Np mrd loader

Showing NP-Card for Lipoyl-GMP (NP0339363)

Jump To Section:
IdentificationSpectraBioTaxonomyChemoTaxonomyPhysical propertiesLinksReferencesXML
Record Information
Version2.0
Created at2024-09-11 21:27:18 UTC
Updated at2024-09-11 21:27:18 UTC
NP-MRD IDNP0339363
Secondary Accession NumbersNone
Natural Product Identification
Common NameLipoyl-GMP
DescriptionLipoyl-GMP belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. 44 Hence, there appear to be two pathways in which LAE is capable of activating carboxylic acids: One that uses guanosine triphosphate to form acyl-GMP; the other is dependent on adenosine triphosphate for the activation of carboxylic acids to the CoA thioester (acyl-CoA) via an. Lipoyl-GMP is an extremely weak basic (essentially neutral) compound (based on its pKa). In humans, lipoyl-GMP is involved in the metabolic disorder called the 2-methyl-3-hydroxybutyryl-coa dehydrogenase deficiency pathway. The free lipoic acid in the cell is first activated by reacting it.
Structure
Thumb
MOLSDFPDBSMILESInChI

MOL for NP0339363 (Lipoyl-GMP)


  Mrv1652303102016522D          

 35 38  0  0  1  0            999 V2000
    9.6795  -12.7761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8949  -13.0310    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.6795  -11.9511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6399  -13.8156    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.3939  -13.1886    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.8949  -11.6961    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.1085  -11.9511    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.3939  -11.5386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1249  -14.4830    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.1085  -12.7761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4100  -12.3636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8553  -14.0705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8553  -14.8955    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.6399  -15.1505    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6067  -16.6859    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    7.1879  -15.3805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2741  -16.2010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3939  -10.7136    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1217  -16.0185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8229  -13.1886    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9499  -14.4830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0916  -17.3533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9393  -17.1708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8949  -15.9351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8229  -14.0136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1085  -14.4261    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5374  -14.4261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5374  -15.2511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2519  -15.6636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2519  -16.4886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9663  -16.9011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7200  -16.5655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2721  -17.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8596  -17.8931    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   14.0525  -17.7216    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  1  2  0  0  0  0
  5  1  1  0  0  0  0
  4  2  1  1  0  0  0
 11  2  1  0  0  0  0
  6  3  1  0  0  0  0
  8  3  1  0  0  0  0
  9  4  1  0  0  0  0
 12  4  1  0  0  0  0
 10  5  2  0  0  0  0
 11  6  2  0  0  0  0
 10  7  1  0  0  0  0
  8  7  1  0  0  0  0
 18  8  2  0  0  0  0
 14  9  1  0  0  0  0
  9 21  1  6  0  0  0
 20 10  1  0  0  0  0
 13 12  1  0  0  0  0
 13 16  1  1  0  0  0
 14 13  1  0  0  0  0
 14 24  1  6  0  0  0
 17 15  1  0  0  0  0
 19 15  2  0  0  0  0
 22 15  1  0  0  0  0
 23 15  1  0  0  0  0
 17 16  1  0  0  0  0
 20 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 35  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
M  END
Download

3D MOL for NP0339363 (Lipoyl-GMP)

Download
3D SDF for NP0339363 (Lipoyl-GMP)

  Mrv1652303102016522D          

 35 38  0  0  1  0            999 V2000
    9.6795  -12.7761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8949  -13.0310    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.6795  -11.9511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6399  -13.8156    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.3939  -13.1886    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.8949  -11.6961    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.1085  -11.9511    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.3939  -11.5386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1249  -14.4830    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.1085  -12.7761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4100  -12.3636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8553  -14.0705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8553  -14.8955    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.6399  -15.1505    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6067  -16.6859    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    7.1879  -15.3805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2741  -16.2010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3939  -10.7136    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1217  -16.0185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8229  -13.1886    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9499  -14.4830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0916  -17.3533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9393  -17.1708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8949  -15.9351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8229  -14.0136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1085  -14.4261    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5374  -14.4261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5374  -15.2511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2519  -15.6636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2519  -16.4886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9663  -16.9011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7200  -16.5655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2721  -17.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8596  -17.8931    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   14.0525  -17.7216    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  1  2  0  0  0  0
  5  1  1  0  0  0  0
  4  2  1  1  0  0  0
 11  2  1  0  0  0  0
  6  3  1  0  0  0  0
  8  3  1  0  0  0  0
  9  4  1  0  0  0  0
 12  4  1  0  0  0  0
 10  5  2  0  0  0  0
 11  6  2  0  0  0  0
 10  7  1  0  0  0  0
  8  7  1  0  0  0  0
 18  8  2  0  0  0  0
 14  9  1  0  0  0  0
  9 21  1  6  0  0  0
 20 10  1  0  0  0  0
 13 12  1  0  0  0  0
 13 16  1  1  0  0  0
 14 13  1  0  0  0  0
 14 24  1  6  0  0  0
 17 15  1  0  0  0  0
 19 15  2  0  0  0  0
 22 15  1  0  0  0  0
 23 15  1  0  0  0  0
 17 16  1  0  0  0  0
 20 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 35  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0339363

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)N1C=NC2=C1N=C(NC(=O)CCCCC1CCSS1)NC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H26N5O9PS2/c24-11(4-2-1-3-9-5-6-34-35-9)20-18-21-15-12(16(27)22-18)19-8-23(15)17-14(26)13(25)10(32-17)7-31-33(28,29)30/h8-10,13-14,17,25-26H,1-7H2,(H2,28,29,30)(H2,20,21,22,24,27)/t9?,10-,13-,14-,17-/m1/s1

> <INCHI_KEY>
DVZGUOFXTLKZTJ-LQLSJNDNSA-N

> <FORMULA>
C18H26N5O9PS2

> <MOLECULAR_WEIGHT>
551.531

> <EXACT_MASS>
551.090955347

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
52.2259510923818

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3S,4R,5R)-5-{2-[5-(1,2-dithiolan-3-yl)pentanamido]-6-oxo-6,9-dihydro-1H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid

> <ALOGPS_LOGP>
0.55

> <JCHEM_LOGP>
-0.8557079189658724

> <ALOGPS_LOGS>
-2.69

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.249797481727976

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.289255960272211

> <JCHEM_PKA_STRONGEST_BASIC>
0.36496215782533403

> <JCHEM_POLAR_SURFACE_AREA>
204.82999999999998

> <JCHEM_REFRACTIVITY>
126.66549999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.12e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4R,5R)-5-{2-[5-(1,2-dithiolan-3-yl)pentanamido]-6-oxo-1H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

Download
3D-SDF for NP0339363 (Lipoyl-GMP)
Download
PDB for NP0339363 (Lipoyl-GMP)
HEADER    PROTEIN                                 10-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-MAR-20         0                                  
HETATM    1  C   UNK     0      18.068 -23.849   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      16.604 -24.325   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      18.068 -22.309   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.128 -25.789   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      19.402 -24.619   0.000  0.00  0.00           N+0
HETATM    6  N   UNK     0      16.604 -21.833   0.000  0.00  0.00           N+0
HETATM    7  N   UNK     0      20.736 -22.309   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      19.402 -21.539   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.033 -27.035   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.736 -23.849   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      15.699 -23.079   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      14.663 -26.265   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      14.663 -27.805   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.128 -28.281   0.000  0.00  0.00           C+0
HETATM   15  P   UNK     0      12.333 -31.147   0.000  0.00  0.00           P+0
HETATM   16  C   UNK     0      13.417 -28.710   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      13.578 -30.242   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      19.402 -19.999   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      11.427 -29.901   0.000  0.00  0.00           O+0
HETATM   20  N   UNK     0      22.069 -24.619   0.000  0.00  0.00           N+0
HETATM   21  O   UNK     0      18.573 -27.035   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      13.238 -32.393   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      11.087 -32.052   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      16.604 -29.746   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      22.069 -26.159   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      20.736 -26.929   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      23.403 -26.929   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      23.403 -28.469   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      24.737 -29.239   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      24.737 -30.779   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      26.070 -31.549   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      27.477 -30.922   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      28.508 -32.067   0.000  0.00  0.00           C+0
HETATM   34  S   UNK     0      27.738 -33.400   0.000  0.00  0.00           S+0
HETATM   35  S   UNK     0      26.231 -33.080   0.000  0.00  0.00           S+0
CONECT    1    2    3    5                                                  
CONECT    2    1    4   11                                                  
CONECT    3    1    6    8                                                  
CONECT    4    2    9   12                                                  
CONECT    5    1   10                                                       
CONECT    6    3   11                                                       
CONECT    7   10    8                                                       
CONECT    8    3    7   18                                                  
CONECT    9    4   14   21                                                  
CONECT   10    5    7   20                                                  
CONECT   11    2    6                                                       
CONECT   12    4   13                                                       
CONECT   13   12   16   14                                                  
CONECT   14    9   13   24                                                  
CONECT   15   17   19   22   23                                             
CONECT   16   13   17                                                       
CONECT   17   15   16                                                       
CONECT   18    8                                                            
CONECT   19   15                                                            
CONECT   20   10   25                                                       
CONECT   21    9                                                            
CONECT   22   15                                                            
CONECT   23   15                                                            
CONECT   24   14                                                            
CONECT   25   20   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   35                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   31   34                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

Download
3D PDB for NP0339363 (Lipoyl-GMP)
Download
SMILES for NP0339363 (Lipoyl-GMP)
O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)N1C=NC2=C1N=C(NC(=O)CCCCC1CCSS1)NC2=O
Download
INCHI for NP0339363 (Lipoyl-GMP)
InChI=1S/C18H26N5O9PS2/c24-11(4-2-1-3-9-5-6-34-35-9)20-18-21-15-12(16(27)22-18)19-8-23(15)17-14(26)13(25)10(32-17)7-31-33(28,29)30/h8-10,13-14,17,25-26H,1-7H2,(H2,28,29,30)(H2,20,21,22,24,27)/t9?,10-,13-,14-,17-/m1/s1
Download
View in JSmol
SynonymsNot Available
Chemical FormulaC18H26N5O9PS2
Average Mass551.5310 Da
Monoisotopic Mass551.09096 Da
IUPAC Name{[(2R,3S,4R,5R)-5-{2-[5-(1,2-dithiolan-3-yl)pentanamido]-6-oxo-6,9-dihydro-1H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
Traditional Name[(2R,3S,4R,5R)-5-{2-[5-(1,2-dithiolan-3-yl)pentanamido]-6-oxo-1H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxyphosphonic acid
CAS Registry NumberNot Available
SMILES
O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)N1C=NC2=C1N=C(NC(=O)CCCCC1CCSS1)NC2=O
InChI Identifier
InChI=1S/C18H26N5O9PS2/c24-11(4-2-1-3-9-5-6-34-35-9)20-18-21-15-12(16(27)22-18)19-8-23(15)17-14(26)13(25)10(32-17)7-31-33(28,29)30/h8-10,13-14,17,25-26H,1-7H2,(H2,28,29,30)(H2,20,21,22,24,27)/t9?,10-,13-,14-,17-/m1/s1
InChI KeyDVZGUOFXTLKZTJ-LQLSJNDNSA-N
Experimental Spectra
Not Available
Predicted Spectra
Not Available
Chemical Shift Submissions
Not Available
Species
Species of OriginNot Available
Chemical Taxonomy
Description Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.
KingdomOrganic compounds  
Super ClassOrganic oxygen compounds  
ClassOrganooxygen compounds  
Sub ClassCarbonyl compounds  
Direct ParentAlkyl-phenylketones  
Alternative Parents
Substituents
  • Alkyl-phenylketone
    • 

  • Anilide
    • 

  • Benzoyl
    • 

  • Aryl alkyl ketone
    • 

  • N-arylamide
    • 

  • 1-hydroxy-2-unsubstituted benzenoid
    • 

  • Phenol
    • 

  • Monocyclic benzene moiety
    • 

  • Beta-aminoketone
    • 

  • Benzenoid
    • 

  • Vinylogous amide
    • 

  • Amino acid or derivatives
    • 

  • Carboxamide group
    • 

  • Secondary carboxylic acid amide
    • 

  • Carboxylic acid derivative
    • 

  • Organonitrogen compound
    • 

  • Primary aliphatic amine
    • 

  • Amine
    • 

  • Organic oxide
    • 

  • Organopnictogen compound
    • 

  • Organic nitrogen compound
    • 

  • Hydrocarbon derivative
    • 

  • Primary amine
    • 

  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External Descriptors
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
logP0.55ALOGPS
logP-0.86ChemAxon
logS-2.7ALOGPS
pKa (Strongest Acidic)1.29ChemAxon
pKa (Strongest Basic)0.36ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count10ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area204.83 ŲChemAxon
Rotatable Bond Count10ChemAxon
Refractivity126.67 m³·mol⁻¹ChemAxon
Polarizability52.23 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
HMDB IDHMDB0013617  
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDFDB029596  
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound53481910  
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General ReferencesNot Available