NP-MRD: Showing NP-Card for TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6] (NP0338925)

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Record Information

Version

2.0

Created at

2024-09-11 18:45:44 UTC

Updated at

2024-09-11 18:45:45 UTC

NP-MRD ID

NP0338925

Secondary Accession Numbers

None

Natural Product Identification

Common Name

TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6]

Description

TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6] belongs to the class of organic compounds known as triacylglycerols. These are glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages. TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6] is an extremely weak basic (essentially neutral) compound (based on its pKa). TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6] can be biosynthesized from DG(18:1(11Z)/16:0/0:0) And arachidonyl-CoA; which is catalyzed by the enzyme diacylglycerol O-acyltransferase. In humans, TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6] is involved in the metabolic disorder called de novo triacylglycerol biosynthesis pathway.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02251205412D          

 64 63  0  0  1  0            999 V2000
    6.9552  -15.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250  -15.7184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2472  -15.6505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7170  -16.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5392  -16.2609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0091  -16.9390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8313  -16.8712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3011  -17.5494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1233  -17.4815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5932  -18.1597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4154  -18.0919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8852  -18.7700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7074  -18.7022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1772  -19.3803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   16.4693  -19.9907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   17.2915  -19.9229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   18.1137  -19.8550    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
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 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
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 61 62  1  0  0  0  0
 62 63  1  0  0  0  0
 19 64  1  1  0  0  0
M  END


  Mrv0541 02251205412D          

 64 63  0  0  1  0            999 V2000
    6.9552  -15.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 62 63  1  0  0  0  0
 19 64  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0338925

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@](COC(=O)CCCCCCCCCC=CCCCCCC)(COC(=O)CCCC=CCC=CCC=CCC=CCCCCC)OC(=O)CCCCCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C57H100O6/c1-4-7-10-13-16-19-22-25-27-28-30-33-35-38-41-44-47-50-56(59)62-53-54(63-57(60)51-48-45-42-39-36-31-24-21-18-15-12-9-6-3)52-61-55(58)49-46-43-40-37-34-32-29-26-23-20-17-14-11-8-5-2/h16,19-20,23,25,27,30,33,38,41,54H,4-15,17-18,21-22,24,26,28-29,31-32,34-37,39-40,42-53H2,1-3H3/t54-/m1/s1

> <INCHI_KEY>
MZKZFZRBZNYKEI-AXAMJWTMSA-N

> <FORMULA>
C57H100O6

> <MOLECULAR_WEIGHT>
881.4003

> <EXACT_MASS>
880.751990932

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
116.01172464329113

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-2-(hexadecanoyloxy)-3-(octadec-11-enoyloxy)propyl icosa-5,8,11,14-tetraenoate

> <ALOGPS_LOGP>
10.81

> <JCHEM_LOGP>
19.781951391

> <ALOGPS_LOGS>
-8.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.56590758366778

> <JCHEM_POLAR_SURFACE_AREA>
78.9

> <JCHEM_REFRACTIVITY>
274.4793

> <JCHEM_ROTATABLE_BOND_COUNT>
51

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.00e-06 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-(hexadecanoyloxy)-3-(octadec-11-enoyloxy)propyl icosa-5,8,11,14-tetraenoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-FEB-12         0                                  
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HETATM    4  C   UNK     0      16.272 -30.480   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.807 -30.354   0.000  0.00  0.00           C+0
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HETATM   11  C   UNK     0      25.042 -33.772   0.000  0.00  0.00           C+0
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HETATM   14  C   UNK     0      28.331 -36.177   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      29.866 -36.050   0.000  0.00  0.00           C+0
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HETATM   17  O   UNK     0      30.085 -38.708   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      32.277 -37.189   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      33.154 -38.455   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      34.689 -38.329   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      35.347 -36.936   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      36.882 -36.810   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      37.759 -38.076   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      37.540 -35.417   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      39.074 -35.290   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      39.732 -33.898   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      41.267 -33.772   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      41.925 -32.379   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      43.460 -32.252   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      44.117 -30.860   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      45.652 -30.733   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      46.310 -29.341   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      47.845 -29.214   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      48.722 -30.480   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      50.256 -30.354   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      51.133 -31.619   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      52.668 -31.493   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      53.545 -32.759   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      55.080 -32.632   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      55.957 -33.898   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      32.497 -39.848   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      30.962 -39.974   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      30.304 -41.367   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      31.181 -42.633   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      28.769 -41.493   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      28.112 -42.886   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      26.577 -43.012   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      25.919 -44.405   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      24.384 -44.531   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      23.726 -45.924   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      24.604 -47.190   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      23.946 -48.582   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      24.823 -49.848   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      24.165 -51.241   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      22.630 -51.367   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      21.973 -52.760   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      22.849 -54.025   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      22.192 -55.418   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      23.069 -56.684   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      22.411 -58.076   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0      23.288 -59.342   0.000  0.00  0.00           C+0
HETATM   62  C   UNK     0      22.630 -60.735   0.000  0.00  0.00           C+0
HETATM   63  C   UNK     0      23.507 -62.000   0.000  0.00  0.00           C+0
HETATM   64  H   UNK     0      33.812 -37.063   0.000  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   41   64                                             
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39                                                            
CONECT   41   19   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   56                                                       
CONECT   56   55   57                                                       
CONECT   57   56   58                                                       
CONECT   58   57   59                                                       
CONECT   59   58   60                                                       
CONECT   60   59   61                                                       
CONECT   61   60   62                                                       
CONECT   62   61   63                                                       
CONECT   63   62                                                            
CONECT   64   19                                                            
MASTER        0    0    0    0    0    0    0    0   64    0  126    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₅₇H₁₀₀O₆

Average Mass

881.4003 Da

Monoisotopic Mass

880.75199 Da

IUPAC Name

(2R)-2-(hexadecanoyloxy)-3-(octadec-11-enoyloxy)propyl icosa-5,8,11,14-tetraenoate

Traditional Name

(2R)-2-(hexadecanoyloxy)-3-(octadec-11-enoyloxy)propyl icosa-5,8,11,14-tetraenoate

CAS Registry Number

Not Available

SMILES

[H][C@@](COC(=O)CCCCCCCCCC=CCCCCCC)(COC(=O)CCCC=CCC=CCC=CCC=CCCCCC)OC(=O)CCCCCCCCCCCCCCC

InChI Identifier

InChI=1S/C57H100O6/c1-4-7-10-13-16-19-22-25-27-28-30-33-35-38-41-44-47-50-56(59)62-53-54(63-57(60)51-48-45-42-39-36-31-24-21-18-15-12-9-6-3)52-61-55(58)49-46-43-40-37-34-32-29-26-23-20-17-14-11-8-5-2/h16,19-20,23,25,27,30,33,38,41,54H,4-15,17-18,21-22,24,26,28-29,31-32,34-37,39-40,42-53H2,1-3H3/t54-/m1/s1

InChI Key

MZKZFZRBZNYKEI-AXAMJWTMSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triacylglycerols. These are glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerolipids

Sub Class

Triradylcglycerols

Direct Parent

Triacylglycerols

Alternative Parents

Substituents

Triacyl-sn-glycerol
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	10.81	ALOGPS
logP	19.78	ChemAxon
logS	-8.2	ALOGPS
pKa (Strongest Basic)	-6.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	78.9 Å²	ChemAxon
Rotatable Bond Count	51	ChemAxon
Refractivity	274.48 m³·mol⁻¹	ChemAxon
Polarizability	116.01 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB027592

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6] (NP0338925)

MOL for NP0338925 (TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6])

3D MOL for NP0338925 (TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6])

3D SDF for NP0338925 (TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6])

3D-SDF for NP0338925 (TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6])

PDB for NP0338925 (TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6])

3D PDB for NP0338925 (TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6])

SMILES for NP0338925 (TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6])

INCHI for NP0338925 (TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6])

Structure for NP0338925 (TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6])

3D Structure for NP0338925 (TG(18:1(11Z)/16:0/20:4(5Z,8Z,11Z,14Z))[iso6])