  O2  UNL     1      -2.274   0.773   1.762  1.00  0.00           O  
HETATM    6  C4  UNL     1      -2.527  -1.492   1.449  1.00  0.00           C  
HETATM    7  C5  UNL     1      -1.019  -1.599   1.129  1.00  0.00           C  
HETATM    8  C6  UNL     1      -1.103  -1.375  -0.355  1.00  0.00           C  
HETATM    9  C7  UNL     1       0.146  -1.358  -1.124  1.00  0.00           C  
HETATM   10  C8  UNL     1       1.093  -2.402  -0.588  1.00  0.00           C  
HETATM   11  C9  UNL     1       2.563  -1.963  -0.728  1.00  0.00           C  
HETATM   12  C10 UNL     1       2.631  -0.759   0.174  1.00  0.00           C  
HETATM   13  C11 UNL     1       3.993  -0.435   0.671  1.00  0.00           C  
HETATM   14  C12 UNL     1       3.938   0.816   1.476  1.00  0.00           C  
HETATM   15  O3  UNL     1       5.241   1.370   1.458  1.00  0.00           O  
HETATM   16  C13 UNL     1       3.009   1.863   1.041  1.00  0.00           C  
HETATM   17  C14 UNL     1       1.641   1.379   0.550  1.00  0.00           C  
HETATM   18  C15 UNL     1       1.946   0.366  -0.549  1.00  0.00           C  
HETATM   19  C16 UNL     1       2.970   1.132  -1.412  1.00  0.00           C  
HETATM   20  C17 UNL     1       0.794  -0.037  -1.381  1.00  0.00           C  
HETATM   21  C18 UNL     1      -0.232   1.059  -1.565  1.00  0.00           C  
HETATM   22  C19 UNL     1      -1.282   1.136  -0.541  1.00  0.00           C  
HETATM   23  C20 UNL     1      -2.014  -0.181  -0.459  1.00  0.00           C  
HETATM   24  C21 UNL     1      -2.817  -0.339  -1.707  1.00  0.00           C  
HETATM   25  H1  UNL     1      -3.635   2.257   0.818  1.00  0.00           H  
HETATM   26  H2  UNL     1      -4.427   1.758  -0.697  1.00  0.00           H  
HETATM   27  H3  UNL     1      -5.426   1.999   0.818  1.00  0.00           H  
HETATM   28  H4  UNL     1      -4.826  -0.390  -0.041  1.00  0.00           H  
HETATM   29  H5  UNL     1      -5.859   0.256   1.745  1.00  0.00           H  
HETATM   30  H6  UNL     1      -2.574   0.442   2.663  1.00  0.00           H  
HETATM   31  H7  UNL     1      -3.010  -2.303   0.866  1.00  0.00           H  
HETATM   32  H8  UNL     1      -2.716  -1.523   2.520  1.00  0.00           H  
HETATM   33  H9  UNL     1      -0.811  -2.677   1.403  1.00  0.00           H  
HETATM   34  H10 UNL     1      -0.427  -0.879   1.680  1.00  0.00           H  
HETATM   35  H11 UNL     1      -1.759  -2.245  -0.690  1.00  0.00           H  
HETATM   36  H12 UNL     1      -0.138  -1.795  -2.143  1.00  0.00           H  
HETATM   37  H13 UNL     1       0.999  -2.538   0.530  1.00  0.00           H  
HETATM   38  H14 UNL     1       0.946  -3.406  -1.010  1.00  0.00           H  
HETATM   39  H15 UNL     1       2.718  -1.721  -1.780  1.00  0.00           H  
HETATM   40  H16 UNL     1       3.159  -2.820  -0.363  1.00  0.00           H  
HETATM   41  H17 UNL     1       2.005  -0.958   1.097  1.00  0.00           H  
HETATM   42  H18 UNL     1       4.270  -1.264   1.395  1.00  0.00           H  
HETATM   43  H19 UNL     1       4.796  -0.472  -0.088  1.00  0.00           H  
HETATM   44  H20 UNL     1       3.759   0.589   2.569  1.00  0.00           H  
HETATM   45  H21 UNL     1       5.812   0.948   0.796  1.00  0.00           H  
HETATM   46  H22 UNL     1       2.760   2.507   1.938  1.00  0.00           H  
HETATM   47  H23 UNL     1       3.443   2.612   0.314  1.00  0.00           H  
HETATM   48  H24 UNL     1       1.178   2.298   0.139  1.00  0.00           H  
HETATM   49  H25 UNL     1       1.140   0.946   1.409  1.00  0.00           H  
HETATM   50  H26 UNL     1       2.527   2.140  -1.597  1.00  0.00           H  
HETATM   51  H27 UNL     1       3.962   1.143  -0.995  1.00  0.00           H  
HETATM   52  H28 UNL     1       3.004   0.638  -2.405  1.00  0.00           H  
HETATM   53  H29 UNL     1       1.228  -0.116  -2.435  1.00  0.00           H  
HETATM   54  H30 UNL     1      -0.751   0.942  -2.565  1.00  0.00           H  
HETATM   55  H31 UNL     1       0.342   2.023  -1.701  1.00  0.00           H  
HETATM   56  H32 UNL     1      -2.041   1.876  -0.916  1.00  0.00           H  
HETATM   57  H33 UNL     1      -1.012   1.424   0.465  1.00  0.00           H  
HETATM   58  H34 UNL     1      -3.695  -1.006  -1.594  1.00  0.00           H  
HETATM   59  H35 UNL     1      -2.171  -0.902  -2.451  1.00  0.00           H  
HETATM   60  H36 UNL     1      -3.038   0.608  -2.240  1.00  0.00           H  
CONECT    1    2   25   26   27
CONECT    2    3    4   28
CONECT    3   29
CONECT    4    5    6   23
CONECT    5   30
CONECT    6    7   31   32
CONECT    7    8   33   34
CONECT    8    9   23   35
CONECT    9   10   20   36
CONECT   10   11   37   38
CONECT   11   12   39   40
CONECT   12   13   18   41
CONECT   13   14   42   43
CONECT   14   15   16   44
CONECT   15   45
CONECT   16   17   46   47
CONECT   17   18   48   49
CONECT   18   19   20
CONECT   19   50   51   52
CONECT   20   21   53
CONECT   21   22   54   55
CONECT   22   23   56   57
CONECT   23   24
CONECT   24   58   59   60
END

HMDB0256756
     RDKit          3D
3,17,20-Trihydroxypregnane
 60 63  0  0  0  0  0  0  0  0999 V2000
   -4.4595    1.6529    0.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2493    0.1609    0.6933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9143   -0.0194    1.9323 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8052   -0.1422    0.8157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2744    0.7732    1.7617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5270   -1.4921    1.4491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0191   -1.5995    1.1288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1027   -1.3748   -0.3552 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1465   -1.3584   -1.1235 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0932   -2.4017   -0.5880 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5628   -1.9629   -0.7275 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6306   -0.7586    0.1741 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9927   -0.4353    0.6713 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9380    0.8161    1.4764 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2406    1.3700    1.4584 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0087    1.8628    1.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6413    1.3795    0.5499 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9464    0.3658   -0.5493 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9699    1.1323   -1.4117 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7939   -0.0368   -1.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2317    1.0593   -1.5646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2824    1.1365   -0.5409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0144   -0.1808   -0.4593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8173   -0.3389   -1.7075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6353    2.2574    0.8179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4266    1.7580   -0.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4256    1.9989    0.8182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8262   -0.3905   -0.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8593    0.2559    1.7446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5737    0.4416    2.6634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0096   -2.3031    0.8658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7156   -1.5232    2.5198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8114   -2.6766    1.4025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4273   -0.8795    1.6799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7593   -2.2453   -0.6898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376   -1.7945   -2.1429 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9989   -2.5375    0.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9464   -3.4064   -1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7181   -1.7213   -1.7795 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1592   -2.8197   -0.3631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0054   -0.9582    1.0966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2702   -1.2637    1.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7956   -0.4718   -0.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7590    0.5892    2.5691 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8115    0.9483    0.7961 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7601    2.5067    1.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4428    2.6119    0.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1781    2.2984    0.1395 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1401    0.9465    1.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5265    2.1404   -1.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9619    1.1430   -0.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0036    0.6377   -2.4055 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2279   -0.1157   -2.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7511    0.9417   -2.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3425    2.0234   -1.7007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0412    1.8761   -0.9164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0116    1.4241    0.4649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6951   -1.0061   -1.5945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1708   -0.9021   -2.4508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0380    0.6083   -2.2403 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 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
 23 24  1  0
 23  4  1  0
 23  8  1  0
 20  9  1  0
 18 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  3 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 15 45  1  0
 16 46  1  0
 16 47  1  0
 17 48  1  0
 17 49  1  0
 19 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  0
 21 54  1  0
 21 55  1  0
 22 56  1  0
 22 57  1  0
 24 58  1  0
 24 59  1  0
 24 60  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Pregnanetriol	HMDB
5-beta-Pregnane-3,17,20-triol	HMDB

Chemical Formula

C₂₁H₃₆O₃

Average Molecular Weight

336.516

Monoisotopic Molecular Weight

336.266445019

IUPAC Name

14-(1-hydroxyethyl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol

Traditional Name

14-(1-hydroxyethyl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol

CAS Registry Number

Not Available

SMILES

CC(O)C1(O)CCC2C3CCC4CC(O)CCC4(C)C3CCC12C

InChI Identifier

InChI=1S/C21H36O3/c1-13(22)21(24)11-8-18-16-5-4-14-12-15(23)6-9-19(14,2)17(16)7-10-20(18,21)3/h13-18,22-24H,4-12H2,1-3H3

InChI Key

SCPADBBISMMJAW-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gluco/mineralocorticoids, progestogins and derivatives. These are steroids with a structure based on a hydroxylated prostane moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Pregnane steroids

Direct Parent

Gluco/mineralocorticoids, progestogins and derivatives

Alternative Parents

Substituents

Progestogin-skeleton
20-hydroxysteroid
17-hydroxysteroid
Hydroxysteroid
3-hydroxysteroid
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

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
logP	3.39	ALOGPS
logP	2.85	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	13.42	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	60.69 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	95.23 m³·mol⁻¹	ChemAxon
Polarizability	40.2 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
DeepCCS	[M-2H]-	212.005	30932474
DeepCCS	[M+Na]+	187.232	30932474
AllCCS	[M+H]+	188.0	32859911
AllCCS	[M+H-H2O]+	185.3	32859911
AllCCS	[M+NH4]+	190.4	32859911
AllCCS	[M+Na]+	191.2	32859911
AllCCS	[M-H]-	189.3	32859911
AllCCS	[M+Na-2H]-	189.9	32859911
AllCCS	[M+HCOO]-	190.8	32859911

Predicted Kovats Retention Indices

Not Available

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (Non-derivatized) - 70eV, Positive	splash10-0c04-2197000000-6752e55da01525e0c491	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TBDMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3,17,20-Trihydroxypregnane GC-MS (TBDMS_3_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood
Urine

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Specified	Not Specified	Cancer patients undergoing total body irradiation	31424920	details
Urine	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Cancer patients undergoing total body irradiation	31424920	details

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

451885

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

517927

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

Simon-Manso Y, Marupaka R, Yan X, Liang Y, Telu KH, Mirokhin Y, Stein SE: Mass Spectrometry Fingerprints of Small-Molecule Metabolites in Biofluids: Building a Spectral Library of Recurrent Spectra for Urine Analysis. Anal Chem. 2019 Sep 17;91(18):12021-12029. doi: 10.1021/acs.analchem.9b02977. Epub 2019 Aug 30. [PubMed:31424920 ]

Showing metabocard for 5-Pregnene-3beta,17,20alpha-triol (HMDB0341279)

MOL for HMDB0341279 (5-Pregnene-3beta,17,20alpha-triol)

3D MOL for HMDB0341279 (5-Pregnene-3beta,17,20alpha-triol)

3D SDF for HMDB0341279 (5-Pregnene-3beta,17,20alpha-triol)

3D-SDF for HMDB0341279 (5-Pregnene-3beta,17,20alpha-triol)

PDB for HMDB0341279 (5-Pregnene-3beta,17,20alpha-triol)

3D PDB for HMDB0341279 (5-Pregnene-3beta,17,20alpha-triol)

SMILES for HMDB0341279 (5-Pregnene-3beta,17,20alpha-triol)

INCHI for HMDB0341279 (5-Pregnene-3beta,17,20alpha-triol)

Structure for HMDB0341279 (5-Pregnene-3beta,17,20alpha-triol)

3D Structure for HMDB0341279 (5-Pregnene-3beta,17,20alpha-triol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

GC-MS Spectra