NP-MRD: Showing NP-Card for Visnadin (NP0051462)

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Record Information

Version

2.0

Created at

2022-04-27 22:49:13 UTC

Updated at

2022-04-27 22:49:13 UTC

NP-MRD ID

NP0051462

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Visnadin

Description

Visnadine, also known as visnagan or carduben, belongs to the class of organic compounds known as angular pyranocoumarins. These are organic compounds containing a pyran (or a hydrogenated derivative) angularly fused to a coumarin moiety. Visnadine is an extremely weak basic (essentially neutral) compound (based on its pKa). Visnadin is found in Ammi visnaga , Anethum spp., Ferula spp., Ferula xeromorpha, Ferulopsis hystrix, Ligusticum lucidum, Peucedanum japonicum and Phlojodicarpus spp.. Visnadine (or visnadin) is a natural vasodilator.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306031608572D          

 31 33  0  0  1  0            999 V2000
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1888    1.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7191    0.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  9  7  2  0  0  0  0
 10  8  2  0  0  0  0
 11  2  1  1  0  0  0
 11  6  1  0  0  0  0
 12  3  1  0  0  0  0
 13  7  1  0  0  0  0
 13  8  1  0  0  0  0
 14  9  1  0  0  0  0
 15 10  1  0  0  0  0
 16 14  2  0  0  0  0
 17 13  2  0  0  0  0
 17 16  1  0  0  0  0
 18 16  1  0  0  0  0
 19 18  1  0  0  0  0
 20 11  1  0  0  0  0
 21  4  1  0  0  0  0
 21  5  1  0  0  0  0
 21 19  1  0  0  0  0
 22 12  2  0  0  0  0
 23 15  2  0  0  0  0
 24 20  2  0  0  0  0
 25 12  1  0  0  0  0
 18 25  1  6  0  0  0
 26 15  1  0  0  0  0
 26 17  1  0  0  0  0
 19 27  1  6  0  0  0
 27 20  1  0  0  0  0
 28 14  1  0  0  0  0
 28 21  1  0  0  0  0
 11 29  1  6  0  0  0
 18 30  1  1  0  0  0
 19 31  1  1  0  0  0
M  END

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
   -4.9234   -2.0889   -0.6152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8868   -1.3301    0.1865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4894   -0.0957   -0.5831 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6984    0.7822   -0.8095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4043    0.6594    0.0387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5941    1.8753    0.2954 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1687    0.1419    0.3734 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1860    0.9509    0.9706 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1096    0.9547    0.2172 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9775    1.4166   -1.1091 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6091    2.5594   -1.5538 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5230    3.1041   -2.9120 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3212    3.1734   -0.6894 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7675   -0.3760    0.2799 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4478   -1.2759    1.2688 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0534   -2.5204    1.3404 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9933   -2.8656    0.4056 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3340   -1.9822   -0.5984 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2964   -2.3393   -1.5533 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5799   -1.4064   -2.5191 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9177   -0.1997   -2.4957 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1873    0.6550   -3.3929 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0235    0.1046   -1.5905 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7203   -0.7638   -0.6428 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4975   -0.9654    2.2392 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0855    0.3830    2.3482 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2583    1.1227    3.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0932    0.5460    3.2656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9021   -2.1274   -0.1088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5853   -3.1433   -0.7332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0601   -1.6855   -1.6295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3719   -1.0412    1.1494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9782   -1.9552    0.3660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1556   -0.4252   -1.6067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2253    0.4929   -1.7595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4003    1.8408   -0.9365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4259    0.6638    0.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5738    1.9650    1.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7865    1.6757    0.7612 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6084    2.8255   -3.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4467    2.8011   -3.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5973    4.2260   -2.8203 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7998   -3.2221    2.1170 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5117   -3.8322    0.4018 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7660   -3.3152   -1.4903 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3265   -1.6495   -3.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2255    0.6741    2.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2044    2.1984    2.8555 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1757    0.8938    4.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2300    1.6576    3.4046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7871    0.1733    4.2646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0117    0.0887    2.8834 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  4  1  0
  3  2  1  0
  2  1  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
  9 14  1  0
 14 15  2  0
 15 25  1  0
 25 26  1  0
 26 27  1  1
 26 28  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 24  2  0
 24 23  1  0
 23 21  1  0
 21 22  2  0
 21 20  1  0
 20 19  2  0
 26  8  1  0
 19 18  1  0
 24 14  1  0
  3 34  1  6
  4 35  1  0
  4 36  1  0
  4 37  1  0
  2 32  1  0
  2 33  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  8 38  1  1
  9 39  1  1
 12 40  1  0
 12 41  1  0
 12 42  1  0
 27 47  1  0
 27 48  1  0
 27 49  1  0
 28 50  1  0
 28 51  1  0
 28 52  1  0
 16 43  1  0
 17 44  1  0
 20 46  1  0
 19 45  1  0
M  END


  Mrv1652306031608572D          

 31 33  0  0  1  0            999 V2000
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1888    1.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7191    0.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  9  7  2  0  0  0  0
 10  8  2  0  0  0  0
 11  2  1  1  0  0  0
 11  6  1  0  0  0  0
 12  3  1  0  0  0  0
 13  7  1  0  0  0  0
 13  8  1  0  0  0  0
 14  9  1  0  0  0  0
 15 10  1  0  0  0  0
 16 14  2  0  0  0  0
 17 13  2  0  0  0  0
 17 16  1  0  0  0  0
 18 16  1  0  0  0  0
 19 18  1  0  0  0  0
 20 11  1  0  0  0  0
 21  4  1  0  0  0  0
 21  5  1  0  0  0  0
 21 19  1  0  0  0  0
 22 12  2  0  0  0  0
 23 15  2  0  0  0  0
 24 20  2  0  0  0  0
 25 12  1  0  0  0  0
 18 25  1  6  0  0  0
 26 15  1  0  0  0  0
 26 17  1  0  0  0  0
 19 27  1  6  0  0  0
 27 20  1  0  0  0  0
 28 14  1  0  0  0  0
 28 21  1  0  0  0  0
 11 29  1  6  0  0  0
 18 30  1  1  0  0  0
 19 31  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0051462

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@](C)(CC)C(=O)O[C@]1([H])[C@]([H])(OC(C)=O)C2=C(OC1(C)C)C=CC1=C2OC(=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H24O7/c1-6-11(2)20(24)27-19-18(25-12(3)22)16-14(28-21(19,4)5)9-7-13-8-10-15(23)26-17(13)16/h7-11,18-19H,6H2,1-5H3/t11-,18-,19-/m1/s1

> <INCHI_KEY>
GVBNSPFBYXGREE-CXWAGAITSA-N

> <FORMULA>
C21H24O7

> <MOLECULAR_WEIGHT>
388.416

> <EXACT_MASS>
388.152203113

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
39.97931317314964

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9R,10R)-10-(acetyloxy)-8,8-dimethyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-9-yl (2R)-2-methylbutanoate

> <ALOGPS_LOGP>
3.59

> <JCHEM_LOGP>
3.383739070999999

> <ALOGPS_LOGS>
-4.18

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.902201746209702

> <JCHEM_POLAR_SURFACE_AREA>
88.13000000000001

> <JCHEM_REFRACTIVITY>
99.65379999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.57e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(9R,10R)-10-(acetyloxy)-8,8-dimethyl-2-oxo-9H,10H-pyrano[2,3-h]chromen-9-yl (2R)-2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-JUN-16   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-JUN-16         0                                  
HETATM    1  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336   8.470   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.819   2.577   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.809   0.863   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.670   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.004   4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.337   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.004   6.160   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336   6.930   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.670   3.850   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.003   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.670   6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.003   3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.337   4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.002   6.160   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      14.670   8.470   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       6.668   2.310   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      10.669   6.160   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      13.337   6.160   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       8.002   4.620   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      10.669   1.540   0.000  0.00  0.00           O+0
HETATM   29  H   UNK     0       4.001   5.390   0.000  0.00  0.00           H+0
HETATM   30  H   UNK     0      12.003   5.390   0.000  0.00  0.00           H+0
HETATM   31  H   UNK     0       9.336   5.390   0.000  0.00  0.00           H+0
CONECT    1    6                                                            
CONECT    2   11                                                            
CONECT    3   12                                                            
CONECT    4   21                                                            
CONECT    5   21                                                            
CONECT    6    1   11                                                       
CONECT    7    9   13                                                       
CONECT    8   10   13                                                       
CONECT    9    7   14                                                       
CONECT   10    8   15                                                       
CONECT   11    2    6   20   29                                             
CONECT   12    3   22   25                                                  
CONECT   13    7    8   17                                                  
CONECT   14    9   16   28                                                  
CONECT   15   10   23   26                                                  
CONECT   16   14   17   18                                                  
CONECT   17   13   16   26                                                  
CONECT   18   16   19   25   30                                             
CONECT   19   18   21   27   31                                             
CONECT   20   11   24   27                                                  
CONECT   21    4    5   19   28                                             
CONECT   22   12                                                            
CONECT   23   15                                                            
CONECT   24   20                                                            
CONECT   25   12   18                                                       
CONECT   26   15   17                                                       
CONECT   27   19   20                                                       
CONECT   28   14   21                                                       
CONECT   29   11                                                            
CONECT   30   18                                                            
CONECT   31   19                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
Visnadin	MeSH
Visnagan	MeSH
Carduben	MeSH
Visnadine	KEGG
(9R,10R)-10-(Acetyloxy)-8,8-dimethyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-H]chromen-9-yl (2R)-2-methylbutanoic acid	Generator

Chemical Formula

C₂₁H₂₄O₇

Average Mass

388.4160 Da

Monoisotopic Mass

388.15220 Da

IUPAC Name

(9R,10R)-10-(acetyloxy)-8,8-dimethyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-9-yl (2R)-2-methylbutanoate

Traditional Name

(9R,10R)-10-(acetyloxy)-8,8-dimethyl-2-oxo-9H,10H-pyrano[2,3-h]chromen-9-yl (2R)-2-methylbutanoate

CAS Registry Number

Not Available

SMILES

[H][C@@](C)(CC)C(=O)O[C@]1([H])[C@]([H])(OC(C)=O)C2=C(OC1(C)C)C=CC1=C2OC(=O)C=C1

InChI Identifier

InChI=1S/C21H24O7/c1-6-11(2)20(24)27-19-18(25-12(3)22)16-14(28-21(19,4)5)9-7-13-8-10-15(23)26-17(13)16/h7-11,18-19H,6H2,1-5H3/t11-,18-,19-/m1/s1

InChI Key

GVBNSPFBYXGREE-CXWAGAITSA-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
Ammi visnaga	Plant	KNApSAcK
Anethum spp.	Plant	KNApSAcK
Ferula spp.	Plant	KNApSAcK
Ferula xeromorpha	LOTUS Database	35616633
Ferulopsis hystrix	LOTUS Database	35616633
Ligusticum lucidum	LOTUS Database	35616633
Peucedanum japonicum	LOTUS Database	35616633
Phlojodicarpus spp.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as angular pyranocoumarins. These are organic compounds containing a pyran (or a hydrogenated derivative) angularly fused to a coumarin moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Pyranocoumarins

Direct Parent

Angular pyranocoumarins

Alternative Parents

Substituents

Angular pyranocoumarin
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromane
Benzopyran
1-benzopyran
Alkyl aryl ether
Fatty acid ester
Pyranone
Dicarboxylic acid or derivatives
Fatty acyl
Benzenoid
Pyran
Heteroaromatic compound
Carboxylic acid ester
Lactone
Organoheterocyclic compound
Ether
Oxacycle
Carboxylic acid derivative
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

coumarins (CHEBI:10001 )
coumarins (C09316 )

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	3.59	ALOGPS
logP	3.38	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	88.13 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	99.65 m³·mol⁻¹	ChemAxon
Polarizability	39.98 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	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

DB13355

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00002504

Chemspider ID

Not Available

KEGG Compound ID

C09316

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Visnadine

METLIN ID

Not Available

PubChem Compound

442151

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Visnadin (NP0051462)

MOL for NP0051462 (Visnadin)

3D MOL for NP0051462 (Visnadin)

3D SDF for NP0051462 (Visnadin)

3D-SDF for NP0051462 (Visnadin)

PDB for NP0051462 (Visnadin)

3D PDB for NP0051462 (Visnadin)

SMILES for NP0051462 (Visnadin)

INCHI for NP0051462 (Visnadin)

Structure for NP0051462 (Visnadin)

3D Structure for NP0051462 (Visnadin)