NP-MRD: Showing NP-Card for methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate (NP0260476)

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Record Information

Version

2.0

Created at

2022-09-08 02:39:41 UTC

Updated at

2022-09-08 02:39:41 UTC

NP-MRD ID

NP0260476

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate

Description

Polyfibrospongol A monoacetate belongs to the class of organic compounds known as m-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 3 of the benzene ring is replaced by a methoxy group. Based on a literature review very few articles have been published on polyfibrospongol A monoacetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082204392D          

 31 33  0  0  1  0            999 V2000
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8163   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -3.0781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0915   -3.8065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5287   -4.5061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1414   -5.2346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3169   -5.2634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5785   -5.9342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1912   -6.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3532   -4.4774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7405   -3.7489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5650   -3.7201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0022   -4.4198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3033   -3.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6906   -2.3208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5151   -2.2921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9523   -2.9917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9024   -1.5636    0.0000 O   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
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 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
 18 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 27  2  0  0  0  0
 16 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
M  END

     RDKit          3D

 67 69  0  0  0  0  0  0  0  0999 V2000
   -4.0822    1.6021   -1.3694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1976    1.4626   -0.4103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4788    2.6103    0.1021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9831    2.5422    1.5151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6742    1.1561    1.9819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6190    0.1858    0.8017 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9459    0.1085    0.1528 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1186   -0.0414    1.1509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0696   -0.9240   -0.9238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3303   -2.1796   -0.6582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9926   -2.0234   -0.0087 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5549   -3.4331    0.3680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8801   -1.0579    1.1047 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4934   -1.7712    2.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5458   -0.7733    1.5451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4253   -0.1138    0.5771 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4953    1.2724    0.4681 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2745    1.9268   -0.4828 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2987    3.4015   -0.5349 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6197    4.0676    0.2730 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0614    4.0552   -1.4640 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1654    5.4503   -1.6097 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0121    1.1870   -1.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9773   -0.1878   -1.2892 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7199   -0.9831   -2.1692 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5496   -0.5025   -3.1795 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1966   -0.7911   -0.3357 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2370   -2.1912   -0.3383 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1669   -2.8878    0.4180 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2013   -4.3646    0.4100 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9843   -2.2501    1.1137 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3263    2.5546   -1.8363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6206    0.7165   -1.7354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6201    2.8049   -0.6099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1294    3.5249   -0.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1175    3.2242    1.5949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7648    2.9583    2.1763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7177    1.1425    2.4823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4456    0.7619    2.6680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9674    0.7540    0.0578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1080   -1.0240    1.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0744   -0.0723    0.5367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2457    0.8313    1.7871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1477   -1.1396   -1.0514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7342   -0.4755   -1.8800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1391   -2.7248   -1.6266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9199   -2.8943   -0.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2868   -1.6754   -0.8166 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0982   -3.5001    1.2255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164   -3.8944   -0.5047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4387   -4.0789    0.5465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7385   -1.0780    3.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6678   -2.4102    2.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2783   -2.4830    2.0377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6126   -0.2904    2.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0059   -1.7991    1.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9573    1.9424    1.1159 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2620    5.6916   -1.5912 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6839    6.0304   -0.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7630    5.7964   -2.5859 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6263    1.6937   -2.1095 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1912    0.4630   -3.6382 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5431   -0.2826   -2.7469 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6236   -1.3048   -3.9571 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0977   -4.7355    0.9530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2971   -4.7617    0.9550 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2322   -4.8184   -0.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 19  1  0
 19 20  2  0
 19 18  1  0
 18 23  2  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 24 27  2  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 29 31  2  0
 27 16  1  0
 16 15  1  0
 13 15  1  1
 13 14  1  0
 13 11  1  0
 11 12  1  0
 11 10  1  0
 10  9  1  0
  9  7  1  0
  7  8  1  1
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
 16 17  2  0
 17 18  1  0
  6 13  1  0
  2  7  1  0
 22 58  1  0
 22 59  1  0
 22 60  1  0
 23 61  1  0
 26 62  1  0
 26 63  1  0
 26 64  1  0
 30 65  1  0
 30 66  1  0
 30 67  1  0
 15 55  1  0
 15 56  1  0
 14 52  1  0
 14 53  1  0
 14 54  1  0
 11 48  1  6
 12 49  1  0
 12 50  1  0
 12 51  1  0
 10 46  1  0
 10 47  1  0
  9 44  1  0
  9 45  1  0
  8 41  1  0
  8 42  1  0
  8 43  1  0
  6 40  1  6
  5 38  1  0
  5 39  1  0
  4 36  1  0
  4 37  1  0
  3 34  1  0
  3 35  1  0
  1 32  1  0
  1 33  1  0
 17 57  1  0
M  END


  Mrv1652309082204392D          

 31 33  0  0  1  0            999 V2000
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8163   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -3.0781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0915   -3.8065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5287   -4.5061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1414   -5.2346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3169   -5.2634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5785   -5.9342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1912   -6.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3532   -4.4774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7405   -3.7489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5650   -3.7201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0022   -4.4198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3033   -3.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6906   -2.3208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5151   -2.2921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9523   -2.9917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9024   -1.5636    0.0000 O   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
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 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
 18 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 27  2  0  0  0  0
 16 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0260476

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CC(OC)=C(OC(C)=O)C(C[C@]2(C)[C@@H](C)CC[C@@]3(C)[C@H]2CCCC3=C)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C26H36O5/c1-16-9-8-10-22-25(16,4)12-11-17(2)26(22,5)15-20-13-19(24(28)30-7)14-21(29-6)23(20)31-18(3)27/h13-14,17,22H,1,8-12,15H2,2-7H3/t17-,22+,25+,26+/m0/s1

> <INCHI_KEY>
ZFRLLXLAQUFWHD-MCRPIMJISA-N

> <FORMULA>
C26H36O5

> <MOLECULAR_WEIGHT>
428.569

> <EXACT_MASS>
428.256274259

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
47.584283400507104

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 3-{[(1R,2S,4aS,8aS)-1,2,4a-trimethyl-5-methylidene-decahydronaphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate

> <JCHEM_LOGP>
5.8118066383333336

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.906164114177334

> <JCHEM_POLAR_SURFACE_AREA>
61.830000000000005

> <JCHEM_REFRACTIVITY>
120.79339999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl 3-{[(1R,2S,4aS,8aS)-1,2,4a-trimethyl-5-methylidene-hexahydro-2H-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.390  -4.440   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.944  -4.440   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.760  -5.746   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.037  -7.105   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.854  -8.411   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.131  -9.771   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.591  -9.825   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       2.947 -11.077   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.224 -12.437   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.393  -8.358   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.116  -6.998   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.655  -6.944   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.471  -8.250   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.300  -5.692   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.022  -4.332   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.562  -4.279   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.378  -5.584   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       7.285  -2.919   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    2    8    9                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6   14   15                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   27                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21                                                            
CONECT   23   18   24                                                       
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   16   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
Polyfibrospongol a monoacetic acid	Generator

Chemical Formula

C₂₆H₃₆O₅

Average Mass

428.5690 Da

Monoisotopic Mass

428.25627 Da

IUPAC Name

methyl 3-{[(1R,2S,4aS,8aS)-1,2,4a-trimethyl-5-methylidene-decahydronaphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate

Traditional Name

methyl 3-{[(1R,2S,4aS,8aS)-1,2,4a-trimethyl-5-methylidene-hexahydro-2H-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CC(OC)=C(OC(C)=O)C(C[C@]2(C)[C@@H](C)CC[C@@]3(C)[C@H]2CCCC3=C)=C1

InChI Identifier

InChI=1S/C26H36O5/c1-16-9-8-10-22-25(16,4)12-11-17(2)26(22,5)15-20-13-19(24(28)30-7)14-21(29-6)23(20)31-18(3)27/h13-14,17,22H,1,8-12,15H2,2-7H3/t17-,22+,25+,26+/m0/s1

InChI Key

ZFRLLXLAQUFWHD-MCRPIMJISA-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 m-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 3 of the benzene ring is replaced by a methoxy group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

M-methoxybenzoic acids and derivatives

Alternative Parents

Substituents

M-methoxybenzoic acid or derivatives
Benzoate ester
Phenol ester
Anisole
Phenoxy compound
Benzoyl
Phenol ether
Methoxybenzene
Alkyl aryl ether
Dicarboxylic acid or derivatives
Methyl ester
Carboxylic acid ester
Ether
Carboxylic acid derivative
Organooxygen compound
Organic oxygen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
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	5.81	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	61.83 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	120.79 m³·mol⁻¹	ChemAxon
Polarizability	47.58 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8821558

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10646199

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate (NP0260476)

MOL for NP0260476 (methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate)

3D MOL for NP0260476 (methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate)

3D SDF for NP0260476 (methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate)

3D-SDF for NP0260476 (methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate)

PDB for NP0260476 (methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate)

3D PDB for NP0260476 (methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate)

SMILES for NP0260476 (methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate)

INCHI for NP0260476 (methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate)

Structure for NP0260476 (methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate)

3D Structure for NP0260476 (methyl 3-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-4-(acetyloxy)-5-methoxybenzoate)