NP-MRD: Showing NP-Card for 10,11-epoxychlorovulone (NP0021147)

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Record Information

Version

2.0

Created at

2021-01-06 06:26:24 UTC

Updated at

2021-07-15 17:35:34 UTC

NP-MRD ID

NP0021147

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10,11-epoxychlorovulone

Provided By

NPAtlas

Description

10,11-epoxychlorovulone is found in Clavularia viridis. Based on a literature review very few articles have been published on 10,11-epoxy-chlorovulone i.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI

  Mrv1652306242120413D          

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M  END

     RDKit          3D

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M  END

  Mrv1652306242120413D          

 56 57  0  0  0  0            999 V2000
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   -4.2869    0.7694   -0.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1875    0.1164   -2.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1419   -1.2734   -2.1537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5924   -0.2807   -0.7190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5332    0.0246   -4.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8583    0.6405   -2.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8987   -1.7394   -1.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8516   -2.9532   -1.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4077   -0.3780   -2.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8593   -2.0596   -2.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2243   -2.3919   -0.0867 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0146   -0.8788   -0.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2962    0.5177    0.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2197   -0.8948    0.6258 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2728    0.2287    4.9780 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6863   -0.6384    4.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6103    1.1980    4.3200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4202    2.2060   -1.1093 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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  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  0  0  0  0
 11 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27  9  1  0  0  0  0
 27 24  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
  2 31  1  0  0  0  0
  2 32  1  0  0  0  0
  3 33  1  0  0  0  0
  3 34  1  0  0  0  0
  4 35  1  0  0  0  0
  4 36  1  0  0  0  0
  5 37  1  0  0  0  0
  5 38  1  0  0  0  0
  6 39  1  0  0  0  0
  7 40  1  0  0  0  0
  8 41  1  0  0  0  0
  8 42  1  0  0  0  0
 10 43  1  0  0  0  0
 12 44  1  0  0  0  0
 13 45  1  0  0  0  0
 14 46  1  0  0  0  0
 15 47  1  0  0  0  0
 15 48  1  0  0  0  0
 16 49  1  0  0  0  0
 16 50  1  0  0  0  0
 17 51  1  0  0  0  0
 17 52  1  0  0  0  0
 21 53  1  0  0  0  0
 21 54  1  0  0  0  0
 21 55  1  0  0  0  0
 27 56  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0021147

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]1(\C(=C(\[H])/C(/[H])=C(/[H])C([H])([H])C([H])([H])C([H])([H])C(=O)OC([H])([H])[H])C(=O)[C@@]2(Cl)O[C@@]12[H])C([H])([H])C(\[H])=C(\[H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H29ClO5/c1-3-4-5-6-9-12-15-20(25)16(18(24)21(22)19(20)27-21)13-10-7-8-11-14-17(23)26-2/h7,9-10,12-13,19,25H,3-6,8,11,14-15H2,1-2H3/b10-7-,12-9-,16-13-/t19-,20-,21+/m0/s1

> <INCHI_KEY>
VQTGQBDTRZNQSB-ZKVKOFCJSA-N

> <FORMULA>
C21H29ClO5

> <MOLECULAR_WEIGHT>
396.91

> <EXACT_MASS>
396.1703517

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
43.11668172570771

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (5Z)-7-[(1R,3E,4S,5S)-1-chloro-4-hydroxy-4-[(2Z)-oct-2-en-1-yl]-2-oxo-6-oxabicyclo[3.1.0]hexan-3-ylidene]hept-5-enoate

> <ALOGPS_LOGP>
4.55

> <JCHEM_LOGP>
5.129732703666666

> <ALOGPS_LOGS>
-5.39

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.813924265019885

> <JCHEM_PKA_STRONGEST_BASIC>
-3.754989526480302

> <JCHEM_POLAR_SURFACE_AREA>
76.13

> <JCHEM_REFRACTIVITY>
107.76979999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.63e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10,11-epoxy-chlorovulone I

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 56 57  0  0  0  0  0  0  0  0999 V2000
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    1.9706    2.7837   -3.7521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1575    3.1075   -2.6446 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1393    4.5271   -1.6022 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.4185    2.9361   -3.1554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0901    2.0815   -2.1324 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.6262    0.2621    4.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.1875    0.1164   -2.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1419   -1.2734   -2.1537 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8987   -1.7394   -1.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8516   -2.9532   -1.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4077   -0.3780   -2.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8593   -2.0596   -2.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2243   -2.3919   -0.0867 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0146   -0.8788   -0.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2962    0.5177    0.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2197   -0.8948    0.6258 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2728    0.2287    4.9780 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6863   -0.6384    4.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6103    1.1980    4.3200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4202    2.2060   -1.1093 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 11 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  1
 24 26  1  0
 26 27  1  0
 27  9  1  0
 27 24  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
 10 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 17 52  1  0
 21 53  1  0
 21 54  1  0
 21 55  1  0
 27 56  1  1
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      -6.638  -0.571   3.304  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.196  -1.040   3.118  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.536  -0.091   2.127  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.111  -0.459   1.868  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.470   0.513   0.880  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.195   0.479  -0.406  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.601   0.129  -1.511  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.176  -0.261  -1.609  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.554   0.697  -2.597  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.169   0.543  -3.864  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.850   0.924  -2.619  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.868   0.144  -2.333  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.827  -1.220  -1.899  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.930  -1.890  -1.644  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.264  -1.354  -1.765  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.033  -1.374  -0.445  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.266  -0.535   0.556  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.940  -0.499   1.862  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.008  -1.114   2.032  0.00  0.00           O+0
HETATM   20  O   UNK     0       4.396   0.215   2.908  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.040   0.259   4.184  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.005   2.340  -3.090  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.971   2.784  -3.752  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.158   3.107  -2.645  0.00  0.00           C+0
HETATM   25 Cl   UNK     0       0.139   4.527  -1.602  0.00  0.00          Cl+0
HETATM   26  O   UNK     0      -1.419   2.936  -3.155  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.090   2.082  -2.132  0.00  0.00           C+0
HETATM   28  H   UNK     0      -6.626   0.262   4.046  0.00  0.00           H+0
HETATM   29  H   UNK     0      -7.021  -0.138   2.357  0.00  0.00           H+0
HETATM   30  H   UNK     0      -7.270  -1.397   3.686  0.00  0.00           H+0
HETATM   31  H   UNK     0      -4.701  -1.032   4.090  0.00  0.00           H+0
HETATM   32  H   UNK     0      -5.258  -2.032   2.632  0.00  0.00           H+0
HETATM   33  H   UNK     0      -4.527   0.913   2.638  0.00  0.00           H+0
HETATM   34  H   UNK     0      -5.125  -0.056   1.188  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.060  -1.502   1.441  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.546  -0.435   2.821  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.730   1.541   1.316  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.399   0.394   0.848  0.00  0.00           H+0
HETATM   39  H   UNK     0      -4.287   0.769  -0.426  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.188   0.116  -2.460  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.142  -1.273  -2.154  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.592  -0.281  -0.719  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.533   0.025  -4.403  0.00  0.00           H+0
HETATM   44  H   UNK     0       2.858   0.641  -2.459  0.00  0.00           H+0
HETATM   45  H   UNK     0       0.899  -1.739  -1.773  0.00  0.00           H+0
HETATM   46  H   UNK     0       2.852  -2.953  -1.307  0.00  0.00           H+0
HETATM   47  H   UNK     0       4.408  -0.378  -2.188  0.00  0.00           H+0
HETATM   48  H   UNK     0       4.859  -2.060  -2.437  0.00  0.00           H+0
HETATM   49  H   UNK     0       5.224  -2.392  -0.087  0.00  0.00           H+0
HETATM   50  H   UNK     0       6.015  -0.879  -0.597  0.00  0.00           H+0
HETATM   51  H   UNK     0       4.296   0.518   0.152  0.00  0.00           H+0
HETATM   52  H   UNK     0       3.220  -0.895   0.626  0.00  0.00           H+0
HETATM   53  H   UNK     0       4.273   0.229   4.978  0.00  0.00           H+0
HETATM   54  H   UNK     0       5.686  -0.638   4.303  0.00  0.00           H+0
HETATM   55  H   UNK     0       5.610   1.198   4.320  0.00  0.00           H+0
HETATM   56  H   UNK     0      -1.420   2.206  -1.109  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    1    3   31   32                                             
CONECT    3    2    4   33   34                                             
CONECT    4    3    5   35   36                                             
CONECT    5    4    6   37   38                                             
CONECT    6    5    7   39                                                  
CONECT    7    6    8   40                                                  
CONECT    8    7    9   41   42                                             
CONECT    9    8   10   11   27                                             
CONECT   10    9   43                                                       
CONECT   11    9   12   22                                                  
CONECT   12   11   13   44                                                  
CONECT   13   12   14   45                                                  
CONECT   14   13   15   46                                                  
CONECT   15   14   16   47   48                                             
CONECT   16   15   17   49   50                                             
CONECT   17   16   18   51   52                                             
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   53   54   55                                             
CONECT   22   11   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26   27                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26    9   24   56                                             
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    2                                                            
CONECT   32    2                                                            
CONECT   33    3                                                            
CONECT   34    3                                                            
CONECT   35    4                                                            
CONECT   36    4                                                            
CONECT   37    5                                                            
CONECT   38    5                                                            
CONECT   39    6                                                            
CONECT   40    7                                                            
CONECT   41    8                                                            
CONECT   42    8                                                            
CONECT   43   10                                                            
CONECT   44   12                                                            
CONECT   45   13                                                            
CONECT   46   14                                                            
CONECT   47   15                                                            
CONECT   48   15                                                            
CONECT   49   16                                                            
CONECT   50   16                                                            
CONECT   51   17                                                            
CONECT   52   17                                                            
CONECT   53   21                                                            
CONECT   54   21                                                            
CONECT   55   21                                                            
CONECT   56   27                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  114    0
END

RDKit          3D

56 57  0  0  0  0  0  0  0  0999 V2000
   -6.6385   -0.5714    3.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1963   -1.0405    3.1175 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5544    0.6968   -2.5970 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1689    0.5431   -3.8642 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8274   -1.2205   -1.8991 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9303   -1.8901   -1.6438 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0053    2.3395   -3.0898 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9706    2.7837   -3.7521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1575    3.1075   -2.6446 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1393    4.5271   -1.6022 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.4185    2.9361   -3.1554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0901    2.0815   -2.1324 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.6262    0.2621    4.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0207   -0.1379    2.3575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2703   -1.3970    3.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7012   -1.0322    4.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2576   -2.0318    2.6325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5266    0.9125    2.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1255   -0.0555    1.1881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0597   -1.5025    1.4406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5458   -0.4345    2.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7298    1.5414    1.3159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3990    0.3937    0.8480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2869    0.7694   -0.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1875    0.1164   -2.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1419   -1.2734   -2.1537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5924   -0.2807   -0.7190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5332    0.0246   -4.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8583    0.6405   -2.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8987   -1.7394   -1.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8516   -2.9532   -1.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4077   -0.3780   -2.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8593   -2.0596   -2.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2243   -2.3919   -0.0867 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0146   -0.8788   -0.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2962    0.5177    0.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2197   -0.8948    0.6258 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2728    0.2287    4.9780 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6863   -0.6384    4.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6103    1.1980    4.3200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4202    2.2060   -1.1093 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
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 18 20  1  0
 20 21  1  0
 11 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  1
 24 26  1  0
 26 27  1  0
 27  9  1  0
 27 24  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
 10 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 17 52  1  0
 21 53  1  0
 21 54  1  0
 21 55  1  0
 27 56  1  1
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₁H₂₉ClO₅

Average Mass

396.9100 Da

Monoisotopic Mass

396.17035 Da

IUPAC Name

methyl (5Z)-7-[(1R,3E,4S,5S)-1-chloro-4-hydroxy-4-[(2Z)-oct-2-en-1-yl]-2-oxo-6-oxabicyclo[3.1.0]hexan-3-ylidene]hept-5-enoate

Traditional Name

10,11-epoxy-chlorovulone I

CAS Registry Number

Not Available

SMILES

CCCCC\C=C/C[C@@]1(O)[C@@H]2O[C@]2(Cl)C(=O)\C1=C\C=C/CCCC(=O)OC

InChI Identifier

InChI=1S/C21H29ClO5/c1-3-4-5-6-9-12-15-20(25)16(18(24)21(22)19(20)27-21)13-10-7-8-11-14-17(23)26-2/h7,9-10,12-13,19,25H,3-6,8,11,14-15H2,1-2H3/b10-7-,12-9-,16-13-/t19-,20-,21+/m0/s1

InChI Key

VQTGQBDTRZNQSB-ZKVKOFCJSA-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
Clavularia viridis	NPAtlas	3435962

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	4.55	ALOGPS
logP	5.13	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	12.81	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	76.13 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	107.77 m³·mol⁻¹	ChemAxon
Polarizability	43.12 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA005668

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

4446347

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5283226

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 10,11-epoxychlorovulone (NP0021147)

MOL for NP0021147 (10,11-epoxychlorovulone)

3D MOL for NP0021147 (10,11-epoxychlorovulone)

3D SDF for NP0021147 (10,11-epoxychlorovulone)

3D-SDF for NP0021147 (10,11-epoxychlorovulone)

PDB for NP0021147 (10,11-epoxychlorovulone)

3D PDB for NP0021147 (10,11-epoxychlorovulone)

SMILES for NP0021147 (10,11-epoxychlorovulone)

INCHI for NP0021147 (10,11-epoxychlorovulone)

Structure for NP0021147 (10,11-epoxychlorovulone)

3D Structure for NP0021147 (10,11-epoxychlorovulone)