Np mrd loader

Showing NP-Card for Liquiritic acid (NP0337539)

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Record Information
Version2.0
Created at2024-09-11 11:17:54 UTC
Updated at2024-09-11 11:17:54 UTC
NP-MRD IDNP0337539
Secondary Accession NumbersNone
Natural Product Identification
Common NameLiquiritic acid
DescriptionLiquiritic acid is also known as liquiritate. Liquiritic acid was first documented in 2021 (PMID: 33988079). Based on a literature review very few articles have been published on Liquiritic acid.
Structure
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MOLSDFPDBSMILESInChI

MOL for NP0337539 (Liquiritic acid)


  Mrv2104 05262313502D          

 37 41  0  0  0  0            999 V2000
   -3.0054   -0.9723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7198   -1.3848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7198   -2.2098    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0054   -2.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2909   -2.2098    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2909   -1.3848    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5764   -0.9723    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5764   -2.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8620   -2.2098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8620   -1.3848    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8620    0.2652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5764   -0.1473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1475   -0.9723    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1475   -0.1473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5670    0.2652    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5670   -1.3848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2814   -0.9723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2814   -0.1473    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2814    1.5028    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5670    1.0902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9959    0.2652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9959    1.0902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4343   -2.6223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2909   -3.0348    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2909   -0.5598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5764   -1.7973    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8620   -0.5598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1475   -1.7973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5670   -0.5598    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2909    0.2652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2814    0.6777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2814    2.3278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5670    1.9152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9959    2.7403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5670    2.7403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0054   -3.4473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7198   -3.0348    0.0000 C   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
  1  6  1  0  0  0  0
  7  6  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 12  7  1  0  0  0  0
  7 10  1  0  0  0  0
 10 13  1  0  0  0  0
 11 12  1  0  0  0  0
 11 14  2  0  0  0  0
 15 14  1  0  0  0  0
 14 13  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 21  1  0  0  0  0
 15 18  1  0  0  0  0
 20 15  1  0  0  0  0
 19 20  1  0  0  0  0
 21 22  1  0  0  0  0
 19 22  1  0  0  0  0
  3 23  1  1  0  0  0
  5 24  1  6  0  0  0
  6 25  1  1  0  0  0
  7 26  1  6  0  0  0
 10 27  1  1  0  0  0
 13 28  1  6  0  0  0
 15 29  1  1  0  0  0
 12 30  2  0  0  0  0
 18 31  1  1  0  0  0
 19 32  1  0  0  0  0
 19 33  1  1  0  0  0
 32 34  1  0  0  0  0
 32 35  2  0  0  0  0
  4 36  1  0  0  0  0
  4 37  1  0  0  0  0
M  END
Download

3D MOL for NP0337539 (Liquiritic acid)

Download
3D SDF for NP0337539 (Liquiritic acid)

  Mrv2104 05262313502D          

 37 41  0  0  0  0            999 V2000
   -3.0054   -0.9723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7198   -1.3848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7198   -2.2098    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0054   -2.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2909   -2.2098    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2909   -1.3848    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5764   -0.9723    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5764   -2.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8620   -2.2098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8620   -1.3848    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8620    0.2652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5764   -0.1473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1475   -0.9723    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1475   -0.1473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5670    0.2652    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5670   -1.3848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2814   -0.9723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2814   -0.1473    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2814    1.5028    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5670    1.0902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9959    0.2652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9959    1.0902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4343   -2.6223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2909   -3.0348    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2909   -0.5598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5764   -1.7973    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8620   -0.5598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1475   -1.7973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5670   -0.5598    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2909    0.2652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2814    0.6777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2814    2.3278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5670    1.9152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9959    2.7403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5670    2.7403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0054   -3.4473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7198   -3.0348    0.0000 C   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
  1  6  1  0  0  0  0
  7  6  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 12  7  1  0  0  0  0
  7 10  1  0  0  0  0
 10 13  1  0  0  0  0
 11 12  1  0  0  0  0
 11 14  2  0  0  0  0
 15 14  1  0  0  0  0
 14 13  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 21  1  0  0  0  0
 15 18  1  0  0  0  0
 20 15  1  0  0  0  0
 19 20  1  0  0  0  0
 21 22  1  0  0  0  0
 19 22  1  0  0  0  0
  3 23  1  1  0  0  0
  5 24  1  6  0  0  0
  6 25  1  1  0  0  0
  7 26  1  6  0  0  0
 10 27  1  1  0  0  0
 13 28  1  6  0  0  0
 15 29  1  1  0  0  0
 12 30  2  0  0  0  0
 18 31  1  1  0  0  0
 19 32  1  0  0  0  0
 19 33  1  1  0  0  0
 32 34  1  0  0  0  0
 32 35  2  0  0  0  0
  4 36  1  0  0  0  0
  4 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0337539

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12C[C@@](C)(CC[C@]1(C)CC[C@]1(C)C2=CC(=O)[C@]2([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]12C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1/C30H46O4/c1-25(2)21-8-11-30(7)23(28(21,5)10-9-22(25)32)20(31)16-18-19-17-27(4,24(33)34)13-12-26(19,3)14-15-29(18,30)6/h16,19,21-23,32H,8-15,17H2,1-7H3,(H,33,34)/t19-,21-,22-,23+,26+,27+,28-,29+,30+/s2

> <INCHI_KEY>
MPDGHEJMBKOTSU-KYVADJCXNA-N

> <FORMULA>
C30H46O4

> <MOLECULAR_WEIGHT>
470.694

> <EXACT_MASS>
470.339609961

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
54.69857761590519

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,4aS,6aS,6bR,8aR,10S,12aS,12bR,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-2-carboxylic acid

> <JCHEM_LOGP>
6.031328036333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
18.621396922000322

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.44433188134718

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8351069321304386

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
134.2685

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4aS,6aS,6bR,8aR,10S,12aS,12bR,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,7,8,8a,10,11,12,12b,14b-dodecahydro-1H-picene-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

Download
3D-SDF for NP0337539 (Liquiritic acid)
Download
PDB for NP0337539 (Liquiritic acid)
HEADER    PROTEIN                                 26-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-23         0                                  
HETATM    1  C   UNK     0      -5.610  -1.815   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.944  -2.585   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.944  -4.125   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.610  -4.895   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.276  -4.125   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.276  -2.585   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.943  -1.815   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.943  -4.895   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.609  -4.125   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.609  -2.585   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.609   0.495   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.943  -0.275   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.275  -1.815   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.275  -0.275   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.058   0.495   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.058  -2.585   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.392  -1.815   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.392  -0.275   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.392   2.805   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.058   2.035   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.726   0.495   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.726   2.035   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -8.277  -4.895   0.000  0.00  0.00           O+0
HETATM   24  H   UNK     0      -4.276  -5.665   0.000  0.00  0.00           H+0
HETATM   25  C   UNK     0      -4.276  -1.045   0.000  0.00  0.00           C+0
HETATM   26  H   UNK     0      -2.943  -3.355   0.000  0.00  0.00           H+0
HETATM   27  C   UNK     0      -1.609  -1.045   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.275  -3.355   0.000  0.00  0.00           C+0
HETATM   29  H   UNK     0       1.058  -1.045   0.000  0.00  0.00           H+0
HETATM   30  O   UNK     0      -4.276   0.495   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.392   1.265   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.392   4.345   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.058   3.575   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       3.726   5.115   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       1.058   5.115   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -5.610  -6.435   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -6.944  -5.665   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5   36   37                                             
CONECT    5    4    6    8   24                                             
CONECT    6    1    7    5   25                                             
CONECT    7    6   12   10   26                                             
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    7   13   27                                             
CONECT   11   12   14                                                       
CONECT   12    7   11   30                                                  
CONECT   13   10   14   16   28                                             
CONECT   14   11   15   13                                                  
CONECT   15   14   18   20   29                                             
CONECT   16   13   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   21   15   31                                             
CONECT   19   20   22   32   33                                             
CONECT   20   15   19                                                       
CONECT   21   18   22                                                       
CONECT   22   21   19                                                       
CONECT   23    3                                                            
CONECT   24    5                                                            
CONECT   25    6                                                            
CONECT   26    7                                                            
CONECT   27   10                                                            
CONECT   28   13                                                            
CONECT   29   15                                                            
CONECT   30   12                                                            
CONECT   31   18                                                            
CONECT   32   19   34   35                                                  
CONECT   33   19                                                            
CONECT   34   32                                                            
CONECT   35   32                                                            
CONECT   36    4                                                            
CONECT   37    4                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

Download
3D PDB for NP0337539 (Liquiritic acid)
Download
SMILES for NP0337539 (Liquiritic acid)
[H][C@@]12C[C@@](C)(CC[C@]1(C)CC[C@]1(C)C2=CC(=O)[C@]2([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]12C)C(O)=O
Download
INCHI for NP0337539 (Liquiritic acid)
InChI=1/C30H46O4/c1-25(2)21-8-11-30(7)23(28(21,5)10-9-22(25)32)20(31)16-18-19-17-27(4,24(33)34)13-12-26(19,3)14-15-29(18,30)6/h16,19,21-23,32H,8-15,17H2,1-7H3,(H,33,34)/t19-,21-,22-,23+,26+,27+,28-,29+,30+/s2
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View in JSmol
Synonyms
ValueSource
LiquiritateGenerator
Chemical FormulaC30H46O4
Average Mass470.6940 Da
Monoisotopic Mass470.33961 Da
IUPAC Name(2R,4aS,6aS,6bR,8aR,10S,12aS,12bR,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-2-carboxylic acid
Traditional Name(2R,4aS,6aS,6bR,8aR,10S,12aS,12bR,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,7,8,8a,10,11,12,12b,14b-dodecahydro-1H-picene-2-carboxylic acid
CAS Registry NumberNot Available
SMILES
[H][C@@]12C[C@@](C)(CC[C@]1(C)CC[C@]1(C)C2=CC(=O)[C@]2([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]12C)C(O)=O
InChI Identifier
InChI=1/C30H46O4/c1-25(2)21-8-11-30(7)23(28(21,5)10-9-22(25)32)20(31)16-18-19-17-27(4,24(33)34)13-12-26(19,3)14-15-29(18,30)6/h16,19,21-23,32H,8-15,17H2,1-7H3,(H,33,34)/t19-,21-,22-,23+,26+,27+,28-,29+,30+/s2
InChI KeyMPDGHEJMBKOTSU-KYVADJCXNA-N
Experimental Spectra
Not Available
Predicted Spectra
Not Available
Chemical Shift Submissions
Not Available
Species
Species of OriginNot Available
Chemical Taxonomy
DescriptionThis compound belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.
KingdomOrganic compounds  
Super ClassLipids and lipid-like molecules  
ClassPrenol lipids  
Sub ClassTriterpenoids  
Direct ParentTriterpenoids  
Alternative Parents
Substituents
  • Triterpenoid
    • 

  • Cyclohexenone
    • 

  • Cyclic alcohol
    • 

  • Secondary alcohol
    • 

  • Ketone
    • 

  • Monocarboxylic acid or derivatives
    • 

  • Carboxylic acid
    • 

  • Carboxylic acid derivative
    • 

  • Organic oxygen compound
    • 

  • Organic oxide
    • 

  • Hydrocarbon derivative
    • 

  • Organooxygen compound
    • 

  • Carbonyl group
    • 

  • Alcohol
    • 

  • Aliphatic homopolycyclic compound
Molecular FrameworkAliphatic homopolycyclic compounds
External DescriptorsNot Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP6.03ChemAxon
pKa (Strongest Acidic)4.44ChemAxon
pKa (Strongest Basic)-0.84ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area74.6 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity134.27 m³·mol⁻¹ChemAxon
Polarizability54.7 ųChemAxon
Number of Rings5ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem CompoundNot Available
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General References
  1. Joshi C, Chaudhari A, Joshi C, Joshi M, Bagatharia S: Repurposing of the herbal formulations: molecular docking and molecular dynamics simulation studies to validate the efficacy of phytocompounds against SARS-CoV-2 proteins. J Biomol Struct Dyn. 2021 May 14:1-15. doi: 10.1080/07391102.2021.1922095. [PubMed:33988079  ]