NP-MRD: Showing NP-Card for Griseofulvin (NP0006405)

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Record Information

Version

2.0

Created at

2020-12-09 03:25:49 UTC

Updated at

2021-07-15 16:54:42 UTC

NP-MRD ID

NP0006405

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Griseofulvin

Provided By

NPAtlas

Description

Griseofulvin is found in Apis cerana, Axinella verrucosa, Memnoniella echinata, Penicillium, Penicillium aethiopicum, Penicillium griseofulvum, Penicillium griseofulvun, Penicillium janczewskii, Penicillium raistrickii, Penicillium sclerotigenum, Penicillium solitum and Penicillium sp.. Griseofulvin was first documented in 1939 (PMID: 16746904). Based on a literature review very few articles have been published on (6'R)-7-chloro-2',4,6-trimethoxy-6'-methyl-3H-spiro[1-benzofuran-2,1'-cyclohexan]-2'-ene-3,4'-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118273D          

 41 43  0  0  0  0            999 V2000
   -2.4554    2.0629   -2.8951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4542    0.6683   -2.6566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6983    0.1164   -1.4132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8485   -0.5038   -1.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0717   -1.0742    0.2098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0832   -1.7799    0.4288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1068   -0.8272    1.3100 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3557    0.4427    0.9531 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3894    0.8411    2.0439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6546    0.2073   -0.3636 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7298    1.2474   -0.6316 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5620    0.8404   -0.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7288    1.5853   -0.2110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6792    3.3179   -0.4784 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.9092    0.9487    0.1099 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0900    1.6930    0.2253 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3212    1.1192    0.5466 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8889   -0.4164    0.3093 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7342   -1.1502    0.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7033   -2.5247    0.3961 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8745   -3.2123    0.7229 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5453   -0.5285   -0.1229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8167   -1.0191   -0.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1299   -2.2325   -0.3992 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7009    2.5973   -2.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2086    2.2203   -3.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4390    2.5276   -2.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6183   -0.5770   -1.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4178   -1.6906    1.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6188   -0.6788    2.2850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1165    1.2341    0.8434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270    1.6272    1.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9818    1.3463    2.8575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8561   -0.0017    2.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5113    0.2523   -0.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1174    1.8700    0.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3896    0.7389    1.5806 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8094   -0.9153    0.5599 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5115   -3.4412   -0.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5950   -4.2129    1.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5081   -2.7182    1.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 10  3  1  0  0  0  0
 22 12  1  0  0  0  0
 23 10  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  4 28  1  0  0  0  0
  7 29  1  0  0  0  0
  7 30  1  0  0  0  0
  8 31  1  6  0  0  0
  9 32  1  0  0  0  0
  9 33  1  0  0  0  0
  9 34  1  0  0  0  0
 17 35  1  0  0  0  0
 17 36  1  0  0  0  0
 17 37  1  0  0  0  0
 18 38  1  0  0  0  0
 21 39  1  0  0  0  0
 21 40  1  0  0  0  0
 21 41  1  0  0  0  0
M  END

     RDKit          3D

 41 43  0  0  0  0  0  0  0  0999 V2000
   -2.4554    2.0629   -2.8951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4542    0.6683   -2.6566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6983    0.1164   -1.4132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8485   -0.5038   -1.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0717   -1.0742    0.2098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0832   -1.7799    0.4288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1068   -0.8272    1.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3557    0.4427    0.9531 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3894    0.8411    2.0439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6546    0.2073   -0.3636 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7298    1.2474   -0.6316 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5620    0.8404   -0.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7288    1.5853   -0.2110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6792    3.3179   -0.4784 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.9092    0.9487    0.1099 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0900    1.6930    0.2253 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3212    1.1192    0.5466 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8889   -0.4164    0.3093 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7342   -1.1502    0.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7033   -2.5247    0.3961 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8745   -3.2123    0.7229 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5453   -0.5285   -0.1229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8167   -1.0191   -0.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1299   -2.2325   -0.3992 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7009    2.5973   -2.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2086    2.2203   -3.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4390    2.5276   -2.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6183   -0.5770   -1.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4178   -1.6906    1.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6188   -0.6788    2.2850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1165    1.2341    0.8434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270    1.6272    1.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9818    1.3463    2.8575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8561   -0.0017    2.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5113    0.2523   -0.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1174    1.8700    0.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3896    0.7389    1.5806 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8094   -0.9153    0.5599 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5115   -3.4412   -0.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5950   -4.2129    1.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5081   -2.7182    1.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  6
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  2  0
 22 23  1  0
 23 24  2  0
 10  3  1  0
 22 12  1  0
 23 10  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  6
  9 32  1  0
  9 33  1  0
  9 34  1  0
 17 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
 21 39  1  0
 21 40  1  0
 21 41  1  0
M  END


  Mrv1652306242118273D          

 41 43  0  0  0  0            999 V2000
   -2.4554    2.0629   -2.8951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4542    0.6683   -2.6566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6983    0.1164   -1.4132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8485   -0.5038   -1.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0717   -1.0742    0.2098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0832   -1.7799    0.4288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1068   -0.8272    1.3100 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3557    0.4427    0.9531 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3894    0.8411    2.0439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6546    0.2073   -0.3636 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7298    1.2474   -0.6316 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5620    0.8404   -0.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7288    1.5853   -0.2110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6792    3.3179   -0.4784 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.9092    0.9487    0.1099 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0900    1.6930    0.2253 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3212    1.1192    0.5466 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8889   -0.4164    0.3093 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7342   -1.1502    0.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7033   -2.5247    0.3961 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8745   -3.2123    0.7229 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5453   -0.5285   -0.1229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8167   -1.0191   -0.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1299   -2.2325   -0.3992 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7009    2.5973   -2.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2086    2.2203   -3.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4390    2.5276   -2.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6183   -0.5770   -1.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4178   -1.6906    1.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6188   -0.6788    2.2850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1165    1.2341    0.8434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270    1.6272    1.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9818    1.3463    2.8575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8561   -0.0017    2.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5113    0.2523   -0.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1174    1.8700    0.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3896    0.7389    1.5806 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8094   -0.9153    0.5599 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5115   -3.4412   -0.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5950   -4.2129    1.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5081   -2.7182    1.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 10  3  1  0  0  0  0
 22 12  1  0  0  0  0
 23 10  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  4 28  1  0  0  0  0
  7 29  1  0  0  0  0
  7 30  1  0  0  0  0
  8 31  1  6  0  0  0
  9 32  1  0  0  0  0
  9 33  1  0  0  0  0
  9 34  1  0  0  0  0
 17 35  1  0  0  0  0
 17 36  1  0  0  0  0
 17 37  1  0  0  0  0
 18 38  1  0  0  0  0
 21 39  1  0  0  0  0
 21 40  1  0  0  0  0
 21 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0006405

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C1=C(OC([H])([H])[H])C(Cl)=C2O[C@]3(C(=O)C2=C1OC([H])([H])[H])C(OC([H])([H])[H])=C([H])C(=O)C([H])([H])[C@@]3([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C17H17ClO6/c1-8-5-9(19)6-12(23-4)17(8)16(20)13-10(21-2)7-11(22-3)14(18)15(13)24-17/h6-8H,5H2,1-4H3/t8-,17+/m1/s1

> <INCHI_KEY>
DDUHZTYCFQRHIY-OEWHWVHBSA-N

> <FORMULA>
C17H17ClO6

> <MOLECULAR_WEIGHT>
352.77

> <EXACT_MASS>
352.071366

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
34.141391622383836

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6'R)-7-chloro-2',4,6-trimethoxy-6'-methyl-3H-spiro[1-benzofuran-2,1'-cyclohexan]-2'-ene-3,4'-dione

> <ALOGPS_LOGP>
2.71

> <JCHEM_LOGP>
2.172137458333333

> <ALOGPS_LOGS>
-3.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.68867051547463

> <JCHEM_PKA_STRONGEST_BASIC>
-4.322861287850263

> <JCHEM_POLAR_SURFACE_AREA>
71.06000000000002

> <JCHEM_REFRACTIVITY>
87.8459

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.04e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6'R)-7-chloro-2',4,6-trimethoxy-6'-methylspiro[1-benzofuran-2,1'-cyclohexan]-2'-ene-3,4'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 41 43  0  0  0  0  0  0  0  0999 V2000
   -2.4554    2.0629   -2.8951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4542    0.6683   -2.6566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6983    0.1164   -1.4132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8485   -0.5038   -1.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0717   -1.0742    0.2098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0832   -1.7799    0.4288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1068   -0.8272    1.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3557    0.4427    0.9531 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3894    0.8411    2.0439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6546    0.2073   -0.3636 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7298    1.2474   -0.6316 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5620    0.8404   -0.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7288    1.5853   -0.2110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6792    3.3179   -0.4784 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.9092    0.9487    0.1099 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0900    1.6930    0.2253 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3212    1.1192    0.5466 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8889   -0.4164    0.3093 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7342   -1.1502    0.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7033   -2.5247    0.3961 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8745   -3.2123    0.7229 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5453   -0.5285   -0.1229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8167   -1.0191   -0.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1299   -2.2325   -0.3992 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7009    2.5973   -2.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2086    2.2203   -3.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4390    2.5276   -2.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6183   -0.5770   -1.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4178   -1.6906    1.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6188   -0.6788    2.2850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1165    1.2341    0.8434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270    1.6272    1.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9818    1.3463    2.8575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8561   -0.0017    2.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5113    0.2523   -0.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1174    1.8700    0.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3896    0.7389    1.5806 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8094   -0.9153    0.5599 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5115   -3.4412   -0.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5950   -4.2129    1.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5081   -2.7182    1.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  6
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  2  0
 22 23  1  0
 23 24  2  0
 10  3  1  0
 22 12  1  0
 23 10  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  6
  9 32  1  0
  9 33  1  0
  9 34  1  0
 17 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
 21 39  1  0
 21 40  1  0
 21 41  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      -2.455   2.063  -2.895  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.454   0.668  -2.657  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.698   0.116  -1.413  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.849  -0.504  -1.111  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.072  -1.074   0.210  0.00  0.00           C+0
HETATM    6  O   UNK     0      -5.083  -1.780   0.429  0.00  0.00           O+0
HETATM    7  C   UNK     0      -3.107  -0.827   1.310  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.356   0.443   0.953  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.389   0.841   2.044  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.655   0.207  -0.364  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.730   1.247  -0.632  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.562   0.840  -0.324  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.729   1.585  -0.211  0.00  0.00           C+0
HETATM   14 Cl   UNK     0       1.679   3.318  -0.478  0.00  0.00          Cl+0
HETATM   15  C   UNK     0       2.909   0.949   0.110  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.090   1.693   0.225  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.321   1.119   0.547  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.889  -0.416   0.309  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.734  -1.150   0.197  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.703  -2.525   0.396  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.874  -3.212   0.723  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.545  -0.529  -0.123  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.817  -1.019  -0.311  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.130  -2.232  -0.399  0.00  0.00           O+0
HETATM   25  H   UNK     0      -1.701   2.597  -2.292  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.209   2.220  -3.953  0.00  0.00           H+0
HETATM   27  H   UNK     0      -3.439   2.528  -2.676  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.618  -0.577  -1.869  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.418  -1.691   1.471  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.619  -0.679   2.285  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.116   1.234   0.843  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.727   1.627   1.626  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.982   1.346   2.857  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.856  -0.002   2.483  0.00  0.00           H+0
HETATM   35  H   UNK     0       5.511   0.252  -0.127  0.00  0.00           H+0
HETATM   36  H   UNK     0       6.117   1.870   0.345  0.00  0.00           H+0
HETATM   37  H   UNK     0       5.390   0.739   1.581  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.809  -0.915   0.560  0.00  0.00           H+0
HETATM   39  H   UNK     0       3.511  -3.441  -0.162  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.595  -4.213   1.155  0.00  0.00           H+0
HETATM   41  H   UNK     0       3.508  -2.718   1.466  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5   28                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   29   30                                             
CONECT    8    7    9   10   31                                             
CONECT    9    8   32   33   34                                             
CONECT   10    8   11    3   23                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   22                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16   35   36   37                                             
CONECT   18   15   19   38                                                  
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20   39   40   41                                             
CONECT   22   19   23   12                                                  
CONECT   23   22   24   10                                                  
CONECT   24   23                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    4                                                            
CONECT   29    7                                                            
CONECT   30    7                                                            
CONECT   31    8                                                            
CONECT   32    9                                                            
CONECT   33    9                                                            
CONECT   34    9                                                            
CONECT   35   17                                                            
CONECT   36   17                                                            
CONECT   37   17                                                            
CONECT   38   18                                                            
CONECT   39   21                                                            
CONECT   40   21                                                            
CONECT   41   21                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   86    0
END

RDKit          3D

41 43  0  0  0  0  0  0  0  0999 V2000
   -2.4554    2.0629   -2.8951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4542    0.6683   -2.6566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6983    0.1164   -1.4132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8485   -0.5038   -1.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0717   -1.0742    0.2098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0832   -1.7799    0.4288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1068   -0.8272    1.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3557    0.4427    0.9531 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3894    0.8411    2.0439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6546    0.2073   -0.3636 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7298    1.2474   -0.6316 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5620    0.8404   -0.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7288    1.5853   -0.2110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6792    3.3179   -0.4784 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.9092    0.9487    0.1099 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0900    1.6930    0.2253 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3212    1.1192    0.5466 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8889   -0.4164    0.3093 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7342   -1.1502    0.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7033   -2.5247    0.3961 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8745   -3.2123    0.7229 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5453   -0.5285   -0.1229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8167   -1.0191   -0.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1299   -2.2325   -0.3992 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7009    2.5973   -2.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2086    2.2203   -3.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4390    2.5276   -2.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6183   -0.5770   -1.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4178   -1.6906    1.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6188   -0.6788    2.2850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1165    1.2341    0.8434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270    1.6272    1.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9818    1.3463    2.8575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8561   -0.0017    2.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5113    0.2523   -0.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1174    1.8700    0.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3896    0.7389    1.5806 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8094   -0.9153    0.5599 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5115   -3.4412   -0.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5950   -4.2129    1.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5081   -2.7182    1.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  6
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  2  0
 22 23  1  0
 23 24  2  0
 10  3  1  0
 22 12  1  0
 23 10  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  6
  9 32  1  0
  9 33  1  0
  9 34  1  0
 17 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
 21 39  1  0
 21 40  1  0
 21 41  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₇H₁₇ClO₆

Average Mass

352.7700 Da

Monoisotopic Mass

352.07137 Da

IUPAC Name

(6'R)-7-chloro-2',4,6-trimethoxy-6'-methyl-3H-spiro[1-benzofuran-2,1'-cyclohexan]-2'-ene-3,4'-dione

Traditional Name

(6'R)-7-chloro-2',4,6-trimethoxy-6'-methylspiro[1-benzofuran-2,1'-cyclohexan]-2'-ene-3,4'-dione

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C(Cl)C2=C1C(=O)C1(O2)[C@H](C)CC(=O)C=C1OC

InChI Identifier

InChI=1S/C17H17ClO6/c1-8-5-9(19)6-12(23-4)17(8)16(20)13-10(21-2)7-11(22-3)14(18)15(13)24-17/h6-8H,5H2,1-4H3/t8-,17?/m1/s1

InChI Key

DDUHZTYCFQRHIY-OEWHWVHBSA-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
Apis cerana	LOTUS Database	35616633
Axinella verrucosa	LOTUS Database	35616633
Memnoniella echinata	LOTUS Database	35616633
Penicillium	NPAtlas	16746904
Penicillium aethiopicum	LOTUS Database	35616633
Penicillium griseofulvum	LOTUS Database	35616633
Penicillium griseofulvun	Fungi	KNApSAcK
Penicillium janczewskii	Fungi	KNApSAcK
Penicillium raistrickii	LOTUS Database	35616633
Penicillium sclerotigenum	LOTUS Database	35616633
Penicillium solitum	LOTUS Database	35616633
Penicillium sp.	Fungi	KNApSAcK

Chemical Taxonomy

Classification

Not classified

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	2.71	ALOGPS
logP	2.17	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	17.69	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	71.06 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	87.85 m³·mol⁻¹	ChemAxon
Polarizability	34.14 Å³	ChemAxon
Number of Rings	3	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

NPA002483

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

23954655

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5702061

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Oxford AE, Raistrick H, Simonart P: Studies in the biochemistry of micro-organisms: Griseofulvin, C(17)H(17)O(6)Cl, a metabolic product of Penicillium griseo-fulvum Dierckx. Biochem J. 1939 Feb;33(2):240-8. doi: 10.1042/bj0330240. [PubMed:16746904 ]

Showing NP-Card for Griseofulvin (NP0006405)

MOL for NP0006405 (Griseofulvin)

3D MOL for NP0006405 (Griseofulvin)

3D SDF for NP0006405 (Griseofulvin)

3D-SDF for NP0006405 (Griseofulvin)

PDB for NP0006405 (Griseofulvin)

3D PDB for NP0006405 (Griseofulvin)

SMILES for NP0006405 (Griseofulvin)

INCHI for NP0006405 (Griseofulvin)

Structure for NP0006405 (Griseofulvin)

3D Structure for NP0006405 (Griseofulvin)