NP-MRD: Showing NP-Card for vicanicin (NP0332833)

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Record Information

Version

2.0

Created at

2024-04-23 00:01:17 UTC

Updated at

2024-09-16 20:03:34 UTC

NP-MRD ID

NP0332833

Natural Product DOI

https://doi.org/10.57994/2107

Secondary Accession Numbers

None

Natural Product Identification

Common Name

vicanicin

Description

5,13-Dichloro-14-hydroxy-6-methoxy-4,7,12,15-tetramethyl-2,9-dioxatricyclo[9.4.0.0³,⁸]Pentadeca-1(11),3(8),4,6,12,14-hexaen-10-one belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone). 5,13-Dichloro-14-hydroxy-6-methoxy-4,7,12,15-tetramethyl-2,9-dioxatricyclo[9.4.0.0³,⁸]Pentadeca-1(11),3(8),4,6,12,14-hexaen-10-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 43  0  0  0  0  0  0  0  0999 V2000
    5.3890    0.5175   -1.2636 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8472   -0.1660   -0.1457 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4966   -0.0371    0.1239 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5537   -0.8933   -0.4058 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9623   -2.0051   -1.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1986   -0.7693   -0.1393 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7991    0.2576    0.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7678    1.1159    1.2186 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2791    2.2081    2.1094 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1012    0.9854    0.9499 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2873    2.0915    1.6383 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.4884    0.5970    1.1119 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6881    0.1522    0.5352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7472    0.9960    0.7986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5519    2.2133    1.6082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0220    0.7214    0.3092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0831    1.5871    0.5860 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1751   -0.4103   -0.4365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7619   -0.8204   -1.0885 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.1497   -1.3077   -0.7420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3308   -2.5076   -1.5433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9080   -0.9954   -0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9138   -1.9919   -0.6068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3770   -3.1380   -0.7536 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4484   -1.7624   -0.7973 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6133    1.1053   -1.8122 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1498    1.2695   -0.9339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8463   -0.2528   -1.9290 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0518   -1.8948   -1.5707 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7861   -2.9953   -0.8615 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4095   -1.9523   -2.2623 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4316    1.8850    2.7447 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8883    3.0297    1.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0818    2.5999    2.7634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3132    2.9737    1.3299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5220    2.6146    1.4716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7054    2.0255    2.7086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9828    1.3314    0.2018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7285   -2.6033   -2.4663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5914   -3.4444   -1.0216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3482   -2.3302   -2.0447 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
  4  6  1  0
  6  7  2  0
  7 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  2  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 10  3  1  0
 25  6  1  0
 22 13  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  5 29  1  0
  5 30  1  0
  5 31  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
 17 38  1  0
 21 39  1  0
 21 40  1  0
 21 41  1  0
  9 32  1  0
  9 33  1  0
  9 34  1  0
M  END


  Mrv1533004241510332D          

 25 27  0  0  0  0            999 V2000
   -0.9753   -1.1939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3705   -0.6328    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4178   -0.8760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0226   -0.3148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8390    0.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8109   -0.5580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3253    0.0870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1503    0.0870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5083    0.8303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6647   -0.5580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4530   -0.3148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6366    0.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0578   -0.8760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8461   -0.6328    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.8742   -1.6803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4790   -2.2414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0859   -1.9235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9023   -2.7278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4811   -1.3623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7378   -1.7203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9945   -1.3623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3897   -1.9235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5733   -2.7278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014   -1.6803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0034   -2.2414    0.0000 Cl  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
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  6 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0332833

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C)C2=C(OC3=C(C)C(O)=C(Cl)C(C)=C3C(=O)O2)C(C)=C1Cl

> <INCHI_IDENTIFIER>
InChI=1S/C18H16Cl2O5/c1-6-10-14(8(3)13(21)11(6)19)24-16-7(2)12(20)15(23-5)9(4)17(16)25-18(10)22/h21H,1-5H3

> <INCHI_KEY>
DJIUVCGPONSSSV-UHFFFAOYSA-N

> <FORMULA>
C18H16Cl2O5

> <MOLECULAR_WEIGHT>
383.22

> <EXACT_MASS>
382.037479

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
37.56570302019004

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5,13-dichloro-14-hydroxy-6-methoxy-4,7,12,15-tetramethyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,11,13-hexaen-10-one

> <ALOGPS_LOGP>
5.47

> <JCHEM_LOGP>
5.762260918333334

> <ALOGPS_LOGS>
-4.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.156955059345313

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7426461219444858

> <JCHEM_POLAR_SURFACE_AREA>
64.99000000000001

> <JCHEM_REFRACTIVITY>
96.26219999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.08e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,13-dichloro-14-hydroxy-6-methoxy-4,7,12,15-tetramethyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,11,13-hexaen-10-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -1.821  -2.229   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.692  -1.181   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.780  -1.635   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.909  -0.588   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.566   0.914   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.380  -1.042   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.341   0.162   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.881   0.162   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.549   1.550   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.841  -1.042   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.312  -0.588   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.655   0.914   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.441  -1.635   0.000  0.00  0.00           C+0
HETATM   14 Cl   UNK     0      10.913  -1.181   0.000  0.00  0.00          Cl+0
HETATM   15  C   UNK     0       9.099  -3.137   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.227  -4.184   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.627  -3.590   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.284  -5.092   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.498  -2.543   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.111  -3.211   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.723  -2.543   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.594  -3.590   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.937  -5.092   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.123  -3.137   0.000  0.00  0.00           C+0
HETATM   25 Cl   UNK     0      -0.006  -4.184   0.000  0.00  0.00          Cl+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   21                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   19                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   10   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20    6   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    3   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₆Cl₂O₅

Average Mass

383.2200 Da

Monoisotopic Mass

382.03748 Da

IUPAC Name

5,13-dichloro-14-hydroxy-6-methoxy-4,7,12,15-tetramethyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,11,13-hexaen-10-one

Traditional Name

5,13-dichloro-14-hydroxy-6-methoxy-4,7,12,15-tetramethyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,11,13-hexaen-10-one

CAS Registry Number

Not Available

SMILES

COC1=C(C)C2=C(OC3=C(C)C(O)=C(Cl)C(C)=C3C(=O)O2)C(C)=C1Cl

InChI Identifier

InChI=1S/C18H16Cl2O5/c1-6-10-14(8(3)13(21)11(6)19)24-16-7(2)12(20)15(23-5)9(4)17(16)25-18(10)22/h21H,1-5H3

InChI Key

DJIUVCGPONSSSV-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, C3D6O, experimental)	Not Available	Université de Rennes	Solenn Ferron	2024-04-23	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, C3D6O, experimental)	Not Available	Université de Rennes	Solenn Ferron	2024-04-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C3D6O, experimental)	Not Available	Université de Rennes	Solenn Ferron	2024-04-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, C3D6O, experimental)	Not Available	Université de Rennes	Solenn Ferron	2024-04-23	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 500.12300072, C3D6O, simulated)	solenn.ferron@univ-rennes.fr	Université de Rennes	Solenn	2024-04-23	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
flavicans		Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Depsides and depsidones

Sub Class

Not Available

Direct Parent

Depsides and depsidones

Alternative Parents

Substituents

Depsidone
Diaryl ether
Anisole
1,4-dioxepine
Alkyl aryl ether
Dioxepine
Aryl chloride
Aryl halide
Benzenoid
Carboxylic acid ester
Lactone
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organochloride
Organohalogen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5.47	ALOGPS
logP	5.76	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	7.16	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.99 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	96.26 m³·mol⁻¹	ChemAxon
Polarizability	37.57 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

Not Available

Chemspider ID

Not Available

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

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for vicanicin (NP0332833)

MOL for NP0332833 (vicanicin)

3D MOL for NP0332833 (vicanicin)

3D SDF for NP0332833 (vicanicin)

3D-SDF for NP0332833 (vicanicin)

PDB for NP0332833 (vicanicin)

3D PDB for NP0332833 (vicanicin)

SMILES for NP0332833 (vicanicin)

INCHI for NP0332833 (vicanicin)

Structure for NP0332833 (vicanicin)

3D Structure for NP0332833 (vicanicin)