NP-MRD: Showing NP-Card for methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate (NP0173691)

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Record Information

Version

2.0

Created at

2022-09-03 10:52:03 UTC

Updated at

2022-09-03 10:52:03 UTC

NP-MRD ID

NP0173691

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate

Description

(5Alpha,8beta,10beta,14alpha)-6alpha-Hydroxy-16-[methyl[2-(beta-D-galactopyranosyloxy)ethyl]amino]-7,16-dioxocassa-13(15)-ene-19-oic acid methyl ester belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate is found in Erythrophleum fordii. Based on a literature review very few articles have been published on (5alpha,8beta,10beta,14alpha)-6alpha-Hydroxy-16-[methyl[2-(beta-D-galactopyranosyloxy)ethyl]amino]-7,16-dioxocassa-13(15)-ene-19-oic acid methyl ester.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032212522D          

 42 45  0  0  1  0            999 V2000
   -7.1565    3.3670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3441    3.2238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8138    3.8558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0959    4.6310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2835    2.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 23  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  1  0  0  0
 15 35  1  0  0  0  0
 35 36  1  6  0  0  0
 35 37  1  0  0  0  0
 12 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  6  0  0  0
 42 40  1  1  0  0  0
  5 42  1  0  0  0  0
 10 42  1  0  0  0  0
M  END

     RDKit          3D

 89 92  0  0  0  0  0  0  0  0999 V2000
   -6.9036   -2.6281   -3.8071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5435   -1.7546   -2.7484 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9378   -0.4308   -2.6929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6441    0.0146   -3.6197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5629    0.5003   -1.5790 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.2810    1.8111   -1.8304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1072   -0.0883   -0.3199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4961    0.3659    0.9486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2416    1.1534    0.8333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3823    0.5918   -0.2869 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0365   -0.8130    0.0722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0922    1.3810   -0.4017 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3346    1.5564    0.8425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8374    1.3611    0.7483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2646    1.7411   -0.5406 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0235    1.8673   -0.6392 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1288    1.7271    0.2065 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2506    2.0596   -0.4999 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070    1.3767    1.4808 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7575    0.9119    2.6080 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9833    1.4795    1.7976 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5230    0.1179    1.4354 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8763    0.1165    1.6916 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3910   -1.1293    1.3477 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9782   -1.7582    2.4576 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5733   -2.9270    1.9844 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8350   -3.9333    3.0820 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6822   -3.3891    4.0370 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9080   -2.5231    1.3850 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.8661   -2.6071    2.3651 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8125   -1.1662    0.7242 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.1175   -0.2060    1.6871 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3989   -0.8894    0.2479 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1307   -1.7835   -0.7845 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1915    1.9366   -1.7282 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7828    3.3062   -1.7181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2361    0.8549   -1.4944 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9882    0.4887   -2.7197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4697    0.6974   -3.7936 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3633   -0.1269   -2.6054 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9282   -0.0506   -3.8696 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0893    0.7519   -1.6058 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.5389   -3.6538   -3.6345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0094   -2.5724   -3.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5165   -2.2475   -4.7962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8874    2.3048   -2.7681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3641    1.6707   -2.0289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1835    2.5437   -1.0300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2005    0.2101   -0.2802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1888   -1.2166   -0.3906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2029    0.9885    1.5767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3241   -0.5406    1.6035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6703    1.0001    1.7744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3932    2.2479    0.7441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1044   -1.2032   -0.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9427   -0.8524    1.1947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8274   -1.5489   -0.1673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4372    2.4115   -0.7450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6542    0.8571    1.6726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5313    2.5718    1.2885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4154    2.1035    1.4897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5922    0.3487    1.0609 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2915    2.1759   -1.7211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1170    1.6810    3.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1648    0.0229    2.3555 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4933    0.5476    3.4206 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4198    2.2586    1.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0533    1.6220    2.8758 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2932   -0.0690    0.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9557   -0.6659    1.9749 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5963   -1.7732    0.9728 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9181   -3.3472    1.2158 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3470   -4.7948    2.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
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    8.4631   -3.7481    4.9320 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1364   -3.2673    0.5731 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9768   -1.7955    2.9105 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5433   -1.0755   -0.0934 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1058   -0.0880    1.7677 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3175    0.1249   -0.1833 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6292   -1.5567   -1.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6860    1.7699   -2.6756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9139    3.7391   -0.7056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0360    3.9982   -2.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6829    3.3870   -2.3570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6561   -0.0560   -1.1738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3232   -1.1863   -2.2975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5591   -0.7356   -4.4737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9310    1.7889   -2.0050 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  5  3  1  6
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  1
 10 12  1  0
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 17 18  2  0
 17 19  1  0
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 31 33  1  0
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 35 36  1  0
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 37 38  1  0
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 33 24  1  0
  1 43  1  0
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  1 45  1  0
  6 46  1  0
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  9 54  1  0
 11 55  1  0
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 16 63  1  0
 20 64  1  0
 20 65  1  0
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 27 73  1  0
 27 74  1  0
 28 75  1  0
 29 76  1  6
 30 77  1  0
 31 78  1  6
 32 79  1  0
 33 80  1  6
 34 81  1  0
 35 82  1  6
 36 83  1  0
 36 84  1  0
 36 85  1  0
 37 86  1  1
 40 87  1  1
 41 88  1  0
 42 89  1  6
M  END


  Mrv1652309032212522D          

 42 45  0  0  1  0            999 V2000
   -7.1565    3.3670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3441    3.2238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8138    3.8558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0959    4.6310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2835    2.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 23  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  1  0  0  0
 15 35  1  0  0  0  0
 35 36  1  6  0  0  0
 35 37  1  0  0  0  0
 12 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  6  0  0  0
 42 40  1  1  0  0  0
  5 42  1  0  0  0  0
 10 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0173691

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@]1(C)CCC[C@]2(C)[C@H]3CC\C(=C/C(=O)N(C)CCO[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)[C@H](C)[C@@H]3C(=O)[C@H](O)[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C30H47NO11/c1-15-16(13-19(33)31(4)11-12-41-27-25(38)23(36)21(34)18(14-32)42-27)7-8-17-20(15)22(35)24(37)26-29(17,2)9-6-10-30(26,3)28(39)40-5/h13,15,17-18,20-21,23-27,32,34,36-38H,6-12,14H2,1-5H3/b16-13+/t15-,17-,18+,20-,21-,23-,24-,25+,26+,27+,29+,30-/m0/s1

> <INCHI_KEY>
GXTGEIIRPCIEGD-PBDYHIGVSA-N

> <FORMULA>
C30H47NO11

> <MOLECULAR_WEIGHT>
597.702

> <EXACT_MASS>
597.314911337

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
63.1889725320095

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1S,4aR,4bS,7E,8R,8aS,10R,10aR)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-tetradecahydrophenanthrene-1-carboxylate

> <ALOGPS_LOGP>
0.40

> <JCHEM_LOGP>
0.006651104999998922

> <ALOGPS_LOGS>
-2.88

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.899535023406102

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.158346514014193

> <JCHEM_PKA_STRONGEST_BASIC>
-0.018379117566151404

> <JCHEM_POLAR_SURFACE_AREA>
183.29

> <JCHEM_REFRACTIVITY>
149.17910000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.89e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,4aR,4bS,7E,8R,8aS,10R,10aR)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate

> <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     -13.359   6.285   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0     -11.842   6.018   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0     -10.852   7.197   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0     -11.379   8.645   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -9.336   6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.862   5.483   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -9.336   8.470   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -8.002   9.240   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.668   8.470   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.668   6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.335   7.700   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.335   6.160   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.001   6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.000   6.160   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0       1.334   3.850   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.002   4.620   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      10.669   6.160   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      10.669   1.540   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       8.002   0.000   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -6.668   3.850   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -6.668   2.310   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -8.002   4.620   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -9.336   3.850   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      -8.002   6.160   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7   42                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   42                                             
CONECT   11   10                                                            
CONECT   12   10   13   37                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   35                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   33                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   24   34                                                  
CONECT   34   33                                                            
CONECT   35   15   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   12   38                                                  
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40    5   10                                                  
MASTER        0    0    0    0    0    0    0    0   42    0   90    0
END

View in JSmol

Synonyms

Value	Source
(5a,8b,10b,14a)-6a-Hydroxy-16-[methyl[2-(b-D-galactopyranosyloxy)ethyl]amino]-7,16-dioxocassa-13(15)-ene-19-Oate methyl ester	Generator
(5a,8b,10b,14a)-6a-Hydroxy-16-[methyl[2-(b-D-galactopyranosyloxy)ethyl]amino]-7,16-dioxocassa-13(15)-ene-19-Oic acid methyl ester	Generator
(5alpha,8beta,10beta,14alpha)-6alpha-Hydroxy-16-[methyl[2-(beta-D-galactopyranosyloxy)ethyl]amino]-7,16-dioxocassa-13(15)-ene-19-Oate methyl ester	Generator
(5Α,8β,10β,14α)-6α-hydroxy-16-[methyl[2-(β-D-galactopyranosyloxy)ethyl]amino]-7,16-dioxocassa-13(15)-ene-19-Oate methyl ester	Generator
(5Α,8β,10β,14α)-6α-hydroxy-16-[methyl[2-(β-D-galactopyranosyloxy)ethyl]amino]-7,16-dioxocassa-13(15)-ene-19-Oic acid methyl ester	Generator

Chemical Formula

C₃₀H₄₇NO₁₁

Average Mass

597.7020 Da

Monoisotopic Mass

597.31491 Da

IUPAC Name

methyl (1S,4aR,4bS,7E,8R,8aS,10R,10aR)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-tetradecahydrophenanthrene-1-carboxylate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@]1(C)CCC[C@]2(C)[C@H]3CC\C(=C/C(=O)N(C)CCO[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)[C@H](C)[C@@H]3C(=O)[C@H](O)[C@@H]12

InChI Identifier

InChI=1S/C30H47NO11/c1-15-16(13-19(33)31(4)11-12-41-27-25(38)23(36)21(34)18(14-32)42-27)7-8-17-20(15)22(35)24(37)26-29(17,2)9-6-10-30(26,3)28(39)40-5/h13,15,17-18,20-21,23-27,32,34,36-38H,6-12,14H2,1-5H3/b16-13+/t15-,17-,18+,20-,21-,23-,24-,25+,26+,27+,29+,30-/m0/s1

InChI Key

GXTGEIIRPCIEGD-PBDYHIGVSA-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
Erythrophleum fordii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Cassane diterpenoid
Diterpenoid
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Hydrophenanthrene
Phenanthrene
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Fatty acyl
Oxane
Monosaccharide
Tertiary carboxylic acid amide
Methyl ester
Cyclic alcohol
Secondary alcohol
Carboxamide group
Ketone
Carboxylic acid ester
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Acetal
Primary alcohol
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organic oxide
Hydrocarbon derivative
Alcohol
Organonitrogen compound
Carbonyl group
Organooxygen compound
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	0.4	ALOGPS
logP	0.0067	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	12.16	ChemAxon
pKa (Strongest Basic)	-0.018	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	183.29 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	149.18 m³·mol⁻¹	ChemAxon
Polarizability	63.19 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

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PubChem Compound

102321188

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References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate (NP0173691)

MOL for NP0173691 (methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate)

3D MOL for NP0173691 (methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate)

3D SDF for NP0173691 (methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate)

3D-SDF for NP0173691 (methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate)

PDB for NP0173691 (methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate)

3D PDB for NP0173691 (methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate)

SMILES for NP0173691 (methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate)

INCHI for NP0173691 (methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate)

Structure for NP0173691 (methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate)

3D Structure for NP0173691 (methyl (1s,4ar,4bs,7e,8r,8as,10r,10ar)-10-hydroxy-1,4a,8-trimethyl-7-{[methyl(2-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl)carbamoyl]methylidene}-9-oxo-decahydrophenanthrene-1-carboxylate)