NP-MRD: Showing NP-Card for methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate (NP0328893)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 12:45:52 UTC

Updated at

2022-09-12 12:45:52 UTC

NP-MRD ID

NP0328893

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate

Description

Methyl 2-{[2-hydroperoxy-4,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-5-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton. methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate is found in Asclepias curassavica. Based on a literature review very few articles have been published on methyl 2-{[2-hydroperoxy-4,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-5-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122214452D          

 40 45  0  0  0  0            999 V2000
   -6.5877   -0.4312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7952   -0.2019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2003   -0.7736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3980   -1.5745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4078   -0.5443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2626   -1.3564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7187    0.2199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0880    0.7517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1476    1.5746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3873    0.3162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5850   -0.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0532   -1.1154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2411   -0.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7092   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8971   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3653   -2.0864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4468   -1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7271   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1953   -0.5346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4756    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2877    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8195   -0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1794    0.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6441   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1505    0.3804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9211    1.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6040    1.6359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6308    2.4604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2553    1.1295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9750    0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8734   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1906   -1.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5392   -1.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3416   -1.8210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6168   -0.6798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3365    0.0961    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8683    0.7268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1486   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9608   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4926    0.4364    0.0000 O   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  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 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
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
 24 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 18 33  1  0  0  0  0
 22 33  1  0  0  0  0
 33 34  1  0  0  0  0
 19 35  1  0  0  0  0
 15 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 35 38  1  0  0  0  0
 38 39  1  0  0  0  0
 13 39  1  0  0  0  0
 39 40  1  0  0  0  0
M  END

     RDKit          3D

 82 87  0  0  0  0  0  0  0  0999 V2000
   -6.5778    4.1079    1.5972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1163    2.7712    1.5357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0687    2.1332    0.3209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4375    2.7511   -0.7051 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5969    0.7303    0.1507 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2254    0.1773    1.3781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7125   -0.0631   -0.4931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4178    0.0869   -1.9440 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.2138   -1.3281   -2.5043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2400    0.8054   -2.0921 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5226    0.6320   -0.9015 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9030   -0.5632   -0.8069 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5529   -0.5668   -0.5514 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1544   -1.1871    0.7712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7022   -0.8583    0.9249 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1335   -0.9246    2.2891 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2213   -0.1920    2.1900 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0856   -0.9278    1.1880 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4234   -0.9816   -0.1998 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4359   -1.7892   -0.9859 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4939   -0.7764   -1.3638 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2035   -0.3182   -0.1213 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5359   -1.0597   -0.1287 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4838    1.1513   -0.3019 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8876    1.5586   -0.3170 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4275    2.3167    0.6269 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8265    2.5131    0.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6600    3.1875    0.9570 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0783    1.8470   -0.8842 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8860    1.3033   -1.3693 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7087    1.7853    0.8355 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8052    0.7735    1.9167 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4950   -0.5384    1.1694 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2164   -1.4911    1.8987 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1038   -1.7226   -0.0016 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4521   -2.8711    0.6998 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5324   -3.5875    1.1242 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6065   -2.0323   -1.2779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7088   -1.1102   -1.6533 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2379   -0.0599   -2.4452 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6182    4.2347    1.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9150    4.7581    1.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4625    4.4206    2.6628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6503    0.7327    2.0792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6809    0.4416   -0.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7215   -1.1192   -0.1495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2871    0.5026   -2.4635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9861   -1.5799   -3.2631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2599   -2.1005   -1.7222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1795   -1.4091   -2.9400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8568    1.5271   -0.7246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2847    0.5242   -0.4512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6784   -0.6775    1.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3899   -2.2665    0.8033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5506    0.1976    0.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0040   -1.9392    2.6541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7407   -0.2787    2.9689 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6706   -0.3312    3.1906 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9721    0.8305    1.9247 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9751   -2.0148    1.5149 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3201   -0.0027   -0.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0615   -2.2462   -1.8856 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8820   -2.6082   -0.3550 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1924   -1.1519   -2.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9375    0.1149   -1.7807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3717   -1.9799    0.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3483   -0.5272    0.3481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7549   -1.5303   -1.1157 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9912    1.5604   -1.2395 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0025    2.7581    1.5236 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5606    1.8941   -2.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9763    0.2883   -1.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6306    1.8008    0.5066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0439    2.7915    1.1091 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1954    0.9353    2.7931 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8796    0.7496    2.2706 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7302   -2.3511    1.9009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3558   -4.5401    0.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0520   -3.0662   -1.1520 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0514   -2.1325   -2.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4019   -1.6877   -2.3358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2415    0.7954   -1.9183 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  1  1
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 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
 20 21  1  0
 21 22  1  0
 22 23  1  1
 22 24  1  0
 24 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  1
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 29 30  1  0
 19 35  1  0
 35 38  1  0
 38 39  1  0
 39 40  1  0
 35 36  1  1
 36 37  1  0
 11  5  1  0
 39 13  1  0
 35 15  1  0
 33 18  1  0
 30 25  1  0
 33 22  1  0
  1 41  1  0
  1 42  1  0
  1 43  1  0
  6 44  1  0
  7 45  1  0
  7 46  1  0
  8 47  1  6
  9 48  1  0
  9 49  1  0
  9 50  1  0
 11 51  1  1
 13 52  1  1
 14 53  1  0
 14 54  1  0
 15 55  1  6
 16 56  1  0
 16 57  1  0
 17 58  1  0
 17 59  1  0
 18 60  1  1
 19 61  1  6
 20 62  1  0
 20 63  1  0
 21 64  1  0
 21 65  1  0
 23 66  1  0
 23 67  1  0
 23 68  1  0
 24 69  1  6
 31 73  1  0
 31 74  1  0
 32 75  1  0
 32 76  1  0
 34 77  1  0
 26 70  1  0
 30 71  1  0
 30 72  1  0
 38 79  1  0
 38 80  1  0
 39 81  1  6
 40 82  1  0
 37 78  1  0
M  END


  Mrv1652309122214452D          

 40 45  0  0  0  0            999 V2000
   -6.5877   -0.4312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7952   -0.2019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2003   -0.7736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3980   -1.5745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4078   -0.5443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2626   -1.3564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7187    0.2199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0880    0.7517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1476    1.5746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3873    0.3162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5850   -0.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0532   -1.1154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2411   -0.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7092   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8971   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3653   -2.0864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4468   -1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7271   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1953   -0.5346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4756    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2877    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8195   -0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1794    0.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6441   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1505    0.3804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9211    1.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6040    1.6359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6308    2.4604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2553    1.1295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9750    0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8734   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1906   -1.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5392   -1.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3416   -1.8210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6168   -0.6798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3365    0.0961    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8683    0.7268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1486   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9608   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4926    0.4364    0.0000 O   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  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 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
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
 24 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 18 33  1  0  0  0  0
 22 33  1  0  0  0  0
 33 34  1  0  0  0  0
 19 35  1  0  0  0  0
 15 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 35 38  1  0  0  0  0
 38 39  1  0  0  0  0
 13 39  1  0  0  0  0
 39 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0328893

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1(O)CC(C)OC1OC1CC2CCC3C(CCC4(C)C(CCC34O)C3=CC(=O)OC3)C2(CC1O)OO

> <INCHI_IDENTIFIER>
InChI=1S/C29H42O11/c1-15-12-27(33,24(32)36-3)25(38-15)39-22-11-17-4-5-20-19(28(17,40-35)13-21(22)30)6-8-26(2)18(7-9-29(20,26)34)16-10-23(31)37-14-16/h10,15,17-22,25,30,33-35H,4-9,11-14H2,1-3H3

> <INCHI_KEY>
NTWQXIKROQBTKK-UHFFFAOYSA-N

> <FORMULA>
C29H42O11

> <MOLECULAR_WEIGHT>
566.644

> <EXACT_MASS>
566.272712172

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
59.32802785952444

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-{[2-hydroperoxy-4,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate

> <JCHEM_LOGP>
1.3583739236666672

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.605329580682808

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.182471761445797

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1663592689632276

> <JCHEM_POLAR_SURFACE_AREA>
161.21

> <JCHEM_REFRACTIVITY>
138.06519999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-{[2-hydroperoxy-4,11-dihydroxy-15-methyl-14-(5-oxo-2H-furan-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0     -12.297  -0.805   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0     -10.818  -0.377   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -9.707  -1.444   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0     -10.076  -2.939   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -8.228  -1.016   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -7.957  -2.532   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -8.808   0.411   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -7.631   1.403   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -7.742   2.939   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -6.323   0.590   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -6.692  -0.905   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -5.699  -2.082   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -4.183  -1.811   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.191  -2.988   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.675  -2.717   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.682  -3.895   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.834  -3.624   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.357  -2.175   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.365  -0.998   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.888   0.451   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.404   0.722   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.396  -0.456   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.068   0.930   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.936  -0.506   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.881   0.710   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.453   2.189   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.727   3.054   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.777   4.593   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       7.943   2.108   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       7.420   0.660   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.364  -1.985   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.089  -2.849   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.873  -1.904   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       2.504  -3.399   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -1.151  -1.269   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -0.628   0.179   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      -1.621   1.357   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -2.144  -0.092   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -3.660  -0.363   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -4.653   0.815   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7   11                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10    5   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   39                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   35                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   33                                                  
CONECT   19   18   20   35                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   33                                             
CONECT   23   22                                                            
CONECT   24   22   25   31                                                  
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   25                                                       
CONECT   31   24   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   18   22   34                                             
CONECT   34   33                                                            
CONECT   35   19   15   36   38                                             
CONECT   36   35   37                                                       
CONECT   37   36                                                            
CONECT   38   35   39                                                       
CONECT   39   38   13   40                                                  
CONECT   40   39                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   90    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-{[2-hydroperoxy-4,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0,.0,]heptadecan-5-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylic acid	Generator

Chemical Formula

C₂₉H₄₂O₁₁

Average Mass

566.6440 Da

Monoisotopic Mass

566.27271 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)C1(O)CC(C)OC1OC1CC2CCC3C(CCC4(C)C(CCC34O)C3=CC(=O)OC3)C2(CC1O)OO

InChI Identifier

InChI=1S/C29H42O11/c1-15-12-27(33,24(32)36-3)25(38-15)39-22-11-17-4-5-20-19(28(17,40-35)13-21(22)30)6-8-26(2)18(7-9-29(20,26)34)16-10-23(31)37-14-16/h10,15,17-22,25,30,33-35H,4-9,11-14H2,1-3H3

InChI Key

NTWQXIKROQBTKK-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
Asclepias curassavica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Steroid lactones

Alternative Parents

Substituents

Steroid lactone
Estrane-skeleton
2-hydroxysteroid
14-hydroxysteroid
Hydroxysteroid
2-furanone
Dicarboxylic acid or derivatives
Cyclic alcohol
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Tertiary alcohol
Tetrahydrofuran
Methyl ester
Enoate ester
Carboxylic acid ester
Hydroperoxide
Lactone
Secondary alcohol
Carboxylic acid derivative
Organoheterocyclic compound
Peroxol
Acetal
Alkyl hydroperoxide
Oxacycle
Carbonyl group
Organic oxygen compound
Alcohol
Organic oxide
Hydrocarbon derivative
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

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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73024884

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate (NP0328893)

MOL for NP0328893 (methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate)

3D MOL for NP0328893 (methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate)

3D SDF for NP0328893 (methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate)

3D-SDF for NP0328893 (methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate)

PDB for NP0328893 (methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate)

3D PDB for NP0328893 (methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate)

SMILES for NP0328893 (methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate)

INCHI for NP0328893 (methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate)

Structure for NP0328893 (methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate)

3D Structure for NP0328893 (methyl 2-{[9a-hydroperoxy-3a,8-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-tetradecahydrocyclopenta[a]phenanthren-7-yl]oxy}-3-hydroxy-5-methyloxolane-3-carboxylate)