Np mrd loader

Showing NP-Card for 5-hydroxy-feruloyl-CoA (NP0339858)

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Record Information
Version2.0
Created at2024-09-11 23:53:48 UTC
Updated at2024-09-11 23:53:49 UTC
NP-MRD IDNP0339858
Secondary Accession NumbersNone
Natural Product Identification
Common Name5-hydroxy-feruloyl-CoA
Description5-Hydroxy-feruloyl-CoA belongs to the class of organic compounds known as 2-enoyl coas. These are organic compounds containing a coenzyme A substructure linked to a 2-enoyl chain. Based on a literature review very few articles have been published on 5-hydroxy-feruloyl-CoA.
Structure
Thumb
MOLSDFPDBSMILESInChI

MOL for NP0339858 (5-hydroxy-feruloyl-CoA)


  Mrv2104 05272302262D          

 62 65  0  0  0  0            999 V2000
    6.0846   -6.9384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6721   -7.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2596   -8.3673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3866   -8.0654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3866   -8.8904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1010   -7.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1010   -6.8279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8155   -8.0654    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5300   -7.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2444   -8.0654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9589   -7.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9589   -6.8279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6734   -8.0654    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.3879   -7.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1023   -8.0654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8168   -7.6529    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   13.5313   -8.0654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5313   -8.8904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2457   -7.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2457   -6.8279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9602   -6.4154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9602   -5.5904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   16.3892   -3.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   16.3892   -6.4154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1036   -6.8279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  4  5  1  0  0  0  0
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  8  9  1  0  0  0  0
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 11 13  1  0  0  0  0
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M  CHG  4  44  -1  46  -1  61  -1  62  -1
M  END
Download

3D MOL for NP0339858 (5-hydroxy-feruloyl-CoA)

Download
3D SDF for NP0339858 (5-hydroxy-feruloyl-CoA)

  Mrv2104 05272302262D          

 62 65  0  0  0  0            999 V2000
    6.0846   -6.9384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6721   -7.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.9589   -7.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9589   -6.8279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   17.1036   -6.8279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 36 61  1  0  0  0  0
 33 62  1  0  0  0  0
M  CHG  4  44  -1  46  -1  61  -1  62  -1
M  END
> <DATABASE_ID>
NP0339858

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(C=CC(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP([O-])(=O)OP([O-])(=O)OCC2OC(C(O)C2OP([O-])([O-])=O)N2C=NC3=C2N=CN=C3N)=CC(O)=C1O

> <INCHI_IDENTIFIER>
InChI=1/C31H44N7O20P3S/c1-31(2,26(44)29(45)34-7-6-20(40)33-8-9-62-21(41)5-4-16-10-17(39)23(42)18(11-16)53-3)13-55-61(51,52)58-60(49,50)54-12-19-25(57-59(46,47)48)24(43)30(56-19)38-15-37-22-27(32)35-14-36-28(22)38/h4-5,10-11,14-15,19,24-26,30,39,42-44H,6-9,12-13H2,1-3H3,(H,33,40)(H,34,45)(H,49,50)(H,51,52)(H2,32,35,36)(H2,46,47,48)/p-4

> <INCHI_KEY>
ILSPFIPSQSFPCN-UHFFFAOYNA-J

> <FORMULA>
C31H40N7O20P3S

> <MOLECULAR_WEIGHT>
955.67

> <EXACT_MASS>
955.128363204

> <JCHEM_ACCEPTOR_COUNT>
20

> <JCHEM_ATOM_COUNT>
102

> <JCHEM_AVERAGE_POLARIZABILITY>
87.36827607485824

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
-4

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonatooxy)oxolan-2-yl]methyl {[3-({2-[(2-{[3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enoyl]sulfanyl}ethyl)carbamoyl]ethyl}carbamoyl)-3-hydroxy-2,2-dimethylpropyl phosphonato]oxy}phosphonate

> <JCHEM_LOGP>
-4.237293856116266

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-4

> <JCHEM_PKA>
0.9212904674755011

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.8204626040093734

> <JCHEM_PKA_STRONGEST_BASIC>
4.887025224816595

> <JCHEM_POLAR_SURFACE_AREA>
424.63999999999993

> <JCHEM_REFRACTIVITY>
208.56240000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
23

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[5-(6-aminopurin-9-yl)-4-hydroxy-3-(phosphonatooxy)oxolan-2-yl]methyl [3-({2-[(2-{[3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enoyl]sulfanyl}ethyl)carbamoyl]ethyl}carbamoyl)-3-hydroxy-2,2-dimethylpropyl phosphonato]oxyphosphonate

> <JCHEM_VEBER_RULE>
0

$$$$

Download
3D-SDF for NP0339858 (5-hydroxy-feruloyl-CoA)
Download
PDB for NP0339858 (5-hydroxy-feruloyl-CoA)
HEADER    PROTEIN                                 27-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-MAY-23         0                                  
HETATM    1  C   UNK     0      11.358 -12.952   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.588 -14.285   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.818 -15.619   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.922 -15.055   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      11.922 -16.595   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      13.255 -14.285   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      13.255 -12.745   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0      14.589 -15.055   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      15.923 -14.285   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.256 -15.055   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      18.590 -14.285   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      18.590 -12.745   0.000  0.00  0.00           O+0
HETATM   13  N   UNK     0      19.924 -15.055   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      21.257 -14.285   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      22.591 -15.055   0.000  0.00  0.00           C+0
HETATM   16  S   UNK     0      23.925 -14.285   0.000  0.00  0.00           S+0
HETATM   17  C   UNK     0      25.258 -15.055   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      25.258 -16.595   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      26.592 -14.285   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      26.592 -12.745   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      27.926 -11.975   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      27.926 -10.435   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      29.259  -9.665   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      29.259  -8.125   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      30.593  -7.355   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      30.593 -10.435   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      31.927  -9.665   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      30.593 -11.975   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      31.927 -12.745   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      29.259 -12.745   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.254 -13.515   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       7.921 -14.285   0.000  0.00  0.00           O+0
HETATM   33  P   UNK     0       6.587 -13.515   0.000  0.00  0.00           P+0
HETATM   34  O   UNK     0       7.357 -12.182   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       5.253 -12.745   0.000  0.00  0.00           O+0
HETATM   36  P   UNK     0       3.920 -13.515   0.000  0.00  0.00           P+0
HETATM   37  O   UNK     0       3.150 -12.182   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       2.586 -14.285   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       1.252 -13.515   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -0.082 -14.285   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -0.242 -15.817   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       0.902 -16.847   0.000  0.00  0.00           O+0
HETATM   43  P   UNK     0       0.582 -18.354   0.000  0.00  0.00           P+0
HETATM   44  O   UNK     0      -0.925 -18.034   0.000  0.00  0.00           O-1
HETATM   45  O   UNK     0       2.088 -18.674   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0       0.262 -19.860   0.000  0.00  0.00           O-1
HETATM   47  C   UNK     0      -1.749 -16.137   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -2.375 -17.544   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -2.519 -14.803   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      -1.488 -13.659   0.000  0.00  0.00           O+0
HETATM   51  N   UNK     0      -4.050 -14.642   0.000  0.00  0.00           N+0
HETATM   52  C   UNK     0      -4.820 -13.309   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      -6.327 -13.629   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      -7.357 -12.485   0.000  0.00  0.00           C+0
HETATM   55  N   UNK     0      -8.864 -12.805   0.000  0.00  0.00           N+0
HETATM   56  N   UNK     0      -6.881 -11.020   0.000  0.00  0.00           N+0
HETATM   57  C   UNK     0      -5.375 -10.700   0.000  0.00  0.00           C+0
HETATM   58  N   UNK     0      -4.345 -11.844   0.000  0.00  0.00           N+0
HETATM   59  N   UNK     0      -6.488 -15.161   0.000  0.00  0.00           N+0
HETATM   60  C   UNK     0      -5.081 -15.787   0.000  0.00  0.00           C+0
HETATM   61  O   UNK     0       4.690 -14.849   0.000  0.00  0.00           O-1
HETATM   62  O   UNK     0       5.817 -14.849   0.000  0.00  0.00           O-1
CONECT    1    2                                                            
CONECT    2    1    3    4   31                                             
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   30                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   21                                                       
CONECT   31    2   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35   62                                             
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37   38   61                                             
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   50                                                  
CONECT   41   40   42   47                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   45   46                                             
CONECT   44   43                                                            
CONECT   45   43                                                            
CONECT   46   43                                                            
CONECT   47   41   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   50   51                                                  
CONECT   50   49   40                                                       
CONECT   51   49   52   60                                                  
CONECT   52   51   53   58                                                  
CONECT   53   52   54   59                                                  
CONECT   54   53   55   56                                                  
CONECT   55   54                                                            
CONECT   56   54   57                                                       
CONECT   57   56   58                                                       
CONECT   58   57   52                                                       
CONECT   59   53   60                                                       
CONECT   60   59   51                                                       
CONECT   61   36                                                            
CONECT   62   33                                                            
MASTER        0    0    0    0    0    0    0    0   62    0  130    0
END

Download
3D PDB for NP0339858 (5-hydroxy-feruloyl-CoA)
Download
SMILES for NP0339858 (5-hydroxy-feruloyl-CoA)
COC1=CC(C=CC(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP([O-])(=O)OP([O-])(=O)OCC2OC(C(O)C2OP([O-])([O-])=O)N2C=NC3=C2N=CN=C3N)=CC(O)=C1O
Download
INCHI for NP0339858 (5-hydroxy-feruloyl-CoA)
InChI=1/C31H44N7O20P3S/c1-31(2,26(44)29(45)34-7-6-20(40)33-8-9-62-21(41)5-4-16-10-17(39)23(42)18(11-16)53-3)13-55-61(51,52)58-60(49,50)54-12-19-25(57-59(46,47)48)24(43)30(56-19)38-15-37-22-27(32)35-14-36-28(22)38/h4-5,10-11,14-15,19,24-26,30,39,42-44H,6-9,12-13H2,1-3H3,(H,33,40)(H,34,45)(H,49,50)(H,51,52)(H2,32,35,36)(H2,46,47,48)/p-4
Download
View in JSmol
SynonymsNot Available
Chemical FormulaC31H40N7O20P3S
Average Mass955.6700 Da
Monoisotopic Mass955.12836 Da
IUPAC Name[5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonatooxy)oxolan-2-yl]methyl {[3-({2-[(2-{[3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enoyl]sulfanyl}ethyl)carbamoyl]ethyl}carbamoyl)-3-hydroxy-2,2-dimethylpropyl phosphonato]oxy}phosphonate
Traditional Name[5-(6-aminopurin-9-yl)-4-hydroxy-3-(phosphonatooxy)oxolan-2-yl]methyl [3-({2-[(2-{[3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enoyl]sulfanyl}ethyl)carbamoyl]ethyl}carbamoyl)-3-hydroxy-2,2-dimethylpropyl phosphonato]oxyphosphonate
CAS Registry NumberNot Available
SMILES
COC1=CC(C=CC(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP([O-])(=O)OP([O-])(=O)OCC2OC(C(O)C2OP([O-])([O-])=O)N2C=NC3=C2N=CN=C3N)=CC(O)=C1O
InChI Identifier
InChI=1/C31H44N7O20P3S/c1-31(2,26(44)29(45)34-7-6-20(40)33-8-9-62-21(41)5-4-16-10-17(39)23(42)18(11-16)53-3)13-55-61(51,52)58-60(49,50)54-12-19-25(57-59(46,47)48)24(43)30(56-19)38-15-37-22-27(32)35-14-36-28(22)38/h4-5,10-11,14-15,19,24-26,30,39,42-44H,6-9,12-13H2,1-3H3,(H,33,40)(H,34,45)(H,49,50)(H,51,52)(H2,32,35,36)(H2,46,47,48)/p-4
InChI KeyILSPFIPSQSFPCN-UHFFFAOYNA-J
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 2-enoyl coas. These are organic compounds containing a coenzyme A substructure linked to a 2-enoyl chain.
KingdomOrganic compounds  
Super ClassLipids and lipid-like molecules  
ClassFatty Acyls  
Sub ClassFatty acyl thioesters  
Direct Parent2-enoyl CoAs  
Alternative Parents
Substituents
  • Coenzyme a or derivatives
    • 

  • Purine ribonucleoside diphosphate
    • 

  • Purine ribonucleoside bisphosphate
    • 

  • Purine ribonucleoside 3',5'-bisphosphate
    • 

  • Pentose-5-phosphate
    • 

  • Pentose phosphate
    • 

  • Ribonucleoside 3'-phosphate
    • 

  • Hydroxycinnamic acid or derivatives
    • 

  • Cinnamic acid or derivatives
    • 

  • N-glycosyl compound
    • 

  • Glycosyl compound
    • 

  • Beta amino acid or derivatives
    • 

  • 6-aminopurine
    • 

  • Methoxyphenol
    • 

  • Monosaccharide phosphate
    • 

  • Organic pyrophosphate
    • 

  • Purine
    • 

  • Imidazopyrimidine
    • 

  • Methoxybenzene
    • 

  • Catechol
    • 

  • Phenoxy compound
    • 

  • Anisole
    • 

  • Phenol ether
    • 

  • Styrene
    • 

  • Phenol
    • 

  • 1-hydroxy-4-unsubstituted benzenoid
    • 

  • 1-hydroxy-2-unsubstituted benzenoid
    • 

  • Alkyl aryl ether
    • 

  • Aminopyrimidine
    • 

  • Monocyclic benzene moiety
    • 

  • Fatty amide
    • 

  • Imidolactam
    • 

  • Benzenoid
    • 

  • Alkyl phosphate
    • 

  • Monosaccharide
    • 

  • N-acyl-amine
    • 

  • N-substituted imidazole
    • 

  • Organic phosphoric acid derivative
    • 

  • Phosphoric acid ester
    • 

  • Pyrimidine
    • 

  • Tetrahydrofuran
    • 

  • Azole
    • 

  • Heteroaromatic compound
    • 

  • Imidazole
    • 

  • Secondary alcohol
    • 

  • Secondary carboxylic acid amide
    • 

  • Thiocarboxylic acid ester
    • 

  • Carboxamide group
    • 

  • Carbothioic s-ester
    • 

  • Amino acid or derivatives
    • 

  • Sulfenyl compound
    • 

  • Organoheterocyclic compound
    • 

  • Thiocarboxylic acid or derivatives
    • 

  • Ether
    • 

  • Azacycle
    • 

  • Oxacycle
    • 

  • Carboxylic acid derivative
    • 

  • Organopnictogen compound
    • 

  • Organic oxygen compound
    • 

  • Organic nitrogen compound
    • 

  • Carbonyl group
    • 

  • Organonitrogen compound
    • 

  • Organooxygen compound
    • 

  • Organosulfur compound
    • 

  • Primary amine
    • 

  • Alcohol
    • 

  • Hydrocarbon derivative
    • 

  • Organic oxide
    • 

  • Amine
    • 

  • Organic anion
    • 

  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic 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
logP-4.2ChemAxon
pKa (Strongest Acidic)0.82ChemAxon
pKa (Strongest Basic)4.89ChemAxon
Physiological Charge-4ChemAxon
Hydrogen Acceptor Count20ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area424.64 ŲChemAxon
Rotatable Bond Count23ChemAxon
Refractivity208.56 m³·mol⁻¹ChemAxon
Polarizability87.37 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
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