NP-MRD: Showing NP-Card for methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate (NP0175381)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 12:49:31 UTC

Updated at

2022-09-03 12:49:31 UTC

NP-MRD ID

NP0175381

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate

Description

Rumphioside I belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate is found in Tinospora crispa. Based on a literature review very few articles have been published on Rumphioside I.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032214492D          

 39 43  0  0  1  0            999 V2000
   -1.1091    3.3608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1992    2.5407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5341    2.0526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2211    2.3846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6243    1.2326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3796    0.9006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4697    0.0806    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2250   -0.2514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8046   -0.4076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0494   -0.0756    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5356   -0.6574    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1618   -1.0982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101   -1.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2737   -2.0621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5483   -2.8401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0118   -3.4669    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7992   -3.3157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3357   -3.9425    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1467   -3.7913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4213   -3.0133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0611   -4.7204    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5976   -5.3472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2501   -4.8716    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0245   -5.6496    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2864   -4.2449    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0974   -4.3961    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5373   -1.9110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1364   -2.4782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8610   -2.0838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7098   -1.2728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8917   -1.1659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3551   -0.5628    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2652    0.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7382    1.1852    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5176    0.9149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7922    0.1369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6122    0.0467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0408    0.7444    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0694    1.5689    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  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  6  0  0  0
 14 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 27 31  2  0  0  0  0
 11 32  1  0  0  0  0
 32 33  1  6  0  0  0
 34 33  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 32 36  1  0  0  0  0
 36 37  2  0  0  0  0
 34 38  1  0  0  0  0
  5 38  1  0  0  0  0
 10 38  1  0  0  0  0
 38 39  1  1  0  0  0
M  END

     RDKit          3D

 75 79  0  0  0  0  0  0  0  0999 V2000
   -5.5964    4.0768    0.0188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1560    2.8292   -0.4680 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5627    1.9346    0.4441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4627    2.2991    1.6251 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0963    0.6469   -0.0044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2669    0.3659   -1.2816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8495   -0.8900   -1.8722 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0450   -1.5713   -2.2310 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0462   -1.8088   -1.0312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4317   -1.2147    0.1711 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0879   -0.5514   -0.0042 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0261    0.4945   -1.0526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980   -1.6382   -0.2579 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3101   -1.3018   -0.4848 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0161   -0.6439    0.4840 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8403    0.3219   -0.0481 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1909   -0.0646    0.1343 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9580    0.6580   -0.7753 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3263    0.0468   -0.8394 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9205    0.0918    0.4174 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9602    2.0998   -0.3816 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6034    2.9329   -1.4653 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0439    2.3552    0.7767 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6490    2.0414    1.9814 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7093    1.6455    0.6434 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8170    2.5202    0.0402 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0228   -2.6397   -0.6041 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3866   -3.3126   -1.7358 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0112   -4.4917   -1.3051 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0081   -4.4987    0.0044 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4184   -3.3942    0.4584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7431    0.0516    1.3456 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7579    1.1071    1.7930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9249    0.2377    2.1223 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2714   -0.8291    2.8603 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9674   -0.9520    2.4316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1574   -1.7823    2.9102 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4651   -0.3375    0.8568 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5665   -1.3313    1.2986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7024    4.7532    0.0104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3101    4.5361   -0.7068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0262    4.0308    1.0283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7393    1.0900   -1.9467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3750   -0.7067   -2.8855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8809   -2.5556   -2.2437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3583   -2.3582   -1.7119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7391   -2.6269   -0.6618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2423   -2.0559    0.9062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5996    1.3964   -0.8804 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0575    0.8052   -1.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2737    0.0003   -2.0285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4320   -2.2371   -1.1588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1276   -2.4187    0.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5533   -0.8054   -1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7441    0.4341   -1.1592 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5218    0.5948   -1.8061 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1981   -1.0322   -1.0852 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9519    0.5610   -1.6043 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8939   -0.7704    0.8770 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9834    2.4306   -0.0898 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9588    3.8404   -1.2605 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8262    3.4488    0.8215 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9247    1.1125    2.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3784    1.4805    1.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3864    3.0601    0.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2363   -3.0200   -2.7596 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4323   -5.2777   -1.9082 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3068   -3.1949    1.5214 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2204    0.5316    1.4032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9007    1.8764    1.0437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3117    1.5735    2.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7116    0.6606    2.7368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3181   -1.3604    0.4915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1273   -2.3288    1.4957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0117   -0.9711    2.2417 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  6
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 18 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 14 27  1  0
 27 31  2  0
 31 30  1  0
 30 29  1  0
 29 28  2  0
 11 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  2  0
 34 38  1  0
 38 39  1  1
 38  5  1  0
 38 10  1  0
 25 16  1  0
 28 27  1  0
 36 32  1  0
  1 40  1  0
  1 41  1  0
  1 42  1  0
  6 43  1  0
  7 44  1  6
  8 45  1  0
  9 46  1  0
  9 47  1  0
 10 48  1  1
 12 49  1  0
 12 50  1  0
 12 51  1  0
 13 52  1  0
 13 53  1  0
 14 54  1  6
 16 55  1  6
 18 56  1  6
 19 57  1  0
 19 58  1  0
 20 59  1  0
 21 60  1  1
 22 61  1  0
 23 62  1  1
 24 63  1  0
 25 64  1  1
 26 65  1  0
 31 68  1  0
 29 67  1  0
 28 66  1  0
 32 69  1  6
 33 70  1  0
 33 71  1  0
 34 72  1  1
 39 73  1  0
 39 74  1  0
 39 75  1  0
M  END


  Mrv1652309032214492D          

 39 43  0  0  1  0            999 V2000
   -1.1091    3.3608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1992    2.5407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5341    2.0526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2211    2.3846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6243    1.2326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3796    0.9006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4697    0.0806    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2250   -0.2514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8046   -0.4076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0494   -0.0756    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5356   -0.6574    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1618   -1.0982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101   -1.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2737   -2.0621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5483   -2.8401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0118   -3.4669    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7992   -3.3157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3357   -3.9425    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1467   -3.7913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4213   -3.0133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0611   -4.7204    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5976   -5.3472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2501   -4.8716    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0245   -5.6496    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2864   -4.2449    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0974   -4.3961    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5373   -1.9110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1364   -2.4782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8610   -2.0838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7098   -1.2728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8917   -1.1659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3551   -0.5628    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2652    0.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7382    1.1852    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5176    0.9149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7922    0.1369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6122    0.0467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0408    0.7444    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0694    1.5689    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  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  6  0  0  0
 14 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 27 31  2  0  0  0  0
 11 32  1  0  0  0  0
 32 33  1  6  0  0  0
 34 33  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 32 36  1  0  0  0  0
 36 37  2  0  0  0  0
 34 38  1  0  0  0  0
  5 38  1  0  0  0  0
 10 38  1  0  0  0  0
 38 39  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0175381

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=C[C@H](O)C[C@H]2[C@](C)(CC(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C3=COC=C3)[C@H]3C[C@H](OC3=O)[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C27H36O12/c1-26(9-16(12-4-5-36-11-12)37-25-22(32)21(31)20(30)17(10-28)38-25)14-8-19(39-24(14)34)27(2)15(23(33)35-3)6-13(29)7-18(26)27/h4-6,11,13-14,16-22,25,28-32H,7-10H2,1-3H3/t13-,14-,16?,17+,18-,19-,20+,21-,22+,25+,26+,27-/m0/s1

> <INCHI_KEY>
GMZIBNWBLDPKAJ-KSABOFSBSA-N

> <FORMULA>
C27H36O12

> <MOLECULAR_WEIGHT>
552.573

> <EXACT_MASS>
552.220676599

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
54.993202612334564

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1S,2R,5R,7S,8S,9R)-8-[2-(furan-3-yl)-2-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0^{2,7}]dodec-3-ene-3-carboxylate

> <ALOGPS_LOGP>
-0.01

> <JCHEM_LOGP>
-0.40653183599999976

> <ALOGPS_LOGS>
-2.68

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.190367613862492

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.208978770703936

> <JCHEM_PKA_STRONGEST_BASIC>
-2.862014352984099

> <JCHEM_POLAR_SURFACE_AREA>
185.35

> <JCHEM_REFRACTIVITY>
131.0046

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.14e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,2R,5R,7S,8S,9R)-8-[2-(furan-3-yl)-2-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0^{2,7}]dodec-3-ene-3-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      -2.070   6.273   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.239   4.743   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.997   3.832   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.413   4.451   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.165   2.301   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.575   1.681   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.744   0.150   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -4.153  -0.469   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.502  -0.761   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.092  -0.141   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.000  -1.227   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.302  -2.050   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.512  -2.679   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.511  -3.849   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.023  -5.302   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.022  -6.472   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.492  -6.189   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -2.493  -7.359   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.007  -7.077   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -4.520  -5.625   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.981  -8.811   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.982  -9.981   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.467  -9.094   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.046 -10.546   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.535  -7.924   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.048  -8.206   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.003  -3.567   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.121  -4.626   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -3.474  -3.890   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -3.192  -2.376   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -1.665  -2.176   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.530  -1.051   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.362   0.725   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.378   2.212   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       2.833   1.708   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       3.345   0.256   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       4.876   0.087   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       0.076   1.390   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       0.130   2.929   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   38                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   38                                                  
CONECT   11   10   12   13   32                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   16   26                                                  
CONECT   26   25                                                            
CONECT   27   14   28   31                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   27                                                       
CONECT   32   11   33   36                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   38                                                  
CONECT   35   34   36                                                       
CONECT   36   35   32   37                                                  
CONECT   37   36                                                            
CONECT   38   34    5   10   39                                             
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₆O₁₂

Average Mass

552.5730 Da

Monoisotopic Mass

552.22068 Da

IUPAC Name

methyl (1S,2R,5R,7S,8S,9R)-8-[2-(furan-3-yl)-2-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0^{2,7}]dodec-3-ene-3-carboxylate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC(=O)C1=C[C@H](O)C[C@H]2[C@](C)(CC(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C3=COC=C3)[C@H]3C[C@H](OC3=O)[C@@]12C

InChI Identifier

InChI=1S/C27H36O12/c1-26(9-16(12-4-5-36-11-12)37-25-22(32)21(31)20(30)17(10-28)38-25)14-8-19(39-24(14)34)27(2)15(23(33)35-3)6-13(29)7-18(26)27/h4-6,11,13-14,16-22,25,28-32H,7-10H2,1-3H3/t13-,14-,16?,17+,18-,19-,20+,21-,22+,25+,26+,27-/m0/s1

InChI Key

GMZIBNWBLDPKAJ-KSABOFSBSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Tinospora crispa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Caprolactone
Oxepane
Dicarboxylic acid or derivatives
Gamma butyrolactone
Monosaccharide
Oxane
Oxolane
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Heteroaromatic compound
Furan
Secondary alcohol
Lactone
Carboxylic acid ester
Polyol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Acetal
Organooxygen compound
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxide
Primary alcohol
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	-0.01	ALOGPS
logP	-0.41	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	185.35 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	131 m³·mol⁻¹	ChemAxon
Polarizability	54.99 Å³	ChemAxon
Number of Rings	5	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

Not Available

Chemspider ID

8778151

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10602782

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate (NP0175381)

MOL for NP0175381 (methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate)

3D MOL for NP0175381 (methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate)

3D SDF for NP0175381 (methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate)

3D-SDF for NP0175381 (methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate)

PDB for NP0175381 (methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate)

3D PDB for NP0175381 (methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate)

SMILES for NP0175381 (methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate)

INCHI for NP0175381 (methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate)

Structure for NP0175381 (methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate)

3D Structure for NP0175381 (methyl (1s,2r,5r,7s,8s,9r)-8-[2-(furan-3-yl)-2-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.0²,⁷]dodec-3-ene-3-carboxylate)