NP-MRD: Showing NP-Card for 7a-Hydroxy-5b-cholanic acid (NP0086978)

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Record Information

Version

2.0

Created at

2022-05-11 16:36:18 UTC

Updated at

2022-05-11 16:36:18 UTC

NP-MRD ID

NP0086978

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7a-Hydroxy-5b-cholanic acid

Description

7A-Hydroxy-5b-cholanic acid, also known as 3-deoxy-cdca or 7a-hydroxy-5b-cholan-24-Oate, belongs to the class of organic compounds known as monohydroxy bile acids, alcohols and derivatives. These are bile acids, alcohols or any of their derivatives bearing a hydroxyl group. 7A-Hydroxy-5b-cholanic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02231219322D          

 32 35  0  0  1  0            999 V2000
   25.4463  -15.8829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.5925  -10.4377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.8871  -11.8359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.4283  -14.2070    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   25.4283  -13.3819    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   24.7139  -14.6195    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.9994  -14.2070    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.2486  -14.6251    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   26.2090  -13.1306    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   24.7139  -12.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.2420  -15.4844    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   23.9994  -13.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2090  -14.4583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.7271  -15.4787    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.6905  -13.7945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.9862  -15.9141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4839  -14.1597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.4283  -12.5569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4653  -12.3463    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   22.4702  -15.9380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.2550  -13.8001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.7020  -14.5953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.6950  -15.4904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.2726  -12.1762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.9143  -11.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.5289  -11.3920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.3362  -11.2219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.4982  -14.8633    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   25.2880  -14.9450    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   24.5710  -13.8770    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   26.8611  -13.0281    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   23.2445  -16.1444    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 14  1  1  6  0  0  0
  2 27  1  0  0  0  0
  3 27  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  4 13  1  0  0  0  0
  4 28  1  6  0  0  0
  5  9  1  0  0  0  0
  5 10  1  0  0  0  0
  5 18  1  1  0  0  0
  6  7  1  0  0  0  0
  6 14  1  0  0  0  0
  6 29  1  1  0  0  0
  7  8  1  0  0  0  0
  7 12  1  0  0  0  0
  7 30  1  6  0  0  0
  8 11  1  0  0  0  0
  8 17  1  0  0  0  0
  8 21  1  1  0  0  0
  9 15  1  0  0  0  0
  9 19  1  0  0  0  0
  9 31  1  6  0  0  0
 10 12  1  0  0  0  0
 11 16  1  0  0  0  0
 11 20  1  0  0  0  0
 11 32  1  1  0  0  0
 13 15  1  0  0  0  0
 14 16  1  0  0  0  0
 17 22  1  0  0  0  0
 19 24  1  0  0  0  0
 19 25  1  6  0  0  0
 20 23  1  0  0  0  0
 22 23  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 67 70  0  0  0  0  0  0  0  0999 V2000
    4.2423   -2.1007   -1.0662 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5057   -0.7929   -0.8713 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4109    0.1809   -0.2191 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7027    0.2482   -1.0597 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6781    1.1914   -0.5136 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3398    2.4075   -0.3442 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9669    0.7278   -0.1902 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2144   -1.0554   -0.2641 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2859   -1.7398    1.1110 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9367   -1.4340    1.7840 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1768   -0.8148    0.6780 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0733   -0.1214    0.9891 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6587    0.3814   -0.2900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6736    1.3856   -0.8570 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6219    0.6439   -1.2032 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2550    0.0381    0.0085 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7075    1.0392    1.0201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0546    0.9306   -0.1818 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8554    2.4659   -0.1779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6479    0.6794   -1.5612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1222    0.6077   -1.5906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4635   -0.5682   -0.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2399   -0.0055    0.6979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8616    0.5453    0.9644 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2355   -0.3686    1.9918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0477   -1.1342    1.5398 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2896   -2.1955    0.7231 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0771   -2.2163   -0.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5665   -2.2308   -2.1190 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5567   -2.9779   -0.8716 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3173   -0.3909   -1.9128 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7341   -0.1858    0.7665 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0488    1.2302   -0.2069 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1154   -0.7310   -1.2802 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3388    0.6599   -2.0513 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2721    0.9152    0.7707 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6702   -1.8090   -0.9081 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1035   -1.3211    1.7118 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3372   -2.8367    0.9721 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0572   -0.8228    2.6848 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4355   -2.3800    2.0916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0510   -1.6180   -0.0769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0198    0.7107    1.6899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6071   -0.4915   -1.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0260    1.8287   -1.8051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3698    2.1539   -0.1131 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4516   -0.1653   -1.9440 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579    1.3966   -1.7144 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5690    0.6544    1.6289 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9404    2.0418    0.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9300    1.2891    1.7954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8756    2.8578    0.1215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6697    2.8543   -1.1729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1799    2.7754    0.6128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2691   -0.3079   -1.9647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3095    1.4262   -2.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4447    0.2932   -2.5901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6342    1.5320   -1.2506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8238   -1.4051   -0.9396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5468   -0.7836   -0.7629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5342   -0.8148    1.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0597    0.7585    0.8433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0949    1.4792    1.5835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9174    0.1756    2.9307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680   -1.1316    2.3966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5570   -1.5430    2.4725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6425   -2.0114   -0.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  9  1  0
  9 10  1  0
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 11 12  1  0
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 26 27  1  0
 26 25  1  0
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 21 20  1  0
 20 18  1  0
 18 19  1  1
 18 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  1
  8  2  1  0
  2  1  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  7  1  0
  5  6  2  0
 16  8  1  0
 16 11  1  0
 13 12  1  0
 18 24  1  0
  8 37  1  6
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  6
 12 43  1  1
 26 66  1  1
 27 67  1  0
 25 64  1  0
 25 65  1  0
 24 63  1  1
 23 61  1  0
 23 62  1  0
 22 59  1  0
 22 60  1  0
 21 57  1  0
 21 58  1  0
 20 55  1  0
 20 56  1  0
 19 52  1  0
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 19 54  1  0
 13 44  1  6
 14 45  1  0
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 15 47  1  0
 15 48  1  0
 17 49  1  0
 17 50  1  0
 17 51  1  0
  2 31  1  6
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  7 36  1  0
M  END


  Mrv0541 02231219322D          

 32 35  0  0  1  0            999 V2000
   25.4463  -15.8829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.5925  -10.4377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.8871  -11.8359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.4283  -14.2070    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   25.4283  -13.3819    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   24.7139  -14.6195    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.9994  -14.2070    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.2486  -14.6251    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   26.2090  -13.1306    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   24.7139  -12.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.2420  -15.4844    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   23.9994  -13.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2090  -14.4583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.7271  -15.4787    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.6905  -13.7945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.9862  -15.9141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4839  -14.1597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.4283  -12.5569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4653  -12.3463    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   22.4702  -15.9380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.2550  -13.8001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.7020  -14.5953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.6950  -15.4904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.2726  -12.1762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.9143  -11.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.5289  -11.3920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.3362  -11.2219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.4982  -14.8633    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   25.2880  -14.9450    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   24.5710  -13.8770    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   26.8611  -13.0281    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   23.2445  -16.1444    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 14  1  1  6  0  0  0
  2 27  1  0  0  0  0
  3 27  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  4 13  1  0  0  0  0
  4 28  1  6  0  0  0
  5  9  1  0  0  0  0
  5 10  1  0  0  0  0
  5 18  1  1  0  0  0
  6  7  1  0  0  0  0
  6 14  1  0  0  0  0
  6 29  1  1  0  0  0
  7  8  1  0  0  0  0
  7 12  1  0  0  0  0
  7 30  1  6  0  0  0
  8 11  1  0  0  0  0
  8 17  1  0  0  0  0
  8 21  1  1  0  0  0
  9 15  1  0  0  0  0
  9 19  1  0  0  0  0
  9 31  1  6  0  0  0
 10 12  1  0  0  0  0
 11 16  1  0  0  0  0
 11 20  1  0  0  0  0
 11 32  1  1  0  0  0
 13 15  1  0  0  0  0
 14 16  1  0  0  0  0
 17 22  1  0  0  0  0
 19 24  1  0  0  0  0
 19 25  1  6  0  0  0
 20 23  1  0  0  0  0
 22 23  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0086978

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)C[C@]4([H])CCCC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H40O3/c1-15(7-10-21(26)27)17-8-9-18-22-19(11-13-24(17,18)3)23(2)12-5-4-6-16(23)14-20(22)25/h15-20,22,25H,4-14H2,1-3H3,(H,26,27)/t15-,16+,17-,18+,19+,20-,22+,23+,24-/m1/s1

> <INCHI_KEY>
JVMCMMXFADJQKU-MMSVWBHPSA-N

> <FORMULA>
C24H40O3

> <MOLECULAR_WEIGHT>
376.5726

> <EXACT_MASS>
376.297745146

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
45.32274513880917

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R)-4-[(1S,2S,7S,9R,10R,11S,14R,15R)-9-hydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid

> <ALOGPS_LOGP>
4.15

> <JCHEM_LOGP>
5.100024050666667

> <ALOGPS_LOGS>
-5.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.595945249665332

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6066783828608372

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
107.60429999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.13e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7a-hydroxy-5b-cholanate

> <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  O   UNK     0      47.500 -29.648   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      53.373 -19.484   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      53.923 -22.094   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      47.466 -26.520   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      47.466 -24.980   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      46.133 -27.290   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      44.799 -26.520   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      43.397 -27.300   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      48.923 -24.510   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      46.133 -24.210   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      43.385 -28.904   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      44.799 -24.980   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      48.923 -26.989   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      46.157 -28.894   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      49.822 -25.750   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      44.774 -29.706   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      41.970 -26.431   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      47.466 -23.440   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      49.402 -23.046   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      41.944 -29.751   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      43.409 -25.760   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      40.510 -27.245   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      40.497 -28.915   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      50.909 -22.729   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      48.373 -21.900   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      51.387 -21.265   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      52.894 -20.948   0.000  0.00  0.00           C+0
HETATM   28  H   UNK     0      47.597 -27.745   0.000  0.00  0.00           H+0
HETATM   29  H   UNK     0      47.204 -27.897   0.000  0.00  0.00           H+0
HETATM   30  H   UNK     0      45.866 -25.904   0.000  0.00  0.00           H+0
HETATM   31  H   UNK     0      50.141 -24.319   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0      43.390 -30.136   0.000  0.00  0.00           H+0
CONECT    1   14                                                            
CONECT    2   27                                                            
CONECT    3   27                                                            
CONECT    4    5    6   13   28                                             
CONECT    5    4    9   10   18                                             
CONECT    6    4    7   14   29                                             
CONECT    7    6    8   12   30                                             
CONECT    8    7   11   17   21                                             
CONECT    9    5   15   19   31                                             
CONECT   10    5   12                                                       
CONECT   11    8   16   20   32                                             
CONECT   12    7   10                                                       
CONECT   13    4   15                                                       
CONECT   14    1    6   16                                                  
CONECT   15    9   13                                                       
CONECT   16   11   14                                                       
CONECT   17    8   22                                                       
CONECT   18    5                                                            
CONECT   19    9   24   25                                                  
CONECT   20   11   23                                                       
CONECT   21    8                                                            
CONECT   22   17   23                                                       
CONECT   23   20   22                                                       
CONECT   24   19   26                                                       
CONECT   25   19                                                            
CONECT   26   24   27                                                       
CONECT   27    2    3   26                                                  
CONECT   28    4                                                            
CONECT   29    6                                                            
CONECT   30    7                                                            
CONECT   31    9                                                            
CONECT   32   11                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Value	Source
3-Deoxy-cdca	ChEBI
3-DeoxyCDCA	ChEBI
7alpha-Hydroxy-5beta-cholan-24-Oic acid	ChEBI
7alpha-Hydroxy-5beta-cholanic acid	ChEBI
7a-Hydroxy-5b-cholan-24-Oate	Generator
7a-Hydroxy-5b-cholan-24-Oic acid	Generator
7alpha-Hydroxy-5beta-cholan-24-Oate	Generator
7Α-hydroxy-5β-cholan-24-Oate	Generator
7Α-hydroxy-5β-cholan-24-Oic acid	Generator
7a-Hydroxy-5b-cholanate	Generator
7alpha-Hydroxy-5beta-cholanate	Generator
7Α-hydroxy-5β-cholanate	Generator
7Α-hydroxy-5β-cholanic acid	Generator
7a-Hydroxy-5b-cholanoate	HMDB
7a-Hydroxy-5b-cholanoic acid	HMDB
3-Deoxychenodeoxycholate	HMDB
(4R)-4-[(1S,2S,7S,9R,10R,11S,14R,15R)-9-Hydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoate	HMDB
7a-Hydroxy-5b-cholanic acid	Generator

Chemical Formula

C₂₄H₄₀O₃

Average Mass

376.5726 Da

Monoisotopic Mass

376.29775 Da

IUPAC Name

(4R)-4-[(1S,2S,7S,9R,10R,11S,14R,15R)-9-hydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid

Traditional Name

7a-hydroxy-5b-cholanate

CAS Registry Number

Not Available

SMILES

[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)C[C@]4([H])CCCC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCC(O)=O

InChI Identifier

InChI=1S/C24H40O3/c1-15(7-10-21(26)27)17-8-9-18-22-19(11-13-24(17,18)3)23(2)12-5-4-6-16(23)14-20(22)25/h15-20,22,25H,4-14H2,1-3H3,(H,26,27)/t15-,16+,17-,18+,19+,20-,22+,23+,24-/m1/s1

InChI Key

JVMCMMXFADJQKU-MMSVWBHPSA-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 monohydroxy bile acids, alcohols and derivatives. These are bile acids, alcohols or any of their derivatives bearing a hydroxyl group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Monohydroxy bile acids, alcohols and derivatives

Alternative Parents

Substituents

Monohydroxy bile acid, alcohol, or derivatives
7-hydroxysteroid
Hydroxysteroid
Cyclic alcohol
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

7alpha-hydroxy steroid (CHEBI:73676 )
bile acid (CHEBI:73676 )
monohydroxy-5beta-cholanic acid (CHEBI:73676 )
C24 bile acids, alcohols, and derivatives (LMST04010011 )

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	4.15	ALOGPS
logP	5.1	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	4.6	ChemAxon
pKa (Strongest Basic)	-0.61	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	107.6 m³·mol⁻¹	ChemAxon
Polarizability	45.32 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0002492

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB023013

KNApSAcK ID

Not Available

Chemspider ID

394733

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

6700

PubChem Compound

447718

PDB ID

Not Available

ChEBI ID

73676

Good Scents ID

Not Available

References

General References

Showing NP-Card for 7a-Hydroxy-5b-cholanic acid (NP0086978)

MOL for NP0086978 (7a-Hydroxy-5b-cholanic acid)

3D MOL for NP0086978 (7a-Hydroxy-5b-cholanic acid)

3D SDF for NP0086978 (7a-Hydroxy-5b-cholanic acid)

3D-SDF for NP0086978 (7a-Hydroxy-5b-cholanic acid)

PDB for NP0086978 (7a-Hydroxy-5b-cholanic acid)

3D PDB for NP0086978 (7a-Hydroxy-5b-cholanic acid)

SMILES for NP0086978 (7a-Hydroxy-5b-cholanic acid)

INCHI for NP0086978 (7a-Hydroxy-5b-cholanic acid)

Structure for NP0086978 (7a-Hydroxy-5b-cholanic acid)

3D Structure for NP0086978 (7a-Hydroxy-5b-cholanic acid)