NP-MRD: Showing NP-Card for Purpactin C (NP0008984)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2020-12-09 06:27:30 UTC

Updated at

2021-07-15 17:01:58 UTC

NP-MRD ID

NP0008984

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Purpactin C

Provided By

NPAtlas

Description

1-{2'-Formyl-4-methoxy-4'-methyl-3,6'-dioxo-3H-spiro[1-benzofuran-2,1'-cyclohexane]-2',4'-dien-5-yl}-3-methylbutyl acetate belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Purpactin C is found in Penicillium and Talaromyces purpureogenus. It was first documented in 1991 (PMID: 2010354). Based on a literature review very few articles have been published on 1-{2'-formyl-4-methoxy-4'-methyl-3,6'-dioxo-3H-spiro[1-benzofuran-2,1'-cyclohexane]-2',4'-dien-5-yl}-3-methylbutyl acetate (PMID: 31771918).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106313D          

 54 56  0  0  0  0            999 V2000
   -0.2341   -2.3832   -1.5401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3864   -0.9764   -1.5380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1271   -0.1762   -0.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0648    0.1663    0.4733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4602   -0.3427    0.3045 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2932   -0.0031    1.5066 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7077   -0.4659    1.4820 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5460    0.0956    0.3705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4125   -0.1091    2.7998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0216    0.2241   -0.8604 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4347   -0.4714   -1.9691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9986    0.2450   -3.1252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3355   -1.7086   -2.0049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7925    0.9672    1.5515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5080    1.4560    1.6987 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4585    1.1326    0.7862 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1543    0.3109   -0.3081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3701    0.1520   -1.0898 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4839   -0.3537   -2.2257 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4721    0.7075   -0.2834 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8085    1.4876    0.7103 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3731    1.5967   -1.0513 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8416    2.5256   -1.7043 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8281    1.4312   -1.0729 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3489    0.4507   -0.3793 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8325    0.2938   -0.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5289   -0.4663    0.4016 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2173   -0.3507    0.4465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4519   -1.2920    1.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0743   -2.1926    1.8622 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8200   -2.6792   -1.7917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8629   -2.8691   -2.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5345   -2.8242   -0.5683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3766   -1.4574    0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7759   -0.3303    2.4465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3613    1.1298    1.6019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7680   -1.5936    1.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7860   -0.6819   -0.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5236    0.5049    0.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1055    0.9506   -0.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8427   -0.4513    3.6655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3817   -0.6572    2.7702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6467    0.9750    2.8083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9771    1.3313   -2.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3801    0.0789   -4.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0233   -0.1045   -3.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5437    1.2447    2.3107 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7095    2.0904    2.5593 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3955    2.1339   -1.6651 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0867   -0.6733    0.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3058    1.0978    0.1689 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2083    0.3274   -1.4615 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0558   -1.2607    0.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3709   -1.2569    1.3225 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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  4 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 17  3  1  0  0  0  0
 28 20  1  0  0  0  0
 21 16  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
  1 33  1  0  0  0  0
  5 34  1  6  0  0  0
  6 35  1  0  0  0  0
  6 36  1  0  0  0  0
  7 37  1  6  0  0  0
  8 38  1  0  0  0  0
  8 39  1  0  0  0  0
  8 40  1  0  0  0  0
  9 41  1  0  0  0  0
  9 42  1  0  0  0  0
  9 43  1  0  0  0  0
 12 44  1  0  0  0  0
 12 45  1  0  0  0  0
 12 46  1  0  0  0  0
 14 47  1  0  0  0  0
 15 48  1  0  0  0  0
 24 49  1  0  0  0  0
 26 50  1  0  0  0  0
 26 51  1  0  0  0  0
 26 52  1  0  0  0  0
 27 53  1  0  0  0  0
 29 54  1  0  0  0  0
M  END

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
   -0.2341   -2.3832   -1.5401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3864   -0.9764   -1.5380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1271   -0.1762   -0.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0648    0.1663    0.4733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4602   -0.3427    0.3045 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2932   -0.0031    1.5066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7077   -0.4659    1.4820 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5460    0.0956    0.3705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4125   -0.1091    2.7998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0216    0.2241   -0.8604 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4347   -0.4714   -1.9691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9986    0.2450   -3.1252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3355   -1.7086   -2.0049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7925    0.9672    1.5515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5080    1.4560    1.6987 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4585    1.1326    0.7862 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1543    0.3109   -0.3081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3701    0.1520   -1.0898 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4839   -0.3537   -2.2257 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4721    0.7075   -0.2834 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8085    1.4876    0.7103 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3731    1.5967   -1.0513 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8416    2.5256   -1.7043 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8281    1.4312   -1.0729 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3489    0.4507   -0.3793 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8325    0.2938   -0.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5289   -0.4663    0.4016 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2173   -0.3507    0.4465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4519   -1.2920    1.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0743   -2.1926    1.8622 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8200   -2.6792   -1.7917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8629   -2.8691   -2.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5345   -2.8242   -0.5683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3766   -1.4574    0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7759   -0.3303    2.4465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3613    1.1298    1.6019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7680   -1.5936    1.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7860   -0.6819   -0.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5236    0.5049    0.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1055    0.9506   -0.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8427   -0.4513    3.6655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3817   -0.6572    2.7702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6467    0.9750    2.8083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9771    1.3313   -2.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3801    0.0789   -4.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0233   -0.1045   -3.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5437    1.2447    2.3107 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7095    2.0904    2.5593 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3955    2.1339   -1.6651 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0867   -0.6733    0.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3058    1.0978    0.1689 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2083    0.3274   -1.4615 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0558   -1.2607    0.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3709   -1.2569    1.3225 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  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  5 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
  4 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  1
 20 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 17  3  1  0
 28 20  1  0
 21 16  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  5 34  1  6
  6 35  1  0
  6 36  1  0
  7 37  1  6
  8 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  0
  9 42  1  0
  9 43  1  0
 12 44  1  0
 12 45  1  0
 12 46  1  0
 14 47  1  0
 15 48  1  0
 24 49  1  0
 26 50  1  0
 26 51  1  0
 26 52  1  0
 27 53  1  0
 29 54  1  0
M  END


  Mrv1652306242106313D          

 54 56  0  0  0  0            999 V2000
   -0.2341   -2.3832   -1.5401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3864   -0.9764   -1.5380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1271   -0.1762   -0.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0648    0.1663    0.4733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4602   -0.3427    0.3045 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2932   -0.0031    1.5066 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7077   -0.4659    1.4820 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5460    0.0956    0.3705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4125   -0.1091    2.7998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0216    0.2241   -0.8604 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4347   -0.4714   -1.9691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9986    0.2450   -3.1252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3355   -1.7086   -2.0049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7925    0.9672    1.5515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5080    1.4560    1.6987 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4585    1.1326    0.7862 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1543    0.3109   -0.3081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3701    0.1520   -1.0898 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4839   -0.3537   -2.2257 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4721    0.7075   -0.2834 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8085    1.4876    0.7103 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3731    1.5967   -1.0513 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8416    2.5256   -1.7043 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8281    1.4312   -1.0729 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3489    0.4507   -0.3793 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8325    0.2938   -0.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5289   -0.4663    0.4016 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2173   -0.3507    0.4465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4519   -1.2920    1.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0743   -2.1926    1.8622 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8200   -2.6792   -1.7917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8629   -2.8691   -2.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5345   -2.8242   -0.5683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3766   -1.4574    0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7759   -0.3303    2.4465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3613    1.1298    1.6019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7680   -1.5936    1.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7860   -0.6819   -0.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5236    0.5049    0.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1055    0.9506   -0.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8427   -0.4513    3.6655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3817   -0.6572    2.7702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6467    0.9750    2.8083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9771    1.3313   -2.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3801    0.0789   -4.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0233   -0.1045   -3.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5437    1.2447    2.3107 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7095    2.0904    2.5593 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3955    2.1339   -1.6651 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0867   -0.6733    0.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3058    1.0978    0.1689 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2083    0.3274   -1.4615 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0558   -1.2607    0.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3709   -1.2569    1.3225 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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  4 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 17  3  1  0  0  0  0
 28 20  1  0  0  0  0
 21 16  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
  1 33  1  0  0  0  0
  5 34  1  6  0  0  0
  6 35  1  0  0  0  0
  6 36  1  0  0  0  0
  7 37  1  6  0  0  0
  8 38  1  0  0  0  0
  8 39  1  0  0  0  0
  8 40  1  0  0  0  0
  9 41  1  0  0  0  0
  9 42  1  0  0  0  0
  9 43  1  0  0  0  0
 12 44  1  0  0  0  0
 12 45  1  0  0  0  0
 12 46  1  0  0  0  0
 14 47  1  0  0  0  0
 15 48  1  0  0  0  0
 24 49  1  0  0  0  0
 26 50  1  0  0  0  0
 26 51  1  0  0  0  0
 26 52  1  0  0  0  0
 27 53  1  0  0  0  0
 29 54  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0008984

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C(=O)C1=C([H])C(=C([H])C(=O)[C@]11OC2=C(C1=O)C(OC([H])([H])[H])=C(C([H])=C2[H])[C@]([H])(OC(=O)C([H])([H])[H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H24O7/c1-12(2)8-18(29-14(4)25)16-6-7-17-20(21(16)28-5)22(27)23(30-17)15(11-24)9-13(3)10-19(23)26/h6-7,9-12,18H,8H2,1-5H3/t18-,23-/m1/s1

> <INCHI_KEY>
JFVAWGUDTZFPLP-UHFFFAOYSA-N

> <FORMULA>
C23H24O7

> <MOLECULAR_WEIGHT>
412.438

> <EXACT_MASS>
412.152203113

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
43.6162430414217

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R)-1-[(2R)-2'-formyl-4-methoxy-4'-methyl-3,6'-dioxo-3H-spiro[1-benzofuran-2,1'-cyclohexane]-2',4'-dien-5-yl]-3-methylbutyl acetate

> <ALOGPS_LOGP>
3.19

> <JCHEM_LOGP>
3.0889906123333337

> <ALOGPS_LOGS>
-5.06

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.643305977234173

> <JCHEM_POLAR_SURFACE_AREA>
95.97

> <JCHEM_REFRACTIVITY>
109.89279999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.60e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R)-1-[(2R)-2'-formyl-4-methoxy-4'-methyl-3,6'-dioxospiro[1-benzofuran-2,1'-cyclohexane]-2',4'-dien-5-yl]-3-methylbutyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
   -0.2341   -2.3832   -1.5401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3864   -0.9764   -1.5380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1271   -0.1762   -0.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0648    0.1663    0.4733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4602   -0.3427    0.3045 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2932   -0.0031    1.5066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7077   -0.4659    1.4820 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5460    0.0956    0.3705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4125   -0.1091    2.7998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0216    0.2241   -0.8604 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4347   -0.4714   -1.9691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9986    0.2450   -3.1252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3355   -1.7086   -2.0049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7925    0.9672    1.5515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5080    1.4560    1.6987 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4585    1.1326    0.7862 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1543    0.3109   -0.3081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3701    0.1520   -1.0898 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4839   -0.3537   -2.2257 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4721    0.7075   -0.2834 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8085    1.4876    0.7103 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3731    1.5967   -1.0513 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8416    2.5256   -1.7043 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8281    1.4312   -1.0729 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3489    0.4507   -0.3793 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8325    0.2938   -0.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5289   -0.4663    0.4016 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2173   -0.3507    0.4465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4519   -1.2920    1.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0743   -2.1926    1.8622 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8200   -2.6792   -1.7917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8629   -2.8691   -2.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5345   -2.8242   -0.5683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3766   -1.4574    0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7759   -0.3303    2.4465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3613    1.1298    1.6019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7680   -1.5936    1.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7860   -0.6819   -0.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5236    0.5049    0.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1055    0.9506   -0.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8427   -0.4513    3.6655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3817   -0.6572    2.7702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6467    0.9750    2.8083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9771    1.3313   -2.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3801    0.0789   -4.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0233   -0.1045   -3.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5437    1.2447    2.3107 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7095    2.0904    2.5593 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3955    2.1339   -1.6651 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0867   -0.6733    0.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3058    1.0978    0.1689 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2083    0.3274   -1.4615 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0558   -1.2607    0.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3709   -1.2569    1.3225 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  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  5 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
  4 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  1
 20 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 17  3  1  0
 28 20  1  0
 21 16  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  5 34  1  6
  6 35  1  0
  6 36  1  0
  7 37  1  6
  8 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  0
  9 42  1  0
  9 43  1  0
 12 44  1  0
 12 45  1  0
 12 46  1  0
 14 47  1  0
 15 48  1  0
 24 49  1  0
 26 50  1  0
 26 51  1  0
 26 52  1  0
 27 53  1  0
 29 54  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      -0.234  -2.383  -1.540  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.386  -0.976  -1.538  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.127  -0.176  -0.461  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.065   0.166   0.473  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.460  -0.343   0.305  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.293  -0.003   1.507  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.708  -0.466   1.482  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.546   0.096   0.371  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.412  -0.109   2.800  0.00  0.00           C+0
HETATM   10  O   UNK     0      -3.022   0.224  -0.860  0.00  0.00           O+0
HETATM   11  C   UNK     0      -3.435  -0.471  -1.969  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.999   0.245  -3.125  0.00  0.00           C+0
HETATM   13  O   UNK     0      -3.336  -1.709  -2.005  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.793   0.967   1.552  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.508   1.456   1.699  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.458   1.133   0.786  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.154   0.311  -0.308  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.370   0.152  -1.090  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.484  -0.354  -2.226  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.472   0.708  -0.283  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.809   1.488   0.710  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.373   1.597  -1.051  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.842   2.526  -1.704  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.828   1.431  -1.073  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.349   0.451  -0.379  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.832   0.294  -0.410  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.529  -0.466   0.402  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.217  -0.351   0.447  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.452  -1.292   1.240  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.074  -2.193   1.862  0.00  0.00           O+0
HETATM   31  H   UNK     0       0.820  -2.679  -1.792  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.863  -2.869  -2.314  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.535  -2.824  -0.568  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.377  -1.457   0.212  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.776  -0.330   2.446  0.00  0.00           H+0
HETATM   36  H   UNK     0      -3.361   1.130   1.602  0.00  0.00           H+0
HETATM   37  H   UNK     0      -4.768  -1.594   1.452  0.00  0.00           H+0
HETATM   38  H   UNK     0      -5.786  -0.682  -0.391  0.00  0.00           H+0
HETATM   39  H   UNK     0      -6.524   0.505   0.794  0.00  0.00           H+0
HETATM   40  H   UNK     0      -5.106   0.951  -0.147  0.00  0.00           H+0
HETATM   41  H   UNK     0      -4.843  -0.451   3.666  0.00  0.00           H+0
HETATM   42  H   UNK     0      -6.382  -0.657   2.770  0.00  0.00           H+0
HETATM   43  H   UNK     0      -5.647   0.975   2.808  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.977   1.331  -2.950  0.00  0.00           H+0
HETATM   45  H   UNK     0      -3.380   0.079  -4.055  0.00  0.00           H+0
HETATM   46  H   UNK     0      -5.023  -0.105  -3.365  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.544   1.245   2.311  0.00  0.00           H+0
HETATM   48  H   UNK     0       0.710   2.090   2.559  0.00  0.00           H+0
HETATM   49  H   UNK     0       6.396   2.134  -1.665  0.00  0.00           H+0
HETATM   50  H   UNK     0       8.087  -0.673   0.034  0.00  0.00           H+0
HETATM   51  H   UNK     0       8.306   1.098   0.169  0.00  0.00           H+0
HETATM   52  H   UNK     0       8.208   0.327  -1.462  0.00  0.00           H+0
HETATM   53  H   UNK     0       6.056  -1.261   0.953  0.00  0.00           H+0
HETATM   54  H   UNK     0       2.371  -1.257   1.323  0.00  0.00           H+0
CONECT    1    2   31   32   33                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5   14                                                  
CONECT    5    4    6   10   34                                             
CONECT    6    5    7   35   36                                             
CONECT    7    6    8    9   37                                             
CONECT    8    7   38   39   40                                             
CONECT    9    7   41   42   43                                             
CONECT   10    5   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11   44   45   46                                             
CONECT   13   11                                                            
CONECT   14    4   15   47                                                  
CONECT   15   14   16   48                                                  
CONECT   16   15   17   21                                                  
CONECT   17   16   18    3                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22   28                                             
CONECT   21   20   16                                                       
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   49                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25   50   51   52                                             
CONECT   27   25   28   53                                                  
CONECT   28   27   29   20                                                  
CONECT   29   28   30   54                                                  
CONECT   30   29                                                            
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    1                                                            
CONECT   34    5                                                            
CONECT   35    6                                                            
CONECT   36    6                                                            
CONECT   37    7                                                            
CONECT   38    8                                                            
CONECT   39    8                                                            
CONECT   40    8                                                            
CONECT   41    9                                                            
CONECT   42    9                                                            
CONECT   43    9                                                            
CONECT   44   12                                                            
CONECT   45   12                                                            
CONECT   46   12                                                            
CONECT   47   14                                                            
CONECT   48   15                                                            
CONECT   49   24                                                            
CONECT   50   26                                                            
CONECT   51   26                                                            
CONECT   52   26                                                            
CONECT   53   27                                                            
CONECT   54   29                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  112    0
END

RDKit          3D

54 56  0  0  0  0  0  0  0  0999 V2000
   -0.2341   -2.3832   -1.5401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3864   -0.9764   -1.5380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1271   -0.1762   -0.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0648    0.1663    0.4733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4602   -0.3427    0.3045 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2932   -0.0031    1.5066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7077   -0.4659    1.4820 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5460    0.0956    0.3705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4125   -0.1091    2.7998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0216    0.2241   -0.8604 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4347   -0.4714   -1.9691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9986    0.2450   -3.1252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3355   -1.7086   -2.0049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7925    0.9672    1.5515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5080    1.4560    1.6987 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4585    1.1326    0.7862 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1543    0.3109   -0.3081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3701    0.1520   -1.0898 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4839   -0.3537   -2.2257 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4721    0.7075   -0.2834 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8085    1.4876    0.7103 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3731    1.5967   -1.0513 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8416    2.5256   -1.7043 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8281    1.4312   -1.0729 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3489    0.4507   -0.3793 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8325    0.2938   -0.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5289   -0.4663    0.4016 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2173   -0.3507    0.4465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4519   -1.2920    1.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0743   -2.1926    1.8622 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8200   -2.6792   -1.7917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8629   -2.8691   -2.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5345   -2.8242   -0.5683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3766   -1.4574    0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7759   -0.3303    2.4465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3613    1.1298    1.6019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7680   -1.5936    1.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7860   -0.6819   -0.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5236    0.5049    0.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1055    0.9506   -0.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8427   -0.4513    3.6655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3817   -0.6572    2.7702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6467    0.9750    2.8083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9771    1.3313   -2.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3801    0.0789   -4.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0233   -0.1045   -3.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5437    1.2447    2.3107 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7095    2.0904    2.5593 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3955    2.1339   -1.6651 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0867   -0.6733    0.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3058    1.0978    0.1689 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2083    0.3274   -1.4615 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0558   -1.2607    0.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3709   -1.2569    1.3225 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  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  5 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
  4 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  1
 20 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 17  3  1  0
 28 20  1  0
 21 16  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  5 34  1  6
  6 35  1  0
  6 36  1  0
  7 37  1  6
  8 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  0
  9 42  1  0
  9 43  1  0
 12 44  1  0
 12 45  1  0
 12 46  1  0
 14 47  1  0
 15 48  1  0
 24 49  1  0
 26 50  1  0
 26 51  1  0
 26 52  1  0
 27 53  1  0
 29 54  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
1-{2'-formyl-4-methoxy-4'-methyl-3,6'-dioxo-3H-spiro[1-benzofuran-2,1'-cyclohexane]-2',4'-dien-5-yl}-3-methylbutyl acetic acid	Generator
5-1''-Acetoxy-6'-formyl-4-methoxy-4'-methyl-3''-methylbutyl-spiro(benzofuran-2,1'-cyclohexa-3',5'-diene)-2',3(2H)-dione	MeSH
Purpactin C	MeSH

Chemical Formula

C₂₃H₂₄O₇

Average Mass

412.4380 Da

Monoisotopic Mass

412.15220 Da

IUPAC Name

(1R)-1-[(2R)-2'-formyl-4-methoxy-4'-methyl-3,6'-dioxo-3H-spiro[1-benzofuran-2,1'-cyclohexane]-2',4'-dien-5-yl]-3-methylbutyl acetate

Traditional Name

(1R)-1-[(2R)-2'-formyl-4-methoxy-4'-methyl-3,6'-dioxospiro[1-benzofuran-2,1'-cyclohexane]-2',4'-dien-5-yl]-3-methylbutyl acetate

CAS Registry Number

Not Available

SMILES

COC1=C(C=CC2=C1C(=O)C1(O2)C(=O)C=C(C)C=C1C=O)C(CC(C)C)OC(C)=O

InChI Identifier

InChI=1S/C23H24O7/c1-12(2)8-18(29-14(4)25)16-6-7-17-20(21(16)28-5)22(27)23(30-17)15(11-24)9-13(3)10-19(23)26/h6-7,9-12,18H,8H2,1-5H3

InChI Key

JFVAWGUDTZFPLP-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
Penicillium	NPAtlas	2010354
Penicillium purpurogenum	LOTUS Database	35616633

Species Where Detected

Species Name	Source	Reference
Penicillium purpurogenum FO-608	KNApSAcK Database	22123792

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Not Available

Direct Parent

Benzofurans

Alternative Parents

Substituents

Coumaran
Benzofuran
Anisole
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
Benzenoid
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Oxacycle
Ether
Monocarboxylic acid or derivatives
Aldehyde
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Organooxygen compound
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	3.19	ALOGPS
logP	3.09	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	95.97 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	109.89 m³·mol⁻¹	ChemAxon
Polarizability	43.62 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	Yes	ChemAxon

External Links

NPAtlas ID

NPA017136

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

116342

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131674

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Nishida H, Tomoda H, Cao J, Okuda S, Omura S: Purpactins, new inhibitors of acyl-CoA:cholesterol acyltransferase produced by Penicillium purpurogenum. II. Structure elucidation of purpactins A, B and C. J Antibiot (Tokyo). 1991 Feb;44(2):144-51. doi: 10.7164/antibiotics.44.144. [PubMed:2010354 ]
Pandit SG, Puttananjaiah MH, Serva Peddha M, Dhale MA: Safety efficacy and chemical profiling of water-soluble Talaromyces purpureogenus CFRM02 pigment. Food Chem. 2020 Apr 25;310:125869. doi: 10.1016/j.foodchem.2019.125869. Epub 2019 Nov 7. [PubMed:31771918 ]

Showing NP-Card for Purpactin C (NP0008984)

MOL for NP0008984 (Purpactin C)

3D MOL for NP0008984 (Purpactin C)

3D SDF for NP0008984 (Purpactin C)

3D-SDF for NP0008984 (Purpactin C)

PDB for NP0008984 (Purpactin C)

3D PDB for NP0008984 (Purpactin C)

SMILES for NP0008984 (Purpactin C)

INCHI for NP0008984 (Purpactin C)

Structure for NP0008984 (Purpactin C)

3D Structure for NP0008984 (Purpactin C)