NP-MRD: Showing NP-Card for (1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid (NP0326014)

You are using an unsupported browser. Please upgrade your browser to a newer version to get the best experience on NP-MRD.

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 07:12:46 UTC

Updated at

2022-09-12 07:12:47 UTC

NP-MRD ID

NP0326014

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid

Description

CHEMBL3969157 belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid is found in Ziziphus jujuba. Based on a literature review very few articles have been published on CHEMBL3969157.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122209122D          

 44 49  0  0  1  0            999 V2000
    0.5233   -2.3607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1279   -2.9220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9163   -2.6790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9442   -3.7263    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1855   -4.0503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2592   -4.8720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0635   -5.0558    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5685   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8925   -6.4745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2506   -5.6171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4651   -5.7765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2900   -5.7890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7133   -5.0809    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1149   -5.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3117   -4.3603    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7350   -3.6521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5599   -3.6647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9615   -4.3853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7864   -4.3979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3848   -3.6772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2097   -3.6898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0346   -3.7023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4580   -2.9942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0564   -2.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2315   -2.2610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4797   -1.5654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0781   -0.8448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5014   -0.1367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3263   -0.1492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7497    0.5589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7279   -0.8699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5528   -0.8824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3046   -1.5780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4362   -4.4230    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2611   -4.4355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0129   -5.1311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7838   -5.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8573   -5.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1880   -5.1186    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7647   -5.8267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9398   -5.8141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5382   -5.0935    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6119   -5.9152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4868   -4.3477    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 26 33  1  0  0  0  0
 22 34  1  0  0  0  0
 34 35  1  6  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 36 39  1  0  0  0  0
 19 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 18 42  1  0  0  0  0
 13 42  1  0  0  0  0
 42 43  1  6  0  0  0
 15 44  1  0  0  0  0
 44  4  1  6  0  0  0
  7 44  1  0  0  0  0
M  END

     RDKit          3D

 96101  0  0  0  0  0  0  0  0999 V2000
   -3.6370    2.3107   -3.7206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3470    2.0517   -2.6270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8611    3.2015   -1.8486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6333    0.6523   -2.1646 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1504    0.5794   -2.0529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4246    0.3506   -0.5558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2242   -0.5283   -0.2621 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.4698   -1.7904   -0.9670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8139   -2.3275   -1.8584 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6291   -2.4864   -0.5598 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9792   -0.7907    1.1696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6572   -1.5769    1.2087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5330   -0.6147    0.7781 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5772    0.5255    1.7272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8115   -0.2880   -0.6598 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6677    0.4231   -1.2943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4817   -0.5620   -1.2256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1481   -0.6505    0.2346 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2591   -1.1137    0.4977 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6347   -2.3191   -0.2663 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1707    0.0299    0.0213 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5992   -0.1896    0.4346 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3332    0.9294   -0.0205 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4112    0.8352   -0.8863 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7119   -0.3337   -1.2567 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1526    2.0064   -1.3421 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7989    3.2683   -0.9210 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5077    4.3891   -1.3567 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5787    4.2559   -2.2193 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2899    5.3864   -2.6557 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9311    3.0097   -2.6376 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0145    2.8493   -3.5130 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2237    1.8967   -2.2022 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7742   -0.3615    1.9211 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0683   -0.8391    2.1278 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8156   -1.3790    2.4780 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7608   -1.1096    3.9942 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3683   -2.7586    2.3206 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4320   -1.1795    1.9826 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4468   -2.1027    2.6501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9209   -1.4447    2.4556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2142   -1.3671    0.9601 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4642   -2.7779    0.5218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1426    0.3358   -0.8118 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2698    1.4459   -4.2761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4106    3.2847   -4.0784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2227    3.3223   -0.9436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9196    3.1123   -1.5442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7799    4.1439   -2.4193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2563   -0.0143   -2.9666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5426   -0.3409   -2.5548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6734    1.4520   -2.4311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3537    1.3039   -0.0332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3758   -0.1609   -0.4084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4848   -3.2583    0.1048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9769    0.0635    1.8367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7410   -1.5131    1.5802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5101   -1.9801    2.2046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7946   -2.3620    0.4100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6257    1.0785    1.8507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3537    1.2703    1.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7837    0.0848    2.7500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8557   -1.2890   -1.1845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7897    0.6281   -2.3526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3748    1.2955   -0.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2939   -0.1323   -1.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8714   -1.5046   -1.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1606    0.4188    0.6055 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5773   -2.1786   -0.8768 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8486   -2.4723   -1.0664 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8020   -3.2360    0.3055 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1687    0.0965   -1.0896 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8480    0.9986    0.4155 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0707   -1.0756   -0.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9565    3.3688   -0.2429 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2466    5.3757   -1.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0290    6.3135   -2.3455 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5512    3.6256   -3.8509 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5118    0.9034   -2.5412 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6774    0.5770    2.4908 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1596   -1.0903    3.0796 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6479   -0.5692    4.3429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8829   -0.4695    4.2487 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5968   -2.0674    4.5358 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1648   -2.8739    3.1155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6358   -3.5440    2.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9259   -2.9048    1.3639 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1296   -0.1452    2.3467 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6567   -2.0607    3.7417 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4866   -3.1358    2.3309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8349   -0.4545    2.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6371   -2.0539    2.9998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1725   -3.2193    1.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8222   -2.8984   -0.4979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5618   -3.4362    0.6135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2077    1.3101   -0.2376 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  3
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  6
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  2  0
 22 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36 38  1  0
 36 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  6
 15 44  1  0
  7  8  1  6
  8 10  1  0
  8  9  2  0
 44  4  1  0
 44  7  1  0
 42 13  1  0
 42 18  1  0
 39 19  1  0
 33 26  1  0
  3 47  1  0
  3 48  1  0
  3 49  1  0
  1 45  1  0
  1 46  1  0
  4 50  1  6
  5 51  1  0
  5 52  1  0
  6 53  1  0
  6 54  1  0
 11 56  1  0
 11 57  1  0
 12 58  1  0
 12 59  1  0
 14 60  1  0
 14 61  1  0
 14 62  1  0
 15 63  1  6
 16 64  1  0
 16 65  1  0
 17 66  1  0
 17 67  1  0
 18 68  1  1
 20 69  1  0
 20 70  1  0
 20 71  1  0
 21 72  1  0
 21 73  1  0
 22 74  1  6
 27 75  1  0
 28 76  1  0
 30 77  1  0
 32 78  1  0
 33 79  1  0
 34 80  1  1
 35 81  1  0
 37 82  1  0
 37 83  1  0
 37 84  1  0
 38 85  1  0
 38 86  1  0
 38 87  1  0
 39 88  1  1
 40 89  1  0
 40 90  1  0
 41 91  1  0
 41 92  1  0
 43 93  1  0
 43 94  1  0
 43 95  1  0
 44 96  1  1
 10 55  1  0
M  END


  Mrv1652309122209122D          

 44 49  0  0  1  0            999 V2000
    0.5233   -2.3607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1279   -2.9220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9163   -2.6790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9442   -3.7263    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1855   -4.0503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2592   -4.8720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0635   -5.0558    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5685   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8925   -6.4745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2506   -5.6171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4651   -5.7765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2900   -5.7890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7133   -5.0809    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1149   -5.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3117   -4.3603    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7350   -3.6521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5599   -3.6647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9615   -4.3853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7864   -4.3979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3848   -3.6772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2097   -3.6898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0346   -3.7023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4580   -2.9942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0564   -2.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2315   -2.2610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4797   -1.5654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0781   -0.8448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5014   -0.1367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3263   -0.1492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7497    0.5589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7279   -0.8699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5528   -0.8824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3046   -1.5780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4362   -4.4230    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2611   -4.4355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0129   -5.1311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7838   -5.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8573   -5.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1880   -5.1186    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7647   -5.8267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9398   -5.8141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5382   -5.0935    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6119   -5.9152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4868   -4.3477    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 26 33  1  0  0  0  0
 22 34  1  0  0  0  0
 34 35  1  6  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 36 39  1  0  0  0  0
 19 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 18 42  1  0  0  0  0
 13 42  1  0  0  0  0
 42 43  1  6  0  0  0
 15 44  1  0  0  0  0
 44  4  1  6  0  0  0
  7 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0326014

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)[C@@H]1CC[C@@]2(CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)C[C@@H](OC(=O)C6=CC=C(O)C(O)=C6)[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]12)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C37H52O7/c1-20(2)22-12-15-37(32(42)43)17-16-35(6)23(29(22)37)9-11-28-34(5)19-26(44-31(41)21-8-10-24(38)25(39)18-21)30(40)33(3,4)27(34)13-14-36(28,35)7/h8,10,18,22-23,26-30,38-40H,1,9,11-17,19H2,2-7H3,(H,42,43)/t22-,23+,26+,27-,28+,29+,30-,34-,35+,36+,37-/m0/s1

> <INCHI_KEY>
MKDOBXUKRMFQNI-JFJOLGLVSA-N

> <FORMULA>
C37H52O7

> <MOLECULAR_WEIGHT>
608.816

> <EXACT_MASS>
608.371304014

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
96

> <JCHEM_AVERAGE_POLARIZABILITY>
68.23867598514892

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,5S,8R,9R,10R,13R,14R,16R,17R,19R)-16-(3,4-dihydroxybenzoyloxy)-17-hydroxy-1,2,14,18,18-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5-carboxylic acid

> <JCHEM_LOGP>
7.453004678333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.556581421042152

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.748244906549395

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3508671040321305

> <JCHEM_POLAR_SURFACE_AREA>
124.29

> <JCHEM_REFRACTIVITY>
167.77080000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5S,8R,9R,10R,13R,14R,16R,17R,19R)-16-(3,4-dihydroxybenzoyloxy)-17-hydroxy-1,2,14,18,18-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       0.977  -4.407   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.105  -5.454   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.577  -5.001   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.762  -6.956   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.346  -7.561   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.484  -9.094   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.985  -9.438   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.061 -10.670   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.666 -12.086   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -0.468 -10.485   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.735 -10.783   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.275 -10.806   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.065  -9.484   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.814 -10.830   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.315  -8.139   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.105  -6.817   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.645  -6.841   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.395  -8.186   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.935  -8.209   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.185  -6.864   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.725  -6.888   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.265  -6.911   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      12.055  -5.589   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      11.305  -4.244   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.765  -4.221   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      12.095  -2.922   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.346  -1.577   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.136  -0.255   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.676  -0.279   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      14.466   1.043   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      14.425  -1.624   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      15.965  -1.647   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      13.635  -2.946   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      12.014  -8.256   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      13.554  -8.280   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      11.224  -9.578   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      12.663 -10.127   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      10.934 -11.090   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       9.684  -9.555   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.894 -10.876   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.354 -10.853   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       6.605  -9.508   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       6.742 -11.042   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.775  -8.116   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   44                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   11   44                                             
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   42                                             
CONECT   14   13                                                            
CONECT   15   13   16   44                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   42                                                  
CONECT   19   18   20   21   39                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   34                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   33                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   26                                                       
CONECT   34   22   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38   39                                             
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   36   19   40                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   18   13   43                                             
CONECT   43   42                                                            
CONECT   44   15    4    7                                                  
MASTER        0    0    0    0    0    0    0    0   44    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₅₂O₇

Average Mass

608.8160 Da

Monoisotopic Mass

608.37130 Da

IUPAC Name

(1R,2R,5S,8R,9R,10R,13R,14R,16R,17R,19R)-16-(3,4-dihydroxybenzoyloxy)-17-hydroxy-1,2,14,18,18-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5-carboxylic acid

Traditional Name

(1R,2R,5S,8R,9R,10R,13R,14R,16R,17R,19R)-16-(3,4-dihydroxybenzoyloxy)-17-hydroxy-1,2,14,18,18-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(=C)[C@@H]1CC[C@@]2(CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)C[C@@H](OC(=O)C6=CC=C(O)C(O)=C6)[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]12)C(O)=O

InChI Identifier

InChI=1S/C37H52O7/c1-20(2)22-12-15-37(32(42)43)17-16-35(6)23(29(22)37)9-11-28-34(5)19-26(44-31(41)21-8-10-24(38)25(39)18-21)30(40)33(3,4)27(34)13-14-36(28,35)7/h8,10,18,22-23,26-30,38-40H,1,9,11-17,19H2,2-7H3,(H,42,43)/t22-,23+,26+,27-,28+,29+,30-,34-,35+,36+,37-/m0/s1

InChI Key

MKDOBXUKRMFQNI-JFJOLGLVSA-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

Species Name	Source	Reference
Ziziphus jujuba	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
18-oxosteroid
18-hydroxysteroid
Hydroxysteroid
Oxosteroid
Steroid
M-hydroxybenzoic acid ester
P-hydroxybenzoic acid ester
Dihydroxybenzoic acid
P-hydroxybenzoic acid alkyl ester
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Catechol
Phenol
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Cyclic alcohol
Carboxylic acid ester
Secondary alcohol
Carboxylic acid
Carboxylic acid derivative
Organooxygen compound
Carbonyl group
Alcohol
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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	7.45	ChemAxon
pKa (Strongest Acidic)	4.75	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	124.29 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	167.77 m³·mol⁻¹	ChemAxon
Polarizability	68.24 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00057168

Chemspider ID

76781939

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102247122

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid (NP0326014)

MOL for NP0326014 ((1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

3D MOL for NP0326014 ((1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

3D SDF for NP0326014 ((1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

3D-SDF for NP0326014 ((1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

PDB for NP0326014 ((1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

3D PDB for NP0326014 ((1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

SMILES for NP0326014 ((1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

INCHI for NP0326014 ((1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

Structure for NP0326014 ((1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

3D Structure for NP0326014 ((1r,3as,5ar,5br,7ar,9r,10r,11ar,11br,13ar,13br)-10-(3,4-dihydroxybenzoyloxy)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)