NP-MRD: Showing NP-Card for Antrocamphin A (NP0007108)

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Record Information

Version

2.0

Created at

2020-12-09 03:59:37 UTC

Updated at

2021-07-15 16:56:41 UTC

NP-MRD ID

NP0007108

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Antrocamphin A

Provided By

NPAtlas

Description

Antrocapmphin A is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Antrocamphin A is found in Antrodia and Antrodia camphorata. It was first documented in 2007 (PMID: 17559265). Based on a literature review a significant number of articles have been published on antrocapmphin A (PMID: 20128588) (PMID: 21088769) (PMID: 34403458) (PMID: 34402874).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118373D          

 36 36  0  0  0  0            999 V2000
    4.8587   -0.6883   -1.8391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3257    0.0094   -0.8681 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1750    0.8840   -0.0245 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9146   -0.0224   -0.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7322   -0.0698   -0.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3307   -0.1458   -0.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2354    0.7813    0.8467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188    1.7476    1.3672 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0584    2.7075    2.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5687    0.7616    1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3938   -0.1982    0.6446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7544   -0.2642    0.9370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4152    0.6269    1.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8554   -1.1373   -0.2060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6874   -2.1308   -0.7528 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3021   -1.8056   -1.9890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5161   -1.1104   -0.5228 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1021   -2.1185   -1.4461 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2417   -1.3166   -2.4435 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9066   -0.6315   -2.0287 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6421    0.2899    0.8060 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6095    1.6960    0.4536 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0467    1.2791   -0.6114 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8192    3.5301    2.3572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8381    3.2072    1.8013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2397    2.2807    3.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9689    1.5089    1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4405    0.1973    1.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5947    1.6166    1.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9508    0.7209    2.7828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4262   -2.7393   -2.5674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3006   -1.3688   -1.7817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7137   -1.0457   -2.5374 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0316   -2.5084   -0.9768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6141   -2.9249   -1.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4023   -1.6186   -2.3740 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
  2  4  1  0  0  0  0
  4  5  3  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17  6  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  9 24  1  0  0  0  0
  9 25  1  0  0  0  0
  9 26  1  0  0  0  0
 10 27  1  0  0  0  0
 13 28  1  0  0  0  0
 13 29  1  0  0  0  0
 13 30  1  0  0  0  0
 16 31  1  0  0  0  0
 16 32  1  0  0  0  0
 16 33  1  0  0  0  0
 18 34  1  0  0  0  0
 18 35  1  0  0  0  0
 18 36  1  0  0  0  0
M  END

     RDKit          3D

 36 36  0  0  0  0  0  0  0  0999 V2000
    4.8587   -0.6883   -1.8391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3257    0.0094   -0.8681 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1750    0.8840   -0.0245 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9146   -0.0224   -0.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7322   -0.0698   -0.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3307   -0.1458   -0.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2354    0.7813    0.8467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188    1.7476    1.3672 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0584    2.7075    2.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5687    0.7616    1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3938   -0.1982    0.6446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7544   -0.2642    0.9370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4152    0.6269    1.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8554   -1.1373   -0.2060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6874   -2.1308   -0.7528 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3021   -1.8056   -1.9890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5161   -1.1104   -0.5228 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1021   -2.1185   -1.4461 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2417   -1.3166   -2.4435 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9066   -0.6315   -2.0287 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6421    0.2899    0.8060 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6095    1.6960    0.4536 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0467    1.2791   -0.6114 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8192    3.5301    2.3572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8381    3.2072    1.8013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2397    2.2807    3.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9689    1.5089    1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4405    0.1973    1.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5947    1.6166    1.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9508    0.7209    2.7828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4262   -2.7393   -2.5674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3006   -1.3688   -1.7817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7137   -1.0457   -2.5374 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0316   -2.5084   -0.9768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6141   -2.9249   -1.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4023   -1.6186   -2.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  3  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  2  0
 17 18  1  0
 17  6  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  9 24  1  0
  9 25  1  0
  9 26  1  0
 10 27  1  0
 13 28  1  0
 13 29  1  0
 13 30  1  0
 16 31  1  0
 16 32  1  0
 16 33  1  0
 18 34  1  0
 18 35  1  0
 18 36  1  0
M  END


  Mrv1652306242118373D          

 36 36  0  0  0  0            999 V2000
    4.8587   -0.6883   -1.8391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3257    0.0094   -0.8681 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1750    0.8840   -0.0245 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9146   -0.0224   -0.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7322   -0.0698   -0.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3307   -0.1458   -0.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2354    0.7813    0.8467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188    1.7476    1.3672 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0584    2.7075    2.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5687    0.7616    1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3938   -0.1982    0.6446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7544   -0.2642    0.9370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4152    0.6269    1.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8554   -1.1373   -0.2060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6874   -2.1308   -0.7528 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3021   -1.8056   -1.9890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5161   -1.1104   -0.5228 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1021   -2.1185   -1.4461 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2417   -1.3166   -2.4435 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9066   -0.6315   -2.0287 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6421    0.2899    0.8060 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6095    1.6960    0.4536 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0467    1.2791   -0.6114 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8192    3.5301    2.3572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8381    3.2072    1.8013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2397    2.2807    3.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9689    1.5089    1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4405    0.1973    1.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5947    1.6166    1.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9508    0.7209    2.7828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4262   -2.7393   -2.5674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3006   -1.3688   -1.7817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7137   -1.0457   -2.5374 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0316   -2.5084   -0.9768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6141   -2.9249   -1.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4023   -1.6186   -2.3740 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
  2  4  1  0  0  0  0
  4  5  3  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17  6  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  9 24  1  0  0  0  0
  9 25  1  0  0  0  0
  9 26  1  0  0  0  0
 10 27  1  0  0  0  0
 13 28  1  0  0  0  0
 13 29  1  0  0  0  0
 13 30  1  0  0  0  0
 16 31  1  0  0  0  0
 16 32  1  0  0  0  0
 16 33  1  0  0  0  0
 18 34  1  0  0  0  0
 18 35  1  0  0  0  0
 18 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007108

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C([H])=C(C#CC1=C(OC([H])([H])[H])C([H])=C(OC([H])([H])[H])C(OC([H])([H])[H])=C1C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H18O3/c1-10(2)7-8-12-11(3)15(18-6)14(17-5)9-13(12)16-4/h9H,1H2,2-6H3

> <INCHI_KEY>
CPPLWBNAWKMJON-UHFFFAOYSA-N

> <FORMULA>
C15H18O3

> <MOLECULAR_WEIGHT>
246.306

> <EXACT_MASS>
246.12559444

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
28.489988696493498

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,2,5-trimethoxy-3-methyl-4-(3-methylbut-3-en-1-yn-1-yl)benzene

> <ALOGPS_LOGP>
3.37

> <JCHEM_LOGP>
3.384860742666666

> <ALOGPS_LOGS>
-4.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.402121570697104

> <JCHEM_POLAR_SURFACE_AREA>
27.69

> <JCHEM_REFRACTIVITY>
70.089

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.67e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,2,5-trimethoxy-3-methyl-4-(3-methylbut-3-en-1-yn-1-yl)benzene

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 36 36  0  0  0  0  0  0  0  0999 V2000
    4.8587   -0.6883   -1.8391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3257    0.0094   -0.8681 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1750    0.8840   -0.0245 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9146   -0.0224   -0.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7322   -0.0698   -0.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3307   -0.1458   -0.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2354    0.7813    0.8467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188    1.7476    1.3672 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0584    2.7075    2.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5687    0.7616    1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3938   -0.1982    0.6446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7544   -0.2642    0.9370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4152    0.6269    1.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8554   -1.1373   -0.2060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6874   -2.1308   -0.7528 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3021   -1.8056   -1.9890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5161   -1.1104   -0.5228 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1021   -2.1185   -1.4461 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2417   -1.3166   -2.4435 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9066   -0.6315   -2.0287 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6421    0.2899    0.8060 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6095    1.6960    0.4536 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0467    1.2791   -0.6114 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8192    3.5301    2.3572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8381    3.2072    1.8013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2397    2.2807    3.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9689    1.5089    1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4405    0.1973    1.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5947    1.6166    1.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9508    0.7209    2.7828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4262   -2.7393   -2.5674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3006   -1.3688   -1.7817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7137   -1.0457   -2.5374 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0316   -2.5084   -0.9768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6141   -2.9249   -1.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4023   -1.6186   -2.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  3  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  2  0
 17 18  1  0
 17  6  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  9 24  1  0
  9 25  1  0
  9 26  1  0
 10 27  1  0
 13 28  1  0
 13 29  1  0
 13 30  1  0
 16 31  1  0
 16 32  1  0
 16 33  1  0
 18 34  1  0
 18 35  1  0
 18 36  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       4.859  -0.688  -1.839  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.326   0.009  -0.868  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.175   0.884  -0.025  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.915  -0.022  -0.559  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.732  -0.070  -0.297  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.331  -0.146  -0.002  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.235   0.781   0.847  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.619   1.748   1.367  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.058   2.708   2.239  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.569   0.762   1.167  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.394  -0.198   0.645  0.00  0.00           C+0
HETATM   12  O   UNK     0      -3.754  -0.264   0.937  0.00  0.00           O+0
HETATM   13  C   UNK     0      -4.415   0.627   1.782  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.855  -1.137  -0.206  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.687  -2.131  -0.753  0.00  0.00           O+0
HETATM   16  C   UNK     0      -3.302  -1.806  -1.989  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.516  -1.110  -0.523  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.102  -2.119  -1.446  0.00  0.00           C+0
HETATM   19  H   UNK     0       4.242  -1.317  -2.443  0.00  0.00           H+0
HETATM   20  H   UNK     0       5.907  -0.632  -2.029  0.00  0.00           H+0
HETATM   21  H   UNK     0       5.642   0.290   0.806  0.00  0.00           H+0
HETATM   22  H   UNK     0       4.609   1.696   0.454  0.00  0.00           H+0
HETATM   23  H   UNK     0       6.047   1.279  -0.611  0.00  0.00           H+0
HETATM   24  H   UNK     0       0.819   3.530   2.357  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.838   3.207   1.801  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.240   2.281   3.214  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.969   1.509   1.837  0.00  0.00           H+0
HETATM   28  H   UNK     0      -5.441   0.197   1.968  0.00  0.00           H+0
HETATM   29  H   UNK     0      -4.595   1.617   1.322  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.951   0.721   2.783  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.426  -2.739  -2.567  0.00  0.00           H+0
HETATM   32  H   UNK     0      -4.301  -1.369  -1.782  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.714  -1.046  -2.537  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.032  -2.508  -0.977  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.614  -2.925  -1.698  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.402  -1.619  -2.374  0.00  0.00           H+0
CONECT    1    2   19   20                                                  
CONECT    2    1    3    4                                                  
CONECT    3    2   21   22   23                                             
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8   24   25   26                                             
CONECT   10    7   11   27                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12   28   29   30                                             
CONECT   14   11   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15   31   32   33                                             
CONECT   17   14   18    6                                                  
CONECT   18   17   34   35   36                                             
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    3                                                            
CONECT   22    3                                                            
CONECT   23    3                                                            
CONECT   24    9                                                            
CONECT   25    9                                                            
CONECT   26    9                                                            
CONECT   27   10                                                            
CONECT   28   13                                                            
CONECT   29   13                                                            
CONECT   30   13                                                            
CONECT   31   16                                                            
CONECT   32   16                                                            
CONECT   33   16                                                            
CONECT   34   18                                                            
CONECT   35   18                                                            
CONECT   36   18                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   72    0
END

RDKit          3D

36 36  0  0  0  0  0  0  0  0999 V2000
    4.8587   -0.6883   -1.8391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3257    0.0094   -0.8681 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1750    0.8840   -0.0245 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9146   -0.0224   -0.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7322   -0.0698   -0.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3307   -0.1458   -0.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2354    0.7813    0.8467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188    1.7476    1.3672 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0584    2.7075    2.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5687    0.7616    1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3938   -0.1982    0.6446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7544   -0.2642    0.9370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4152    0.6269    1.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8554   -1.1373   -0.2060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6874   -2.1308   -0.7528 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3021   -1.8056   -1.9890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5161   -1.1104   -0.5228 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1021   -2.1185   -1.4461 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2417   -1.3166   -2.4435 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9066   -0.6315   -2.0287 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6421    0.2899    0.8060 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6095    1.6960    0.4536 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0467    1.2791   -0.6114 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8192    3.5301    2.3572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8381    3.2072    1.8013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2397    2.2807    3.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9689    1.5089    1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4405    0.1973    1.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5947    1.6166    1.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9508    0.7209    2.7828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4262   -2.7393   -2.5674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3006   -1.3688   -1.7817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7137   -1.0457   -2.5374 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0316   -2.5084   -0.9768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6141   -2.9249   -1.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4023   -1.6186   -2.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  3  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  2  0
 17 18  1  0
 17  6  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  9 24  1  0
  9 25  1  0
  9 26  1  0
 10 27  1  0
 13 28  1  0
 13 29  1  0
 13 30  1  0
 16 31  1  0
 16 32  1  0
 16 33  1  0
 18 34  1  0
 18 35  1  0
 18 36  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Antrocamphin a	MeSH

Chemical Formula

C₁₅H₁₈O₃

Average Mass

246.3060 Da

Monoisotopic Mass

246.12559 Da

IUPAC Name

1,2,5-trimethoxy-3-methyl-4-(3-methylbut-3-en-1-yn-1-yl)benzene

Traditional Name

1,2,5-trimethoxy-3-methyl-4-(3-methylbut-3-en-1-yn-1-yl)benzene

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C(OC)C(C)=C1C#CC(C)=C

InChI Identifier

InChI=1S/C15H18O3/c1-10(2)7-8-12-11(3)15(18-6)14(17-5)9-13(12)16-4/h9H,1H2,2-6H3

InChI Key

CPPLWBNAWKMJON-UHFFFAOYSA-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
Antrodia	NPAtlas	17559265
Taiwanofungus camphoratus	Fungi	KNApSAcK

Species Where Detected

Species Name	Source	Reference
Antrodia camphorata	KNApSAcK Database	22123792

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Phenoxy compound
Methoxybenzene
Anisole
Toluene
Alkyl aryl ether
Monocyclic benzene moiety
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

methoxybenzene (CHEBI:65414 )

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	3.37	ALOGPS
logP	3.38	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	27.69 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	70.09 m³·mol⁻¹	ChemAxon
Polarizability	28.49 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA001842

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00038467

Chemspider ID

20568906

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16737471

PDB ID

Not Available

ChEBI ID

65414

Good Scents ID

Not Available

References

General References

Chen JJ, Lin WJ, Liao CH, Shieh PC: Anti-inflammatory benzenoids from Antrodia camphorata. J Nat Prod. 2007 Jun;70(6):989-92. doi: 10.1021/np070045e. Epub 2007 Jun 9. [PubMed:17559265 ]
Hsieh YH, Chu FH, Wang YS, Chien SC, Chang ST, Shaw JF, Chen CY, Hsiao WW, Kuo YH, Wang SY: Antrocamphin A, an anti-inflammatory principal from the fruiting body of Taiwanofungus camphoratus , and its mechanisms. J Agric Food Chem. 2010 Mar 10;58(5):3153-8. doi: 10.1021/jf903638p. [PubMed:20128588 ]
Lee CL, Huang CH, Wang HC, Chuang DW, Wu MJ, Wang SY, Hwang TL, Wu CC, Chen YL, Chang FR, Wu YC: First total synthesis of antrocamphin A and its analogs as anti-inflammatory and anti-platelet aggregation agents. Org Biomol Chem. 2011 Jan 7;9(1):70-3. doi: 10.1039/c0ob00616e. Epub 2010 Nov 18. [PubMed:21088769 ]

Showing NP-Card for Antrocamphin A (NP0007108)

MOL for NP0007108 (Antrocamphin A)

3D MOL for NP0007108 (Antrocamphin A)

3D SDF for NP0007108 (Antrocamphin A)

3D-SDF for NP0007108 (Antrocamphin A)

PDB for NP0007108 (Antrocamphin A)

3D PDB for NP0007108 (Antrocamphin A)

SMILES for NP0007108 (Antrocamphin A)

INCHI for NP0007108 (Antrocamphin A)

Structure for NP0007108 (Antrocamphin A)

3D Structure for NP0007108 (Antrocamphin A)