NP-MRD: Showing NP-Card for Veranisatin B (NP0079679)

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Record Information

Version

2.0

Created at

2022-04-29 00:41:02 UTC

Updated at

2022-04-29 00:41:02 UTC

NP-MRD ID

NP0079679

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Veranisatin B

Description

Methyl (1'S,2'S,3R,5'R,7'R,8'R,11'R)-5',7',11'-trihydroxy-2'-methyl-4,10'-dioxo-9'-oxaspiro[oxetane-3,6'-tricyclo[6.3.1.0¹,⁵]Dodecane]-7'-carboxylate belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. Veranisatin B is found in Illicium verum and Illicium verum Hook f. . Based on a literature review very few articles have been published on methyl (1'S,2'S,3R,5'R,7'R,8'R,11'R)-5',7',11'-trihydroxy-2'-methyl-4,10'-dioxo-9'-oxaspiro[oxetane-3,6'-tricyclo[6.3.1.0¹,⁵]Dodecane]-7'-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 48  0  0  0  0  0  0  0  0999 V2000
    4.7844    0.8139    0.5710 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3838    0.6250    0.5333 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6781    0.8755   -0.6370 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3706    1.2702   -1.6218 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2330    0.7108   -0.7759 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8715    1.0575   -2.0789 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5387    1.7093    0.1306 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9741    1.6180    0.0318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3426    0.2177    0.4755 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8047   -0.0937    0.3058 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5161    0.8024   -0.6430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8505   -1.5607   -0.1058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4048   -1.9953   -0.2994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7172   -0.7124   -0.5254 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1546   -0.2377   -1.7931 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7449   -0.6974   -0.5648 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5548   -1.6229    0.2216 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4143   -1.7131   -0.9277 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2593   -1.5525   -1.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7977   -1.9176   -2.7966 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9624    0.0296    1.8827 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3609   -1.1744    2.1973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0610    1.1073    2.3705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1707    1.5758    3.5559 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8949    1.5708    1.4777 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3364   -0.1564    0.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0024    1.5005    1.4118 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1587    1.2838   -0.3729 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4912    1.7578   -2.4496 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8913    2.7201   -0.2107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2855    1.7294   -1.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3961    2.3910    0.6720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3311   -0.0308    1.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6112    0.6759   -0.4800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2299    1.8401   -0.4399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3411    0.5845   -1.7119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3036   -2.1985    0.6770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4100   -1.6899   -1.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3696   -2.6277   -1.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0326   -2.6299    0.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4690   -0.9912   -2.3518 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0610   -2.6081    0.3340 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1448   -1.2757    1.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8789    0.0885    2.5430 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3662   -1.0697    2.8832 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
  3  5  1  0
  5  6  1  6
  5  7  1  0
  7  8  1  0
  9  8  1  6
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  1
 17 18  1  0
 18 19  1  0
 19 20  2  0
  9 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 23 25  1  0
 16  5  1  0
 16 19  1  0
 25  7  1  0
 14  9  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  6 29  1  0
  7 30  1  6
  8 31  1  0
  8 32  1  0
 10 33  1  1
 11 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 15 41  1  0
 17 42  1  0
 17 43  1  0
 21 44  1  1
 22 45  1  0
M  END


  Mrv1652304292202412D          

 25 28  0  0  1  0            999 V2000
    1.9244    0.3780    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0553    0.3779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5758   -0.3331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2489   -0.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0188   -1.0667    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9003   -1.1190    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7752   -1.0887    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0848   -1.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4521   -2.3914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7465   -1.9560    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9926   -2.2910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2377   -0.3582    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7913    0.3674    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4854    0.8133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8174    1.1920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5446    1.5816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1164    1.6270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3892    1.2373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8180    0.2282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4045   -0.3521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8242   -0.9385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8285   -1.7635    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5968   -1.1632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9028   -0.3682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5922   -1.7728    0.0000 O   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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  6  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
  1 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  1  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  2  0  0  0  0
  7 23  1  6  0  0  0
  6 24  1  6  0  0  0
  1 24  1  6  0  0  0
  5 25  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0079679

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@]1(O)[C@H]2C[C@]3([C@@H](C)CC[C@]3(O)[C@]11COC1=O)[C@@H](O)C(=O)O2

> <INCHI_IDENTIFIER>
InChI=1S/C16H20O9/c1-7-3-4-15(21)13(7)5-8(25-10(18)9(13)17)16(22,12(20)23-2)14(15)6-24-11(14)19/h7-9,17,21-22H,3-6H2,1-2H3/t7-,8+,9-,13-,14+,15+,16+/m0/s1

> <INCHI_KEY>
BPDHZCGFGOWILW-WUAXORPDSA-N

> <FORMULA>
C16H20O9

> <MOLECULAR_WEIGHT>
356.327

> <EXACT_MASS>
356.110732224

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
32.51137176402288

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1'S,2'S,3R,5'R,7'R,8'R,11'R)-5',7',11'-trihydroxy-2'-methyl-4,10'-dioxo-9'-oxaspiro[oxetane-3,6'-tricyclo[6.3.1.0^{1,5}]dodecane]-7'-carboxylate

> <ALOGPS_LOGP>
-0.54

> <JCHEM_LOGP>
-1.4116249570000003

> <ALOGPS_LOGS>
-1.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.177893900518832

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.712948988312336

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4660889836121287

> <JCHEM_POLAR_SURFACE_AREA>
139.59

> <JCHEM_REFRACTIVITY>
76.80609999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.03e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1'S,2'S,3R,5'R,7'R,8'R,11'R)-5',7',11'-trihydroxy-2'-methyl-4,10'-dioxo-9'-oxaspiro[oxetane-3,6'-tricyclo[6.3.1.0^{1,5}]dodecane]-7'-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       3.592   0.706   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.970   0.705   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.075  -0.622   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.465  -0.583   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.902  -1.991   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.547  -2.089   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.180  -2.032   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.758  -3.464   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.577  -4.464   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.260  -3.651   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.853  -4.277   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.044  -0.669   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.210   0.686   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.506   1.518   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.259   2.225   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.617   2.952   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       3.951   3.037   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.593   2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.127   0.426   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.222  -0.657   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.138  -1.752   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.147  -3.292   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       6.714  -2.171   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.552  -0.687   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.105  -3.309   0.000  0.00  0.00           O+0
CONECT    1    2   13   24                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   25                                                  
CONECT    6    5    7   10   24                                             
CONECT    7    6    8   12   23                                             
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6   11                                                  
CONECT   11   10                                                            
CONECT   12    7   13   19   21                                             
CONECT   13   12    1   14   15                                             
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17                                                            
CONECT   19   12   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   12   22                                                  
CONECT   22   21                                                            
CONECT   23    7                                                            
CONECT   24    6    1                                                       
CONECT   25    5                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1's,2's,3R,5'r,7'r,8'r,11'r)-5',7',11'-trihydroxy-2'-methyl-4,10'-dioxo-9'-oxaspiro[oxetane-3,6'-tricyclo[6.3.1.0,]dodecane]-7'-carboxylic acid	Generator

Chemical Formula

C₁₆H₂₀O₉

Average Mass

356.3270 Da

Monoisotopic Mass

356.11073 Da

IUPAC Name

methyl (1'S,2'S,3R,5'R,7'R,8'R,11'R)-5',7',11'-trihydroxy-2'-methyl-4,10'-dioxo-9'-oxaspiro[oxetane-3,6'-tricyclo[6.3.1.0^{1,5}]dodecane]-7'-carboxylate

Traditional Name

methyl (1'S,2'S,3R,5'R,7'R,8'R,11'R)-5',7',11'-trihydroxy-2'-methyl-4,10'-dioxo-9'-oxaspiro[oxetane-3,6'-tricyclo[6.3.1.0^{1,5}]dodecane]-7'-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@]1(O)[C@H]2C[C@]3([C@@H](C)CC[C@]3(O)[C@]11COC1=O)[C@@H](O)C(=O)O2

InChI Identifier

InChI=1S/C16H20O9/c1-7-3-4-15(21)13(7)5-8(25-10(18)9(13)17)16(22,12(20)23-2)14(15)6-24-11(14)19/h7-9,17,21-22H,3-6H2,1-2H3/t7-,8+,9-,13-,14+,15+,16+/m0/s1

InChI Key

BPDHZCGFGOWILW-WUAXORPDSA-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
Illicium verum	LOTUS Database	35616633
Illicium verum Hook f.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Prezizaane sesquiterpenoid
Sesquiterpenoid
Tricarboxylic acid or derivatives
Delta_valerolactone
Delta valerolactone
Oxane
Methyl ester
Tertiary alcohol
Cyclic alcohol
Beta_propiolactone
Secondary alcohol
Oxetane
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	-0.54	ALOGPS
logP	-1.4	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	10.71	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	139.59 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	76.81 m³·mol⁻¹	ChemAxon
Polarizability	32.51 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

162908116

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Veranisatin B (NP0079679)

MOL for NP0079679 (Veranisatin B)

3D MOL for NP0079679 (Veranisatin B)

3D SDF for NP0079679 (Veranisatin B)

3D-SDF for NP0079679 (Veranisatin B)

PDB for NP0079679 (Veranisatin B)

3D PDB for NP0079679 (Veranisatin B)

SMILES for NP0079679 (Veranisatin B)

INCHI for NP0079679 (Veranisatin B)

Structure for NP0079679 (Veranisatin B)

3D Structure for NP0079679 (Veranisatin B)