NP-MRD: Showing NP-Card for Chaetoxanthone A (NP0007913)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2020-12-09 05:28:23 UTC

Updated at

2021-07-15 16:58:54 UTC

NP-MRD ID

NP0007913

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Chaetoxanthone A

Provided By

NPAtlas

Description

Chaetoxanthone A is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Chaetoxanthone A is found in Chaetomium sp. Based on a literature review very few articles have been published on chaetoxanthone A.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106053D          

 45 49  0  0  0  0            999 V2000
    5.9928   -0.3948   -2.0463 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7014   -0.3422   -1.4734 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4972    0.3691   -0.2887 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5567    1.0163    0.3155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3354    1.7167    1.4897 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0717    1.7612    2.0395 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0055    1.1119    1.4346 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7971    1.1364    1.9323 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7739    0.5250    1.3699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871    0.5778    1.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5713   -0.0494    1.3679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4013   -0.7557    0.2040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376   -0.8267   -0.3870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0472   -1.5414   -1.5338 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9505   -0.1843    0.1990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2008   -0.2422   -0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4218   -0.8702   -1.4281 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2368    0.4194    0.2689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5197   -1.4565   -0.4606 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9859   -0.7334   -1.7055 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0771    0.2641   -1.4246 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3522   -0.2979   -1.6432 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0481    0.7782   -0.0025 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9095   -0.3438    0.9984 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1956   -0.5383    1.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8599   -0.0095    1.9200 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6305   -1.5535    0.3856 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2748    0.5852   -2.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7456   -0.6664   -1.2774 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0272   -1.1681   -2.8379 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5406    0.9917   -0.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1727    2.2191    1.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9170    2.3078    2.9490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6213    1.1286    2.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6394   -1.7806   -2.1670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2603   -2.4991   -0.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1259   -0.2614   -2.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3924   -1.4872   -2.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9467    1.1299   -2.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6368   -0.0993   -2.5517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0100    1.3372    0.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2146    1.4980    0.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9686   -0.9480    1.1222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5245    0.3925    2.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9347   -1.2753    2.6010 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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 24 27  1  0  0  0  0
 18  3  1  0  0  0  0
 27 19  1  0  0  0  0
 18  7  2  0  0  0  0
 15  9  1  0  0  0  0
 26 11  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  4 31  1  0  0  0  0
  5 32  1  0  0  0  0
  6 33  1  0  0  0  0
 10 34  1  0  0  0  0
 14 35  1  0  0  0  0
 19 36  1  6  0  0  0
 20 37  1  0  0  0  0
 20 38  1  0  0  0  0
 21 39  1  6  0  0  0
 22 40  1  0  0  0  0
 23 41  1  0  0  0  0
 23 42  1  0  0  0  0
 25 43  1  0  0  0  0
 25 44  1  0  0  0  0
 25 45  1  0  0  0  0
M  END

     RDKit          3D

 45 49  0  0  0  0  0  0  0  0999 V2000
    5.9928   -0.3948   -2.0463 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7014   -0.3422   -1.4734 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4972    0.3691   -0.2887 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5567    1.0163    0.3155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3354    1.7167    1.4897 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0717    1.7612    2.0395 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0055    1.1119    1.4346 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7971    1.1364    1.9323 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7739    0.5250    1.3699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871    0.5778    1.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5713   -0.0494    1.3679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4013   -0.7557    0.2040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376   -0.8267   -0.3870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0472   -1.5414   -1.5338 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9505   -0.1843    0.1990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2008   -0.2422   -0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4218   -0.8702   -1.4281 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2368    0.4194    0.2689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5197   -1.4565   -0.4606 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9859   -0.7334   -1.7055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0771    0.2641   -1.4246 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3522   -0.2979   -1.6432 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0481    0.7782   -0.0025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9095   -0.3438    0.9984 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1956   -0.5383    1.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8599   -0.0095    1.9200 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6305   -1.5535    0.3856 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2748    0.5852   -2.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7456   -0.6664   -1.2774 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0272   -1.1681   -2.8379 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5406    0.9917   -0.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1727    2.2191    1.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9170    2.3078    2.9490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6213    1.1286    2.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6394   -1.7806   -2.1670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2603   -2.4991   -0.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1259   -0.2614   -2.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3924   -1.4872   -2.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9467    1.1299   -2.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6368   -0.0993   -2.5517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0100    1.3372    0.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2146    1.4980    0.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9686   -0.9480    1.1222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5245    0.3925    2.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9347   -1.2753    2.6010 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
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 12 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  1
 24 26  1  0
 24 27  1  0
 18  3  1  0
 27 19  1  0
 18  7  2  0
 15  9  1  0
 26 11  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  5 32  1  0
  6 33  1  0
 10 34  1  0
 14 35  1  0
 19 36  1  6
 20 37  1  0
 20 38  1  0
 21 39  1  6
 22 40  1  0
 23 41  1  0
 23 42  1  0
 25 43  1  0
 25 44  1  0
 25 45  1  0
M  END


  Mrv1652306242106053D          

 45 49  0  0  0  0            999 V2000
    5.9928   -0.3948   -2.0463 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7014   -0.3422   -1.4734 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4972    0.3691   -0.2887 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5567    1.0163    0.3155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3354    1.7167    1.4897 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0717    1.7612    2.0395 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0055    1.1119    1.4346 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7971    1.1364    1.9323 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7739    0.5250    1.3699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871    0.5778    1.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5713   -0.0494    1.3679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4013   -0.7557    0.2040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376   -0.8267   -0.3870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0472   -1.5414   -1.5338 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9505   -0.1843    0.1990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2008   -0.2422   -0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4218   -0.8702   -1.4281 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2368    0.4194    0.2689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5197   -1.4565   -0.4606 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9859   -0.7334   -1.7055 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0771    0.2641   -1.4246 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3522   -0.2979   -1.6432 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0481    0.7782   -0.0025 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9095   -0.3438    0.9984 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1956   -0.5383    1.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8599   -0.0095    1.9200 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6305   -1.5535    0.3856 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2748    0.5852   -2.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7456   -0.6664   -1.2774 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0272   -1.1681   -2.8379 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5406    0.9917   -0.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1727    2.2191    1.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9170    2.3078    2.9490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6213    1.1286    2.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6394   -1.7806   -2.1670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2603   -2.4991   -0.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1259   -0.2614   -2.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3924   -1.4872   -2.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9467    1.1299   -2.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6368   -0.0993   -2.5517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0100    1.3372    0.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2146    1.4980    0.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9686   -0.9480    1.1222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5245    0.3925    2.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9347   -1.2753    2.6010 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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 24 27  1  0  0  0  0
 18  3  1  0  0  0  0
 27 19  1  0  0  0  0
 18  7  2  0  0  0  0
 15  9  1  0  0  0  0
 26 11  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  4 31  1  0  0  0  0
  5 32  1  0  0  0  0
  6 33  1  0  0  0  0
 10 34  1  0  0  0  0
 14 35  1  0  0  0  0
 19 36  1  6  0  0  0
 20 37  1  0  0  0  0
 20 38  1  0  0  0  0
 21 39  1  6  0  0  0
 22 40  1  0  0  0  0
 23 41  1  0  0  0  0
 23 42  1  0  0  0  0
 25 43  1  0  0  0  0
 25 44  1  0  0  0  0
 25 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007913

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)C3=C(OC2=C([H])C2=C1[C@@]1([H])O[C@](O2)(C([H])([H])[H])C([H])([H])[C@]([H])(O[H])C1([H])[H])C([H])=C([H])C([H])=C3OC([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H18O7/c1-20-8-9(21)6-13(26-20)16-14(27-20)7-12-17(19(16)23)18(22)15-10(24-2)4-3-5-11(15)25-12/h3-5,7,9,13,21,23H,6,8H2,1-2H3/t9-,13+,20+/m1/s1

> <INCHI_KEY>
PYEDKAHYOPGAKC-PDXJJUDESA-N

> <FORMULA>
C20H18O7

> <MOLECULAR_WEIGHT>
370.357

> <EXACT_MASS>
370.10525292

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
37.81123923861456

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,17S,19R)-3,19-dihydroxy-7-methoxy-17-methyl-12,16,21-trioxapentacyclo[15.3.1.0^{2,15}.0^{4,13}.0^{6,11}]henicosa-2(15),3,6(11),7,9,13-hexaen-5-one

> <ALOGPS_LOGP>
1.87

> <JCHEM_LOGP>
2.8570950009999994

> <ALOGPS_LOGS>
-3.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.99008352665265

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.835536345985009

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8032214321178417

> <JCHEM_POLAR_SURFACE_AREA>
94.45

> <JCHEM_REFRACTIVITY>
94.062

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.63e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,17S,19R)-3,19-dihydroxy-7-methoxy-17-methyl-12,16,21-trioxapentacyclo[15.3.1.0^{2,15}.0^{4,13}.0^{6,11}]henicosa-2(15),3,6(11),7,9,13-hexaen-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 45 49  0  0  0  0  0  0  0  0999 V2000
    5.9928   -0.3948   -2.0463 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7014   -0.3422   -1.4734 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4972    0.3691   -0.2887 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5567    1.0163    0.3155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3354    1.7167    1.4897 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0717    1.7612    2.0395 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0055    1.1119    1.4346 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7971    1.1364    1.9323 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7739    0.5250    1.3699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871    0.5778    1.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5713   -0.0494    1.3679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4013   -0.7557    0.2040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376   -0.8267   -0.3870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0472   -1.5414   -1.5338 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9505   -0.1843    0.1990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2008   -0.2422   -0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4218   -0.8702   -1.4281 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2368    0.4194    0.2689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5197   -1.4565   -0.4606 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9859   -0.7334   -1.7055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0771    0.2641   -1.4246 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3522   -0.2979   -1.6432 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0481    0.7782   -0.0025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9095   -0.3438    0.9984 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1956   -0.5383    1.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8599   -0.0095    1.9200 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6305   -1.5535    0.3856 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2748    0.5852   -2.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7456   -0.6664   -1.2774 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0272   -1.1681   -2.8379 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5406    0.9917   -0.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1727    2.2191    1.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9170    2.3078    2.9490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6213    1.1286    2.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6394   -1.7806   -2.1670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2603   -2.4991   -0.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1259   -0.2614   -2.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3924   -1.4872   -2.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9467    1.1299   -2.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6368   -0.0993   -2.5517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0100    1.3372    0.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2146    1.4980    0.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9686   -0.9480    1.1222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5245    0.3925    2.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9347   -1.2753    2.6010 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
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 12 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  1
 24 26  1  0
 24 27  1  0
 18  3  1  0
 27 19  1  0
 18  7  2  0
 15  9  1  0
 26 11  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  5 32  1  0
  6 33  1  0
 10 34  1  0
 14 35  1  0
 19 36  1  6
 20 37  1  0
 20 38  1  0
 21 39  1  6
 22 40  1  0
 23 41  1  0
 23 42  1  0
 25 43  1  0
 25 44  1  0
 25 45  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       5.993  -0.395  -2.046  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.701  -0.342  -1.473  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.497   0.369  -0.289  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.557   1.016   0.316  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335   1.717   1.490  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.072   1.761   2.039  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.006   1.112   1.435  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.797   1.136   1.932  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.774   0.525   1.370  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.487   0.578   1.932  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.571  -0.049   1.368  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.401  -0.756   0.204  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.138  -0.827  -0.387  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.047  -1.541  -1.534  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.951  -0.184   0.199  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.201  -0.242  -0.367  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.422  -0.870  -1.428  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.237   0.419   0.269  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.520  -1.456  -0.461  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.986  -0.733  -1.706  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.077   0.264  -1.425  0.00  0.00           C+0
HETATM   22  O   UNK     0      -5.352  -0.298  -1.643  0.00  0.00           O+0
HETATM   23  C   UNK     0      -4.048   0.778  -0.003  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.910  -0.344   0.998  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.196  -0.538   1.797  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.860  -0.010   1.920  0.00  0.00           O+0
HETATM   27  O   UNK     0      -3.631  -1.554   0.386  0.00  0.00           O+0
HETATM   28  H   UNK     0       6.275   0.585  -2.453  0.00  0.00           H+0
HETATM   29  H   UNK     0       6.746  -0.666  -1.277  0.00  0.00           H+0
HETATM   30  H   UNK     0       6.027  -1.168  -2.838  0.00  0.00           H+0
HETATM   31  H   UNK     0       6.541   0.992  -0.097  0.00  0.00           H+0
HETATM   32  H   UNK     0       6.173   2.219   1.953  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.917   2.308   2.949  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.621   1.129   2.840  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.639  -1.781  -2.167  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.260  -2.499  -0.742  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.126  -0.261  -2.223  0.00  0.00           H+0
HETATM   38  H   UNK     0      -3.392  -1.487  -2.410  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.947   1.130  -2.108  0.00  0.00           H+0
HETATM   40  H   UNK     0      -5.637  -0.099  -2.552  0.00  0.00           H+0
HETATM   41  H   UNK     0      -5.010   1.337   0.150  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.215   1.498   0.085  0.00  0.00           H+0
HETATM   43  H   UNK     0      -5.969  -0.948   1.122  0.00  0.00           H+0
HETATM   44  H   UNK     0      -5.524   0.393   2.274  0.00  0.00           H+0
HETATM   45  H   UNK     0      -4.935  -1.275   2.601  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   18                                                  
CONECT    4    3    5   31                                                  
CONECT    5    4    6   32                                                  
CONECT    6    5    7   33                                                  
CONECT    7    6    8   18                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11   34                                                  
CONECT   11   10   12   26                                                  
CONECT   12   11   13   19                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13   35                                                       
CONECT   15   13   16    9                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16    3    7                                                  
CONECT   19   12   20   27   36                                             
CONECT   20   19   21   37   38                                             
CONECT   21   20   22   23   39                                             
CONECT   22   21   40                                                       
CONECT   23   21   24   41   42                                             
CONECT   24   23   25   26   27                                             
CONECT   25   24   43   44   45                                             
CONECT   26   24   11                                                       
CONECT   27   24   19                                                       
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    4                                                            
CONECT   32    5                                                            
CONECT   33    6                                                            
CONECT   34   10                                                            
CONECT   35   14                                                            
CONECT   36   19                                                            
CONECT   37   20                                                            
CONECT   38   20                                                            
CONECT   39   21                                                            
CONECT   40   22                                                            
CONECT   41   23                                                            
CONECT   42   23                                                            
CONECT   43   25                                                            
CONECT   44   25                                                            
CONECT   45   25                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

RDKit          3D

45 49  0  0  0  0  0  0  0  0999 V2000
    5.9928   -0.3948   -2.0463 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7014   -0.3422   -1.4734 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4972    0.3691   -0.2887 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5567    1.0163    0.3155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3354    1.7167    1.4897 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0717    1.7612    2.0395 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0055    1.1119    1.4346 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7971    1.1364    1.9323 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7739    0.5250    1.3699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871    0.5778    1.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5713   -0.0494    1.3679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4013   -0.7557    0.2040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376   -0.8267   -0.3870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0472   -1.5414   -1.5338 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9505   -0.1843    0.1990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2008   -0.2422   -0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4218   -0.8702   -1.4281 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2368    0.4194    0.2689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5197   -1.4565   -0.4606 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9859   -0.7334   -1.7055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0771    0.2641   -1.4246 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3522   -0.2979   -1.6432 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0481    0.7782   -0.0025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9095   -0.3438    0.9984 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1956   -0.5383    1.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8599   -0.0095    1.9200 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6305   -1.5535    0.3856 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2748    0.5852   -2.4525 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7456   -0.6664   -1.2774 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0272   -1.1681   -2.8379 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5406    0.9917   -0.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1727    2.2191    1.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9170    2.3078    2.9490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6213    1.1286    2.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6394   -1.7806   -2.1670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2603   -2.4991   -0.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1259   -0.2614   -2.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3924   -1.4872   -2.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9467    1.1299   -2.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6368   -0.0993   -2.5517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0100    1.3372    0.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2146    1.4980    0.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9686   -0.9480    1.1222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5245    0.3925    2.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9347   -1.2753    2.6010 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
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 12 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  1
 24 26  1  0
 24 27  1  0
 18  3  1  0
 27 19  1  0
 18  7  2  0
 15  9  1  0
 26 11  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  5 32  1  0
  6 33  1  0
 10 34  1  0
 14 35  1  0
 19 36  1  6
 20 37  1  0
 20 38  1  0
 21 39  1  6
 22 40  1  0
 23 41  1  0
 23 42  1  0
 25 43  1  0
 25 44  1  0
 25 45  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₀H₁₈O₇

Average Mass

370.3570 Da

Monoisotopic Mass

370.10525 Da

IUPAC Name

(1S,17S,19R)-3,19-dihydroxy-7-methoxy-17-methyl-12,16,21-trioxapentacyclo[15.3.1.0^{2,15}.0^{4,13}.0^{6,11}]henicosa-2(15),3,6(11),7,9,13-hexaen-5-one

Traditional Name

(1S,17S,19R)-3,19-dihydroxy-7-methoxy-17-methyl-12,16,21-trioxapentacyclo[15.3.1.0^{2,15}.0^{4,13}.0^{6,11}]henicosa-2(15),3,6(11),7,9,13-hexaen-5-one

CAS Registry Number

Not Available

SMILES

COC1=CC=CC2=C1C(=O)C1=C(O)C3=C(O[C@@]4(C)C[C@H](O)C[C@@H]3O4)C=C1O2

InChI Identifier

InChI=1S/C20H18O7/c1-20-8-9(21)6-13(26-20)16-14(27-20)7-12-17(19(16)23)18(22)15-10(24-2)4-3-5-11(15)25-12/h3-5,7,9,13,21,23H,6,8H2,1-2H3/t9-,13+,20+/m1/s1

InChI Key

PYEDKAHYOPGAKC-PDXJJUDESA-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
Chaetomium sp.	NPAtlas	18683985

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	1.87	ALOGPS
logP	2.86	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	7.84	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	94.45 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	94.06 m³·mol⁻¹	ChemAxon
Polarizability	37.81 Å³	ChemAxon
Number of Rings	5	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

NPA000007

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00038729

Chemspider ID

24711218

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44586905

PDB ID

Not Available

ChEBI ID

65611

Good Scents ID

Not Available

References

General References

Showing NP-Card for Chaetoxanthone A (NP0007913)

MOL for NP0007913 (Chaetoxanthone A)

3D MOL for NP0007913 (Chaetoxanthone A)

3D SDF for NP0007913 (Chaetoxanthone A)

3D-SDF for NP0007913 (Chaetoxanthone A)

PDB for NP0007913 (Chaetoxanthone A)

3D PDB for NP0007913 (Chaetoxanthone A)

SMILES for NP0007913 (Chaetoxanthone A)

INCHI for NP0007913 (Chaetoxanthone A)

Structure for NP0007913 (Chaetoxanthone A)

3D Structure for NP0007913 (Chaetoxanthone A)