NP-MRD: Showing NP-Card for (1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid (NP0300161)

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Record Information

Version

2.0

Created at

2022-09-10 12:24:38 UTC

Updated at

2022-09-10 12:24:38 UTC

NP-MRD ID

NP0300161

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid

Description

D-Glucoside belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid is found in Trichosanthes tricuspidata. Based on a literature review very few articles have been published on D-Glucoside.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102214242D          

 50 55  0  0  1  0            999 V2000
    1.9163   -2.6790    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
    0.5233   -2.3607    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  0  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  0  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  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
    7.6845   -3.7274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2829   -3.0068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5094   -3.7400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9327   -3.0319    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5311   -2.3112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9544   -1.6031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7576   -3.0444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1809   -2.3363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0058   -2.3488    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4291   -1.6407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2540   -1.6533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4074   -3.0695    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.2323   -3.0820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9841   -3.7776    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.3857   -4.4983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1592   -3.7651    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7359   -4.4732    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  0  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  0  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  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  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  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 33 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 38 39  1  6  0  0  0
 38 40  1  0  0  0  0
 31 40  1  0  0  0  0
 40 41  1  1  0  0  0
 23 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 42 45  1  0  0  0  0
 19 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 18 48  1  0  0  0  0
 13 48  1  0  0  0  0
 48 49  1  6  0  0  0
 15 50  1  0  0  0  0
  4 50  1  0  0  0  0
  7 50  1  0  0  0  0
M  END

     RDKit          3D

113118  0  0  0  0  0  0  0  0999 V2000
   -7.7397   -3.1034    0.4535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5888   -1.8974    0.9366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5880   -1.6799    2.4038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4262   -0.7608    0.0708 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.4232   -1.0307   -1.4125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1104    0.3758   -1.9476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8046    1.2353   -0.7467 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.1134    1.7876   -0.3010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1125    1.6733   -1.0579 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2526    2.4129    0.9151 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8740    2.3553   -0.9369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5726    2.2951   -0.2005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9922    0.8968   -0.1957 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6506    0.6039   -1.6153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9689   -0.0825    0.4365 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4525   -1.4832    0.2413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0599   -1.5878    0.8970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1549   -0.5167    0.4334 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7052   -0.6597    0.8119 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4365   -0.6126    2.2644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2978   -2.0715    0.3979 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2189   -2.2305    0.3371 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8014   -1.2398   -0.6472 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2103   -1.3005   -0.6273 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9825   -1.8544   -1.6429 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3784   -2.3655   -2.6126 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4983   -1.8365   -1.5790 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9492   -0.5301   -1.2406 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2811    0.1170   -0.2997 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8814    0.1209    0.9365 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3539   -0.3374   -1.3017 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.9563   -0.7404   -0.1539 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2826   -0.4540    0.0091 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.7349   -1.0607    1.3274 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9752   -0.5463    2.3459 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5087    1.0296    0.0040 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.8724    1.3349    0.1155 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0236    1.5666   -1.3427 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.0061    2.9741   -1.2541 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6571    1.0953   -1.6816 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5102    1.1917   -3.0767 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4361    0.1754   -0.2923 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500    0.9983   -1.4889 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2967    0.6708    0.8690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0109    0.3682   -0.0386 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3403    1.7196    0.4963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8047    1.9818    0.2249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7026    0.8802    0.6270 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0226    1.1271    2.1088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3665    0.2368    0.3464 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.8602   -3.9431    1.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7445   -3.2675   -0.6096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9925   -2.5223    2.9794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5156   -1.5204    2.7029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0820   -0.7035    2.6735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4059   -0.1803    0.1811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4377   -1.3530   -1.7409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7309   -1.7873   -1.7437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3639    0.3536   -2.7305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0548    0.7139   -2.4705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1232    2.8534    1.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7562    2.5226   -2.0485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3364    3.3436   -0.6213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8379    2.9245   -0.7848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6642    2.7757    0.7649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8831   -0.4059   -1.9800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2113    1.2670   -2.3466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6069    0.8154   -1.9184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7094    0.0069    1.5521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0403   -2.2037    0.8784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4847   -1.8933   -0.7522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1495   -1.6996    1.9820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6718   -2.5651    0.5128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1134   -0.6761   -0.6910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4557    0.3229    2.7867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1635   -1.2948    2.7702 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5530   -1.0891    2.5084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7107   -2.3406   -0.5970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6308   -2.7712    1.1903 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3867   -3.2408   -0.0898 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7084   -2.2145    1.3221 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3795   -1.5584   -1.6209 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8536   -2.1233   -2.5736 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8429   -2.6190   -0.8589 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7353    0.8331    1.0021 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1468    0.5141    1.6797 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1166   -0.9065    1.2519 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7455   -0.9552   -2.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9040   -0.8725   -0.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8023   -0.7603    1.4853 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7300   -2.1483    1.2286 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1997    0.3933    2.4946 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9581    1.4866    0.8309 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9630    2.0575    0.7843 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7895    1.3227   -2.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8557    3.3604   -1.5321 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8997    1.7975   -1.2676 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8677    0.5426   -3.4450 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3130    1.9515   -1.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9584    1.1474   -1.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6310    0.4057   -2.4249 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9049    1.5328    0.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9468   -0.1732    1.1826 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7024    0.9711    1.7477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4896    0.3017   -1.0565 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2103    2.5627   -0.0153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1028    1.8866    1.5629 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.8834    2.3390   -0.8093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9538    1.6792    2.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0077    0.2213    2.7034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2508    1.8208    2.5717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7212    0.7667    1.2941 H   0  0  0  0  0  0  0  0  0  0  0  0
 30 29  1  0
 29 28  1  0
 28 27  1  0
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 50  4  1  0
  4  5  1  0
  5  6  1  0
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  7  8  1  1
  8 10  1  0
  8  9  2  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
 45 42  1  0
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 45105  1  6
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 47108  1  0
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 49110  1  0
 49111  1  0
 49112  1  0
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 16 70  1  0
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 50113  1  1
  4 56  1  6
  5 57  1  0
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 10 61  1  0
  3 53  1  0
  3 54  1  0
  3 55  1  0
  1 51  1  0
  1 52  1  0
 43 99  1  0
 43100  1  0
 43101  1  0
 44102  1  0
 44103  1  0
 44104  1  0
 31 88  1  6
 33 89  1  6
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 35 92  1  0
 36 93  1  1
 37 94  1  0
 38 95  1  6
 39 96  1  0
 40 97  1  1
 41 98  1  0
M  END


  Mrv1652309102214242D          

 50 55  0  0  1  0            999 V2000
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    1.1279   -2.9220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5233   -2.3607    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  0  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  0  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  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
    7.6845   -3.7274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2829   -3.0068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5094   -3.7400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9327   -3.0319    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5311   -2.3112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9544   -1.6031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7576   -3.0444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1809   -2.3363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0058   -2.3488    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4291   -1.6407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2540   -1.6533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4074   -3.0695    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.2323   -3.0820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9841   -3.7776    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.3857   -4.4983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1592   -3.7651    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7359   -4.4732    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  0  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  0  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  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  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  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 33 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 38 39  1  6  0  0  0
 38 40  1  0  0  0  0
 31 40  1  0  0  0  0
 40 41  1  1  0  0  0
 23 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 42 45  1  0  0  0  0
 19 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 18 48  1  0  0  0  0
 13 48  1  0  0  0  0
 48 49  1  6  0  0  0
 15 50  1  0  0  0  0
  4 50  1  0  0  0  0
  7 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0300161

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CON(CC(=O)O[C@H]1CC[C@@]2(C)C(CC[C@]3(C)C2CCC2C4[C@@H](CC[C@@]4(CC[C@@]32C)C(O)=O)C(C)=C)C1(C)C)C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C39H63NO10/c1-21(2)22-11-16-39(34(46)47)18-17-37(6)23(29(22)39)9-10-26-36(5)14-13-27(35(3,4)25(36)12-15-38(26,37)7)50-28(42)19-40(48-8)33-32(45)31(44)30(43)24(20-41)49-33/h22-27,29-33,41,43-45H,1,9-20H2,2-8H3,(H,46,47)/t22-,23?,24+,25?,26?,27-,29?,30+,31-,32+,33?,36-,37+,38+,39-/m0/s1

> <INCHI_KEY>
KRCLQJBBBGFWTC-OMCNKCBHSA-N

> <FORMULA>
C39H63NO10

> <MOLECULAR_WEIGHT>
705.93

> <EXACT_MASS>
705.445197233

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
113

> <JCHEM_AVERAGE_POLARIZABILITY>
77.69935766902786

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,5S,8R,14R,17S)-17-[(2-{methoxy[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-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>
4.171465856666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.415619126086575

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.74831243598883

> <JCHEM_PKA_STRONGEST_BASIC>
-2.980307029483474

> <JCHEM_POLAR_SURFACE_AREA>
166.22

> <JCHEM_REFRACTIVITY>
183.82030000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5S,8R,14R,17S)-17-[(2-{methoxy[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-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                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       3.577  -5.001   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       0.977  -4.407   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  C   UNK     0      12.014  -8.256   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      13.554  -8.280   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      14.344  -6.958   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      13.595  -5.613   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      15.884  -6.981   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0      16.674  -5.659   0.000  0.00  0.00           N+0
HETATM   29  O   UNK     0      15.925  -4.314   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      16.715  -2.992   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      18.214  -5.683   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      19.004  -4.361   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      20.544  -4.384   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      21.334  -3.063   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      22.874  -3.086   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      21.294  -5.730   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      22.834  -5.753   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      20.504  -7.052   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      21.253  -8.397   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      18.964  -7.028   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      18.174  -8.350   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      11.224  -9.578   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      12.663 -10.127   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      10.934 -11.090   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       9.684  -9.555   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       8.894 -10.876   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       7.354 -10.853   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       6.605  -9.508   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       6.742 -11.042   0.000  0.00  0.00           C+0
HETATM   50  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   50                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   11   50                                             
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   48                                             
CONECT   14   13                                                            
CONECT   15   13   16   50                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   48                                                  
CONECT   19   18   20   21   45                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   42                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   31                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   28   32   40                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   36                                                  
CONECT   34   33   35                                                       
CONECT   35   34                                                            
CONECT   36   33   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   31   41                                                  
CONECT   41   40                                                            
CONECT   42   23   43   44   45                                             
CONECT   43   42                                                            
CONECT   44   42                                                            
CONECT   45   42   19   46                                                  
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   18   13   49                                             
CONECT   49   48                                                            
CONECT   50   15    4    7                                                  
MASTER        0    0    0    0    0    0    0    0   50    0  110    0
END

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Synonyms

Not Available

Chemical Formula

C₃₉H₆₃NO₁₀

Average Mass

705.9300 Da

Monoisotopic Mass

705.44520 Da

IUPAC Name

(1R,2R,5S,8R,14R,17S)-17-[(2-{methoxy[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-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

CAS Registry Number

Not Available

SMILES

CON(CC(=O)O[C@H]1CC[C@@]2(C)C(CC[C@]3(C)C2CCC2C4[C@@H](CC[C@@]4(CC[C@@]32C)C(O)=O)C(C)=C)C1(C)C)C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C39H63NO10/c1-21(2)22-11-16-39(34(46)47)18-17-37(6)23(29(22)39)9-10-26-36(5)14-13-27(35(3,4)25(36)12-15-38(26,37)7)50-28(42)19-40(48-8)33-32(45)31(44)30(43)24(20-41)49-33/h22-27,29-33,41,43-45H,1,9-20H2,2-8H3,(H,46,47)/t22-,23?,24+,25?,26?,27-,29?,30+,31-,32+,33?,36-,37+,38+,39-/m0/s1

InChI Key

KRCLQJBBBGFWTC-OMCNKCBHSA-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
Trichosanthes tricuspidata	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-hydroxysteroid
18-oxosteroid
Oxosteroid
Hydroxysteroid
Steroid
Alpha-amino acid ester
Hexose monosaccharide
N-glycosyl compound
Glycosyl compound
Alpha-amino acid or derivatives
Oxane
Monosaccharide
Dicarboxylic acid or derivatives
Secondary alcohol
Carboxylic acid ester
Oxacycle
N-organohydroxylamine
Organoheterocyclic compound
Polyol
Carboxylic acid
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen 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
logP	4.17	ChemAxon
pKa (Strongest Acidic)	4.75	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	166.22 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	183.82 m³·mol⁻¹	ChemAxon
Polarizability	77.7 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00000631

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Glucoside

METLIN ID

Not Available

PubChem Compound

49769056

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,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid (NP0300161)

MOL for NP0300161 ((1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

3D MOL for NP0300161 ((1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

3D SDF for NP0300161 ((1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

3D-SDF for NP0300161 ((1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

PDB for NP0300161 ((1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

3D PDB for NP0300161 ((1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

SMILES for NP0300161 ((1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

INCHI for NP0300161 ((1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

Structure for NP0300161 ((1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)

3D Structure for NP0300161 ((1r,3as,5ar,5br,9s,11ar)-9-[(2-{methoxy[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}acetyl)oxy]-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid)