NP-MRD: Showing NP-Card for chrysoarticulin A (NP0042295)

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Record Information

Version

1.0

Created at

2021-06-20 23:59:30 UTC

Updated at

2021-06-30 00:17:18 UTC

NP-MRD ID

NP0042295

Secondary Accession Numbers

None

Natural Product Identification

Common Name

chrysoarticulin A

Provided By

JEOL Database JEOL Logo

Description

(3R,4S)-3-[(2R)-butan-2-yl]-4,8-dihydroxy-5,7-dimethyl-3,4-dihydro-1H-2-benzopyran-1-one belongs to the class of organic compounds known as 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position. chrysoarticulin A is found in Chrysosporium articulatum. It was first documented in 2013 (Jeon, J., et al.). Based on a literature review very few articles have been published on (3R,4S)-3-[(2R)-butan-2-yl]-4,8-dihydroxy-5,7-dimethyl-3,4-dihydro-1H-2-benzopyran-1-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212101593D          

 39 40  0  0  0  0            999 V2000
   -2.0054    3.0193   -0.6338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8350    1.5957   -1.1461 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5526    0.8720   -0.6718 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6995    1.5530   -1.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871    0.7197    0.8720 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7212    0.1454    1.3721 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9495   -1.1883    1.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0687   -1.6647    1.4248 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7843   -2.0695    0.9984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9942   -3.4235    0.6887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2479   -3.9777    0.6115 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0885   -4.2740    0.4434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1282   -5.7227    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3884   -3.7605    0.5437 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6227   -2.4151    0.8722 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0429   -1.9287    0.9804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5245   -1.5552    1.0791 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6951   -0.0990    1.4165 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7631    0.0042    2.8405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0972    3.0471    0.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1680    3.6573   -0.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9185    3.4567   -1.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8420    1.6196   -2.2433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7154    1.0105   -0.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6042   -0.1274   -1.1231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9091    2.4972   -0.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5844    1.7633   -2.3023 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5786    0.9098   -1.1283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4300    1.7161    1.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9095   -3.3156    0.9121 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8157   -6.2259   -0.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7772   -5.8182   -0.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5838   -6.2429    0.9566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2348   -4.4250    0.3719 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7566   -2.7581    0.9328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2033   -1.4207    1.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.2438    0.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6333    0.3008    1.0252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1488    0.0433    3.1821 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  9 17  2  0  0  0  0
  5  3  1  0  0  0  0
  3  4  1  0  0  0  0
 14 15  2  0  0  0  0
  3  2  1  0  0  0  0
 15 17  1  0  0  0  0
  2  1  1  0  0  0  0
 12 14  1  0  0  0  0
 15 16  1  0  0  0  0
  9 10  1  0  0  0  0
 12 13  1  0  0  0  0
 10 12  2  0  0  0  0
 10 11  1  0  0  0  0
  9  7  1  0  0  0  0
  7  8  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18  5  1  0  0  0  0
  5 29  1  1  0  0  0
 14 34  1  0  0  0  0
 18 38  1  6  0  0  0
  3 25  1  6  0  0  0
  4 26  1  0  0  0  0
  4 27  1  0  0  0  0
  4 28  1  0  0  0  0
  2 23  1  0  0  0  0
  2 24  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
 16 35  1  0  0  0  0
 16 36  1  0  0  0  0
 16 37  1  0  0  0  0
 13 31  1  0  0  0  0
 13 32  1  0  0  0  0
 13 33  1  0  0  0  0
 11 30  1  0  0  0  0
 19 39  1  0  0  0  0
M  END

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
   -2.0054    3.0193   -0.6338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8350    1.5957   -1.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5526    0.8720   -0.6718 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6995    1.5530   -1.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871    0.7197    0.8720 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7212    0.1454    1.3721 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9495   -1.1883    1.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0687   -1.6647    1.4248 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7843   -2.0695    0.9984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9942   -3.4235    0.6887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2479   -3.9777    0.6115 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0885   -4.2740    0.4434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1282   -5.7227    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3884   -3.7605    0.5437 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6227   -2.4151    0.8722 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0429   -1.9287    0.9804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5245   -1.5552    1.0791 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6951   -0.0990    1.4165 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7631    0.0042    2.8405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0972    3.0471    0.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1680    3.6573   -0.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9185    3.4567   -1.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8420    1.6196   -2.2433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7154    1.0105   -0.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6042   -0.1274   -1.1231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9091    2.4972   -0.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5844    1.7633   -2.3023 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5786    0.9098   -1.1283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4300    1.7161    1.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9095   -3.3156    0.9121 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8157   -6.2259   -0.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7772   -5.8182   -0.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5838   -6.2429    0.9566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2348   -4.4250    0.3719 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7566   -2.7581    0.9328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2033   -1.4207    1.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.2438    0.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6333    0.3008    1.0252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1488    0.0433    3.1821 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  6  1  0
  6  7  1  0
  9 17  2  0
  5  3  1  0
  3  4  1  0
 14 15  2  0
  3  2  1  0
 15 17  1  0
  2  1  1  0
 12 14  1  0
 15 16  1  0
  9 10  1  0
 12 13  1  0
 10 12  2  0
 10 11  1  0
  9  7  1  0
  7  8  2  0
 17 18  1  0
 18 19  1  0
 18  5  1  0
  5 29  1  1
 14 34  1  0
 18 38  1  6
  3 25  1  6
  4 26  1  0
  4 27  1  0
  4 28  1  0
  2 23  1  0
  2 24  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
 13 31  1  0
 13 32  1  0
 13 33  1  0
 11 30  1  0
 19 39  1  0
M  END


  Mrv1652306212101593D          

 39 40  0  0  0  0            999 V2000
   -2.0054    3.0193   -0.6338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8350    1.5957   -1.1461 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5526    0.8720   -0.6718 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6995    1.5530   -1.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871    0.7197    0.8720 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7212    0.1454    1.3721 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9495   -1.1883    1.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0687   -1.6647    1.4248 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7843   -2.0695    0.9984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9942   -3.4235    0.6887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2479   -3.9777    0.6115 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0885   -4.2740    0.4434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1282   -5.7227    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3884   -3.7605    0.5437 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6227   -2.4151    0.8722 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0429   -1.9287    0.9804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5245   -1.5552    1.0791 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6951   -0.0990    1.4165 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7631    0.0042    2.8405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0972    3.0471    0.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1680    3.6573   -0.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9185    3.4567   -1.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8420    1.6196   -2.2433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7154    1.0105   -0.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6042   -0.1274   -1.1231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9091    2.4972   -0.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5844    1.7633   -2.3023 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5786    0.9098   -1.1283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4300    1.7161    1.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9095   -3.3156    0.9121 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8157   -6.2259   -0.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7772   -5.8182   -0.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5838   -6.2429    0.9566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2348   -4.4250    0.3719 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7566   -2.7581    0.9328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2033   -1.4207    1.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.2438    0.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6333    0.3008    1.0252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1488    0.0433    3.1821 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  9 17  2  0  0  0  0
  5  3  1  0  0  0  0
  3  4  1  0  0  0  0
 14 15  2  0  0  0  0
  3  2  1  0  0  0  0
 15 17  1  0  0  0  0
  2  1  1  0  0  0  0
 12 14  1  0  0  0  0
 15 16  1  0  0  0  0
  9 10  1  0  0  0  0
 12 13  1  0  0  0  0
 10 12  2  0  0  0  0
 10 11  1  0  0  0  0
  9  7  1  0  0  0  0
  7  8  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18  5  1  0  0  0  0
  5 29  1  1  0  0  0
 14 34  1  0  0  0  0
 18 38  1  6  0  0  0
  3 25  1  6  0  0  0
  4 26  1  0  0  0  0
  4 27  1  0  0  0  0
  4 28  1  0  0  0  0
  2 23  1  0  0  0  0
  2 24  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
 16 35  1  0  0  0  0
 16 36  1  0  0  0  0
 16 37  1  0  0  0  0
 13 31  1  0  0  0  0
 13 32  1  0  0  0  0
 13 33  1  0  0  0  0
 11 30  1  0  0  0  0
 19 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0042295

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(C([H])=C(C2=C1C(=O)O[C@]([H])([C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H])[C@@]2([H])O[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O4/c1-5-7(2)14-13(17)10-8(3)6-9(4)12(16)11(10)15(18)19-14/h6-7,13-14,16-17H,5H2,1-4H3/t7-,13+,14-/m1/s1

> <INCHI_KEY>
GFNHLBAMMYVPFE-IYCUSSIYSA-N

> <FORMULA>
C15H20O4

> <MOLECULAR_WEIGHT>
264.321

> <EXACT_MASS>
264.136159124

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
28.8932543826229

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,4S)-3-[(2R)-butan-2-yl]-4,8-dihydroxy-5,7-dimethyl-3,4-dihydro-1H-2-benzopyran-1-one

> <ALOGPS_LOGP>
2.37

> <JCHEM_LOGP>
4.019531507333333

> <ALOGPS_LOGS>
-2.10

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.331246619300181

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.323925615974494

> <JCHEM_PKA_STRONGEST_BASIC>
-3.592494783526064

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
72.6791

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.09e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4S)-3-[(2R)-butan-2-yl]-4,8-dihydroxy-5,7-dimethyl-3,4-dihydro-2-benzopyran-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
   -2.0054    3.0193   -0.6338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8350    1.5957   -1.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5526    0.8720   -0.6718 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6995    1.5530   -1.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871    0.7197    0.8720 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7212    0.1454    1.3721 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9495   -1.1883    1.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0687   -1.6647    1.4248 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7843   -2.0695    0.9984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9942   -3.4235    0.6887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2479   -3.9777    0.6115 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0885   -4.2740    0.4434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1282   -5.7227    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3884   -3.7605    0.5437 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6227   -2.4151    0.8722 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0429   -1.9287    0.9804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5245   -1.5552    1.0791 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6951   -0.0990    1.4165 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7631    0.0042    2.8405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0972    3.0471    0.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1680    3.6573   -0.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9185    3.4567   -1.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8420    1.6196   -2.2433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7154    1.0105   -0.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6042   -0.1274   -1.1231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9091    2.4972   -0.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5844    1.7633   -2.3023 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5786    0.9098   -1.1283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4300    1.7161    1.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9095   -3.3156    0.9121 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8157   -6.2259   -0.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7772   -5.8182   -0.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5838   -6.2429    0.9566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2348   -4.4250    0.3719 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7566   -2.7581    0.9328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2033   -1.4207    1.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.2438    0.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6333    0.3008    1.0252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1488    0.0433    3.1821 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  6  1  0
  6  7  1  0
  9 17  2  0
  5  3  1  0
  3  4  1  0
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  3  2  1  0
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  2  1  1  0
 12 14  1  0
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 12 13  1  0
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  9  7  1  0
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  2 23  1  0
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  1 20  1  0
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 16 35  1  0
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 13 31  1  0
 13 32  1  0
 13 33  1  0
 11 30  1  0
 19 39  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -2.005   3.019  -0.634  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.835   1.596  -1.146  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.553   0.872  -0.672  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.700   1.553  -1.234  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.487   0.720   0.872  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.721   0.145   1.372  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.950  -1.188   1.273  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.069  -1.665   1.425  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.784  -2.070   0.998  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.994  -3.424   0.689  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.248  -3.978   0.612  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.089  -4.274   0.443  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.128  -5.723   0.108  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.388  -3.761   0.544  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.623  -2.415   0.872  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.043  -1.929   0.980  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.525  -1.555   1.079  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.695  -0.099   1.417  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.763   0.004   2.841  0.00  0.00           O+0
HETATM   20  H   UNK     0      -2.097   3.047   0.456  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.168   3.657  -0.930  0.00  0.00           H+0
HETATM   22  H   UNK     0      -2.918   3.457  -1.051  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.842   1.620  -2.243  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.715   1.010  -0.855  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.604  -0.127  -1.123  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.909   2.497  -0.721  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.584   1.763  -2.302  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.579   0.910  -1.128  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.430   1.716   1.327  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.910  -3.316   0.912  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.816  -6.226  -0.127  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.777  -5.818  -0.769  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.584  -6.243   0.957  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.235  -4.425   0.372  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.757  -2.758   0.933  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.203  -1.421   1.937  0.00  0.00           H+0
HETATM   37  H   UNK     0       3.270  -1.244   0.158  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.633   0.301   1.025  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.149   0.043   3.182  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2    3    1   23   24                                             
CONECT    3    5    4    2   25                                             
CONECT    4    3   26   27   28                                             
CONECT    5    6    3   18   29                                             
CONECT    6    5    7                                                       
CONECT    7    6    9    8                                                  
CONECT    8    7                                                            
CONECT    9   17   10    7                                                  
CONECT   10    9   12   11                                                  
CONECT   11   10   30                                                       
CONECT   12   14   13   10                                                  
CONECT   13   12   31   32   33                                             
CONECT   14   15   12   34                                                  
CONECT   15   14   17   16                                                  
CONECT   16   15   35   36   37                                             
CONECT   17    9   15   18                                                  
CONECT   18   17   19    5   38                                             
CONECT   19   18   39                                                       
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    2                                                            
CONECT   24    2                                                            
CONECT   25    3                                                            
CONECT   26    4                                                            
CONECT   27    4                                                            
CONECT   28    4                                                            
CONECT   29    5                                                            
CONECT   30   11                                                            
CONECT   31   13                                                            
CONECT   32   13                                                            
CONECT   33   13                                                            
CONECT   34   14                                                            
CONECT   35   16                                                            
CONECT   36   16                                                            
CONECT   37   16                                                            
CONECT   38   18                                                            
CONECT   39   19                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   80    0
END

RDKit          3D

39 40  0  0  0  0  0  0  0  0999 V2000
   -2.0054    3.0193   -0.6338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8350    1.5957   -1.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5526    0.8720   -0.6718 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6995    1.5530   -1.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871    0.7197    0.8720 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7212    0.1454    1.3721 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9495   -1.1883    1.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0687   -1.6647    1.4248 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7843   -2.0695    0.9984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9942   -3.4235    0.6887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2479   -3.9777    0.6115 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0885   -4.2740    0.4434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1282   -5.7227    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3884   -3.7605    0.5437 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6227   -2.4151    0.8722 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0429   -1.9287    0.9804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5245   -1.5552    1.0791 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6951   -0.0990    1.4165 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7631    0.0042    2.8405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0972    3.0471    0.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1680    3.6573   -0.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9185    3.4567   -1.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8420    1.6196   -2.2433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7154    1.0105   -0.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6042   -0.1274   -1.1231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9091    2.4972   -0.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5844    1.7633   -2.3023 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5786    0.9098   -1.1283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4300    1.7161    1.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9095   -3.3156    0.9121 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8157   -6.2259   -0.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7772   -5.8182   -0.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5838   -6.2429    0.9566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2348   -4.4250    0.3719 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7566   -2.7581    0.9328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2033   -1.4207    1.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.2438    0.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6333    0.3008    1.0252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1488    0.0433    3.1821 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  6  1  0
  6  7  1  0
  9 17  2  0
  5  3  1  0
  3  4  1  0
 14 15  2  0
  3  2  1  0
 15 17  1  0
  2  1  1  0
 12 14  1  0
 15 16  1  0
  9 10  1  0
 12 13  1  0
 10 12  2  0
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  9  7  1  0
  7  8  2  0
 17 18  1  0
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 18  5  1  0
  5 29  1  1
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  3 25  1  6
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  4 27  1  0
  4 28  1  0
  2 23  1  0
  2 24  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
 13 31  1  0
 13 32  1  0
 13 33  1  0
 11 30  1  0
 19 39  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀O₄

Average Mass

264.3210 Da

Monoisotopic Mass

264.13616 Da

IUPAC Name

(3R,4S)-3-[(2R)-butan-2-yl]-4,8-dihydroxy-5,7-dimethyl-3,4-dihydro-1H-2-benzopyran-1-one

Traditional Name

(3R,4S)-3-[(2R)-butan-2-yl]-4,8-dihydroxy-5,7-dimethyl-3,4-dihydro-2-benzopyran-1-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C(C([H])=C(C2=C1C(=O)O[C@]([H])([C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H])[C@@]2([H])O[H])C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C15H20O4/c1-5-7(2)14-13(17)10-8(3)6-9(4)12(16)11(10)15(18)19-14/h6-7,13-14,16-17H,5H2,1-4H3/t7-,13+,14-/m1/s1

InChI Key

GFNHLBAMMYVPFE-IYCUSSIYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Chrysosporium articulatum	JEOL database	Jeon, J., et al, Tetrahedron Lett. 54, 2111 (2013)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

2-benzopyrans

Direct Parent

2-benzopyrans

Alternative Parents

Substituents

2-benzopyran
Phenol
Benzenoid
Vinylogous acid
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	2.37	ALOGPS
logP	4.02	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	10.32	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	72.68 m³·mol⁻¹	ChemAxon
Polarizability	28.89 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

29355719

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71725517

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Jeon, J., et al. (2013). Jeon, J., et al, Tetrahedron Lett. 54, 2111 (2013). Tetrahedron Lett.

Showing NP-Card for chrysoarticulin A (NP0042295)

MOL for NP0042295 (chrysoarticulin A)

3D MOL for NP0042295 (chrysoarticulin A)

3D SDF for NP0042295 (chrysoarticulin A)

3D-SDF for NP0042295 (chrysoarticulin A)

PDB for NP0042295 (chrysoarticulin A)

3D PDB for NP0042295 (chrysoarticulin A)

SMILES for NP0042295 (chrysoarticulin A)

INCHI for NP0042295 (chrysoarticulin A)

Structure for NP0042295 (chrysoarticulin A)

3D Structure for NP0042295 (chrysoarticulin A)