NP-MRD: Showing NP-Card for Trichoderic acid (NP0010313)

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Record Information

Version

2.0

Created at

2021-01-05 19:52:26 UTC

Updated at

2021-07-15 17:05:45 UTC

NP-MRD ID

NP0010313

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Trichoderic acid

Provided By

NPAtlas

Description

Trichoderic acid, also known as trichoderate, belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Trichoderic acid is found in Trichoderma. Trichoderic acid was first documented in 2011 (PMID: 21922660). Based on a literature review very few articles have been published on Trichoderic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107373D          

 40 41  0  0  0  0            999 V2000
   -4.3277    2.2702    0.9920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3939    1.0959    0.7924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1716    1.1395    1.2681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1819    0.0651    1.1357 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0461    0.5081    0.6593 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2901   -0.1717   -0.5228 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6723   -0.0851   -1.0198 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7423   -0.5879   -0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6859    0.2383    0.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7138    1.6771   -0.1343 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7591   -0.2938    1.1033 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7813   -1.5021    1.4479 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7782    0.5261    1.5617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3243   -1.5114   -0.3567 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3257   -2.4174    0.6377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6487   -1.0813    0.2986 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6830   -0.6835   -0.7160 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8499   -0.1120    0.0610 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0527    2.2440    0.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8526    2.1917    1.9685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7804    3.2179    0.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8585    2.0390    1.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9846   -0.3372    2.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541    0.3662   -1.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8450    0.9968   -1.3097 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7988   -0.6132   -2.0130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7645   -1.6186    0.1246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7311    1.7736   -1.2593 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6307    2.1412    0.2221 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8567    2.2430    0.2859 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7220    0.5061    1.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6049   -2.0118   -1.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9788   -3.1923    0.1958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4750   -3.0233    1.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7905   -1.8324    1.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0756   -1.8954    0.9088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0132   -1.6337   -1.2188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3644    0.0733   -1.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2165   -0.8827    0.7940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6995    0.1734   -0.5967 H   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18  2  1  0  0  0  0
 16  4  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  3 22  1  0  0  0  0
  4 23  1  1  0  0  0
  6 24  1  6  0  0  0
  7 25  1  0  0  0  0
  7 26  1  0  0  0  0
  8 27  1  0  0  0  0
 10 28  1  0  0  0  0
 10 29  1  0  0  0  0
 10 30  1  0  0  0  0
 13 31  1  0  0  0  0
 14 32  1  6  0  0  0
 15 33  1  0  0  0  0
 15 34  1  0  0  0  0
 15 35  1  0  0  0  0
 16 36  1  1  0  0  0
 17 37  1  0  0  0  0
 17 38  1  0  0  0  0
 18 39  1  0  0  0  0
 18 40  1  0  0  0  0
M  END

     RDKit          3D

 40 41  0  0  0  0  0  0  0  0999 V2000
   -4.3277    2.2702    0.9920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3939    1.0959    0.7924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1716    1.1395    1.2681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1819    0.0651    1.1357 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0461    0.5081    0.6593 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2901   -0.1717   -0.5228 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6723   -0.0851   -1.0198 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7423   -0.5879   -0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6859    0.2383    0.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7138    1.6771   -0.1343 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7591   -0.2938    1.1033 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7813   -1.5021    1.4479 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7782    0.5261    1.5617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3243   -1.5114   -0.3567 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3257   -2.4174    0.6377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6487   -1.0813    0.2986 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6830   -0.6835   -0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8499   -0.1120    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0527    2.2440    0.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8526    2.1917    1.9685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7804    3.2179    0.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8585    2.0390    1.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9846   -0.3372    2.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541    0.3662   -1.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8450    0.9968   -1.3097 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7988   -0.6132   -2.0130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7645   -1.6186    0.1246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7311    1.7736   -1.2593 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6307    2.1412    0.2221 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8567    2.2430    0.2859 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7220    0.5061    1.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6049   -2.0118   -1.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9788   -3.1923    0.1958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4750   -3.0233    1.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7905   -1.8324    1.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0756   -1.8954    0.9088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0132   -1.6337   -1.2188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3644    0.0733   -1.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2165   -0.8827    0.7940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6995    0.1734   -0.5967 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 11 13  1  0
  6 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18  2  1  0
 16  4  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  3 22  1  0
  4 23  1  1
  6 24  1  6
  7 25  1  0
  7 26  1  0
  8 27  1  0
 10 28  1  0
 10 29  1  0
 10 30  1  0
 13 31  1  0
 14 32  1  6
 15 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  1
 17 37  1  0
 17 38  1  0
 18 39  1  0
 18 40  1  0
M  END


  Mrv1652306242107373D          

 40 41  0  0  0  0            999 V2000
   -4.3277    2.2702    0.9920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3939    1.0959    0.7924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1716    1.1395    1.2681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1819    0.0651    1.1357 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0461    0.5081    0.6593 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2901   -0.1717   -0.5228 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6723   -0.0851   -1.0198 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7423   -0.5879   -0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6859    0.2383    0.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7138    1.6771   -0.1343 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7591   -0.2938    1.1033 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7813   -1.5021    1.4479 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7782    0.5261    1.5617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3243   -1.5114   -0.3567 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3257   -2.4174    0.6377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6487   -1.0813    0.2986 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6830   -0.6835   -0.7160 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8499   -0.1120    0.0610 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0527    2.2440    0.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8526    2.1917    1.9685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7804    3.2179    0.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8585    2.0390    1.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9846   -0.3372    2.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541    0.3662   -1.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8450    0.9968   -1.3097 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7988   -0.6132   -2.0130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7645   -1.6186    0.1246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7311    1.7736   -1.2593 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6307    2.1412    0.2221 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8567    2.2430    0.2859 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7220    0.5061    1.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6049   -2.0118   -1.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9788   -3.1923    0.1958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4750   -3.0233    1.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7905   -1.8324    1.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0756   -1.8954    0.9088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0132   -1.6337   -1.2188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3644    0.0733   -1.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2165   -0.8827    0.7940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6995    0.1734   -0.5967 H   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18  2  1  0  0  0  0
 16  4  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  3 22  1  0  0  0  0
  4 23  1  1  0  0  0
  6 24  1  6  0  0  0
  7 25  1  0  0  0  0
  7 26  1  0  0  0  0
  8 27  1  0  0  0  0
 10 28  1  0  0  0  0
 10 29  1  0  0  0  0
 10 30  1  0  0  0  0
 13 31  1  0  0  0  0
 14 32  1  6  0  0  0
 15 33  1  0  0  0  0
 15 34  1  0  0  0  0
 15 35  1  0  0  0  0
 16 36  1  1  0  0  0
 17 37  1  0  0  0  0
 17 38  1  0  0  0  0
 18 39  1  0  0  0  0
 18 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0010313

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C(=C(/[H])C([H])([H])[C@]1([H])O[C@@]2([H])C([H])=C(C([H])([H])[H])C([H])([H])C([H])([H])[C@@]2([H])[C@]1([H])C([H])([H])[H])\C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O3/c1-9-4-6-12-11(3)13(18-14(12)8-9)7-5-10(2)15(16)17/h5,8,11-14H,4,6-7H2,1-3H3,(H,16,17)/b10-5+/t11-,12-,13-,14-/m0/s1

> <INCHI_KEY>
ACWHPYSUDDTJQF-MBAHPQJTSA-N

> <FORMULA>
C15H22O3

> <MOLECULAR_WEIGHT>
250.338

> <EXACT_MASS>
250.156894568

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
28.664981336334932

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-4-[(2S,3S,3aS,7aR)-3,6-dimethyl-2,3,3a,4,5,7a-hexahydro-1-benzofuran-2-yl]-2-methylbut-2-enoic acid

> <ALOGPS_LOGP>
2.95

> <JCHEM_LOGP>
3.118946775

> <ALOGPS_LOGS>
-3.43

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.682234835331536

> <JCHEM_PKA_STRONGEST_BASIC>
-4.199917975587815

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
71.74350000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.27e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-4-[(2S,3S,3aS,7aR)-3,6-dimethyl-2,3,3a,4,5,7a-hexahydro-1-benzofuran-2-yl]-2-methylbut-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 40 41  0  0  0  0  0  0  0  0999 V2000
   -4.3277    2.2702    0.9920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3939    1.0959    0.7924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1716    1.1395    1.2681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1819    0.0651    1.1357 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0461    0.5081    0.6593 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2901   -0.1717   -0.5228 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6723   -0.0851   -1.0198 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7423   -0.5879   -0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6859    0.2383    0.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7138    1.6771   -0.1343 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7591   -0.2938    1.1033 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7813   -1.5021    1.4479 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7782    0.5261    1.5617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3243   -1.5114   -0.3567 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3257   -2.4174    0.6377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6487   -1.0813    0.2986 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6830   -0.6835   -0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8499   -0.1120    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0527    2.2440    0.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8526    2.1917    1.9685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7804    3.2179    0.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8585    2.0390    1.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9846   -0.3372    2.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541    0.3662   -1.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8450    0.9968   -1.3097 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7988   -0.6132   -2.0130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7645   -1.6186    0.1246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7311    1.7736   -1.2593 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6307    2.1412    0.2221 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8567    2.2430    0.2859 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7220    0.5061    1.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6049   -2.0118   -1.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9788   -3.1923    0.1958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4750   -3.0233    1.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7905   -1.8324    1.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0756   -1.8954    0.9088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0132   -1.6337   -1.2188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3644    0.0733   -1.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2165   -0.8827    0.7940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6995    0.1734   -0.5967 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 11 13  1  0
  6 14  1  0
 14 15  1  0
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 16 17  1  0
 17 18  1  0
 18  2  1  0
 16  4  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  3 22  1  0
  4 23  1  1
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 15 34  1  0
 15 35  1  0
 16 36  1  1
 17 37  1  0
 17 38  1  0
 18 39  1  0
 18 40  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      -4.328   2.270   0.992  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.394   1.096   0.792  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.172   1.139   1.268  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.182   0.065   1.136  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.046   0.508   0.659  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.290  -0.172  -0.523  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.672  -0.085  -1.020  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.742  -0.588  -0.166  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.686   0.238   0.240  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.714   1.677  -0.134  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.759  -0.294   1.103  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.781  -1.502   1.448  0.00  0.00           O+0
HETATM   13  O   UNK     0       5.778   0.526   1.562  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.324  -1.511  -0.357  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.326  -2.417   0.638  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.649  -1.081   0.299  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.683  -0.684  -0.716  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.850  -0.112   0.061  0.00  0.00           C+0
HETATM   19  H   UNK     0      -5.053   2.244   0.143  0.00  0.00           H+0
HETATM   20  H   UNK     0      -4.853   2.192   1.968  0.00  0.00           H+0
HETATM   21  H   UNK     0      -3.780   3.218   0.943  0.00  0.00           H+0
HETATM   22  H   UNK     0      -1.859   2.039   1.804  0.00  0.00           H+0
HETATM   23  H   UNK     0      -0.985  -0.337   2.171  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.354   0.366  -1.289  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.845   0.997  -1.310  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.799  -0.613  -2.013  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.765  -1.619   0.125  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.731   1.774  -1.259  0.00  0.00           H+0
HETATM   29  H   UNK     0       4.631   2.141   0.222  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.857   2.243   0.286  0.00  0.00           H+0
HETATM   31  H   UNK     0       6.722   0.506   1.214  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.605  -2.012  -1.295  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.979  -3.192   0.196  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.475  -3.023   1.166  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.791  -1.832   1.440  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.076  -1.895   0.909  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.013  -1.634  -1.219  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.364   0.073  -1.431  0.00  0.00           H+0
HETATM   39  H   UNK     0      -4.216  -0.883   0.794  0.00  0.00           H+0
HETATM   40  H   UNK     0      -4.699   0.173  -0.597  0.00  0.00           H+0
CONECT    1    2   19   20   21                                             
CONECT    2    1    3   18                                                  
CONECT    3    2    4   22                                                  
CONECT    4    3    5   16   23                                             
CONECT    5    4    6                                                       
CONECT    6    5    7   14   24                                             
CONECT    7    6    8   25   26                                             
CONECT    8    7    9   27                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9   28   29   30                                             
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   31                                                       
CONECT   14    6   15   16   32                                             
CONECT   15   14   33   34   35                                             
CONECT   16   14   17    4   36                                             
CONECT   17   16   18   37   38                                             
CONECT   18   17    2   39   40                                             
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    3                                                            
CONECT   23    4                                                            
CONECT   24    6                                                            
CONECT   25    7                                                            
CONECT   26    7                                                            
CONECT   27    8                                                            
CONECT   28   10                                                            
CONECT   29   10                                                            
CONECT   30   10                                                            
CONECT   31   13                                                            
CONECT   32   14                                                            
CONECT   33   15                                                            
CONECT   34   15                                                            
CONECT   35   15                                                            
CONECT   36   16                                                            
CONECT   37   17                                                            
CONECT   38   17                                                            
CONECT   39   18                                                            
CONECT   40   18                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   82    0
END

RDKit          3D

40 41  0  0  0  0  0  0  0  0999 V2000
   -4.3277    2.2702    0.9920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3939    1.0959    0.7924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1716    1.1395    1.2681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1819    0.0651    1.1357 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0461    0.5081    0.6593 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2901   -0.1717   -0.5228 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6723   -0.0851   -1.0198 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7423   -0.5879   -0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6859    0.2383    0.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7138    1.6771   -0.1343 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7591   -0.2938    1.1033 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7813   -1.5021    1.4479 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7782    0.5261    1.5617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3243   -1.5114   -0.3567 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3257   -2.4174    0.6377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6487   -1.0813    0.2986 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6830   -0.6835   -0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8499   -0.1120    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0527    2.2440    0.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8526    2.1917    1.9685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7804    3.2179    0.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8585    2.0390    1.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9846   -0.3372    2.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541    0.3662   -1.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8450    0.9968   -1.3097 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7988   -0.6132   -2.0130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7645   -1.6186    0.1246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7311    1.7736   -1.2593 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6307    2.1412    0.2221 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8567    2.2430    0.2859 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7220    0.5061    1.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6049   -2.0118   -1.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9788   -3.1923    0.1958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4750   -3.0233    1.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7905   -1.8324    1.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0756   -1.8954    0.9088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0132   -1.6337   -1.2188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3644    0.0733   -1.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2165   -0.8827    0.7940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6995    0.1734   -0.5967 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 11 13  1  0
  6 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18  2  1  0
 16  4  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  3 22  1  0
  4 23  1  1
  6 24  1  6
  7 25  1  0
  7 26  1  0
  8 27  1  0
 10 28  1  0
 10 29  1  0
 10 30  1  0
 13 31  1  0
 14 32  1  6
 15 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  1
 17 37  1  0
 17 38  1  0
 18 39  1  0
 18 40  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Trichoderate	Generator
(2E)-4-[(2S,3S,3AS,7ar)-3,6-dimethyl-2,3,3a,4,5,7a-hexahydro-1-benzofuran-2-yl]-2-methylbut-2-enoate	Generator

Chemical Formula

C₁₅H₂₂O₃

Average Mass

250.3380 Da

Monoisotopic Mass

250.15689 Da

IUPAC Name

(2E)-4-[(2S,3S,3aS,7aR)-3,6-dimethyl-2,3,3a,4,5,7a-hexahydro-1-benzofuran-2-yl]-2-methylbut-2-enoic acid

Traditional Name

(2E)-4-[(2S,3S,3aS,7aR)-3,6-dimethyl-2,3,3a,4,5,7a-hexahydro-1-benzofuran-2-yl]-2-methylbut-2-enoic acid

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@H](C\C=C(/C)C(O)=O)O[C@H]2C=C(C)CC[C@@H]12

InChI Identifier

InChI=1S/C15H22O3/c1-9-4-6-12-11(3)13(18-14(12)8-9)7-5-10(2)15(16)17/h5,8,11-14H,4,6-7H2,1-3H3,(H,16,17)/b10-5+/t11-,12-,13-,14-/m0/s1

InChI Key

ACWHPYSUDDTJQF-MBAHPQJTSA-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
Trichoderma	NPAtlas	21922660

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Not Available

Direct Parent

Benzofurans

Alternative Parents

Substituents

Benzofuran
Branched fatty acid
Heterocyclic fatty acid
Methyl-branched fatty acid
Fatty acyl
Fatty acid
Unsaturated fatty acid
Tetrahydrofuran
Carboxylic acid derivative
Carboxylic acid
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Oxacycle
Organic oxide
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	2.95	ALOGPS
logP	3.12	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	4.68	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	71.74 m³·mol⁻¹	ChemAxon
Polarizability	28.66 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA001418

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28289048

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139583488

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wu SH, Zhao LX, Chen YW, Huang R, Miao CP, Wang J: Sesquiterpenoids from the endophytic fungus Trichoderma sp. PR-35 of Paeonia delavayi. Chem Biodivers. 2011 Sep;8(9):1717-23. doi: 10.1002/cbdv.201000236. [PubMed:21922660 ]

Showing NP-Card for Trichoderic acid (NP0010313)

MOL for NP0010313 (Trichoderic acid)

3D MOL for NP0010313 (Trichoderic acid)

3D SDF for NP0010313 (Trichoderic acid)

3D-SDF for NP0010313 (Trichoderic acid)

PDB for NP0010313 (Trichoderic acid)

3D PDB for NP0010313 (Trichoderic acid)

SMILES for NP0010313 (Trichoderic acid)

INCHI for NP0010313 (Trichoderic acid)

Structure for NP0010313 (Trichoderic acid)

3D Structure for NP0010313 (Trichoderic acid)