NP-MRD: Showing NP-Card for (2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate (NP0241995)

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Record Information

Version

2.0

Created at

2022-09-07 02:11:58 UTC

Updated at

2022-09-07 02:11:58 UTC

NP-MRD ID

NP0241995

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate

Description

Kakisaponin C belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated. (2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate is found in Diospyros kaki. (2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate was first documented in 2009 (PMID: 19420791). Based on a literature review very few articles have been published on Kakisaponin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072204112D          

 46 50  0  0  1  0            999 V2000
   -1.5694   -5.9978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8486   -5.5965    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1406   -6.0201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8357   -4.7716    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5436   -4.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1149   -4.3703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1020   -3.5454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188   -3.1441    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0984   -2.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3926   -1.7332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7162   -2.6345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2366   -1.9943    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9423   -1.2236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4627   -0.5834    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1685    0.1874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6889    0.8276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2773   -0.7140    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7977   -0.0738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5715   -1.4847    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3861   -1.6153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0512   -2.1249    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3454   -2.8956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1589   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9690   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091   -2.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -2.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5893   -2.9882    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3994   -3.1441    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1294   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9395   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7497   -2.6764    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2897   -2.0527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0197   -3.4559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8298   -3.6118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4796   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1876   -4.5031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1854   -4.8503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6695   -3.9236    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1294   -4.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -4.3914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0492   -3.6118    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5091   -4.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2391   -3.4559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9993   -4.2453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8889   -3.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  1  0  0  0
  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  6  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  6  0  0  0
  8 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 27 26  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 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
 28 38  1  0  0  0  0
 38 39  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 27 41  1  0  0  0  0
 41 42  1  6  0  0  0
 41 43  1  0  0  0  0
 24 43  1  0  0  0  0
 43 44  1  1  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
  8 46  1  0  0  0  0
M  END

     RDKit          3D

104108  0  0  0  0  0  0  0  0999 V2000
    2.3097    3.8279    5.3712 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0101    2.5563    5.7209 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9843    2.8381    6.6766 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6973    1.9454    4.5333 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7351    2.9248    3.9837 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7105    1.6658    3.4201 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3702    1.0593    2.2330 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4766    0.7517    1.0892 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3983    0.2140    0.0074 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6250    0.1212    0.2195 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9221   -0.1835   -1.2253 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7449   -0.6862   -2.2555 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6637    0.0032   -3.4367 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7084   -0.4032   -4.2611 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4633    0.2510   -5.6073 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4602   -0.1004   -6.4939 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7890   -1.8769   -4.4817 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0976   -2.1430   -4.9488 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5723   -2.7201   -3.2686 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3609   -4.0318   -3.6134 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3689   -2.1293   -2.5235 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1895   -2.8567   -1.3662 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5281   -0.3558    1.3280 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2326   -0.4375    1.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5081   -1.6703    1.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7669   -1.8125    1.1642 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5175   -0.7721    0.4646 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6299   -1.3202   -0.4035 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1184   -2.1535   -1.5589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3576   -2.3129    0.5068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6857   -2.7723   -0.0422 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3995   -3.2935    1.0632 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4801   -1.7244   -0.7225 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.7959   -1.7507   -0.2192 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9716   -0.3441   -0.5059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3025    0.1573    0.8553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7313    0.5593   -1.4793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4851   -0.2113   -0.8660 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1247    1.1759   -0.5500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7592    1.5333   -0.1202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7656    0.3537   -0.1166 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3692    0.2369   -1.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4974    0.7293    0.5939 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8787    1.6914    1.7231 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4777    1.4855   -0.2601 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7404    1.8528    0.4730 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2007    3.6294    5.3211 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4594    4.5784    6.2008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6953    4.2893    4.4522 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3167    1.8043    6.1528 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9103    3.7477    7.0425 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1593    0.9809    4.7999 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2473    3.6545    3.2839 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1704    3.5495    4.8042 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5171    2.4045    3.3958 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1764    2.6061    3.2234 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9378    0.9675    3.8578 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2412    1.6855    1.9571 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8172    0.0827    2.5737 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8175   -0.7127   -1.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6823   -0.0342   -3.8716 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4520   -0.1011   -5.9491 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3730    1.3394   -5.4346 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3261    0.0106   -5.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1165   -2.2213   -5.2951 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5065   -2.8761   -4.4636 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4645   -2.6784   -2.5794 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8532   -4.6715   -3.0115 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5077   -2.1961   -3.2143 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6508   -3.7271   -1.4395 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9550   -1.3115    1.7432 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0350   -2.4878    2.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2321   -2.7685    1.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1446   -0.3202    1.3141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4971   -3.1921   -1.4471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6071   -1.8428   -2.5331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0365   -2.2527   -1.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3522   -2.0342    1.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7412   -3.2661    0.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5877   -3.6251   -0.7510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9289   -4.0826    1.4426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6062   -1.8856   -1.8330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3263   -2.4066   -0.7367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1132   -0.5165    1.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7723    1.1611    0.8429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4868    0.0761    1.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1848    0.6279   -2.4454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8798    1.5645   -1.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7551    0.1440   -1.6560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5586   -0.3509   -2.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3600    1.7771   -1.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9189    1.6222    0.1433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8719    1.8153    0.9733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3871    2.3659   -0.7169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5395   -0.4216   -1.7834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0480    1.2842   -1.8753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2202    0.0564   -2.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6006    1.2570    2.4191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1106    2.7042    1.3471 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0331    1.8974    2.3681 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0631    2.4569   -0.6442 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8248    0.9397   -1.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4040    2.3428   -0.2759 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4615    2.6883    1.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8 46  1  0
 46 45  1  0
 45 43  1  0
 43 44  1  1
 43 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 28 29  1  6
 28 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 35 37  1  0
 35 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  6
 24 23  2  0
  8  9  1  6
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 23  8  1  0
 21 12  1  0
 41 43  1  0
 41 27  1  0
 38 28  1  0
  1 47  1  0
  1 48  1  0
  1 49  1  0
  2 50  1  1
  3 51  1  0
  4 52  1  1
  5 53  1  0
  5 54  1  0
  5 55  1  0
  6 56  1  0
  6 57  1  0
  7 58  1  0
  7 59  1  0
 46103  1  0
 46104  1  0
 45101  1  0
 45102  1  0
 44 98  1  0
 44 99  1  0
 44100  1  0
 25 72  1  0
 26 73  1  0
 27 74  1  1
 29 75  1  0
 29 76  1  0
 29 77  1  0
 30 78  1  0
 30 79  1  0
 31 80  1  6
 32 81  1  0
 33 82  1  6
 34 83  1  0
 36 84  1  0
 36 85  1  0
 36 86  1  0
 37 87  1  0
 37 88  1  0
 37 89  1  0
 38 90  1  6
 39 91  1  0
 39 92  1  0
 40 93  1  0
 40 94  1  0
 42 95  1  0
 42 96  1  0
 42 97  1  0
 23 71  1  0
 12 60  1  1
 14 61  1  1
 15 62  1  0
 15 63  1  0
 16 64  1  0
 17 65  1  6
 18 66  1  0
 19 67  1  1
 20 68  1  0
 21 69  1  6
 22 70  1  0
M  END


  Mrv1652309072204112D          

 46 50  0  0  1  0            999 V2000
   -1.5694   -5.9978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8486   -5.5965    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1406   -6.0201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8357   -4.7716    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5436   -4.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1149   -4.3703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1020   -3.5454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188   -3.1441    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0984   -2.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3926   -1.7332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7162   -2.6345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2366   -1.9943    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9423   -1.2236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4627   -0.5834    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1685    0.1874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6889    0.8276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2773   -0.7140    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7977   -0.0738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5715   -1.4847    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3861   -1.6153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0512   -2.1249    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3454   -2.8956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1589   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9690   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091   -2.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -2.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5893   -2.9882    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3994   -3.1441    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1294   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9395   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7497   -2.6764    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2897   -2.0527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0197   -3.4559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8298   -3.6118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4796   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1876   -4.5031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1854   -4.8503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6695   -3.9236    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1294   -4.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -4.3914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0492   -3.6118    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5091   -4.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2391   -3.4559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9993   -4.2453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8889   -3.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  1  0  0  0
  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  6  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  6  0  0  0
  8 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 27 26  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 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
 28 38  1  0  0  0  0
 38 39  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 27 41  1  0  0  0  0
 41 42  1  6  0  0  0
 41 43  1  0  0  0  0
 24 43  1  0  0  0  0
 43 44  1  1  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
  8 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0241995

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](O)[C@H](C)CC[C@@]1(CC[C@]2(C)C(C=C[C@@H]3[C@@]4(C)C[C@@H](O)[C@@H](O)C(C)(C)[C@H]4CC[C@@]23C)=C1)C(=O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C36H58O10/c1-19(20(2)38)10-13-36(31(44)46-30-28(42)27(41)26(40)23(18-37)45-30)15-14-34(6)21(16-36)8-9-25-33(5)17-22(39)29(43)32(3,4)24(33)11-12-35(25,34)7/h8-9,16,19-20,22-30,37-43H,10-15,17-18H2,1-7H3/t19-,20+,22-,23-,24-,25-,26-,27+,28-,29-,30+,33+,34-,35-,36+/m1/s1

> <INCHI_KEY>
SIVJXPZDODNUNP-KBQKSEQVSA-N

> <FORMULA>
C36H58O10

> <MOLECULAR_WEIGHT>
650.85

> <EXACT_MASS>
650.402998068

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
72.50861890609873

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2S,4aS,4bR,6aS,8S,9R,10aS,10bR)-8,9-dihydroxy-2-[(3R,4S)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-2,3,4,4a,4b,5,6,6a,7,8,9,10,10a,10b-tetradecahydrochrysene-2-carboxylate

> <JCHEM_LOGP>
2.269018565666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.073750938378296

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.180324275925813

> <JCHEM_PKA_STRONGEST_BASIC>
-1.376210002013449

> <JCHEM_POLAR_SURFACE_AREA>
177.14

> <JCHEM_REFRACTIVITY>
172.18380000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2S,4aS,4bR,6aS,8S,9R,10aS,10bR)-8,9-dihydroxy-2-[(3R,4S)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3H-chrysene-2-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.929 -11.196   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.584 -10.447   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.262 -11.238   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -1.560  -8.907   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.881  -8.116   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.214  -8.158   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.190  -6.618   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.155  -5.869   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.184  -4.674   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.733  -3.235   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      -1.337  -4.918   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.308  -3.723   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.759  -2.284   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.730  -1.089   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.181   0.350   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -3.153   1.545   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -4.251  -1.333   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -5.222  -0.138   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -4.800  -2.771   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -6.321  -3.015   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -3.829  -3.966   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -4.378  -5.405   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.163  -4.705   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.676  -4.996   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.684  -3.832   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.196  -4.123   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.700  -5.578   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.212  -5.869   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.708  -4.414   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.220  -4.705   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.733  -4.996   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      11.741  -3.832   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      11.237  -6.451   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      12.749  -6.742   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      10.229  -7.615   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      11.550  -8.406   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       9.679  -9.054   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.716  -7.324   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.708  -8.488   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       6.196  -8.197   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       5.692  -6.742   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       4.684  -7.906   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.180  -6.451   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       3.732  -7.925   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       3.171  -7.615   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       1.659  -7.324   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   23   46                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   12   22                                                  
CONECT   22   21                                                            
CONECT   23    8   24                                                       
CONECT   24   23   25   43                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   41                                                  
CONECT   28   27   29   30   38                                             
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   37   38                                             
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   35   28   39                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   27   42   43                                             
CONECT   42   41                                                            
CONECT   43   41   24   44   45                                             
CONECT   44   43                                                            
CONECT   45   43   46                                                       
CONECT   46   45    8                                                       
MASTER        0    0    0    0    0    0    0    0   46    0  100    0
END

View in JSmol

Synonyms

Value	Source
28-O-beta-D-Glucopyranosyl-2alpha,3alpha,19-trihydoxy-18,19-secours-11,13(18)-dien-28-Oic acid	MeSH

Chemical Formula

C₃₆H₅₈O₁₀

Average Mass

650.8500 Da

Monoisotopic Mass

650.40300 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H](O)[C@H](C)CC[C@@]1(CC[C@]2(C)C(C=C[C@@H]3[C@@]4(C)C[C@@H](O)[C@@H](O)C(C)(C)[C@H]4CC[C@@]23C)=C1)C(=O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C36H58O10/c1-19(20(2)38)10-13-36(31(44)46-30-28(42)27(41)26(40)23(18-37)45-30)15-14-34(6)21(16-36)8-9-25-33(5)17-22(39)29(43)32(3,4)24(33)11-12-35(25,34)7/h8-9,16,19-20,22-30,37-43H,10-15,17-18H2,1-7H3/t19-,20+,22-,23-,24-,25-,26-,27+,28-,29-,30+,33+,34-,35-,36+/m1/s1

InChI Key

SIVJXPZDODNUNP-KBQKSEQVSA-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
Diospyros kaki	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Diterpene glycosides

Alternative Parents

Substituents

Diterpene glycoside
Diterpenoid
18-oxosteroid
Oxosteroid
Steroid
Fatty acyl glycoside of mono- or disaccharide
Fatty acyl glycoside
Hexose monosaccharide
Alkyl glycoside
Fatty alcohol
Fatty acid ester
Fatty acyl
Oxane
Monosaccharide
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00056543

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

102424799

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chen G, Wang ZQ, Jia JM: Three minor novel triterpenoids from the leaves of Diospyros kaki. Chem Pharm Bull (Tokyo). 2009 May;57(5):532-5. doi: 10.1248/cpb.57.532. [PubMed:19420791 ]
LOTUS database [Link]

Showing NP-Card for (2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate (NP0241995)

MOL for NP0241995 ((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate)

3D MOL for NP0241995 ((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate)

3D SDF for NP0241995 ((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate)

3D-SDF for NP0241995 ((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate)

PDB for NP0241995 ((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate)

3D PDB for NP0241995 ((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate)

SMILES for NP0241995 ((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate)

INCHI for NP0241995 ((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate)

Structure for NP0241995 ((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate)

3D Structure for NP0241995 ((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (2s,4as,4br,6as,8s,9r,10as,10br)-8,9-dihydroxy-2-[(3r,4s)-4-hydroxy-3-methylpentyl]-4a,4b,7,7,10a-pentamethyl-4,5,6,6a,8,9,10,10b-octahydro-3h-chrysene-2-carboxylate)