NP-MRD: Showing NP-Card for 07H239-A (NP0005515)

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Record Information

Version

2.0

Created at

2020-12-09 02:44:43 UTC

Updated at

2021-07-15 16:52:14 UTC

NP-MRD ID

NP0005515

Secondary Accession Numbers

None

Natural Product Identification

Common Name

07H239-A

Provided By

NPAtlas

Description

(1S,4R,7S,8aR)-4-{[(2E,4E)-6,8-dimethyldeca-2,4-dienoyl]oxy}-8a-methyl-6-oxo-7-(3-oxoprop-1-en-2-yl)-1,2,3,4,6,7,8,8a-octahydronaphthalene-1-carboxylic acid belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5. 07H239-A is found in Unknown-fungus sp. LL-07H239. 07H239-A was first documented in 2004 (PMID: 15387660). Based on a literature review very few articles have been published on (1S,4R,7S,8aR)-4-{[(2E,4E)-6,8-dimethyldeca-2,4-dienoyl]oxy}-8a-methyl-6-oxo-7-(3-oxoprop-1-en-2-yl)-1,2,3,4,6,7,8,8a-octahydronaphthalene-1-carboxylic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118193D          

 69 70  0  0  0  0            999 V2000
   -7.9549    2.3253   -0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8349    1.9521    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4764    2.4572    1.6345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4293    2.1437    2.2496 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9128    0.9921   -0.3691 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7736   -0.2823    0.4121 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4334   -0.9606    0.1902 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3024   -1.1809   -1.3115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3893   -0.0309    0.6894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5084    1.2358    0.3270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6180    1.7037   -0.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4910    2.6344   -1.3332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2482   -0.3893    1.5421 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0269   -0.3861    0.8059 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0729    0.3420    1.1584 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0135    1.0543    2.1926 O   0  0  0  0  0  0  0  0  0  0  0  0
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 33 69  1  0  0  0  0
M  END

     RDKit          3D

 69 70  0  0  0  0  0  0  0  0999 V2000
   -7.9549    2.3253   -0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8349    1.9521    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
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 29 67  1  0
 30 68  1  1
 33 69  1  0
M  END


  Mrv1652306242118193D          

 69 70  0  0  0  0            999 V2000
   -7.9549    2.3253   -0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8349    1.9521    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4764    2.4572    1.6345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4293    2.1437    2.2496 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9128    0.9921   -0.3691 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7736   -0.2823    0.4121 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4334   -0.9606    0.1902 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3024   -1.1809   -1.3115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3893   -0.0309    0.6894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5084    1.2358    0.3270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6180    1.7037   -0.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4910    2.6344   -1.3332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2482   -0.3893    1.5421 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0269   -0.3861    0.8059 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0729    0.3420    1.1584 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0135    1.0543    2.1926 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3276    0.3303    0.3803 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3615    1.0524    0.7650 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6341    1.0621    0.0059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6432    1.7880    0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9626    1.9275   -0.1859 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1528    3.4072   -0.5274 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3114    1.1186   -1.3646 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3523   -0.3593   -1.2132 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7152   -0.9881   -2.5614 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6014   -0.6548   -0.3413 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7078   -2.1674   -0.1467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3810   -1.7851    2.1235 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9346   -2.6811    1.0678 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4074   -2.2945    0.8767 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0445   -3.3669    0.1170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4301   -4.3958   -0.2524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3825   -3.2607   -0.2183 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.6167   -0.9816    0.1988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2216   -0.8948   -1.8620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3899   -0.6890   -1.6904 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.7732    1.9715    0.6580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1605    0.2908    2.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4416   -0.2545   -0.5091 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2562    1.6434    1.6577 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7050    0.4932   -0.8894 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4357    2.3660    1.3435 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7321    1.7216    0.6020 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5318    3.6004   -1.4142 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7615    4.0097    0.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2235    3.5732   -0.6635 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5521    1.3798   -2.1723 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2674    1.5242   -1.8067 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4785   -0.7970   -0.7595 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4637   -0.2980   -3.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8187   -1.1248   -3.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1693   -1.9907   -2.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4619   -0.3281   -0.9523 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5379   -0.1261    0.6047 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8353   -2.3471    0.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6122   -2.5666   -0.6830 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7704   -2.6484   -0.5084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0461   -1.8159    3.0049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3802   -2.1482    2.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3736   -2.6173    0.1154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8698   -3.7521    1.4140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8223   -2.1540    1.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9246   -3.9295   -0.7109 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 13 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 11  5  1  0  0  0  0
 30  7  1  0  0  0  0
  1 34  1  0  0  0  0
  1 35  1  0  0  0  0
  3 36  1  0  0  0  0
  5 37  1  6  0  0  0
  6 38  1  0  0  0  0
  6 39  1  0  0  0  0
  8 40  1  0  0  0  0
  8 41  1  0  0  0  0
  8 42  1  0  0  0  0
 10 43  1  0  0  0  0
 13 44  1  1  0  0  0
 17 45  1  0  0  0  0
 18 46  1  0  0  0  0
 19 47  1  0  0  0  0
 20 48  1  0  0  0  0
 21 49  1  1  0  0  0
 22 50  1  0  0  0  0
 22 51  1  0  0  0  0
 22 52  1  0  0  0  0
 23 53  1  0  0  0  0
 23 54  1  0  0  0  0
 24 55  1  1  0  0  0
 25 56  1  0  0  0  0
 25 57  1  0  0  0  0
 25 58  1  0  0  0  0
 26 59  1  0  0  0  0
 26 60  1  0  0  0  0
 27 61  1  0  0  0  0
 27 62  1  0  0  0  0
 27 63  1  0  0  0  0
 28 64  1  0  0  0  0
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 29 66  1  0  0  0  0
 29 67  1  0  0  0  0
 30 68  1  1  0  0  0
 33 69  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005515

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)[C@@]1([H])C([H])([H])C([H])([H])[C@@]([H])(OC(=O)C(\[H])=C(/[H])\C(\[H])=C(/[H])[C@]([H])(C([H])([H])[H])C([H])([H])[C@@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H])C2=C([H])C(=O)[C@]([H])(C(=C([H])[H])C([H])=O)C([H])([H])[C@]12C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C27H36O6/c1-6-17(2)13-18(3)9-7-8-10-25(30)33-24-12-11-21(26(31)32)27(5)15-20(19(4)16-28)23(29)14-22(24)27/h7-10,14,16-18,20-21,24H,4,6,11-13,15H2,1-3,5H3,(H,31,32)/b9-7+,10-8+/t17-,18-,20-,21+,24+,27+/m0/s1

> <INCHI_KEY>
KFNRVRQZGWBRJR-XQLFHWRFSA-N

> <FORMULA>
C27H36O6

> <MOLECULAR_WEIGHT>
456.579

> <EXACT_MASS>
456.251188879

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
51.4938918923644

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4R,7S,8aR)-4-{[(2E,4E,6R,8S)-6,8-dimethyldeca-2,4-dienoyl]oxy}-8a-methyl-6-oxo-7-(3-oxoprop-1-en-2-yl)-1,2,3,4,6,7,8,8a-octahydronaphthalene-1-carboxylic acid

> <ALOGPS_LOGP>
3.99

> <JCHEM_LOGP>
5.390709962666667

> <ALOGPS_LOGS>
-5.65

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.116881464291584

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.1452064641764315

> <JCHEM_PKA_STRONGEST_BASIC>
-5.013896443327932

> <JCHEM_POLAR_SURFACE_AREA>
97.74000000000001

> <JCHEM_REFRACTIVITY>
129.3875

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.03e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4R,7S,8aR)-4-{[(2E,4E,6R,8S)-6,8-dimethyldeca-2,4-dienoyl]oxy}-8a-methyl-6-oxo-7-(3-oxoprop-1-en-2-yl)-1,2,3,4,7,8-hexahydronaphthalene-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 69 70  0  0  0  0  0  0  0  0999 V2000
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   -6.8349    1.9521    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4764    2.4572    1.6345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4293    2.1437    2.2496 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9128    0.9921   -0.3691 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7736   -0.2823    0.4121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4334   -0.9606    0.1902 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3024   -1.1809   -1.3115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3893   -0.0309    0.6894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5084    1.2358    0.3270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6180    1.7037   -0.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4910    2.6344   -1.3332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2482   -0.3893    1.5421 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0269   -0.3861    0.8059 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0729    0.3420    1.1584 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0135    1.0543    2.1926 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3276    0.3303    0.3803 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3615    1.0524    0.7650 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6341    1.0621    0.0059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6432    1.7880    0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9626    1.9275   -0.1859 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1528    3.4072   -0.5274 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3114    1.1186   -1.3646 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3523   -0.3593   -1.2132 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7152   -0.9881   -2.5614 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.7078   -2.1674   -0.1467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3810   -1.7851    2.1235 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0445   -3.3669    0.1170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4301   -4.3958   -0.2524 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3899   -0.6890   -1.6904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1664   -2.2814   -1.5282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7732    1.9715    0.6580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1605    0.2908    2.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4416   -0.2545   -0.5091 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7050    0.4932   -0.8894 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4357    2.3660    1.3435 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7321    1.7216    0.6020 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5318    3.6004   -1.4142 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5521    1.3798   -2.1723 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8187   -1.1248   -3.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1693   -1.9907   -2.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4619   -0.3281   -0.9523 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5379   -0.1261    0.6047 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8353   -2.3471    0.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6122   -2.5666   -0.6830 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7704   -2.6484   -0.5084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0461   -1.8159    3.0049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3802   -2.1482    2.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3736   -2.6173    0.1154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8698   -3.7521    1.4140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8223   -2.1540    1.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9246   -3.9295   -0.7109 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
  9 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
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 17 18  2  0
 18 19  1  0
 19 20  2  0
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 29 30  1  0
 30 31  1  0
 31 32  2  0
 31 33  1  0
 11  5  1  0
 30  7  1  0
  1 34  1  0
  1 35  1  0
  3 36  1  0
  5 37  1  6
  6 38  1  0
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 29 67  1  0
 30 68  1  1
 33 69  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -7.955   2.325  -0.269  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.835   1.952   0.322  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.476   2.457   1.635  0.00  0.00           C+0
HETATM    4  O   UNK     0      -5.429   2.144   2.250  0.00  0.00           O+0
HETATM    5  C   UNK     0      -5.913   0.992  -0.369  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.774  -0.282   0.412  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.433  -0.961   0.190  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.302  -1.181  -1.312  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.389  -0.031   0.689  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.508   1.236   0.327  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.618   1.704  -0.527  0.00  0.00           C+0
HETATM   12  O   UNK     0      -4.491   2.634  -1.333  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.248  -0.389   1.542  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.027  -0.386   0.806  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.073   0.342   1.158  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.014   1.054   2.193  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.328   0.330   0.380  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.361   1.052   0.765  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.634   1.062   0.006  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.643   1.788   0.412  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.963   1.928  -0.186  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.153   3.407  -0.527  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.311   1.119  -1.365  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.352  -0.359  -1.213  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.715  -0.988  -2.561  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.601  -0.655  -0.341  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.708  -2.167  -0.147  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.381  -1.785   2.123  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.935  -2.681   1.068  0.00  0.00           C+0
HETATM   30  C   UNK     0      -4.407  -2.295   0.877  0.00  0.00           C+0
HETATM   31  C   UNK     0      -5.045  -3.367   0.117  0.00  0.00           C+0
HETATM   32  O   UNK     0      -4.430  -4.396  -0.252  0.00  0.00           O+0
HETATM   33  O   UNK     0      -6.383  -3.261  -0.218  0.00  0.00           O+0
HETATM   34  H   UNK     0      -8.614   3.018   0.234  0.00  0.00           H+0
HETATM   35  H   UNK     0      -8.258   1.974  -1.243  0.00  0.00           H+0
HETATM   36  H   UNK     0      -7.150   3.146   2.116  0.00  0.00           H+0
HETATM   37  H   UNK     0      -6.354   0.724  -1.367  0.00  0.00           H+0
HETATM   38  H   UNK     0      -5.811  -0.034   1.498  0.00  0.00           H+0
HETATM   39  H   UNK     0      -6.617  -0.982   0.199  0.00  0.00           H+0
HETATM   40  H   UNK     0      -5.222  -0.895  -1.862  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.390  -0.689  -1.690  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.166  -2.281  -1.528  0.00  0.00           H+0
HETATM   43  H   UNK     0      -2.773   1.972   0.658  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.160   0.291   2.440  0.00  0.00           H+0
HETATM   45  H   UNK     0       1.442  -0.255  -0.509  0.00  0.00           H+0
HETATM   46  H   UNK     0       2.256   1.643   1.658  0.00  0.00           H+0
HETATM   47  H   UNK     0       3.705   0.493  -0.889  0.00  0.00           H+0
HETATM   48  H   UNK     0       4.436   2.366   1.343  0.00  0.00           H+0
HETATM   49  H   UNK     0       6.732   1.722   0.602  0.00  0.00           H+0
HETATM   50  H   UNK     0       5.532   3.600  -1.414  0.00  0.00           H+0
HETATM   51  H   UNK     0       5.761   4.010   0.295  0.00  0.00           H+0
HETATM   52  H   UNK     0       7.223   3.573  -0.664  0.00  0.00           H+0
HETATM   53  H   UNK     0       5.552   1.380  -2.172  0.00  0.00           H+0
HETATM   54  H   UNK     0       7.267   1.524  -1.807  0.00  0.00           H+0
HETATM   55  H   UNK     0       5.479  -0.797  -0.760  0.00  0.00           H+0
HETATM   56  H   UNK     0       7.464  -0.298  -3.034  0.00  0.00           H+0
HETATM   57  H   UNK     0       5.819  -1.125  -3.198  0.00  0.00           H+0
HETATM   58  H   UNK     0       7.169  -1.991  -2.424  0.00  0.00           H+0
HETATM   59  H   UNK     0       8.462  -0.328  -0.952  0.00  0.00           H+0
HETATM   60  H   UNK     0       7.538  -0.126   0.605  0.00  0.00           H+0
HETATM   61  H   UNK     0       7.835  -2.347   0.927  0.00  0.00           H+0
HETATM   62  H   UNK     0       8.612  -2.567  -0.683  0.00  0.00           H+0
HETATM   63  H   UNK     0       6.770  -2.648  -0.508  0.00  0.00           H+0
HETATM   64  H   UNK     0      -3.046  -1.816   3.005  0.00  0.00           H+0
HETATM   65  H   UNK     0      -1.380  -2.148   2.484  0.00  0.00           H+0
HETATM   66  H   UNK     0      -2.374  -2.617   0.115  0.00  0.00           H+0
HETATM   67  H   UNK     0      -2.870  -3.752   1.414  0.00  0.00           H+0
HETATM   68  H   UNK     0      -4.822  -2.154   1.897  0.00  0.00           H+0
HETATM   69  H   UNK     0      -6.925  -3.930  -0.711  0.00  0.00           H+0
CONECT    1    2   34   35                                                  
CONECT    2    1    3    5                                                  
CONECT    3    2    4   36                                                  
CONECT    4    3                                                            
CONECT    5    2    6   11   37                                             
CONECT    6    5    7   38   39                                             
CONECT    7    6    8    9   30                                             
CONECT    8    7   40   41   42                                             
CONECT    9    7   10   13                                                  
CONECT   10    9   11   43                                                  
CONECT   11   10   12    5                                                  
CONECT   12   11                                                            
CONECT   13    9   14   28   44                                             
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   45                                                  
CONECT   18   17   19   46                                                  
CONECT   19   18   20   47                                                  
CONECT   20   19   21   48                                                  
CONECT   21   20   22   23   49                                             
CONECT   22   21   50   51   52                                             
CONECT   23   21   24   53   54                                             
CONECT   24   23   25   26   55                                             
CONECT   25   24   56   57   58                                             
CONECT   26   24   27   59   60                                             
CONECT   27   26   61   62   63                                             
CONECT   28   13   29   64   65                                             
CONECT   29   28   30   66   67                                             
CONECT   30   29   31    7   68                                             
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   69                                                       
CONECT   34    1                                                            
CONECT   35    1                                                            
CONECT   36    3                                                            
CONECT   37    5                                                            
CONECT   38    6                                                            
CONECT   39    6                                                            
CONECT   40    8                                                            
CONECT   41    8                                                            
CONECT   42    8                                                            
CONECT   43   10                                                            
CONECT   44   13                                                            
CONECT   45   17                                                            
CONECT   46   18                                                            
CONECT   47   19                                                            
CONECT   48   20                                                            
CONECT   49   21                                                            
CONECT   50   22                                                            
CONECT   51   22                                                            
CONECT   52   22                                                            
CONECT   53   23                                                            
CONECT   54   23                                                            
CONECT   55   24                                                            
CONECT   56   25                                                            
CONECT   57   25                                                            
CONECT   58   25                                                            
CONECT   59   26                                                            
CONECT   60   26                                                            
CONECT   61   27                                                            
CONECT   62   27                                                            
CONECT   63   27                                                            
CONECT   64   28                                                            
CONECT   65   28                                                            
CONECT   66   29                                                            
CONECT   67   29                                                            
CONECT   68   30                                                            
CONECT   69   33                                                            
MASTER        0    0    0    0    0    0    0    0   69    0  140    0
END

RDKit          3D

69 70  0  0  0  0  0  0  0  0999 V2000
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 28 64  1  0
 28 65  1  0
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M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(1S,4R,7S,8AR)-4-{[(2E,4E)-6,8-dimethyldeca-2,4-dienoyl]oxy}-8a-methyl-6-oxo-7-(3-oxoprop-1-en-2-yl)-1,2,3,4,6,7,8,8a-octahydronaphthalene-1-carboxylate	Generator

Chemical Formula

C₂₇H₃₆O₆

Average Mass

456.5790 Da

Monoisotopic Mass

456.25119 Da

IUPAC Name

(1S,4R,7S,8aR)-4-{[(2E,4E,6R,8S)-6,8-dimethyldeca-2,4-dienoyl]oxy}-8a-methyl-6-oxo-7-(3-oxoprop-1-en-2-yl)-1,2,3,4,6,7,8,8a-octahydronaphthalene-1-carboxylic acid

Traditional Name

(1S,4R,7S,8aR)-4-{[(2E,4E,6R,8S)-6,8-dimethyldeca-2,4-dienoyl]oxy}-8a-methyl-6-oxo-7-(3-oxoprop-1-en-2-yl)-1,2,3,4,7,8-hexahydronaphthalene-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

CCC(C)CC(C)\C=C\C=C\C(=O)O[C@@H]1CC[C@H](C(O)=O)[C@@]2(C)C[C@@H](C(=C)C=O)C(=O)C=C12

InChI Identifier

InChI=1S/C27H36O6/c1-6-17(2)13-18(3)9-7-8-10-25(30)33-24-12-11-21(26(31)32)27(5)15-20(19(4)16-28)23(29)14-22(24)27/h7-10,14,16-18,20-21,24H,4,6,11-13,15H2,1-3,5H3,(H,31,32)/b9-7+,10-8+/t17?,18?,20-,21+,24+,27+/m0/s1

InChI Key

KFNRVRQZGWBRJR-XQLFHWRFSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Unknown-fungus sp. LL-07H239.	NPAtlas	15387660

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids

Alternative Parents

Substituents

Eremophilane sesquiterpenoid
Cyclohexenone
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Alpha,beta-unsaturated aldehyde
Enal
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Cyclic ketone
Ketone
Carboxylic acid
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Aldehyde
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic 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	3.99	ALOGPS
logP	5.39	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	4.15	ChemAxon
pKa (Strongest Basic)	-5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	97.74 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	129.39 m³·mol⁻¹	ChemAxon
Polarizability	51.49 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA011027

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9469014

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11294029

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

McDonald LA, Barbieri LR, Bernan VS, Janso J, Lassota P, Carter GT: 07H239-A, a new cytotoxic eremophilane sesquiterpene from the marine-derived Xylariaceous fungus LL-07H239. J Nat Prod. 2004 Sep;67(9):1565-7. doi: 10.1021/np049924g. [PubMed:15387660 ]

Showing NP-Card for 07H239-A (NP0005515)

MOL for NP0005515 (07H239-A)

3D MOL for NP0005515 (07H239-A)

3D SDF for NP0005515 (07H239-A)

3D-SDF for NP0005515 (07H239-A)

PDB for NP0005515 (07H239-A)

3D PDB for NP0005515 (07H239-A)

SMILES for NP0005515 (07H239-A)

INCHI for NP0005515 (07H239-A)

Structure for NP0005515 (07H239-A)

3D Structure for NP0005515 (07H239-A)