NP-MRD: Showing NP-Card for Epimetendiol (NP0087437)

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Record Information

Version

2.0

Created at

2022-05-11 16:49:39 UTC

Updated at

2022-05-11 16:49:39 UTC

NP-MRD ID

NP0087437

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Epimetendiol

Description

Epimetendiol 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. Epimetendiol is an extremely weak basic (essentially neutral) compound (based on its pKa). Epimetendiol is one of the major urinary metabolites of the anabolic androgenic compound metandienone. Anabolic-androgenic steroids such as metandienone are some of the most frequently detected drugs in amateur and professional sports. Metandienone misuse can be detected by high resolution mass spectrometry for a prolonged period after stopping the intake of metandienone. The use of anabolic steroids was banned by the International Olympic Committee for the first time at the Olympic Games in Montreal in 1976.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02231220322D          

 26 29  0  0  1  0            999 V2000
    9.5024  -10.8741    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9220  -10.9039    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5184   -9.6814    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2064  -12.0569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1747   -9.6953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2737   -8.4705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8715   -8.1214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8892  -11.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6037  -11.3453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7457  -10.5203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8892   -9.2828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1027  -10.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4602  -10.1078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6037   -8.8703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5877   -9.6953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4602  -11.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1747  -11.3453    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7457  -11.3453    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.6037  -10.5203    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8892  -10.1078    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.3181  -10.1078    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1747  -10.5203    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.3181   -9.2828    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.1027   -9.0278    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0313  -11.7578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7755   -8.6348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 22  5  1  1  0  0  0
 23  6  1  1  0  0  0
 24  7  1  1  0  0  0
  8 17  1  0  0  0  0
  8  9  1  0  0  0  0
  9 19  1  0  0  0  0
 10 13  2  0  0  0  0
 10 18  1  0  0  0  0
 11 20  1  0  0  0  0
 11 14  1  0  0  0  0
 12 21  1  0  0  0  0
 12 15  1  0  0  0  0
 13 22  1  0  0  0  0
 14 23  1  0  0  0  0
 15 24  1  0  0  0  0
 16 18  1  0  0  0  0
 16 17  1  0  0  0  0
 17 22  1  0  0  0  0
 18 25  1  6  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 20 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 26  1  6  0  0  0
 17  4  1  1  0  0  0
 19  3  1  1  0  0  0
 20  2  1  6  0  0  0
 21  1  1  6  0  0  0
M  END

     RDKit          3D

 57 60  0  0  0  0  0  0  0  0999 V2000
   -2.5538    0.6252   -1.3288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4085    0.2347    0.1085 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7876    1.3317    0.8941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3660    1.5792    0.5124 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4541    0.3393    0.3418 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2669   -0.7518   -0.4133 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5917   -1.9569   -0.5450 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9817   -1.8528   -0.0527 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6671   -0.5369   -0.2415 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6622   -0.5524   -1.3789 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4619   -0.2743    1.0299 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3251    0.9350    0.9109 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9331    1.1396    2.1604 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4703    2.0973    0.5594 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3233    1.9038   -0.0416 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7350    0.6139   -0.4375 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3194    0.7503   -1.8949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5424   -1.0015    0.3121 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3916   -2.1087   -0.1978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8167   -1.6275   -0.0120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7178   -0.2538    0.6556 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9112    0.5463    0.2011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7495   -0.3443    2.0322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4669   -0.2497   -2.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9502    1.4887   -1.6348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6226    0.9606   -1.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3635    2.2750    0.6638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9141    1.1994    2.0010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3325    2.2498   -0.3708 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1024    2.1682    1.3465 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7579   -0.0756    1.3241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5305   -0.4106   -1.4459 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0845   -2.7802    0.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5781   -2.3661   -1.5986 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5977   -2.6140   -0.6180 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0359   -2.2158    1.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5815   -1.1171   -1.1421 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2473   -0.9929   -2.3048 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9528    0.5074   -1.5701 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7312   -0.1085    1.8386 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0750   -1.1842    1.2475 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1027    0.7437    0.1371 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4921    1.9646    2.1318 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8185    3.1203    0.8128 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7183    2.7963   -0.2852 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3942    1.3023   -2.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1275    1.3164   -2.4049 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2434   -0.2163   -2.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3314   -1.0714    1.4071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2715   -2.9800    0.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1703   -2.4531   -1.2051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4163   -2.2933    0.6201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2394   -1.4822   -1.0296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6945    1.6343    0.1130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7227    0.4076    0.9579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3206    0.1216   -0.7373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7066   -0.4803    2.2880 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  1
 21  2  1  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  6
  2 18  1  0
 16  5  1  0
  6 18  1  0
 16  9  1  0
 18 49  1  1
 19 50  1  0
 19 51  1  0
 20 52  1  0
 20 53  1  0
 22 54  1  0
 22 55  1  0
 22 56  1  0
 23 57  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  1
  6 32  1  6
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
 10 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  6
 13 43  1  0
 14 44  1  0
 15 45  1  0
 17 46  1  0
 17 47  1  0
 17 48  1  0
M  END


  Mrv0541 02231220322D          

 26 29  0  0  1  0            999 V2000
    9.5024  -10.8741    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9220  -10.9039    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5184   -9.6814    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2064  -12.0569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1747   -9.6953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2737   -8.4705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8715   -8.1214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8892  -11.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6037  -11.3453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7457  -10.5203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8892   -9.2828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1027  -10.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4602  -10.1078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6037   -8.8703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5877   -9.6953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4602  -11.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1747  -11.3453    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7457  -11.3453    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.6037  -10.5203    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8892  -10.1078    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.3181  -10.1078    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1747  -10.5203    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.3181   -9.2828    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.1027   -9.0278    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0313  -11.7578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7755   -8.6348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 22  5  1  1  0  0  0
 23  6  1  1  0  0  0
 24  7  1  1  0  0  0
  8 17  1  0  0  0  0
  8  9  1  0  0  0  0
  9 19  1  0  0  0  0
 10 13  2  0  0  0  0
 10 18  1  0  0  0  0
 11 20  1  0  0  0  0
 11 14  1  0  0  0  0
 12 21  1  0  0  0  0
 12 15  1  0  0  0  0
 13 22  1  0  0  0  0
 14 23  1  0  0  0  0
 15 24  1  0  0  0  0
 16 18  1  0  0  0  0
 16 17  1  0  0  0  0
 17 22  1  0  0  0  0
 18 25  1  6  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 20 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 26  1  6  0  0  0
 17  4  1  1  0  0  0
 19  3  1  1  0  0  0
 20  2  1  6  0  0  0
 21  1  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0087437

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12CC[C@@](C)(O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@]2(C)C[C@H](O)C=C[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C21H34O2/c1-18-9-6-15-16(19(18,2)10-5-14(22)13-18)7-11-20(3)17(15)8-12-21(20,4)23/h5,10,14-17,22-23H,6-9,11-13H2,1-4H3/t14-,15-,16+,17+,18-,19-,20+,21-/m1/s1

> <INCHI_KEY>
NZDUEHZAWOAARB-BWTDTTKRSA-N

> <FORMULA>
C21H34O2

> <MOLECULAR_WEIGHT>
318.4935

> <EXACT_MASS>
318.255880332

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
38.02681019753757

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,5S,7R,10R,11S,14R,15S)-2,7,14,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-3-ene-5,14-diol

> <ALOGPS_LOGP>
4.20

> <JCHEM_LOGP>
3.5783664226666665

> <ALOGPS_LOGS>
-5.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.82449480141571

> <JCHEM_PKA_STRONGEST_BASIC>
-0.489789976974511

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
94.70709999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.02e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5S,7R,10R,11S,14R,15S)-2,7,14,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-3-ene-5,14-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  H   UNK     0      17.738 -20.298   0.000  0.00  0.00           H+0
HETATM    2  H   UNK     0      14.788 -20.354   0.000  0.00  0.00           H+0
HETATM    3  H   UNK     0      15.901 -18.072   0.000  0.00  0.00           H+0
HETATM    4  C   UNK     0      13.452 -22.506   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.393 -18.098   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      17.311 -15.812   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      18.427 -15.160   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.727 -21.948   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      16.060 -21.178   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.725 -19.638   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.727 -17.328   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.858 -19.344   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.059 -18.868   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.060 -16.558   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      19.764 -18.098   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.059 -21.948   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.393 -21.178   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.725 -21.178   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.060 -19.638   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.727 -18.868   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      17.394 -18.868   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.393 -19.638   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      17.394 -17.328   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      18.858 -16.852   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.392 -21.948   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      20.114 -16.118   0.000  0.00  0.00           O+0
CONECT    1   21                                                            
CONECT    2   20                                                            
CONECT    3   19                                                            
CONECT    4   17                                                            
CONECT    5   22                                                            
CONECT    6   23                                                            
CONECT    7   24                                                            
CONECT    8   17    9                                                       
CONECT    9    8   19                                                       
CONECT   10   13   18                                                       
CONECT   11   20   14                                                       
CONECT   12   21   15                                                       
CONECT   13   10   22                                                       
CONECT   14   11   23                                                       
CONECT   15   12   24                                                       
CONECT   16   18   17                                                       
CONECT   17    8   16   22    4                                             
CONECT   18   10   16   25                                                  
CONECT   19    9   20   21    3                                             
CONECT   20   11   19   22    2                                             
CONECT   21   12   19   23    1                                             
CONECT   22    5   13   17   20                                             
CONECT   23    6   14   21   24                                             
CONECT   24    7   15   23   26                                             
CONECT   25   18                                                            
CONECT   26   24                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Value	Source
(3a,5b,17a)-17-Methyl-androst-1-ene-3,17-diol	HMDB
17-Epimetendiol	HMDB
17b-Methyl-5b-androst-1-ene-3a,17a-diol	HMDB

Chemical Formula

C₂₁H₃₄O₂

Average Mass

318.4935 Da

Monoisotopic Mass

318.25588 Da

IUPAC Name

(1S,2R,5S,7R,10R,11S,14R,15S)-2,7,14,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-3-ene-5,14-diol

Traditional Name

(1S,2R,5S,7R,10R,11S,14R,15S)-2,7,14,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-3-ene-5,14-diol

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC[C@@](C)(O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@]2(C)C[C@H](O)C=C[C@]12C

InChI Identifier

InChI=1S/C21H34O2/c1-18-9-6-15-16(19(18,2)10-5-14(22)13-18)7-11-20(3)17(15)8-12-21(20,4)23/h5,10,14-17,22-23H,6-9,11-13H2,1-4H3/t14-,15-,16+,17+,18-,19-,20+,21-/m1/s1

InChI Key

NZDUEHZAWOAARB-BWTDTTKRSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anser anser	FooDB	FooDB
Bison bison	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Dromaius novaehollandiae	FooDB	FooDB
Equus caballus	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Lagopus muta	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Melanitta fusca	FooDB	FooDB
Meleagris gallopavo	FooDB	FooDB
Numida meleagris	FooDB	FooDB
Odocoileus	FooDB	FooDB
Oryctolagus	FooDB	FooDB
Ovis aries	FooDB	FooDB
Phasianidae	FooDB	FooDB
Phasianus colchicus	FooDB	FooDB
Struthio camelus	FooDB	FooDB
Sus scrofa	FooDB	FooDB
Sus scrofa domestica	FooDB	FooDB

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
3-hydroxy-delta-1-steroid
Delta-1-steroid
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

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	4.2	ALOGPS
logP	3.58	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	17.82	ChemAxon
pKa (Strongest Basic)	-0.49	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	94.71 m³·mol⁻¹	ChemAxon
Polarizability	38.03 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

External Links

HMDB ID

HMDB0006012

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB023801

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53477798

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Epimetendiol (NP0087437)

MOL for NP0087437 (Epimetendiol)

3D MOL for NP0087437 (Epimetendiol)

3D SDF for NP0087437 (Epimetendiol)

3D-SDF for NP0087437 (Epimetendiol)

PDB for NP0087437 (Epimetendiol)

3D PDB for NP0087437 (Epimetendiol)

SMILES for NP0087437 (Epimetendiol)

INCHI for NP0087437 (Epimetendiol)

Structure for NP0087437 (Epimetendiol)

3D Structure for NP0087437 (Epimetendiol)