NP-MRD: Showing NP-Card for chaetoviridin E (NP0035962)

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Record Information

Version

2.0

Created at

2021-06-20 19:15:46 UTC

Updated at

2021-06-30 00:07:21 UTC

NP-MRD ID

NP0035962

Secondary Accession Numbers

None

Natural Product Identification

Common Name

chaetoviridin E

Provided By

JEOL Database JEOL Logo

Description

Chaetoviridin E belongs to the class of organic compounds known as cyclohexenones. Cyclohexenones are compounds containing a cylohexenone moiety, which is a six-membered aliphatic ring that carries a ketone and has one endocyclic double bond. Chaetoviridin E 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. chaetoviridin E is found in Chaetomium cochliodes and Chaetomium globosum. chaetoviridin E was first documented in 2012 (PMID: 22890540). Based on a literature review very few articles have been published on chaetoviridin E (PMID: 32193933).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202121153D          

 52 54  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306202121153D          

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   -0.0135    2.4774   -1.6277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0357    3.7296   -2.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101    4.0399   -1.3486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2534    0.8009    3.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2527   -2.3557    5.6375 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1407   -3.8835    5.4579 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7382   -3.8029    6.5140 H   0  0  0  0  0  0  0  0  0  0  0  0
 20  9  1  0  0  0  0
 28 29  2  0  0  0  0
 20 19  1  0  0  0  0
  7  5  1  0  0  0  0
  9 10  2  0  0  0  0
  5  3  1  0  0  0  0
 10 11  1  0  0  0  0
  3  2  2  0  0  0  0
 11 12  1  0  0  0  0
  2  1  1  0  0  0  0
 12 19  2  0  0  0  0
  5  6  2  0  0  0  0
  8 25  1  0  0  0  0
  3  4  1  0  0  0  0
 12 13  1  0  0  0  0
 23 25  1  0  0  0  0
 13 14  2  0  0  0  0
 23 21  1  0  0  0  0
 14 15  1  0  0  0  0
  8  9  1  0  0  0  0
 15 17  1  0  0  0  0
 20 21  2  0  0  0  0
 17 18  1  0  0  0  0
 25 27  1  0  0  0  0
 21 22  1  0  0  0  0
 27 28  1  0  0  0  0
 23 24  2  0  0  0  0
 28  7  1  0  0  0  0
 15 16  1  0  0  0  0
  7  8  2  0  0  0  0
 25 26  1  1  0  0  0
 10 37  1  0  0  0  0
 19 49  1  0  0  0  0
  2 33  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
  4 34  1  0  0  0  0
  4 35  1  0  0  0  0
  4 36  1  0  0  0  0
 13 38  1  0  0  0  0
 14 39  1  0  0  0  0
 15 40  1  1  0  0  0
 17 44  1  0  0  0  0
 17 45  1  0  0  0  0
 18 46  1  0  0  0  0
 18 47  1  0  0  0  0
 18 48  1  0  0  0  0
 16 41  1  0  0  0  0
 16 42  1  0  0  0  0
 16 43  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
M  END
> <DATABASE_ID>
NP0035962

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]\C(=C(\[H])[C@@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H])C1=C([H])C2=C(Cl)C(=O)[C@]3(OC(=O)C(C(=O)C(=C(/[H])C([H])([H])[H])\C([H])([H])[H])=C3C2=C([H])O1)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H23ClO5/c1-6-12(3)8-9-14-10-15-16(11-28-14)18-17(20(25)13(4)7-2)22(27)29-23(18,5)21(26)19(15)24/h7-12H,6H2,1-5H3/b9-8+,13-7+/t12-,23-/m0/s1

> <INCHI_KEY>
XEBNYZYYHZZSJR-IIWQDEIUSA-N

> <FORMULA>
C23H23ClO5

> <MOLECULAR_WEIGHT>
414.88

> <EXACT_MASS>
414.1234015

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
43.949478709936955

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6aS)-5-chloro-6a-methyl-9-[(2E)-2-methylbut-2-enoyl]-3-[(1E,3S)-3-methylpent-1-en-1-yl]-6H,6aH,8H-furo[2,3-h]isochromene-6,8-dione

> <ALOGPS_LOGP>
4.95

> <JCHEM_LOGP>
4.564409021333332

> <ALOGPS_LOGS>
-5.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-5.230398937717024

> <JCHEM_POLAR_SURFACE_AREA>
69.67000000000002

> <JCHEM_REFRACTIVITY>
115.99249999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.87e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6aS)-5-chloro-6a-methyl-9-[(2E)-2-methylbut-2-enoyl]-3-[(1E,3S)-3-methylpent-1-en-1-yl]furo[2,3-h]isochromene-6,8-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
   -1.4915   -6.6066   -0.7091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5941   -5.7706    0.1501 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7422   -5.6324    0.0360 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6117   -6.2977   -0.9918 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4996   -4.7254    0.9633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5003   -4.1282    0.5770 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0382   -4.5981    2.3540 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7519   -3.5011    3.0612 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6780   -2.0973    2.7049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5888   -1.4842    1.9279 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5625   -0.1457    1.5838 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5124    0.6454    2.0394 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5252    2.0232    1.5870 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4513    2.5664    0.7790 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4288    4.0074    0.3244 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6774    4.7233    0.8457 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3552    4.1201   -1.2094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0655    3.5562   -1.7929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4465    0.1595    2.8474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3919   -1.2397    3.2728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2872   -1.7771    4.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6192   -0.9113    4.8195 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.1580   -3.2153    4.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1177   -3.8276    5.0321 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2303   -3.8633    4.4059 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1421   -3.4424    5.5604 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1897   -5.2851    4.3877 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7274   -5.7377    3.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9097   -6.9102    2.9532 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9886   -7.0491   -1.5709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3095   -5.9874   -1.0915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9271   -7.4140   -0.1125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1395   -5.2238    0.9164 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9023   -5.5802   -1.7660 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1256   -7.1463   -1.4786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5226   -6.6897   -0.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4599   -1.9439    1.4799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2912    2.6513    1.9392 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2773    1.9596    0.4108 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5537    4.5174    0.7487 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7330    4.6705    1.9389 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6621    5.7820    0.5651 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5943    4.2810    0.4397 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4274    5.1766   -1.4966 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2098    3.6097   -1.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0135    2.4774   -1.6277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0357    3.7296   -2.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101    4.0399   -1.3486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2534    0.8009    3.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2527   -2.3557    5.6375 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1407   -3.8835    5.4579 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7382   -3.8029    6.5140 H   0  0  0  0  0  0  0  0  0  0  0  0
 20  9  1  0
 28 29  2  0
 20 19  1  0
  7  5  1  0
  9 10  2  0
  5  3  1  0
 10 11  1  0
  3  2  2  0
 11 12  1  0
  2  1  1  0
 12 19  2  0
  5  6  2  0
  8 25  1  0
  3  4  1  0
 12 13  1  0
 23 25  1  0
 13 14  2  0
 23 21  1  0
 14 15  1  0
  8  9  1  0
 15 17  1  0
 20 21  2  0
 17 18  1  0
 25 27  1  0
 21 22  1  0
 27 28  1  0
 23 24  2  0
 28  7  1  0
 15 16  1  0
  7  8  2  0
 25 26  1  1
 10 37  1  0
 19 49  1  0
  2 33  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 34  1  0
  4 35  1  0
  4 36  1  0
 13 38  1  0
 14 39  1  0
 15 40  1  1
 17 44  1  0
 17 45  1  0
 18 46  1  0
 18 47  1  0
 18 48  1  0
 16 41  1  0
 16 42  1  0
 16 43  1  0
 26 50  1  0
 26 51  1  0
 26 52  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -1.492  -6.607  -0.709  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.594  -5.771   0.150  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.742  -5.632   0.036  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.612  -6.298  -0.992  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.500  -4.725   0.963  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.500  -4.128   0.577  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.038  -4.598   2.354  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.752  -3.501   3.061  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.678  -2.097   2.705  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.589  -1.484   1.928  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.563  -0.146   1.584  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.512   0.645   2.039  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.525   2.023   1.587  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.451   2.566   0.779  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.429   4.007   0.324  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.677   4.723   0.846  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.355   4.120  -1.209  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.066   3.556  -1.793  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.447   0.160   2.847  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.392  -1.240   3.273  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.287  -1.777   4.133  0.00  0.00           C+0
HETATM   22 Cl   UNK     0      -2.619  -0.911   4.819  0.00  0.00          Cl+0
HETATM   23  C   UNK     0      -1.158  -3.215   4.565  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.118  -3.828   5.032  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.230  -3.863   4.406  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.142  -3.442   5.560  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.190  -5.285   4.388  0.00  0.00           O+0
HETATM   28  C   UNK     0       0.727  -5.738   3.223  0.00  0.00           C+0
HETATM   29  O   UNK     0       0.910  -6.910   2.953  0.00  0.00           O+0
HETATM   30  H   UNK     0      -0.989  -7.049  -1.571  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.309  -5.987  -1.091  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.927  -7.414  -0.113  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.139  -5.224   0.916  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.902  -5.580  -1.766  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.126  -7.146  -1.479  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.523  -6.690  -0.525  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.460  -1.944   1.480  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.291   2.651   1.939  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.277   1.960   0.411  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.554   4.517   0.749  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.733   4.670   1.939  0.00  0.00           H+0
HETATM   42  H   UNK     0       2.662   5.782   0.565  0.00  0.00           H+0
HETATM   43  H   UNK     0       3.594   4.281   0.440  0.00  0.00           H+0
HETATM   44  H   UNK     0       1.427   5.177  -1.497  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.210   3.610  -1.671  0.00  0.00           H+0
HETATM   46  H   UNK     0      -0.014   2.477  -1.628  0.00  0.00           H+0
HETATM   47  H   UNK     0       0.036   3.730  -2.873  0.00  0.00           H+0
HETATM   48  H   UNK     0      -0.810   4.040  -1.349  0.00  0.00           H+0
HETATM   49  H   UNK     0      -1.253   0.801   3.186  0.00  0.00           H+0
HETATM   50  H   UNK     0       1.253  -2.356   5.638  0.00  0.00           H+0
HETATM   51  H   UNK     0       2.141  -3.884   5.458  0.00  0.00           H+0
HETATM   52  H   UNK     0       0.738  -3.803   6.514  0.00  0.00           H+0
CONECT    1    2   30   31   32                                             
CONECT    2    3    1   33                                                  
CONECT    3    5    2    4                                                  
CONECT    4    3   34   35   36                                             
CONECT    5    7    3    6                                                  
CONECT    6    5                                                            
CONECT    7    5   28    8                                                  
CONECT    8   25    9    7                                                  
CONECT    9   20   10    8                                                  
CONECT   10    9   11   37                                                  
CONECT   11   10   12                                                       
CONECT   12   11   19   13                                                  
CONECT   13   12   14   38                                                  
CONECT   14   13   15   39                                                  
CONECT   15   14   17   16   40                                             
CONECT   16   15   41   42   43                                             
CONECT   17   15   18   44   45                                             
CONECT   18   17   46   47   48                                             
CONECT   19   20   12   49                                                  
CONECT   20    9   19   21                                                  
CONECT   21   23   20   22                                                  
CONECT   22   21                                                            
CONECT   23   25   21   24                                                  
CONECT   24   23                                                            
CONECT   25    8   23   27   26                                             
CONECT   26   25   50   51   52                                             
CONECT   27   25   28                                                       
CONECT   28   29   27    7                                                  
CONECT   29   28                                                            
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    2                                                            
CONECT   34    4                                                            
CONECT   35    4                                                            
CONECT   36    4                                                            
CONECT   37   10                                                            
CONECT   38   13                                                            
CONECT   39   14                                                            
CONECT   40   15                                                            
CONECT   41   16                                                            
CONECT   42   16                                                            
CONECT   43   16                                                            
CONECT   44   17                                                            
CONECT   45   17                                                            
CONECT   46   18                                                            
CONECT   47   18                                                            
CONECT   48   18                                                            
CONECT   49   19                                                            
CONECT   50   26                                                            
CONECT   51   26                                                            
CONECT   52   26                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  108    0
END

RDKit          3D

52 54  0  0  0  0  0  0  0  0999 V2000
   -1.4915   -6.6066   -0.7091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5941   -5.7706    0.1501 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7422   -5.6324    0.0360 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6117   -6.2977   -0.9918 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4996   -4.7254    0.9633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5003   -4.1282    0.5770 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0382   -4.5981    2.3540 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7519   -3.5011    3.0612 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6780   -2.0973    2.7049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5888   -1.4842    1.9279 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5625   -0.1457    1.5838 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5124    0.6454    2.0394 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5252    2.0232    1.5870 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4513    2.5664    0.7790 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4288    4.0074    0.3244 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6774    4.7233    0.8457 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3552    4.1201   -1.2094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0655    3.5562   -1.7929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4465    0.1595    2.8474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3919   -1.2397    3.2728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2872   -1.7771    4.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6192   -0.9113    4.8195 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.1580   -3.2153    4.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1177   -3.8276    5.0321 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2303   -3.8633    4.4059 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1421   -3.4424    5.5604 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1897   -5.2851    4.3877 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7274   -5.7377    3.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9097   -6.9102    2.9532 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9886   -7.0491   -1.5709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3095   -5.9874   -1.0915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9271   -7.4140   -0.1125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1395   -5.2238    0.9164 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9023   -5.5802   -1.7660 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1256   -7.1463   -1.4786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5226   -6.6897   -0.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4599   -1.9439    1.4799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2912    2.6513    1.9392 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2773    1.9596    0.4108 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5537    4.5174    0.7487 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7330    4.6705    1.9389 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6621    5.7820    0.5651 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5943    4.2810    0.4397 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4274    5.1766   -1.4966 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2098    3.6097   -1.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0135    2.4774   -1.6277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0357    3.7296   -2.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101    4.0399   -1.3486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2534    0.8009    3.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2527   -2.3557    5.6375 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1407   -3.8835    5.4579 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7382   -3.8029    6.5140 H   0  0  0  0  0  0  0  0  0  0  0  0
 20  9  1  0
 28 29  2  0
 20 19  1  0
  7  5  1  0
  9 10  2  0
  5  3  1  0
 10 11  1  0
  3  2  2  0
 11 12  1  0
  2  1  1  0
 12 19  2  0
  5  6  2  0
  8 25  1  0
  3  4  1  0
 12 13  1  0
 23 25  1  0
 13 14  2  0
 23 21  1  0
 14 15  1  0
  8  9  1  0
 15 17  1  0
 20 21  2  0
 17 18  1  0
 25 27  1  0
 21 22  1  0
 27 28  1  0
 23 24  2  0
 28  7  1  0
 15 16  1  0
  7  8  2  0
 25 26  1  1
 10 37  1  0
 19 49  1  0
  2 33  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 34  1  0
  4 35  1  0
  4 36  1  0
 13 38  1  0
 14 39  1  0
 15 40  1  1
 17 44  1  0
 17 45  1  0
 18 46  1  0
 18 47  1  0
 18 48  1  0
 16 41  1  0
 16 42  1  0
 16 43  1  0
 26 50  1  0
 26 51  1  0
 26 52  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₂₃H₂₃ClO₅

Average Mass

414.8800 Da

Monoisotopic Mass

414.12340 Da

IUPAC Name

(6aS)-5-chloro-6a-methyl-9-[(2E)-2-methylbut-2-enoyl]-3-[(1E,3S)-3-methylpent-1-en-1-yl]-6H,6aH,8H-furo[2,3-h]isochromene-6,8-dione

Traditional Name

(6aS)-5-chloro-6a-methyl-9-[(2E)-2-methylbut-2-enoyl]-3-[(1E,3S)-3-methylpent-1-en-1-yl]furo[2,3-h]isochromene-6,8-dione

CAS Registry Number

Not Available

SMILES

[H]\C(=C(\[H])[C@@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H])C1=C([H])C2=C(Cl)C(=O)[C@]3(OC(=O)C(C(=O)C(=C(/[H])C([H])([H])[H])\C([H])([H])[H])=C3C2=C([H])O1)C([H])([H])[H]

InChI Identifier

InChI=1S/C23H23ClO5/c1-6-12(3)8-9-14-10-15-16(11-28-14)18-17(20(25)13(4)7-2)22(27)29-23(18,5)21(26)19(15)24/h7-12H,6H2,1-5H3/b9-8+,13-7+/t12-,23-/m0/s1

InChI Key

XEBNYZYYHZZSJR-IIWQDEIUSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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 cochliodes	LOTUS Database	35616633
Chaetomium globosum	JEOL database	Borges, W. S., et al, J. Nat. Prod. 74, 1182 (2011)

Species Where Detected

Species Name	Source	Reference
Chaetomium cochliodes CTh05	KNApSAcK Database	22123792
Chaetomium sp.	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclohexenones. Cyclohexenones are compounds containing a cylohexenone moiety, which is a six-membered aliphatic ring that carries a ketone and has one endocyclic double bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Cyclohexenones

Alternative Parents

Substituents

Cyclohexenone
Alpha-acyloxy ketone
2-furanone
Pyran
Alpha-branched alpha,beta-unsaturated-ketone
Alpha-haloketone
Alpha-chloroketone
Acryloyl-group
Dihydrofuran
Enone
Enoate ester
Alpha,beta-unsaturated ketone
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Lactone
Vinyl chloride
Haloalkene
Monocarboxylic acid or derivatives
Chloroalkene
Oxacycle
Carboxylic acid derivative
Vinyl halide
Organoheterocyclic compound
Organochloride
Organohalogen compound
Organic oxide
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

organic heterotricyclic compound (CHEBI:67614 )
organochlorine compound (CHEBI:67614 )
enone (CHEBI:67614 )
gamma-lactone (CHEBI:67614 )
azaphilone (CHEBI:67614 )

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	4.95	ALOGPS
logP	4.56	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Basic)	-5.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	69.67 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	115.99 m³·mol⁻¹	ChemAxon
Polarizability	43.95 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00052910

Chemspider ID

26631687

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

67614

Good Scents ID

Not Available

References

General References

Chen GD, Li YJ, Gao H, Chen Y, Li XX, Li J, Guo LD, Cen YZ, Yao XS: New azaphilones and chlorinated phenolic glycosides from Chaetomium elatum with caspase-3 inhibitory activity. Planta Med. 2012 Oct;78(15):1683-9. doi: 10.1055/s-0032-1315211. Epub 2012 Aug 13. [PubMed:22890540 ]
Wang W, Yang J, Liao YY, Cheng G, Chen J, Cheng XD, Qin JJ, Shao Z: Cytotoxic Nitrogenated Azaphilones from the Deep-Sea-Derived Fungus Chaetomium globosum MP4-S01-7. J Nat Prod. 2020 Apr 24;83(4):1157-1166. doi: 10.1021/acs.jnatprod.9b01165. Epub 2020 Mar 20. [PubMed:32193933 ]
Borges, W. S., et al. (2011). Borges, W. S., et al, J. Nat. Prod. 74, 1182 (2011). J. Nat. Prod..

Showing NP-Card for chaetoviridin E (NP0035962)

MOL for NP0035962 (chaetoviridin E)

3D MOL for NP0035962 (chaetoviridin E)

3D SDF for NP0035962 (chaetoviridin E)

3D-SDF for NP0035962 (chaetoviridin E)

PDB for NP0035962 (chaetoviridin E)

3D PDB for NP0035962 (chaetoviridin E)

SMILES for NP0035962 (chaetoviridin E)

INCHI for NP0035962 (chaetoviridin E)

Structure for NP0035962 (chaetoviridin E)

3D Structure for NP0035962 (chaetoviridin E)