NP-MRD: Showing NP-Card for 3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid (NP0176387)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 14:02:08 UTC

Updated at

2022-09-03 14:02:08 UTC

NP-MRD ID

NP0176387

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid

Description

3-{[(3R,3aS,5aS,6R,7R,9aS,9bS)-3-acetyl-3a,6,7,9a-tetramethyl-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Based on a literature review very few articles have been published on 3-{[(3R,3aS,5aS,6R,7R,9aS,9bS)-3-acetyl-3a,6,7,9a-tetramethyl-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032216022D          

 31 34  0  0  1  0            999 V2000
   -0.2319   -3.7331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3781   -2.9211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1544   -2.6418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2519   -2.3885    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1913   -1.5657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9551   -1.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4877   -1.8839    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3123   -1.9097    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9223   -1.1827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7469   -1.2084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5715   -1.2342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9615   -1.9612    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7861   -1.9870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5269   -2.6624    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2930   -2.9687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3583   -3.4700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9735   -4.0198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7571   -3.7620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3723   -4.3118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1559   -4.0540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3245   -3.2464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7711   -4.6037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2037   -5.1194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4200   -5.3772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8049   -4.8274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0212   -5.0852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7023   -2.6367    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2677   -3.3379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4431   -3.3122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0531   -2.5852    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5476   -3.2371    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
  4  2  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 19 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  0  0  0  0
 14 27  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  7 30  1  0  0  0  0
  4 30  1  0  0  0  0
 30 31  1  1  0  0  0
M  END

     RDKit          3D

 69 72  0  0  0  0  0  0  0  0999 V2000
   -3.5720    1.6351    2.4476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6743    2.2202    1.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8774    3.4263    1.0410 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5503    1.4625   -0.1314 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5186    0.2724   -0.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6192   -0.9397   -0.5381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3409   -0.4731    0.1030 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2017   -1.4032    0.1259 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2127   -2.0930    1.4778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2867   -2.5071   -0.9128 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0098   -2.6562   -1.6734 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1150   -2.7297   -0.6507 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3448   -3.2725   -1.3274 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3271   -1.3104   -0.0889 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9209   -1.5880    1.2996 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4667   -0.7333   -0.8860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8782    0.6428   -0.5924 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7505    0.9302    0.4381 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1138    2.1997    0.8086 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0393    2.3762    1.9085 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5194    1.4038    2.5338 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4483    3.6536    2.3335 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5949    3.2684    0.1320 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7218    3.0306   -0.9048 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3633    1.7231   -1.2702 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4913    1.6567   -2.3374 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0800   -0.5744   -0.0846 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0575    0.6009    0.8049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0439    1.5793    0.1988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1861    0.8896   -0.4640 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0864    0.9189   -1.9770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9939    2.3591    3.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2653    0.7536    2.5629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5722    1.4202    2.8146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8787    2.1202   -1.0125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2813    0.3994   -1.0030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0024    0.0798    0.7415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0171   -1.8559   -0.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6124   -1.0151   -1.6209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6534   -0.2690    1.1769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2752   -2.0500    1.9136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6222   -1.6146    2.2499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0698   -3.2035    1.4099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0751   -2.3412   -1.6655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5037   -3.5016   -0.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0154   -3.6587   -2.1853 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2140   -1.8257   -2.3459 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8996   -3.3840    0.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2147   -3.3912   -0.6465 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1187   -4.3403   -1.6430 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5835   -2.7793   -2.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9610   -0.7306    1.9504 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4742   -2.4870    1.7725 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9934   -1.9248    1.1463 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2538   -0.8262   -2.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3882   -1.3926   -0.7987 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1789    0.0762    0.9857 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0653    4.1416    1.6898 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8771    4.2948    0.4185 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3314    3.8963   -1.4158 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1265    0.8635   -2.7924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0680   -0.1948   -1.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8771    1.1000    1.1079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5354    0.3125    1.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3313    2.2771    1.0123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4905    2.1268   -0.6090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2373    1.5721   -2.2673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0396   -0.0515   -2.4615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9744    1.4351   -2.4551 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  8  1  0
  8  9  1  1
  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
  4 30  1  0
 30 31  1  6
 30 29  1  0
 29 28  1  0
 28 27  1  0
 27 14  1  0
 14 15  1  1
 14 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 19 20  1  0
 20 22  1  0
 20 21  2  0
 14 12  1  0
 25 17  1  0
 27  8  1  0
 30  7  1  0
 13 49  1  0
 13 50  1  0
 13 51  1  0
 12 48  1  1
 11 46  1  0
 11 47  1  0
 10 44  1  0
 10 45  1  0
  9 41  1  0
  9 42  1  0
  9 43  1  0
  7 40  1  1
  6 38  1  0
  6 39  1  0
  5 36  1  0
  5 37  1  0
  4 35  1  6
  1 32  1  0
  1 33  1  0
  1 34  1  0
 31 67  1  0
 31 68  1  0
 31 69  1  0
 29 65  1  0
 29 66  1  0
 28 63  1  0
 28 64  1  0
 27 62  1  6
 15 52  1  0
 15 53  1  0
 15 54  1  0
 16 55  1  0
 16 56  1  0
 18 57  1  0
 23 59  1  0
 24 60  1  0
 26 61  1  0
 22 58  1  0
M  END


  Mrv1652309032216022D          

 31 34  0  0  1  0            999 V2000
   -0.2319   -3.7331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3781   -2.9211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1544   -2.6418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2519   -2.3885    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1913   -1.5657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9551   -1.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4877   -1.8839    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3123   -1.9097    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9223   -1.1827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7469   -1.2084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5715   -1.2342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9615   -1.9612    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7861   -1.9870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5269   -2.6624    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2930   -2.9687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3583   -3.4700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9735   -4.0198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7571   -3.7620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3723   -4.3118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1559   -4.0540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3245   -3.2464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7711   -4.6037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2037   -5.1194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4200   -5.3772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8049   -4.8274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0212   -5.0852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7023   -2.6367    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2677   -3.3379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4431   -3.3122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0531   -2.5852    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5476   -3.2371    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
  4  2  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 19 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  0  0  0  0
 14 27  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  7 30  1  0  0  0  0
  4 30  1  0  0  0  0
 30 31  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0176387

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@]2(C)[C@@H]3CC[C@@H](C(C)=O)[C@@]3(C)CC[C@H]2[C@]1(C)CC1=CC(=CC=C1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C27H38O4/c1-16-10-12-26(4)22-9-7-20(17(2)28)25(22,3)13-11-23(26)27(16,5)15-19-14-18(24(30)31)6-8-21(19)29/h6,8,14,16,20,22-23,29H,7,9-13,15H2,1-5H3,(H,30,31)/t16-,20+,22-,23-,25-,26-,27-/m1/s1

> <INCHI_KEY>
PCLWWUDFTVTRTJ-DCJOPLFNSA-N

> <FORMULA>
C27H38O4

> <MOLECULAR_WEIGHT>
426.597

> <EXACT_MASS>
426.277009704

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
49.11365121320672

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-{[(3R,3aS,5aS,6R,7R,9aS,9bS)-3-acetyl-3a,6,7,9a-tetramethyl-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid

> <ALOGPS_LOGP>
5.53

> <JCHEM_LOGP>
6.180682377666665

> <ALOGPS_LOGS>
-5.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.922372274411577

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.376010511421949

> <JCHEM_PKA_STRONGEST_BASIC>
-6.0621119076182675

> <JCHEM_POLAR_SURFACE_AREA>
74.60000000000001

> <JCHEM_REFRACTIVITY>
122.24559999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.12e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-{[(3R,3aS,5aS,6R,7R,9aS,9bS)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.433  -6.968   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.706  -5.453   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -2.155  -4.931   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.470  -4.459   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.357  -2.923   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.783  -2.341   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.777  -3.517   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.316  -3.565   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.588  -2.208   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.128  -2.256   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.667  -2.304   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.395  -3.661   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.934  -3.709   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.584  -4.970   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.014  -5.542   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.269  -6.477   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.417  -7.504   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.880  -7.022   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.028  -8.049   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.491  -7.567   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.806  -6.060   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      12.639  -8.594   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.714  -9.556   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.251 -10.037   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.102  -9.011   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.640  -9.492   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.044  -4.922   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.233  -6.231   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.694  -6.183   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.966  -4.826   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.022  -6.043   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   30                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   30                                                  
CONECT    8    7    9   10   27                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   27                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   19   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   17   26                                                  
CONECT   26   25                                                            
CONECT   27   14    8   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    7    4   31                                             
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Value	Source
3-{[(3R,3as,5as,6R,7R,9as,9BS)-3-acetyl-3a,6,7,9a-tetramethyl-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoate	Generator

Chemical Formula

C₂₇H₃₈O₄

Average Mass

426.5970 Da

Monoisotopic Mass

426.27701 Da

IUPAC Name

3-{[(3R,3aS,5aS,6R,7R,9aS,9bS)-3-acetyl-3a,6,7,9a-tetramethyl-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid

Traditional Name

3-{[(3R,3aS,5aS,6R,7R,9aS,9bS)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@]2(C)[C@@H]3CC[C@@H](C(C)=O)[C@@]3(C)CC[C@H]2[C@]1(C)CC1=CC(=CC=C1O)C(O)=O

InChI Identifier

InChI=1S/C27H38O4/c1-16-10-12-26(4)22-9-7-20(17(2)28)25(22,3)13-11-23(26)27(16,5)15-19-14-18(24(30)31)6-8-21(19)29/h6,8,14,16,20,22-23,29H,7,9-13,15H2,1-5H3,(H,30,31)/t16-,20+,22-,23-,25-,26-,27-/m1/s1

InChI Key

PCLWWUDFTVTRTJ-DCJOPLFNSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Hydroxybenzoic acid
Benzoic acid
Benzoic acid or derivatives
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	5.53	ALOGPS
logP	6.18	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	4.38	ChemAxon
pKa (Strongest Basic)	-6.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	122.25 m³·mol⁻¹	ChemAxon
Polarizability	49.11 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

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

163062132

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid (NP0176387)

MOL for NP0176387 (3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid)

3D MOL for NP0176387 (3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid)

3D SDF for NP0176387 (3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid)

3D-SDF for NP0176387 (3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid)

PDB for NP0176387 (3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid)

3D PDB for NP0176387 (3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid)

SMILES for NP0176387 (3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid)

INCHI for NP0176387 (3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid)

Structure for NP0176387 (3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid)

3D Structure for NP0176387 (3-{[(3r,3as,5as,6r,7r,9as,9bs)-3-acetyl-3a,6,7,9a-tetramethyl-decahydrocyclopenta[a]naphthalen-6-yl]methyl}-4-hydroxybenzoic acid)