NP-MRD: Showing NP-Card for 13'-Carboxy-gamma-tocopherol (NP0339041)

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Record Information

Version

2.0

Created at

2024-09-11 19:24:18 UTC

Updated at

2024-09-11 19:24:18 UTC

NP-MRD ID

NP0339041

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13'-Carboxy-gamma-tocopherol

Description

13'-Carboxy-gamma-tocopherol belongs to the class of organic compounds known as tocopherols. These are vitamin E derivatives containing a saturated trimethyltridecyl chain attached to the carbon C6 atom of a benzopyran ring system. The differ from tocotrienols that contain an unsaturated trimethyltrideca-3,7,11-trien-1-yl chain. 13'-Carboxy-gamma-tocopherol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02251208062D          

 32 33  0  0  1  0            999 V2000
   10.1901  -10.3367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0151  -10.3367    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4276  -11.0512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0151  -11.7657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4276  -12.4802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0151  -13.1947    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.1901  -13.1947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4276  -13.9091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2526  -13.9091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6651  -14.6236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4901  -14.6236    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.0776  -15.3381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4901  -13.7986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2046  -13.3861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9191  -13.7986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6336  -13.3861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3480  -13.7986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0625  -13.3861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.3480  -14.6236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0625  -15.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6336  -15.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6336  -15.8611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9191  -14.6236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2046  -15.0361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4276   -9.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2526   -9.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6651   -8.9078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4901   -8.9078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9026   -9.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9026   -8.1933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7276   -8.1933    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4901   -7.4788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  2 25  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 11 24  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
 15 23  2  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
M  END


  Mrv0541 02251208062D          

 32 33  0  0  1  0            999 V2000
   10.1901  -10.3367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0151  -10.3367    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4276  -11.0512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0151  -11.7657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4276  -12.4802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0151  -13.1947    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.1901  -13.1947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4276  -13.9091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2526  -13.9091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6651  -14.6236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4901  -14.6236    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.0776  -15.3381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4901  -13.7986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2046  -13.3861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9191  -13.7986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6336  -13.3861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3480  -13.7986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0625  -13.3861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.3480  -14.6236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0625  -15.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6336  -15.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6336  -15.8611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9191  -14.6236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2046  -15.0361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4276   -9.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2526   -9.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6651   -8.9078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4901   -8.9078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9026   -9.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9026   -8.1933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7276   -8.1933    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4901   -7.4788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  2 25  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 11 24  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
 15 23  2  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0339041

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CCC[C@H](C)CCC[C@]1(C)CCC2=C(O1)C(C)=C(C)C(O)=C2)CCCC(C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H46O4/c1-19(12-8-14-21(3)27(30)31)10-7-11-20(2)13-9-16-28(6)17-15-24-18-25(29)22(4)23(5)26(24)32-28/h18-21,29H,7-17H2,1-6H3,(H,30,31)/t19-,20+,21?,28-/m1/s1

> <INCHI_KEY>
WPZHQZIUOXUCOK-PXUFRVCMSA-N

> <FORMULA>
C28H46O4

> <MOLECULAR_WEIGHT>
446.6624

> <EXACT_MASS>
446.33960996

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
54.97236489408404

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(6R,10S)-13-[(2R)-6-hydroxy-2,7,8-trimethyl-3,4-dihydro-2H-1-benzopyran-2-yl]-2,6,10-trimethyltridecanoic acid

> <ALOGPS_LOGP>
7.21

> <JCHEM_LOGP>
8.930021287666667

> <ALOGPS_LOGS>
-6.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
10.470461963888265

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.999792396057005

> <JCHEM_PKA_STRONGEST_BASIC>
-4.852416276885971

> <JCHEM_POLAR_SURFACE_AREA>
66.75999999999999

> <JCHEM_REFRACTIVITY>
132.0242

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.06e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6R,10S)-13-[(2R)-6-hydroxy-2,7,8-trimethyl-3,4-dihydro-1-benzopyran-2-yl]-2,6,10-trimethyltridecanoic acid

> <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                                  
HETATM    1  C   UNK     0      19.022 -19.295   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      20.562 -19.295   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      21.332 -20.629   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      20.562 -21.963   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      21.332 -23.296   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      20.562 -24.630   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      19.022 -24.630   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.332 -25.964   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      22.872 -25.964   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      23.642 -27.297   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      25.182 -27.297   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      24.412 -28.631   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      25.182 -25.757   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      26.515 -24.987   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      27.849 -25.757   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      29.183 -24.987   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      30.516 -25.757   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      31.850 -24.987   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      30.516 -27.297   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      31.850 -28.067   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      29.183 -28.067   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      29.183 -29.607   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      27.849 -27.297   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      26.515 -28.067   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      21.332 -17.962   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      22.872 -17.962   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      23.642 -16.628   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      25.182 -16.628   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      25.952 -17.962   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      25.952 -15.294   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      27.492 -15.294   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      25.182 -13.960   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   24                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   15   21   24                                                  
CONECT   24   11   23                                                       
CONECT   25    2   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

View in JSmol

Synonyms

Value	Source
13'-Carboxy-g-tocopherol	Generator
13'-Carboxy-γ-tocopherol	Generator
(6R,10S)-13-[(2R)-6-Hydroxy-2,7,8-trimethyl-3,4-dihydro-2H-1-benzopyran-2-yl]-2,6,10-trimethyltridecanoate	Generator

Chemical Formula

C₂₈H₄₆O₄

Average Mass

446.6624 Da

Monoisotopic Mass

446.33961 Da

IUPAC Name

(6R,10S)-13-[(2R)-6-hydroxy-2,7,8-trimethyl-3,4-dihydro-2H-1-benzopyran-2-yl]-2,6,10-trimethyltridecanoic acid

Traditional Name

(6R,10S)-13-[(2R)-6-hydroxy-2,7,8-trimethyl-3,4-dihydro-1-benzopyran-2-yl]-2,6,10-trimethyltridecanoic acid

CAS Registry Number

Not Available

SMILES

C[C@H](CCC[C@H](C)CCC[C@]1(C)CCC2=C(O1)C(C)=C(C)C(O)=C2)CCCC(C)C(O)=O

InChI Identifier

InChI=1S/C28H46O4/c1-19(12-8-14-21(3)27(30)31)10-7-11-20(2)13-9-16-28(6)17-15-24-18-25(29)22(4)23(5)26(24)32-28/h18-21,29H,7-17H2,1-6H3,(H,30,31)/t19-,20+,21?,28-/m1/s1

InChI Key

WPZHQZIUOXUCOK-PXUFRVCMSA-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 tocopherols. These are vitamin E derivatives containing a saturated trimethyltridecyl chain attached to the carbon C6 atom of a benzopyran ring system. The differ from tocotrienols that contain an unsaturated trimethyltrideca-3,7,11-trien-1-yl chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Quinone and hydroquinone lipids

Direct Parent

Tocopherols

Alternative Parents

Substituents

Tocopherol
Diterpenoid
Long-chain fatty acid
Chromane
Benzopyran
1-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Branched fatty acid
Methyl-branched fatty acid
Heterocyclic fatty acid
Hydroxy fatty acid
Fatty acyl
Fatty acid
Benzenoid
Oxacycle
Carboxylic acid derivative
Carboxylic acid
Organoheterocyclic compound
Ether
Monocarboxylic acid or derivatives
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	7.21	ALOGPS
logP	8.93	ChemAxon
logS	-6.9	ALOGPS
pKa (Strongest Acidic)	5	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	132.02 m³·mol⁻¹	ChemAxon
Polarizability	54.97 Å³	ChemAxon
Number of Rings	2	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

HMDB0012557

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB029123

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

53481463

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 13'-Carboxy-gamma-tocopherol (NP0339041)

MOL for NP0339041 (13'-Carboxy-gamma-tocopherol)

3D MOL for NP0339041 (13'-Carboxy-gamma-tocopherol)

3D SDF for NP0339041 (13'-Carboxy-gamma-tocopherol)

3D-SDF for NP0339041 (13'-Carboxy-gamma-tocopherol)

PDB for NP0339041 (13'-Carboxy-gamma-tocopherol)

3D PDB for NP0339041 (13'-Carboxy-gamma-tocopherol)

SMILES for NP0339041 (13'-Carboxy-gamma-tocopherol)

INCHI for NP0339041 (13'-Carboxy-gamma-tocopherol)

Structure for NP0339041 (13'-Carboxy-gamma-tocopherol)

3D Structure for NP0339041 (13'-Carboxy-gamma-tocopherol)