NP-MRD: Showing NP-Card for 6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate (NP0219786)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 20:53:48 UTC

Updated at

2022-09-05 20:53:48 UTC

NP-MRD ID

NP0219786

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate

Description

62640-13-5 Belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups. 6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate is found in Leplaea thompsonii. Based on a literature review very few articles have been published on 62640-13-5.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052222532D          

 51 56  0  0  0  0            999 V2000
    0.3060   -1.6516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7976   -2.3142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6171   -2.2198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9452   -1.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1291   -1.3418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3871   -0.8552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6122   -1.1383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0204   -0.6088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7953   -0.8919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1218    0.2038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4221   -0.0310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0296    0.5271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7465    1.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8539    0.4922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4120   -0.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3770   -0.9397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0981   -0.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0956   -1.3450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9321   -2.1537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4902   -2.7613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1125   -2.2481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7695   -1.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1087   -2.8824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9283   -2.7880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4198   -3.4505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2394   -3.3562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7806   -3.6393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2722   -4.3019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9441   -5.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1245   -5.1533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4357   -5.7215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2553   -5.6271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7468   -6.2897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5664   -6.1953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4187   -7.0466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1076   -6.4784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2880   -6.5728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5992   -7.1410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2711   -7.8980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9611   -3.7337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3806   -4.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4828   -4.4060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7455   -5.1880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5326   -5.4351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5409   -6.2601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7588   -6.5228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2673   -5.8602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3043   -4.1588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3125   -3.3339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1490   -2.5252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4695   -3.0711    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 16 22  1  0  0  0  0
  4 22  1  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 23 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
 31 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 27 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 43 47  2  0  0  0  0
 42 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
  2 51  1  0  0  0  0
 49 51  1  0  0  0  0
 40 51  1  0  0  0  0
M  END

     RDKit          3D

 97102  0  0  0  0  0  0  0  0999 V2000
   -2.7630   -2.3228    1.2644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6948   -1.7466    0.8424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6081   -0.4110    0.2961 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7613    0.4509   -0.0388 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0781    1.6097   -0.8792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4859    1.1642    1.0127 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8456    2.4723    0.5864 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4162    3.6642    1.1118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8529    4.9871    0.5762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6219    3.6181    2.0849 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6076    0.6351    1.7841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7844    0.0408    1.2427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6550   -0.0979    2.1790 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3749   -0.4574    0.0836 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8744   -0.8248   -1.1551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8180    0.2228   -1.5939 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5444    1.4679   -1.4370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8289    0.0011   -3.0366 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8469   -0.9230   -3.2623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7908   -1.9407   -3.9577 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7291   -0.3729   -2.3869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5716   -0.2219   -1.0959 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4045    0.2257    0.9680 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3527    0.2044    2.3190 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1247    1.2589    3.1480 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0508    2.2964    2.4799 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8214   -0.4290    0.2827 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0090    0.1176    0.8221 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8803    0.9021    0.1318 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6300    1.1552   -1.0744 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0881    1.4500    0.7707 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8589    2.2136   -0.1506 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1385    3.5415    0.0141 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9600    4.2458   -1.0206 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7051    4.1580    1.0294 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8973    0.3350    1.3753 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1100    0.8815    2.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3598   -0.5701    0.2467 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2279    0.1250   -0.7508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7488   -1.9128    0.2427 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0205   -2.4705    0.8378 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5571   -2.5049   -1.1641 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8107   -3.1568   -1.6697 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1637   -4.4587   -1.7953 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4443   -4.4933   -2.3551 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8249   -3.2560   -2.5495 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8866   -2.4275   -2.1574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5620   -3.4980   -0.9621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2597   -3.9164    0.4242 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5151   -3.6132    1.6542 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4076   -2.4901    0.9713 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7706   -1.9648    1.3059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6819   -3.3608    1.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1962   -0.5893   -0.7479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2146    1.2314   -1.4365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7073    2.3790   -0.1632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7682    2.0119   -1.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7052    1.4175    1.8085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9558    4.9328   -0.5222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0280    5.7002    0.7788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7378    5.3326    1.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9998    1.5099    2.4051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2325   -0.0276    2.6170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3558   -1.7978   -1.0637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6465   -0.9666   -1.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4348    1.3739   -2.1708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1233    2.4107   -1.7831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1217    1.6565   -0.5114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4685    0.5582   -2.8609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9749   -1.1446   -2.3418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5781   -1.3125   -0.7715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3243    1.2638    0.6505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0969    1.2169    4.2374 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7825   -0.0738   -0.7671 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8060    2.1680    1.5765 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6453    3.5590   -1.5441 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5470    5.0504   -0.5354 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2805    4.7018   -1.7808 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3241   -0.2612    2.1020 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0033    0.7234    3.2147 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1204    1.9962    1.9911 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0198    0.4084    1.7010 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8745   -1.4687    0.6565 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4440   -0.9254   -0.2553 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9673   -0.5782   -1.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7980    0.9211   -0.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6477    0.5585   -1.5969 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6058   -3.1086    0.1931 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7648   -3.0992    1.7420 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6878   -1.6863    1.2184 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3803   -1.7246   -1.9140 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5775   -5.3147   -1.5295 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9941   -5.4015   -2.5753 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9815   -1.3408   -2.2237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5617   -3.1566   -1.1591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3992   -4.3940   -1.6325 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8178   -4.3131    0.4073 H   0  0  0  0  0  0  0  0  0  0  0  0
 39 38  1  0
 38 36  1  0
 36 37  1  0
 36 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 33 35  2  0
 31 29  1  0
 29 30  2  0
 29 28  1  0
 28 27  1  0
 27 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 23  3  1  0
  3  2  1  0
  2  1  2  3
  2 51  1  0
 51 50  1  1
 50 49  1  0
 49 48  1  0
 48 42  1  0
 42 43  1  0
 43 47  2  0
 47 46  1  0
 46 45  1  0
 45 44  2  0
 42 40  1  0
 40 41  1  1
  3  4  1  0
  4  5  1  6
  4 22  1  0
 22 21  1  0
 21 19  1  0
 19 20  2  0
 19 18  1  0
 18 16  1  0
 16 17  1  6
 16 15  1  0
 15 14  1  0
 14 12  1  0
 12 13  2  0
 12 11  1  0
 11  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 40 27  1  0
  6  4  1  0
 49 51  1  0
 44 43  1  0
 16 22  1  0
 40 51  1  0
 39 85  1  0
 39 86  1  0
 39 87  1  0
 38 83  1  0
 38 84  1  0
 36 79  1  1
 37 80  1  0
 37 81  1  0
 37 82  1  0
 31 75  1  1
 34 76  1  0
 34 77  1  0
 34 78  1  0
 27 74  1  6
 23 72  1  6
 25 73  1  0
  3 54  1  6
  1 52  1  0
  1 53  1  0
 49 97  1  6
 48 95  1  0
 48 96  1  0
 42 91  1  6
 47 94  1  0
 45 93  1  0
 44 92  1  0
 41 88  1  0
 41 89  1  0
 41 90  1  0
  5 55  1  0
  5 56  1  0
  5 57  1  0
 22 71  1  1
 21 69  1  0
 21 70  1  0
 17 66  1  0
 17 67  1  0
 17 68  1  0
 15 64  1  0
 15 65  1  0
 11 62  1  0
 11 63  1  0
  6 58  1  1
  9 59  1  0
  9 60  1  0
  9 61  1  0
M  END


  Mrv1652309052222532D          

 51 56  0  0  0  0            999 V2000
    0.3060   -1.6516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7976   -2.3142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6171   -2.2198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9452   -1.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1291   -1.3418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3871   -0.8552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6122   -1.1383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0204   -0.6088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7953   -0.8919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1218    0.2038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4221   -0.0310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0296    0.5271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7465    1.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8539    0.4922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4120   -0.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3770   -0.9397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0981   -0.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0956   -1.3450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9321   -2.1537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4902   -2.7613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1125   -2.2481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7695   -1.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1087   -2.8824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9283   -2.7880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4198   -3.4505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2394   -3.3562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7806   -3.6393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2722   -4.3019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9441   -5.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1245   -5.1533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4357   -5.7215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2553   -5.6271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7468   -6.2897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5664   -6.1953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4187   -7.0466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1076   -6.4784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2880   -6.5728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5992   -7.1410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2711   -7.8980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9611   -3.7337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3806   -4.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4828   -4.4060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7455   -5.1880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5326   -5.4351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5409   -6.2601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7588   -6.5228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2673   -5.8602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3043   -4.1588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3125   -3.3339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1490   -2.5252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4695   -3.0711    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 16 22  1  0  0  0  0
  4 22  1  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 23 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
 31 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 27 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 43 47  2  0  0  0  0
 42 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
  2 51  1  0  0  0  0
 49 51  1  0  0  0  0
 40 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0219786

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(OC(C)=O)C(=O)OC1C(OC=O)C(C(=C)C23OC2CC(C2=COC=C2)C13C)C1(C)C2CC(=O)OC2(C)COC(=O)CC1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C37H46O14/c1-9-18(2)30(48-21(5)40)33(43)49-32-31(46-17-38)29(19(3)37-26(50-37)12-23(36(32,37)8)22-10-11-44-15-22)35(7)24-13-28(42)51-34(24,6)16-45-27(41)14-25(35)47-20(4)39/h10-11,15,17-18,23-26,29-32H,3,9,12-14,16H2,1-2,4-8H3

> <INCHI_KEY>
BILAMKFGAFCWCS-UHFFFAOYSA-N

> <FORMULA>
C37H46O14

> <MOLECULAR_WEIGHT>
714.761

> <EXACT_MASS>
714.288756161

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
70.53275281690122

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-octahydro-2H-furo[2,3-c]oxocin-4-yl]-3-(formyloxy)--(furan-3-yl)-1b-methyl-5-methylidene-octahydroindeno[1,7a-b]oxiren-2-yl 2-(acetyloxy)-3-methylpentanoate

> <JCHEM_LOGP>
2.9668313579999994

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8598267576006644

> <JCHEM_POLAR_SURFACE_AREA>
183.47

> <JCHEM_REFRACTIVITY>
170.6801

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3H-furo[2,3-c]oxocin-4-yl]-3-(formyloxy)--(furan-3-yl)-1b-methyl-5-methylidene-hexahydroindeno[1,7a-b]oxiren-2-yl 2-(acetyloxy)-3-methylpentanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       0.571  -3.083   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.489  -4.320   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.019  -4.144   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.631  -2.731   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.108  -2.505   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.589  -1.596   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.143  -2.125   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.038  -1.136   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.485  -1.665   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.227   0.380   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.655  -0.058   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.789   0.984   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.260   2.430   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       5.327   0.919   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.369  -0.215   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.304  -1.754   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.650  -1.006   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.645  -2.511   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.340  -4.020   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.382  -5.154   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.810  -4.196   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.170  -2.796   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.936  -5.380   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.466  -5.204   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.384  -6.441   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.914  -6.265   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.324  -6.793   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.241  -8.030   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.629  -9.443   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.099  -9.619   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.547 -10.680   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       6.076 -10.504   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       6.994 -11.741   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.524 -11.564   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       6.382 -13.154   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       3.934 -12.093   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.404 -12.269   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.852 -13.330   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.239 -14.743   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.794  -6.970   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       2.577  -8.296   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       0.901  -8.224   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       1.392  -9.684   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.861 -10.146   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.876 -11.685   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       1.416 -12.176   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       0.499 -10.939   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -0.568  -7.763   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -0.583  -6.223   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      -0.278  -4.714   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       0.876  -5.733   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   51                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5    6   22                                             
CONECT    5    4                                                            
CONECT    6    4    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   22                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   16    4                                                  
CONECT   23    3   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   23   28   40                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   31   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38                                                            
CONECT   40   27   41   42   51                                             
CONECT   41   40                                                            
CONECT   42   40   43   48                                                  
CONECT   43   42   44   47                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   43                                                       
CONECT   48   42   49                                                       
CONECT   49   48   50   51                                                  
CONECT   50   49   51                                                       
CONECT   51   50    2   49   40                                             
MASTER        0    0    0    0    0    0    0    0   51    0  112    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₆O₁₄

Average Mass

714.7610 Da

Monoisotopic Mass

714.28876 Da

IUPAC Name

4-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-octahydro-2H-furo[2,3-c]oxocin-4-yl]-3-(formyloxy)--(furan-3-yl)-1b-methyl-5-methylidene-octahydroindeno[1,7a-b]oxiren-2-yl 2-(acetyloxy)-3-methylpentanoate

Traditional Name

4-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3H-furo[2,3-c]oxocin-4-yl]-3-(formyloxy)--(furan-3-yl)-1b-methyl-5-methylidene-hexahydroindeno[1,7a-b]oxiren-2-yl 2-(acetyloxy)-3-methylpentanoate

CAS Registry Number

Not Available

SMILES

CCC(C)C(OC(C)=O)C(=O)OC1C(OC=O)C(C(=C)C23OC2CC(C2=COC=C2)C13C)C1(C)C2CC(=O)OC2(C)COC(=O)CC1OC(C)=O

InChI Identifier

InChI=1S/C37H46O14/c1-9-18(2)30(48-21(5)40)33(43)49-32-31(46-17-38)29(19(3)37-26(50-37)12-23(36(32,37)8)22-10-11-44-15-22)35(7)24-13-28(42)51-34(24,6)16-45-27(41)14-25(35)47-20(4)39/h10-11,15,17-18,23-26,29-32H,3,9,12-14,16H2,1-2,4-8H3

InChI Key

BILAMKFGAFCWCS-UHFFFAOYSA-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
Leplaea thompsonii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Hexacarboxylic acids and derivatives

Direct Parent

Hexacarboxylic acids and derivatives

Alternative Parents

Substituents

Hexacarboxylic acid or derivatives
Oxocin
Fatty acid ester
Gamma butyrolactone
Fatty acyl
Oxane
Monosaccharide
Furan
Heteroaromatic compound
Tetrahydrofuran
Carboxylic acid ester
Lactone
Dialkyl ether
Oxirane
Ether
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organooxygen 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	2.97	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	183.47 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	170.68 m³·mol⁻¹	ChemAxon
Polarizability	70.53 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

383073

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

433157

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate (NP0219786)

MOL for NP0219786 (6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate)

3D MOL for NP0219786 (6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate)

3D SDF for NP0219786 (6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate)

3D-SDF for NP0219786 (6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate)

PDB for NP0219786 (6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate)

3D PDB for NP0219786 (6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate)

SMILES for NP0219786 (6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate)

INCHI for NP0219786 (6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate)

Structure for NP0219786 (6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate)

3D Structure for NP0219786 (6-[5-(acetyloxy)-4,9a-dimethyl-2,7-dioxo-tetrahydro-3h-furo[2,3-c]oxocin-4-yl]-5-(formyloxy)-3-(furan-3-yl)-3a-methyl-7-methylidene-hexahydroindeno[1,7a-b]oxiren-4-yl 2-(acetyloxy)-3-methylpentanoate)