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Showing NP-Card for Liquoric acid (NP0337175)

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Record Information
Version2.0
Created at2024-09-11 09:39:16 UTC
Updated at2024-09-11 09:39:17 UTC
NP-MRD IDNP0337175
Secondary Accession NumbersNone
Natural Product Identification
Common NameLiquoric acid
DescriptionLiquoric acid is also known as liquate. Liquoric acid was first documented in 2021 (PMID: 33961536). Based on a literature review very few articles have been published on Liquoric acid (PMID: 37110817).
Structure
Thumb
MOLSDFPDBSMILESInChI

MOL for NP0337175 (Liquoric acid)


  Mrv2104 05262312112D          

 36 41  0  0  0  0            999 V2000
   -4.3018   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0163   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0163   -3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3018   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5873   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5873   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8729   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8729   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1584   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1584   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1584   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8729   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4439   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7295   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7295   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0150   -2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0150   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0150    0.4126    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7295    0.0001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995    0.0001    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7307   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8851   -4.2959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8893   -4.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5873   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1584   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5873   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995    0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5984    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995    1.6501    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4140    0.4126    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439   -0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8046   -1.5086    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  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
 10 13  1  0  0  0  0
  7 10  1  0  0  0  0
 12  7  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
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 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 20 15  1  0  0  0  0
 15 18  1  0  0  0  0
 18 21  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
  4 24  1  0  0  0  0
  4 25  1  0  0  0  0
  6 26  1  1  0  0  0
 10 27  1  1  0  0  0
 12 28  2  0  0  0  0
 13 29  1  6  0  0  0
 19 30  1  1  0  0  0
 19 31  1  6  0  0  0
 30 32  2  0  0  0  0
 30 33  1  0  0  0  0
 15 34  1  1  0  0  0
 18 35  1  1  0  0  0
 22 36  1  6  0  0  0
 17 36  1  6  0  0  0
M  END
Download

3D MOL for NP0337175 (Liquoric acid)

Download
3D SDF for NP0337175 (Liquoric acid)

  Mrv2104 05262312112D          

 36 41  0  0  0  0            999 V2000
   -4.3018   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0163   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0163   -3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3018   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5873   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5873   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8729   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8729   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1584   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1584   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1584   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8729   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4439   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7295   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7295   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0150   -2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0150   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0150    0.4126    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7295    0.0001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995    0.0001    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7307   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8851   -4.2959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8893   -4.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5873   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1584   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5873   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995    0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5984    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995    1.6501    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4140    0.4126    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439   -0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8046   -1.5086    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  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
 10 13  1  0  0  0  0
  7 10  1  0  0  0  0
 12  7  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
 20 15  1  0  0  0  0
 15 18  1  0  0  0  0
 18 21  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
  4 24  1  0  0  0  0
  4 25  1  0  0  0  0
  6 26  1  1  0  0  0
 10 27  1  1  0  0  0
 12 28  2  0  0  0  0
 13 29  1  6  0  0  0
 19 30  1  1  0  0  0
 19 31  1  6  0  0  0
 30 32  2  0  0  0  0
 30 33  1  0  0  0  0
 15 34  1  1  0  0  0
 18 35  1  1  0  0  0
 22 36  1  6  0  0  0
 17 36  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0337175

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12C[C@](C)([C@H]3C[C@]1(C)[C@@H](C[C@]1(C)C2=CC(=O)C2[C@@]4(C)CC[C@H](O)C(C)(C)C4CC[C@@]12C)O3)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1/C30H44O5/c1-25(2)19-8-11-29(6)23(26(19,3)10-9-20(25)32)18(31)12-16-17-13-28(5,24(33)34)21-14-27(17,4)22(35-21)15-30(16,29)7/h12,17,19-23,32H,8-11,13-15H2,1-7H3,(H,33,34)/t17-,19?,20-,21+,22+,23?,26-,27-,28+,29+,30+/s2

> <INCHI_KEY>
NGWKGSCSHDHHAJ-MHBNTXKUNA-N

> <FORMULA>
C30H44O5

> <MOLECULAR_WEIGHT>
484.677

> <EXACT_MASS>
484.318874517

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
55.29738411482059

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3S,4R,9S,12S,17S,19R,20R,22S)-9-hydroxy-3,4,8,8,12,19,22-heptamethyl-14-oxo-23-oxahexacyclo[18.2.1.0^{3,16}.0^{4,13}.0^{7,12}.0^{17,22}]tricos-15-ene-19-carboxylic acid

> <JCHEM_LOGP>
4.731409474666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
17.75893183727454

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.239294571523991

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8349132512870444

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
133.78939999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3S,4R,9S,12S,17S,19R,20R,22S)-9-hydroxy-3,4,8,8,12,19,22-heptamethyl-14-oxo-23-oxahexacyclo[18.2.1.0^{3,16}.0^{4,13}.0^{7,12}.0^{17,22}]tricos-15-ene-19-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

Download
3D-SDF for NP0337175 (Liquoric acid)
Download
PDB for NP0337175 (Liquoric 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      -8.030  -3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -9.364  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.364  -6.160   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.030  -6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.696  -6.160   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.696  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.363  -3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.363  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.029  -6.160   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.029  -4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.029  -1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.363  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.695  -3.850   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.695  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.362  -1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.362  -4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.028  -3.850   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.028  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.028   0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.362   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.306  -1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.306   0.000   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0     -10.697  -6.930   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -9.119  -8.019   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -7.260  -8.264   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.696  -3.080   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.029  -3.080   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.696  -1.540   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -2.695  -5.390   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.306   1.540   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.117   1.859   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       1.306   3.080   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       2.639   0.770   0.000  0.00  0.00           O+0
HETATM   34  H   UNK     0      -2.695  -0.770   0.000  0.00  0.00           H+0
HETATM   35  C   UNK     0       1.306  -3.080   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -1.502  -2.816   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5   24   25                                             
CONECT    5    4    6    8                                                  
CONECT    6    1    7    5   26                                             
CONECT    7    6   10   12                                                  
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   13    7   27                                             
CONECT   11   12   14                                                       
CONECT   12    7   11   28                                                  
CONECT   13   10   14   16   29                                             
CONECT   14   11   15   13                                                  
CONECT   15   14   20   18   34                                             
CONECT   16   13   17                                                       
CONECT   17   16   18   36                                                  
CONECT   18   17   15   21   35                                             
CONECT   19   20   22   30   31                                             
CONECT   20   15   19                                                       
CONECT   21   18   22                                                       
CONECT   22   21   19   36                                                  
CONECT   23    3                                                            
CONECT   24    4                                                            
CONECT   25    4                                                            
CONECT   26    6                                                            
CONECT   27   10                                                            
CONECT   28   12                                                            
CONECT   29   13                                                            
CONECT   30   19   32   33                                                  
CONECT   31   19                                                            
CONECT   32   30                                                            
CONECT   33   30                                                            
CONECT   34   15                                                            
CONECT   35   18                                                            
CONECT   36   22   17                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   82    0
END

Download
3D PDB for NP0337175 (Liquoric acid)
Download
SMILES for NP0337175 (Liquoric acid)
[H][C@@]12C[C@](C)([C@H]3C[C@]1(C)[C@@H](C[C@]1(C)C2=CC(=O)C2[C@@]4(C)CC[C@H](O)C(C)(C)C4CC[C@@]12C)O3)C(O)=O
Download
INCHI for NP0337175 (Liquoric acid)
InChI=1/C30H44O5/c1-25(2)19-8-11-29(6)23(26(19,3)10-9-20(25)32)18(31)12-16-17-13-28(5,24(33)34)21-14-27(17,4)22(35-21)15-30(16,29)7/h12,17,19-23,32H,8-11,13-15H2,1-7H3,(H,33,34)/t17-,19?,20-,21+,22+,23?,26-,27-,28+,29+,30+/s2
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View in JSmol
Synonyms
ValueSource
LiquateGenerator
Liquic acidGenerator
Chemical FormulaC30H44O5
Average Mass484.6770 Da
Monoisotopic Mass484.31887 Da
IUPAC Name(1R,3S,4R,9S,12S,17S,19R,20R,22S)-9-hydroxy-3,4,8,8,12,19,22-heptamethyl-14-oxo-23-oxahexacyclo[18.2.1.0^{3,16}.0^{4,13}.0^{7,12}.0^{17,22}]tricos-15-ene-19-carboxylic acid
Traditional Name(1R,3S,4R,9S,12S,17S,19R,20R,22S)-9-hydroxy-3,4,8,8,12,19,22-heptamethyl-14-oxo-23-oxahexacyclo[18.2.1.0^{3,16}.0^{4,13}.0^{7,12}.0^{17,22}]tricos-15-ene-19-carboxylic acid
CAS Registry NumberNot Available
SMILES
[H][C@@]12C[C@](C)([C@H]3C[C@]1(C)[C@@H](C[C@]1(C)C2=CC(=O)C2[C@@]4(C)CC[C@H](O)C(C)(C)C4CC[C@@]12C)O3)C(O)=O
InChI Identifier
InChI=1/C30H44O5/c1-25(2)19-8-11-29(6)23(26(19,3)10-9-20(25)32)18(31)12-16-17-13-28(5,24(33)34)21-14-27(17,4)22(35-21)15-30(16,29)7/h12,17,19-23,32H,8-11,13-15H2,1-7H3,(H,33,34)/t17-,19?,20-,21+,22+,23?,26-,27-,28+,29+,30+/s2
InChI KeyNGWKGSCSHDHHAJ-MHBNTXKUNA-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
    • 

  • Naphthofuran
    • 

  • Cyclohexenone
    • 

  • Oxepane
    • 

  • Cyclic alcohol
    • 

  • Tetrahydrofuran
    • 

  • Ketone
    • 

  • Secondary alcohol
    • 

  • Carboxylic acid derivative
    • 

  • Carboxylic acid
    • 

  • Dialkyl ether
    • 

  • Ether
    • 

  • Monocarboxylic acid or derivatives
    • 

  • Oxacycle
    • 

  • Organoheterocyclic compound
    • 

  • Alcohol
    • 

  • Organic oxide
    • 

  • Hydrocarbon derivative
    • 

  • Organooxygen compound
    • 

  • Organic oxygen compound
    • 

  • Carbonyl group
    • 

  • Aliphatic heteropolycyclic compound
Molecular FrameworkAliphatic heteropolycyclic 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
logP4.73ChemAxon
pKa (Strongest Acidic)4.24ChemAxon
pKa (Strongest Basic)-0.83ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area83.83 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity133.79 m³·mol⁻¹ChemAxon
Polarizability55.3 ųChemAxon
Number of Rings6ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
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. Mustafa G, Younas S, Mahrosh HS, Albeshr MF, Bhat EA: Molecular Docking and Simulation-Binding Analysis of Plant Phytochemicals with the Hepatocellular Carcinoma Targets Epidermal Growth Factor Receptor and Caspase-9. Molecules. 2023 Apr 20;28(8):3583. doi: 10.3390/molecules28083583. [PubMed:37110817  ] 
  2. Chen Z, Han S, Zhang J, Zheng P, Liu X, Zhang Y, Jia G: Metabolomics screening of serum biomarkers for occupational exposure of titanium dioxide nanoparticles. Nanotoxicology. 2021 Aug;15(6):832-849. doi: 10.1080/17435390.2021.1921872. Epub  2021 May 7. [PubMed:33961536  ]