NP-MRD: Showing NP-Card for methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate (NP0296554)

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Record Information

Version

1.0

Created at

2022-09-10 06:11:59 UTC

Updated at

2022-09-10 06:11:59 UTC

NP-MRD ID

NP0296554

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate

Description

Methyl 25-hydroxy-3-epidehydrotumulosate belongs to the class of organic compounds known as trihydroxy bile acids, alcohols and derivatives. These are prenol lipids structurally characterized by a bile acid or alcohol which bears three hydroxyl groups. Based on a literature review very few articles have been published on methyl 25-hydroxy-3-epidehydrotumulosate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102208122D          

 37 40  0  0  1  0            999 V2000
    0.1102   -2.8023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4211   -3.5665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383   -3.6793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7447   -3.0280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5619   -3.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8728   -3.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3665   -4.5563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6900   -4.0179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0009   -4.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8390   -1.6970    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0630   -1.4167    0.0000 O   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  1  0  0  0  0  0  0  0  0  0
    4.3708   -0.9394    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  1  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
    7.1376   -0.3850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1351   -0.7453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.7902    0.0000 C   0  0  2  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  1  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  2  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
   -0.0853   -4.2178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5916   -4.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7366   -3.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5660   -4.7241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  5  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 16 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 10 32  1  0  0  0  0
 14 32  1  0  0  0  0
 32 33  1  1  0  0  0
  2 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 34 37  1  0  0  0  0
M  END

     RDKit          3D

 87 90  0  0  0  0  0  0  0  0999 V2000
    6.4936    0.0115   -2.1337 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0925    0.3815   -0.9354 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7918    0.0035   -0.3619 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0172   -0.7855   -1.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6574   -1.2328   -0.8174 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9796   -2.0532    0.3502 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6738   -1.7782    1.5181 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6831   -3.2288    0.1283 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0357   -4.0784    1.1999 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7429   -0.0869   -0.6271 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5860    0.5506   -2.0201 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9302    1.8744   -2.0469 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0951    0.3140   -2.3191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4856    0.5482   -0.9928 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4519    1.9985   -0.6378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8545    0.0437   -0.7669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6044   -0.4333   -1.7201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9725   -0.9037   -1.3173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4782    0.1519   -0.3504 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9597    0.2054   -0.2228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5504    1.4073   -0.9745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6021   -1.0183   -0.8483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4459    0.3081    1.1969 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.7439    0.8661    1.1311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6338    1.1848    2.0768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1856    1.2793    1.7750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7475    0.0791    0.9670 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0331   -1.1567    1.7560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2887    0.1315    0.6348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3550    0.2475    1.5433 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1143    0.2989    1.2941 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4111   -0.3110   -0.0775 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0617   -1.7281   -0.0093 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0101    1.2378   -0.1020 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2443    2.5258    0.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3172    0.5009    1.1827 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1811    1.5072   -0.7875 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8412   -0.6034   -2.7374 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4797    0.3153   -2.5343 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2857    0.9452   -0.0610 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9105   -0.6476    0.5438 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9563   -0.2135   -2.2835 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5789   -1.7201   -1.5691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2570   -1.8750   -1.6588 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3768   -4.9688    1.1298 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9603   -3.5762    2.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0705   -4.4364    1.0080 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2719    0.6576    0.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1028   -0.0108   -2.8109 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6284    2.0782   -1.3835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0306   -0.7205   -2.6864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2476    1.0496   -3.0614 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4976    2.4012   -0.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2816    2.2612    0.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7272    2.5677   -1.5738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2692   -0.4900   -2.7380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6379   -0.9203   -2.1958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8336   -1.8852   -0.8483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1597    1.1395   -0.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7750    2.2288   -0.2450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7460    1.8058   -1.6324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4120    1.1386   -1.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7148   -0.7999   -1.9488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6593   -1.1188   -0.4731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0634   -1.9466   -0.6664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6096   -0.7178    1.6178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3990    0.3714    1.6462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8005    0.8389    3.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0528    2.2338    2.0768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0015    2.1732    1.1434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6300    1.3666    2.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5075   -0.9104    2.7518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5833   -1.9373    1.2185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0567   -1.6397    2.0578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6949    0.3138    2.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5189    1.3177    1.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5587   -0.2923    2.1170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0580   -1.8891   -0.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6230   -2.4553   -0.4812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1802   -2.0903    1.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7493    2.8132   -0.7748 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9072    3.3171    0.5721 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4534    2.3312    0.9263 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3593    0.6144    1.5016 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6283    0.8469    2.0058 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1282   -0.5938    1.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3855    2.4696   -0.8402 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  6  1  0
  6  7  2  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 34  1  0
 34 35  1  0
 34 36  1  0
 34 37  1  0
  5 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  1
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  1
 27 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  1  0
 32 33  1  1
 32 10  1  0
 32 14  1  0
 29 16  1  0
 27 19  1  0
  9 45  1  0
  9 46  1  0
  9 47  1  0
  5 44  1  6
  4 42  1  0
  4 43  1  0
  3 40  1  0
  3 41  1  0
  1 38  1  0
  1 39  1  0
 35 81  1  0
 35 82  1  0
 35 83  1  0
 36 84  1  0
 36 85  1  0
 36 86  1  0
 37 87  1  0
 10 48  1  1
 11 49  1  6
 12 50  1  0
 13 51  1  0
 13 52  1  0
 15 53  1  0
 15 54  1  0
 15 55  1  0
 17 56  1  0
 18 57  1  0
 18 58  1  0
 19 59  1  6
 21 60  1  0
 21 61  1  0
 21 62  1  0
 22 63  1  0
 22 64  1  0
 22 65  1  0
 23 66  1  1
 24 67  1  0
 25 68  1  0
 25 69  1  0
 26 70  1  0
 26 71  1  0
 28 72  1  0
 28 73  1  0
 28 74  1  0
 30 75  1  0
 31 76  1  0
 31 77  1  0
 33 78  1  0
 33 79  1  0
 33 80  1  0
M  END


  Mrv1652309102208122D          

 37 40  0  0  1  0            999 V2000
    0.1102   -2.8023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4211   -3.5665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383   -3.6793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7447   -3.0280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5619   -3.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8728   -3.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3665   -4.5563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6900   -4.0179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0009   -4.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8390   -1.6970    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0630   -1.4167    0.0000 O   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  1  0  0  0  0  0  0  0  0  0
    4.3708   -0.9394    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  1  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
    7.1376   -0.3850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1351   -0.7453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.7902    0.0000 C   0  0  2  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  1  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  2  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
   -0.0853   -4.2178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5916   -4.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7366   -3.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5660   -4.7241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  5  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 16 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 10 32  1  0  0  0  0
 14 32  1  0  0  0  0
 32 33  1  1  0  0  0
  2 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 34 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0296554

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C(CCC(=C)C(C)(C)O)[C@H]1[C@H](O)C[C@@]2(C)C3=CC[C@H]4C(C)(C)[C@H](O)CC[C@]4(C)C3=CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C32H50O5/c1-19(29(4,5)36)10-11-20(27(35)37-9)26-23(33)18-32(8)22-12-13-24-28(2,3)25(34)15-16-30(24,6)21(22)14-17-31(26,32)7/h12,14,20,23-26,33-34,36H,1,10-11,13,15-18H2,2-9H3/t20?,23-,24+,25-,26+,30-,31-,32+/m1/s1

> <INCHI_KEY>
QYINWYSAHKZFTN-HSTXRIAUSA-N

> <FORMULA>
C32H50O5

> <MOLECULAR_WEIGHT>
514.747

> <EXACT_MASS>
514.36582471

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
87

> <JCHEM_AVERAGE_POLARIZABILITY>
60.66226788793938

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-[(2S,5R,7R,11R,13R,14R,15R)-5,13-dihydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),9-dien-14-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate

> <JCHEM_LOGP>
4.147351082000001

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.33356925462635

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.872239460561776

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6733500436281815

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
148.87240000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-[(2S,5R,7R,11R,13R,14R,15R)-5,13-dihydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),9-dien-14-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       0.206  -5.231   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.786  -6.657   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.312  -6.868   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.257  -5.652   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.782  -5.863   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.363  -7.289   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.417  -8.505   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       6.888  -7.500   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       7.468  -8.926   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.727  -4.647   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.299  -3.168   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.851  -2.645   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.574  -2.304   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.790  -3.249   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.159  -1.754   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.306  -2.978   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.829  -1.529   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.345  -1.258   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.338  -2.436   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.854  -2.164   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.323  -0.719   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      15.185  -1.391   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.846  -3.342   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      16.362  -3.071   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      14.323  -4.790   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.807  -5.061   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.814  -3.884   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.291  -5.332   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.299  -4.155   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.775  -5.603   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.259  -5.874   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.267  -4.697   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.595  -6.083   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.159  -7.873   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.104  -9.089   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -1.375  -6.928   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       1.057  -8.818   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   34                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8                                                            
CONECT   10    5   11   32                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16   32                                             
CONECT   15   14                                                            
CONECT   16   14   17   29                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   27                                                  
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   19   28   29                                             
CONECT   28   27                                                            
CONECT   29   27   16   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   10   14   33                                             
CONECT   33   32                                                            
CONECT   34    2   35   36   37                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   34                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

View in JSmol

Synonyms

Value	Source
Methyl 25-hydroxy-3-epidehydrotumulosic acid	Generator

Chemical Formula

C₃₂H₅₀O₅

Average Mass

514.7470 Da

Monoisotopic Mass

514.36582 Da

IUPAC Name

methyl 2-[(2S,5R,7R,11R,13R,14R,15R)-5,13-dihydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),9-dien-14-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate

Traditional Name

methyl 2-[(2S,5R,7R,11R,13R,14R,15R)-5,13-dihydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),9-dien-14-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate

CAS Registry Number

Not Available

SMILES

COC(=O)C(CCC(=C)C(C)(C)O)[C@H]1[C@H](O)C[C@@]2(C)C3=CC[C@H]4C(C)(C)[C@H](O)CC[C@]4(C)C3=CC[C@]12C

InChI Identifier

InChI=1S/C32H50O5/c1-19(29(4,5)36)10-11-20(27(35)37-9)26-23(33)18-32(8)22-12-13-24-28(2,3)25(34)15-16-30(24,6)21(22)14-17-31(26,32)7/h12,14,20,23-26,33-34,36H,1,10-11,13,15-18H2,2-9H3/t20?,23-,24+,25-,26+,30-,31-,32+/m1/s1

InChI Key

QYINWYSAHKZFTN-HSTXRIAUSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as trihydroxy bile acids, alcohols and derivatives. These are prenol lipids structurally characterized by a bile acid or alcohol which bears three hydroxyl groups.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Trihydroxy bile acids, alcohols and derivatives

Alternative Parents

Substituents

Triterpenoid
Ergostane-skeleton
Ergosterol-skeleton
Trihydroxy bile acid, alcohol, or derivatives
25-hydroxysteroid
3-hydroxy-delta-7-steroid
3-hydroxysteroid
14-alpha-methylsteroid
3-alpha-hydroxysteroid
16-hydroxysteroid
16-alpha-hydroxysteroid
Hydroxysteroid
Delta-7-steroid
Cyclic alcohol
Methyl ester
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen compound
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	4.15	ChemAxon
pKa (Strongest Acidic)	14.87	ChemAxon
pKa (Strongest Basic)	-0.67	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	148.87 m³·mol⁻¹	ChemAxon
Polarizability	60.66 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78442479

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139583733

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate (NP0296554)

MOL for NP0296554 (methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate)

3D MOL for NP0296554 (methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate)

3D SDF for NP0296554 (methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate)

3D-SDF for NP0296554 (methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate)

PDB for NP0296554 (methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate)

3D PDB for NP0296554 (methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate)

SMILES for NP0296554 (methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate)

INCHI for NP0296554 (methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate)

Structure for NP0296554 (methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate)

3D Structure for NP0296554 (methyl 2-[(1r,2r,3ar,5ar,7r,9as,11ar)-2,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methyl-5-methylideneheptanoate)