NP-MRD: Showing NP-Card for (2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate (NP0167253)

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Record Information

Version

2.0

Created at

2022-09-03 02:47:55 UTC

Updated at

2022-09-03 02:47:55 UTC

NP-MRD ID

NP0167253

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate

Description

(2R,3R)-2,6-bis(acetyloxy)-6-methyl-2-[(1R,2R,4S,5R,7R,11S,14S,15R)-4,5,11-tris(acetyloxy)-2,15-dimethyl-8-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-9-en-14-yl]heptan-3-yl acetate belongs to the class of organic compounds known as bile acids, alcohols and derivatives. These are organic compounds containing an alcohol or acid derivative of cholic acid. (2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate is found in Tinospora cordifolia. Based on a literature review very few articles have been published on (2R,3R)-2,6-bis(acetyloxy)-6-methyl-2-[(1R,2R,4S,5R,7R,11S,14S,15R)-4,5,11-tris(acetyloxy)-2,15-dimethyl-8-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-9-en-14-yl]heptan-3-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032204472D          

 52 55  0  0  1  0            999 V2000
    8.0466   -1.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5148   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7951    0.0722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7026   -0.8489    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1708   -0.2182    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3587   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269    0.2673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5466   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.0432    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9193    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4511    0.5577    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2632    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5435    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3557    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0117    2.1096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8557    2.4498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4830    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0148    0.1221    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7345   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9224   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3905   -0.1684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0307   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5660   -0.1416    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0596   -0.7929    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7109   -1.2992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5533   -1.4442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8642   -2.2084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6814   -2.3212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3578   -2.8597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083   -0.2865    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3559   -0.5974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0072   -0.0911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7714   -0.4020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0823    0.3622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4605   -1.1661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5356   -0.7128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1869   -0.2065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9511   -0.5174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0741    0.6108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5211    0.5307    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1302    1.0371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0173    1.8543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8944    0.7262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3367    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6708    0.6076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8685    1.4085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2737    1.9802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4812    1.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4713    2.7812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  9 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 20 19  1  1  0  0  0
  7 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  6  0  0  0
 26 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 35 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 32 42  1  1  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  2  0  0  0  0
 25 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 19 48  1  0  0  0  0
 23 48  1  0  0  0  0
 48 49  1  6  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  2  0  0  0  0
M  END

     RDKit          3D

108111  0  0  0  0  0  0  0  0999 V2000
    7.2544    4.8254   -0.3076 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5951    3.7583    0.4685 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6542    3.8211    1.7241 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9235    2.7042   -0.0816 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2823    1.6645    0.6861 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8224    1.6669    0.5292 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2174    0.6008   -0.3400 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4522    1.2702   -1.4558 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2867   -0.2157   -1.0333 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2349   -0.7599   -0.0342 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0546    0.4292    0.4549 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1039    0.5705   -0.4782 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3883    0.2748   -0.1363 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5475    0.4048   -1.0835 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6394   -0.1294    1.0267 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6761   -1.1589   -1.9613 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2285   -1.4166   -3.0603 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4092   -1.7695   -1.5367 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7716   -1.3674   -0.4618 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2872   -0.3053    0.4112 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2246    0.4578    1.1588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0448   -0.2809    1.4130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5587   -0.9859    0.2165 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6576   -0.1550   -1.0309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6666   -1.9372    0.4363 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9053   -1.5991    1.1001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6519   -2.9435    1.2798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6989   -1.1087    2.3618 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5334   -0.9295    3.4169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0772   -0.3609    4.7358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7337   -1.2592    3.2641 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7089    0.7083    0.6552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6844    1.7691    0.2718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0335    2.0310   -1.1152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8174    2.3837   -1.9956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0030    1.1254   -1.7736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7020    3.3396   -1.1123 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8451    3.6093   -0.4448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3715    5.0215   -0.5632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4281    2.7500    0.2253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0833   -1.2510   -0.8540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0773   -2.0254   -1.3986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0508   -2.5498   -2.7854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9960   -2.2314   -0.5914 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6780   -2.6757   -0.8619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1754   -2.7756   -1.2093 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5235   -2.0320   -0.1145 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6642   -2.8366    1.0594 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3660   -4.0233    1.0826 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4810   -4.8396    2.3495 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9094   -4.4099    0.0204 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9304    5.8410   -0.0036 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1054    4.6901   -1.3868 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3548    4.7208   -0.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5238    2.6832    0.1443 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3021    1.6057    1.5180 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1391    2.0330   -1.9521 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5717    1.8259   -1.1632 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2276    0.5698   -2.2887 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8610    0.5319   -1.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7917   -1.2324    0.8526 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9542   -1.4986   -0.4546 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5290    0.0583    1.4092 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0985   -0.5464   -1.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1784    1.2840   -0.8095 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1781    0.5533   -2.1178 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0414   -2.5771   -2.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8506   -0.8638    1.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9413    1.4091    0.6635 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6441    0.6684    2.1910 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1198   -1.0224    2.2131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7589    0.4833    1.8233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5739    0.9057   -0.7118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6369   -0.2286   -1.5386 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1022   -0.3434   -1.7902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2049   -2.7228    1.1405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9999   -3.6163    1.9046 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7236   -3.4564    0.2999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2014   -1.1657    5.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9976   -0.1379    4.6260 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.9435    5.0280   -1.5258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0667    5.2425    0.2593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2179   -3.2454   -2.9660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9909   -3.1622   -2.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1109   -1.7187   -3.4913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0090   -3.7289   -0.7141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1390   -2.1905   -1.7090 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0460   -2.3019   -2.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1274   -3.8388   -1.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6217   -5.5476    2.3141 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3276   -4.1581    3.1888 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4224   -5.3976    2.3729 H   0  0  0  0  0  0  0  0  0  0  0  0
 44 43  1  0
 43 45  2  0
 43 42  1  0
 42 32  1  0
 32 33  1  0
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 35 37  1  0
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 39 41  2  0
 32 26  1  0
 26 27  1  0
 26 28  1  1
 28 29  1  0
 29 30  1  0
 29 31  2  0
 26 25  1  0
 25 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  1
 49 50  1  0
 50 51  1  0
 50 52  2  0
 48 19  1  0
 19 18  2  0
 18 16  1  0
 16 17  2  0
 16  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 11  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  6
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 23 25  1  0
 23 48  1  0
 20 19  1  0
  7  9  1  0
 44 99  1  0
 44100  1  0
 44101  1  0
 32 85  1  1
 33 86  1  0
 33 87  1  0
 34 88  1  0
 34 89  1  0
 36 90  1  0
 36 91  1  0
 36 92  1  0
 37 93  1  0
 37 94  1  0
 37 95  1  0
 40 96  1  0
 40 97  1  0
 40 98  1  0
 27 79  1  0
 27 80  1  0
 27 81  1  0
 30 82  1  0
 30 83  1  0
 30 84  1  0
 25 78  1  1
 46102  1  0
 46103  1  0
 47104  1  0
 47105  1  0
 51106  1  0
 51107  1  0
 51108  1  0
 18 69  1  0
  9 62  1  6
 10 63  1  0
 10 64  1  0
 11 65  1  1
 14 66  1  0
 14 67  1  0
 14 68  1  0
  5 56  1  1
  6 57  1  0
  6 58  1  0
  8 59  1  0
  8 60  1  0
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 20 70  1  1
 21 71  1  0
 21 72  1  0
 22 73  1  0
 22 74  1  0
 24 75  1  0
 24 76  1  0
 24 77  1  0
  1 53  1  0
  1 54  1  0
  1 55  1  0
M  END


  Mrv1652309032204472D          

 52 55  0  0  1  0            999 V2000
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    7.5148   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7951    0.0722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7026   -0.8489    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1708   -0.2182    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3587   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269    0.2673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5466   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.0432    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9193    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4511    0.5577    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2632    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5435    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3557    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0117    2.1096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8557    2.4498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4830    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0148    0.1221    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7345   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9224   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3905   -0.1684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0307   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5660   -0.1416    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0596   -0.7929    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7109   -1.2992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5533   -1.4442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8642   -2.2084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6814   -2.3212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3578   -2.8597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083   -0.2865    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3559   -0.5974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0072   -0.0911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7714   -0.4020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0823    0.3622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4605   -1.1661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5356   -0.7128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1869   -0.2065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9511   -0.5174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0741    0.6108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5211    0.5307    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1302    1.0371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0173    1.8543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8944    0.7262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3367    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6708    0.6076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8685    1.4085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2737    1.9802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4812    1.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4713    2.7812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  9 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 20 19  1  1  0  0  0
  7 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  6  0  0  0
 26 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 35 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 32 42  1  1  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  2  0  0  0  0
 25 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 19 48  1  0  0  0  0
 23 48  1  0  0  0  0
 48 49  1  6  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0167253

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H](CCC(C)(C)OC(C)=O)[C@](C)(OC(C)=O)[C@H]1CC[C@@]2(OC(C)=O)C3=CC(=O)[C@@H]4C[C@@H](OC(C)=O)[C@H](C[C@]4(C)[C@H]3CC[C@]12C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C39H56O13/c1-21(40)47-31-19-29-30(46)18-28-27(36(29,9)20-32(31)48-22(2)41)12-16-37(10)33(13-17-39(28,37)52-26(6)45)38(11,51-25(5)44)34(49-23(3)42)14-15-35(7,8)50-24(4)43/h18,27,29,31-34H,12-17,19-20H2,1-11H3/t27-,29-,31+,32-,33-,34+,36+,37+,38+,39+/m0/s1

> <INCHI_KEY>
HNFXHLSAYHJBHJ-RWCWHVSBSA-N

> <FORMULA>
C39H56O13

> <MOLECULAR_WEIGHT>
732.864

> <EXACT_MASS>
732.372091863

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
108

> <JCHEM_AVERAGE_POLARIZABILITY>
78.36357802610326

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R)-2,6-bis(acetyloxy)-6-methyl-2-[(1R,2R,4S,5R,7R,11S,14S,15R)-4,5,11-tris(acetyloxy)-2,15-dimethyl-8-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-14-yl]heptan-3-yl acetate

> <ALOGPS_LOGP>
4.03

> <JCHEM_LOGP>
3.256614666666665

> <ALOGPS_LOGS>
-5.94

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.92426504630391

> <JCHEM_PKA_STRONGEST_BASIC>
-5.9096191157376925

> <JCHEM_POLAR_SURFACE_AREA>
174.86999999999998

> <JCHEM_REFRACTIVITY>
183.78480000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.48e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R)-2,6-bis(acetyloxy)-6-methyl-2-[(1R,2R,4S,5R,7R,11S,14S,15R)-4,5,11-tris(acetyloxy)-2,15-dimethyl-8-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-14-yl]heptan-3-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      15.020  -2.491   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.028  -1.314   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      14.551   0.135   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      12.512  -1.585   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.519  -0.407   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.003  -0.678   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.010   0.499   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.487  -0.949   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.533   1.947   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.049   2.218   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.042   1.041   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      13.558   1.312   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      14.081   2.761   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      15.597   3.032   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      13.089   3.938   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.541   3.125   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       9.064   4.573   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.025   2.854   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.502   1.405   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.494   0.228   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.971  -1.221   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.455  -1.492   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.462  -0.314   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.791  -1.700   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.923  -0.264   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.978  -1.480   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.194  -2.425   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.033  -2.696   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.613  -4.122   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.139  -4.333   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       0.668  -5.338   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       0.762  -0.535   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -0.664  -1.115   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.880  -0.170   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -3.307  -0.750   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -3.887   0.676   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -2.726  -2.177   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -4.733  -1.331   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -5.949  -0.385   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -7.375  -0.966   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -5.738   1.140   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       0.973   0.991   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      -0.243   1.936   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -0.032   3.461   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -1.669   1.356   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       2.495   1.215   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       3.770   2.079   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       4.986   1.134   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       5.355   2.629   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       4.244   3.696   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       2.765   3.268   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       4.613   5.192   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9   20                                             
CONECT    8    7                                                            
CONECT    9    7   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10    5   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    9   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   48                                                  
CONECT   20   19    7   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25   48                                             
CONECT   24   23                                                            
CONECT   25   23   26   46                                                  
CONECT   26   25   27   28   32                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   26   33   42                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   37   38                                             
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   35   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   32   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43                                                            
CONECT   46   25   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   19   23   49                                             
CONECT   49   48   50                                                       
CONECT   50   49   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  110    0
END

View in JSmol

Synonyms

Value	Source
(2R,3R)-2,6-Bis(acetyloxy)-6-methyl-2-[(1R,2R,4S,5R,7R,11S,14S,15R)-4,5,11-tris(acetyloxy)-2,15-dimethyl-8-oxotetracyclo[8.7.0.0,.0,]heptadec-9-en-14-yl]heptan-3-yl acetic acid	Generator

Chemical Formula

C₃₉H₅₆O₁₃

Average Mass

732.8640 Da

Monoisotopic Mass

732.37209 Da

IUPAC Name

(2R,3R)-2,6-bis(acetyloxy)-6-methyl-2-[(1R,2R,4S,5R,7R,11S,14S,15R)-4,5,11-tris(acetyloxy)-2,15-dimethyl-8-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-14-yl]heptan-3-yl acetate

Traditional Name

(2R,3R)-2,6-bis(acetyloxy)-6-methyl-2-[(1R,2R,4S,5R,7R,11S,14S,15R)-4,5,11-tris(acetyloxy)-2,15-dimethyl-8-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-14-yl]heptan-3-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H](CCC(C)(C)OC(C)=O)[C@](C)(OC(C)=O)[C@H]1CC[C@@]2(OC(C)=O)C3=CC(=O)[C@@H]4C[C@@H](OC(C)=O)[C@H](C[C@]4(C)[C@H]3CC[C@]12C)OC(C)=O

InChI Identifier

InChI=1S/C39H56O13/c1-21(40)47-31-19-29-30(46)18-28-27(36(29,9)20-32(31)48-22(2)41)12-16-37(10)33(13-17-39(28,37)52-26(6)45)38(11,51-25(5)44)34(49-23(3)42)14-15-35(7,8)50-24(4)43/h18,27,29,31-34H,12-17,19-20H2,1-11H3/t27-,29-,31+,32-,33-,34+,36+,37+,38+,39+/m0/s1

InChI Key

HNFXHLSAYHJBHJ-RWCWHVSBSA-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
Tinospora cordifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bile acids, alcohols and derivatives. These are organic compounds containing an alcohol or acid derivative of cholic acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Bile acids, alcohols and derivatives

Alternative Parents

Substituents

Cholesterol
Cholestane-skeleton
Ecdysteroid
Bile acid, alcohol, or derivatives
Steroid ester
Hexacarboxylic acid or derivatives
6-oxosteroid
Oxosteroid
Delta-7-steroid
Cyclohexenone
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organooxygen compound
Organic oxygen 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	4.03	ALOGPS
logP	3.26	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	17.92	ChemAxon
pKa (Strongest Basic)	-5.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	174.87 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	183.78 m³·mol⁻¹	ChemAxon
Polarizability	78.36 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163028748

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate (NP0167253)

MOL for NP0167253 ((2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate)

3D MOL for NP0167253 ((2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate)

3D SDF for NP0167253 ((2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate)

3D-SDF for NP0167253 ((2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate)

PDB for NP0167253 ((2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate)

3D PDB for NP0167253 ((2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate)

SMILES for NP0167253 ((2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate)

INCHI for NP0167253 ((2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate)

Structure for NP0167253 ((2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate)

3D Structure for NP0167253 ((2r,3r)-2-[(1s,3as,5ar,7r,8s,9ar,9br,11ar)-3a,7,8-tris(acetyloxy)-9a,11a-dimethyl-5-oxo-1h,2h,3h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,6-bis(acetyloxy)-6-methylheptan-3-yl acetate)