NP-MRD: Showing NP-Card for (9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate (NP0240049)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 23:45:53 UTC

Updated at

2022-09-06 23:45:53 UTC

NP-MRD ID

NP0240049

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate

Description

CHEMBL4471756 belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. (9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate is found in Scleroderma areolatum. Based on a literature review very few articles have been published on CHEMBL4471756.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072201452D          

 39 43  0  0  1  0            999 V2000
   -2.6844   -4.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8848   -4.9475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6612   -5.7416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3089   -4.3568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5326   -3.5627    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3065   -3.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2738   -2.4525    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9215   -1.9415    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8028   -1.1251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6879   -2.2470    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3356   -1.7360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1020   -2.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7497   -1.5304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2206   -2.8578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9870   -3.1633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5729   -3.3688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8066   -3.0634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1589   -3.5744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4797   -2.2288    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0070   -1.5944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1145   -1.4891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2913   -1.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1668   -2.1215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1983   -2.8613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1524   -3.6080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9549   -3.7994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6049   -3.2913    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6129   -2.4664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9729   -1.9458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2628   -1.9583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0653   -2.1497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4160   -2.8964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2410   -2.9044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0509   -3.6362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2448   -3.8120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4386   -4.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7100   -4.4401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0216   -2.9150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6377   -3.6452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  1  0  0  0
 10  8  1  6  0  0  0
 10 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
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  1  0  0  0
  7 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 26  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 23 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 27 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 24 38  1  0  0  0  0
  5 38  1  0  0  0  0
 19 38  1  0  0  0  0
 38 39  1  1  0  0  0
M  END

     RDKit          3D

 81 85  0  0  0  0  0  0  0  0999 V2000
   -0.4701    0.6203   -5.1318 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3361    0.9708   -3.9248 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2399    1.8526   -3.9992 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1442    0.3730   -2.7094 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8235    0.6137   -1.5317 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7611   -0.5411   -1.1214 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1587    0.0558    0.2533 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1475   -0.7781    0.9499 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5255   -0.1561    2.2694 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4149   -1.0342    0.1687 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1288    0.1529   -0.0647 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5300    0.1733   -0.1476 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1589    1.1741   -0.5973 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3062   -0.9799    0.2913 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7947   -0.9610    0.2044 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6435   -2.0219    0.7605 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1892   -2.1112    0.8751 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7783   -3.3893    0.4776 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8097    0.1990    0.8105 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1504   -1.1074    1.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5968    1.0573    2.0073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8841    1.1758    2.2546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7538    0.9821    1.0918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2868    0.6546   -0.1323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0491    0.0382   -1.2068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3553   -0.5569   -0.7218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4369    0.4754   -0.5100 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2855    1.0018    0.8658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1412    1.2087    1.5222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3033    1.4280    1.8472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5980    1.6403    1.6813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2864    1.4708    0.3855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4008    2.0436    0.2946 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8162    0.7446   -0.7243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7575   -0.2196   -0.6563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8293   -1.0561   -1.9195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0542   -1.1509    0.4928 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1071    0.9678   -0.3362 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2581    2.4836   -0.1078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9162   -0.3902   -5.0302 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1572    0.7295   -6.0312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3082    1.3671   -5.1541 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5812    1.4212   -1.7965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6104   -0.5820   -1.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2097   -1.4786   -1.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5481    1.0714   -0.0094 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420   -1.7969    1.1982 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0552   -0.6289    3.1424 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2110    0.9110    2.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6408   -0.1022    2.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1894   -1.4464   -0.8495 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2472   -1.6489    0.9470 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1262   -1.1504   -0.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1566    0.0641    0.5060 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2805   -2.8694    1.0784 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9511   -2.0558    1.9775 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4063   -4.0222    0.9415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1355   -1.2210    2.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7686   -1.9997    0.8717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7983   -1.2601    0.5304 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1081    2.0210    2.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9855    0.4815    2.9003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2405    0.4353    3.0311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0525    2.1733    2.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3094    0.7888   -1.9728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5417   -0.8388   -1.7006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7237   -1.3302   -1.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1713   -1.0411    0.2562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3742    1.2819   -1.2674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3082    1.6052    2.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9191    1.5888    2.8570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1834    1.9567    2.5347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5800   -2.1316   -1.6754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2325   -0.6561   -2.7394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9059   -1.0929   -2.2150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2550   -1.1158    1.2628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1464   -2.2129    0.1813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0029   -0.8967    1.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5173    2.8942    0.5337 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2882    2.7616    0.1320 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0641    2.9222   -1.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 38  1  0
 38 39  1  1
 38 24  1  0
 24 23  2  0
 23 22  1  0
 22 21  1  0
 21 19  1  0
 19 20  1  1
 23 29  1  0
 29 28  2  0
 28 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 32 34  1  0
 34 35  1  0
 35 36  1  0
 35 37  1  0
 35 27  1  0
 27 26  1  0
 26 25  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 19  7  1  0
 27 28  1  0
 17 10  1  0
 19 38  1  0
 25 24  1  0
  9 48  1  0
  9 49  1  0
  9 50  1  0
  8 47  1  1
  7 46  1  6
  6 44  1  0
  6 45  1  0
  5 43  1  6
  1 40  1  0
  1 41  1  0
  1 42  1  0
 39 79  1  0
 39 80  1  0
 39 81  1  0
 22 63  1  0
 22 64  1  0
 21 61  1  0
 21 62  1  0
 20 58  1  0
 20 59  1  0
 20 60  1  0
 29 70  1  0
 30 71  1  0
 31 72  1  0
 36 73  1  0
 36 74  1  0
 36 75  1  0
 37 76  1  0
 37 77  1  0
 37 78  1  0
 27 69  1  6
 26 67  1  0
 26 68  1  0
 25 65  1  0
 25 66  1  0
 10 51  1  6
 15 52  1  0
 15 53  1  0
 15 54  1  0
 16 55  1  0
 17 56  1  1
 18 57  1  0
M  END


  Mrv1652309072201452D          

 39 43  0  0  1  0            999 V2000
   -2.6844   -4.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8848   -4.9475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6612   -5.7416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3089   -4.3568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5326   -3.5627    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3065   -3.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2738   -2.4525    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9215   -1.9415    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8028   -1.1251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6879   -2.2470    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3356   -1.7360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1020   -2.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7497   -1.5304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2206   -2.8578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9870   -3.1633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5729   -3.3688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8066   -3.0634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1589   -3.5744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4797   -2.2288    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0070   -1.5944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1145   -1.4891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2913   -1.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1668   -2.1215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1983   -2.8613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1524   -3.6080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9549   -3.7994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6049   -3.2913    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6129   -2.4664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9729   -1.9458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2628   -1.9583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0653   -2.1497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4160   -2.8964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2410   -2.9044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0509   -3.6362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2448   -3.8120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4386   -4.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7100   -4.4401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0216   -2.9150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6377   -3.6452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  1  0  0  0
 10  8  1  6  0  0  0
 10 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
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  1  0  0  0
  7 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 26  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 23 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 27 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 24 38  1  0  0  0  0
  5 38  1  0  0  0  0
 19 38  1  0  0  0  0
 38 39  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0240049

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]([C@H]1C[C@@H](OC(C)=O)[C@@]2(C)C3=C(CC[C@]12C)C=C1C=CC(=O)OC(C)(C)[C@@H]1CC3)[C@H]1OC(=O)C(C)=C[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C32H42O7/c1-17-14-25(34)28(38-29(17)36)18(2)24-16-26(37-19(3)33)32(7)23-10-9-22-20(8-11-27(35)39-30(22,4)5)15-21(23)12-13-31(24,32)6/h8,11,14-15,18,22,24-26,28,34H,9-10,12-13,16H2,1-7H3/t18-,22+,24+,25-,26+,28+,31+,32+/m0/s1

> <INCHI_KEY>
XNFBOJFRJTXMJL-XUONUPSOSA-N

> <FORMULA>
C32H42O7

> <MOLECULAR_WEIGHT>
538.681

> <EXACT_MASS>
538.293053692

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
58.50413910391987

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(9R,13R,14R,16R,17R)-16-[(1S)-1-[(2R,3S)-3-hydroxy-5-methyl-6-oxo-3,6-dihydro-2H-pyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0^{3,9}.0^{13,17}]nonadeca-1(12),2,4-trien-14-yl acetate

> <JCHEM_LOGP>
4.538948783333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.719411700923946

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3589293220158662

> <JCHEM_POLAR_SURFACE_AREA>
99.13000000000001

> <JCHEM_REFRACTIVITY>
148.65080000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(9R,13R,14R,16R,17R)-16-[(1S)-1-[(2R,3S)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0^{3,9}.0^{13,17}]nonadeca-1(12),2,4-trien-14-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.011  -8.856   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.518  -9.235   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -3.101 -10.718   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -2.443  -8.133   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -2.861  -6.650   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.305  -6.117   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.244  -4.578   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.453  -3.624   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.232  -2.100   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.884  -4.194   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -8.093  -3.240   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -9.524  -3.811   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0     -10.733  -2.857   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -9.745  -5.335   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -11.176  -5.905   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.536  -6.288   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -7.106  -5.718   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -5.897  -6.672   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.762  -4.161   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.746  -2.976   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.080  -2.780   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.544  -2.679   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.311  -3.960   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.370  -5.341   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.284  -6.735   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.782  -7.092   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.996  -6.144   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.011  -4.604   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.816  -3.632   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.224  -3.655   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.722  -4.013   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.377  -5.407   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       7.917  -5.422   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       5.695  -6.788   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       4.190  -7.116   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.552  -8.613   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.192  -8.288   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -1.907  -5.441   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -1.190  -6.804   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   38                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   19                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   10   18                                                  
CONECT   18   17                                                            
CONECT   19    7   20   21   38                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   29                                                  
CONECT   24   23   25   38                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   35                                                  
CONECT   28   27   29   30                                                  
CONECT   29   28   23                                                       
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   27   36   37                                             
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   24    5   19   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

C₃₂H₄₂O₇

Average Mass

538.6810 Da

Monoisotopic Mass

538.29305 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]([C@H]1C[C@@H](OC(C)=O)[C@@]2(C)C3=C(CC[C@]12C)C=C1C=CC(=O)OC(C)(C)[C@@H]1CC3)[C@H]1OC(=O)C(C)=C[C@@H]1O

InChI Identifier

InChI=1S/C32H42O7/c1-17-14-25(34)28(38-29(17)36)18(2)24-16-26(37-19(3)33)32(7)23-10-9-22-20(8-11-27(35)39-30(22,4)5)15-21(23)12-13-31(24,32)6/h8,11,14-15,18,22,24-26,28,34H,9-10,12-13,16H2,1-7H3/t18-,22+,24+,25-,26+,28+,31+,32+/m0/s1

InChI Key

XNFBOJFRJTXMJL-XUONUPSOSA-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
Scleroderma areolatum	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Dihydropyranone
Pyran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

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

103881525

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

146684325

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate (NP0240049)

MOL for NP0240049 ((9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate)

3D MOL for NP0240049 ((9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate)

3D SDF for NP0240049 ((9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate)

3D-SDF for NP0240049 ((9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate)

PDB for NP0240049 ((9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate)

3D PDB for NP0240049 ((9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate)

SMILES for NP0240049 ((9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate)

INCHI for NP0240049 ((9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate)

Structure for NP0240049 ((9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate)

3D Structure for NP0240049 ((9r,13r,14r,16r,17r)-16-[(1s)-1-[(2r,3s)-3-hydroxy-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,8,13,17-tetramethyl-6-oxo-7-oxatetracyclo[10.7.0.0³,⁹.0¹³,¹⁷]nonadeca-1(12),2,4-trien-14-yl acetate)