Np mrd loader

Showing NP-Card for PC(16:0/18:2(9Z,12Z)) (NP0334219)

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Record Information
Version2.0
Created at2024-09-09 22:41:47 UTC
Updated at2024-09-09 22:41:47 UTC
NP-MRD IDNP0334219
Secondary Accession NumbersNone
Natural Product Identification
Common NamePC(16:0/18:2(9Z,12Z))
DescriptionPC(16:0/18:2(9Z,12Z)) is a phosphatidylcholine (PC or GPCho). It is a glycerophospholipid in which a phosphorylcholine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphocholines can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PC(16:0/18:2(9Z,12Z)), in particular, consists of one chain of palmitic acid at the C-1 position and one chain of linoleic acid at the C-2 position. The palmitic acid moiety is derived from fish oils, milk fats, vegetable oils and animal fats, while the linoleic acid moiety is derived from seed oils. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling. While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PCs can be synthesized via three different routes. In one route, choline is activated first by phosphorylation and then by coupling to CDP prior to attachment to phosphatidic acid. PCs can also synthesized by the addition of choline to CDP-activated 1,2-diacylglycerol. A third route to PC synthesis involves the conversion of either PS or PE to PC. [HMDB]
Structure
Thumb
MOLSDFPDBSMILESInChI

MOL for NP0334219 (PC(16:0/18:2(9Z,12Z)))


  Mrv1652306022100152D          

 52 51  0  0  1  0            999 V2000
    6.0180   -4.6524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5582    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7773   -2.7813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2062   -1.9563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9042   -3.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0180   -3.8274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8438    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7325   -3.4149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1293    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7325   -2.5899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4148    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4470   -2.1774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7003    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4470   -1.3524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9859    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1614   -0.9399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2714    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1614   -0.1149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5569    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4470    0.2976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4470    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8425    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7325    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1280    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0180    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4135    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3035    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6990    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5891    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9846    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4457    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0792   -1.6543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2542   -1.6543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3023    0.2976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3023    1.1226    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8412    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7312    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8417   -0.9399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 52 49  1  0  0  0  0
 52 50  1  0  0  0  0
M  CHG  2  43   1  46  -1
M  END
Download

3D MOL for NP0334219 (PC(16:0/18:2(9Z,12Z)))

Download
3D SDF for NP0334219 (PC(16:0/18:2(9Z,12Z)))

  Mrv1652306022100152D          

 52 51  0  0  1  0            999 V2000
    6.0180   -4.6524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5582    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7773   -2.7813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2062   -1.9563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9042   -3.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0180   -3.8274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8438    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7325   -3.4149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1293    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7325   -2.5899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4148    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4470   -2.1774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7003    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4470   -1.3524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9859    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1614   -0.9399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2714    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1614   -0.1149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5569    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4470    0.2976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4470    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8425    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7325    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1280    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0180    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4135    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3035    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6990    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5891    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9846    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8746    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2701    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1601    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5556    1.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4457    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4122    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.4917   -2.3688    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
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    1.0167    1.5351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0167   -0.9399    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
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 22 19  1  0  0  0  0
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 34 41  1  0  0  0  0
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 36 37  1  0  0  0  0
 40 38  1  0  0  0  0
 40 39  1  0  0  0  0
 40 51  1  1  0  0  0
 43  3  1  0  0  0  0
 43  4  1  0  0  0  0
 43  5  1  0  0  0  0
 43 36  1  0  0  0  0
 44 41  2  0  0  0  0
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 49 37  1  0  0  0  0
 50 39  1  0  0  0  0
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 52 47  2  0  0  0  0
 52 49  1  0  0  0  0
 52 50  1  0  0  0  0
M  CHG  2  43   1  46  -1
M  END
> <DATABASE_ID>
NP0334219

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C\C\C=C\CCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C42H80NO8P/c1-6-8-10-12-14-16-18-20-21-23-25-27-29-31-33-35-42(45)51-40(39-50-52(46,47)49-37-36-43(3,4)5)38-48-41(44)34-32-30-28-26-24-22-19-17-15-13-11-9-7-2/h14,16,20-21,40H,6-13,15,17-19,22-39H2,1-5H3/b16-14+,21-20+/t40-/m1/s1

> <INCHI_KEY>
JLPULHDHAOZNQI-JLOPVYAASA-N

> <FORMULA>
C42H80NO8P

> <MOLECULAR_WEIGHT>
758.075

> <EXACT_MASS>
757.562155538

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
132

> <JCHEM_AVERAGE_POLARIZABILITY>
92.31988195107387

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-{[(2R)-3-(hexadecanoyloxy)-2-[(9E,12E)-octadeca-9,12-dienoyloxy]propyl phosphono]oxy}ethyl)trimethylazanium

> <ALOGPS_LOGP>
5.48

> <JCHEM_LOGP>
8.279090395861585

> <ALOGPS_LOGS>
-7.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064469137

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744159309169722

> <JCHEM_POLAR_SURFACE_AREA>
111.19000000000003

> <JCHEM_REFRACTIVITY>
227.30030000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
40

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.53e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2-{[(2R)-3-(hexadecanoyloxy)-2-[(9E,12E)-octadeca-9,12-dienoyloxy]propyl phosphono]oxy}ethyl)trimethylazanium

> <JCHEM_VEBER_RULE>
0

$$$$

Download
3D-SDF for NP0334219 (PC(16:0/18:2(9Z,12Z)))
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PDB for NP0334219 (PC(16:0/18:2(9Z,12Z)))
HEADER    PROTEIN                                 02-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-JUN-21         0                                  
HETATM    1  C   UNK     0      11.234  -8.684   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -23.442   2.096   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.184  -5.192   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.852  -3.652   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.288  -5.755   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.234  -7.144   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -22.108   2.866   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.567  -6.374   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -20.775   2.096   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.567  -4.834   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -19.441   2.866   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.901  -4.064   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -18.107   2.096   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.901  -2.524   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -16.774   2.866   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      15.235  -1.754   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -15.440   2.096   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      15.235  -0.214   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -14.106   2.866   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.901   0.556   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.901   2.096   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -12.773   2.096   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.567   2.866   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -11.439   2.866   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.234   2.096   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -10.105   2.096   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.900   2.866   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -8.771   2.866   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.566   2.096   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -7.438   2.096   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.233   2.866   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -6.104   2.866   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.899   2.096   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -4.770   2.096   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.565   2.866   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.748  -3.088   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.208  -3.088   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -0.769   2.866   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       0.564   0.556   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       0.564   2.096   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -3.437   2.866   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       3.232   2.096   0.000  0.00  0.00           C+0
HETATM   43  N   UNK     0       6.518  -4.422   0.000  0.00  0.00           N+1
HETATM   44  O   UNK     0      -3.437   4.406   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       3.232   0.556   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0       0.358  -1.754   0.000  0.00  0.00           O-1
HETATM   47  O   UNK     0       1.898  -3.294   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0      -2.103   2.096   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0       3.438  -1.754   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0       1.898  -0.214   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0       1.898   2.866   0.000  0.00  0.00           O+0
HETATM   52  P   UNK     0       1.898  -1.754   0.000  0.00  0.00           P+0
CONECT    1    6                                                            
CONECT    2    7                                                            
CONECT    3   43                                                            
CONECT    4   43                                                            
CONECT    5   43                                                            
CONECT    6    1    8                                                       
CONECT    7    2    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   11                                                       
CONECT   10    8   12                                                       
CONECT   11    9   13                                                       
CONECT   12   10   14                                                       
CONECT   13   11   15                                                       
CONECT   14   12   16                                                       
CONECT   15   13   17                                                       
CONECT   16   14   18                                                       
CONECT   17   15   19                                                       
CONECT   18   16   20                                                       
CONECT   19   17   22                                                       
CONECT   20   18   21                                                       
CONECT   21   20   23                                                       
CONECT   22   19   24                                                       
CONECT   23   21   25                                                       
CONECT   24   22   26                                                       
CONECT   25   23   27                                                       
CONECT   26   24   28                                                       
CONECT   27   25   29                                                       
CONECT   28   26   30                                                       
CONECT   29   27   31                                                       
CONECT   30   28   32                                                       
CONECT   31   29   33                                                       
CONECT   32   30   34                                                       
CONECT   33   31   35                                                       
CONECT   34   32   41                                                       
CONECT   35   33   42                                                       
CONECT   36   37   43                                                       
CONECT   37   36   49                                                       
CONECT   38   40   48                                                       
CONECT   39   40   50                                                       
CONECT   40   38   39   51                                                  
CONECT   41   34   44   48                                                  
CONECT   42   35   45   51                                                  
CONECT   43    3    4    5   36                                             
CONECT   44   41                                                            
CONECT   45   42                                                            
CONECT   46   52                                                            
CONECT   47   52                                                            
CONECT   48   38   41                                                       
CONECT   49   37   52                                                       
CONECT   50   39   52                                                       
CONECT   51   40   42                                                       
CONECT   52   46   47   49   50                                             
MASTER        0    0    0    0    0    0    0    0   52    0  102    0
END

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3D PDB for NP0334219 (PC(16:0/18:2(9Z,12Z)))
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SMILES for NP0334219 (PC(16:0/18:2(9Z,12Z)))
CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C\C\C=C\CCCCC
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INCHI for NP0334219 (PC(16:0/18:2(9Z,12Z)))
InChI=1S/C42H80NO8P/c1-6-8-10-12-14-16-18-20-21-23-25-27-29-31-33-35-42(45)51-40(39-50-52(46,47)49-37-36-43(3,4)5)38-48-41(44)34-32-30-28-26-24-22-19-17-15-13-11-9-7-2/h14,16,20-21,40H,6-13,15,17-19,22-39H2,1-5H3/b16-14+,21-20+/t40-/m1/s1
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View in JSmol
Synonyms
ValueSource
Glycerophospholipids, cholineMeSH
Choline, phosphatidylMeSH
PhosphatidylcholineMeSH
Choline glycerophospholipidsMeSH
Cholines, phosphatidylMeSH
Phosphatidyl cholineMeSH
PhosphatidylcholinesMeSH
Phosphatidyl cholinesMeSH
Choline phosphoglyceridesMeSH
Phosphoglycerides, cholineMeSH
Chemical FormulaC42H80NO8P
Average Mass758.0750 Da
Monoisotopic Mass757.56216 Da
IUPAC Name(2-{[(2R)-3-(hexadecanoyloxy)-2-[(9E,12E)-octadeca-9,12-dienoyloxy]propyl phosphono]oxy}ethyl)trimethylazanium
Traditional Name(2-{[(2R)-3-(hexadecanoyloxy)-2-[(9E,12E)-octadeca-9,12-dienoyloxy]propyl phosphono]oxy}ethyl)trimethylazanium
CAS Registry NumberNot Available
SMILES
CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C\C\C=C\CCCCC
InChI Identifier
InChI=1S/C42H80NO8P/c1-6-8-10-12-14-16-18-20-21-23-25-27-29-31-33-35-42(45)51-40(39-50-52(46,47)49-37-36-43(3,4)5)38-48-41(44)34-32-30-28-26-24-22-19-17-15-13-11-9-7-2/h14,16,20-21,40H,6-13,15,17-19,22-39H2,1-5H3/b16-14+,21-20+/t40-/m1/s1
InChI KeyJLPULHDHAOZNQI-JLOPVYAASA-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 phosphatidylcholines. These are glycerophosphocholines in which the two free -OH are attached to one fatty acid each through an ester linkage.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerophospholipids
Sub ClassGlycerophosphocholines
Direct ParentPhosphatidylcholines
Alternative ParentsNot Available
SubstituentsNot Available
Molecular FrameworkAliphatic acyclic 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
logP5.48ALOGPS
logP8.28ChemAxon
logS-7.5ALOGPS
pKa (Strongest Acidic)1.86ChemAxon
pKa (Strongest Basic)-6.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area111.19 ŲChemAxon
Rotatable Bond Count40ChemAxon
Refractivity227.3 m³·mol⁻¹ChemAxon
Polarizability92.32 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityNoChemAxon
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 ID17341551  
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 ReferencesNot Available