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Details

Stereochemistry ABSOLUTE
Molecular Formula C42H32N6O12
Molecular Weight 812.7365
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SORBINICATE

SMILES

O=C(OC[C@@H](OC(=O)C1=CN=CC=C1)[C@@H](OC(=O)C2=CN=CC=C2)[C@H](OC(=O)C3=CN=CC=C3)[C@H](COC(=O)C4=CN=CC=C4)OC(=O)C5=CN=CC=C5)C6=CN=CC=C6

InChI

InChIKey=IMRLNFKFNFLWQF-IYKITFJXSA-N
InChI=1S/C42H32N6O12/c49-37(27-7-1-13-43-19-27)55-25-33(57-39(51)29-9-3-15-45-21-29)35(59-41(53)31-11-5-17-47-23-31)36(60-42(54)32-12-6-18-48-24-32)34(58-40(52)30-10-4-16-46-22-30)26-56-38(50)28-8-2-14-44-20-28/h1-24,33-36H,25-26H2/t33-,34+,35-,36-/m1/s1

HIDE SMILES / InChI

Molecular Formula C42H32N6O12
Molecular Weight 812.7365
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

D-glucitol hexanicotinate (sorbinicate, SN) is a derivative of nicotinic acid. In rabbits kept on a diet containing 1 g/day cholesterol for 12 weeks, sorbinicate displayed greater hypolipemic and antiatherogenic activity than an equidose of plain nicotinic acid at much lower and more constant plasma nicotinic acid levels. By modulating the bioavailability of nicotinic acid, sorbinicate maintains and in some cases enhances the pharmacological activity of the acid, avoiding at least some of its major side effects. Sorbinicate has effective lipid-lowering activity; the combination of hypolipidemic and anti-aggregating properties may prove important in primary and secondary prevention of atherosclerotic disease. It is suggested that the antilipolytic activity of sorbinicate is at least partly mediated by an inhibition of glucagon secretion (and/or synthesis).

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparative evaluation of some pharmacological properties and side effects of D-glucitol hexanicotinate (sorbinicate) and nicotinic acid correlated with the plasma concentration of nicotinic acid.
1980 May
Possible glucagon-mediated hypocholesterolemic activity of a nicotinic acid derivative (sorbinicate).
1983
Effect of D-glucitol-hexanicotinate on platelet aggregability in patients with coronary heart disease.
1984 May
Patents

Sample Use Guides

D-glucitol-hexanicotinate (sorbinicate) was administered at a daily dose of 1.6 mg to 16 male patients who had survived myocardial infarction.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:55:09 GMT 2023
Edited
by admin
on Sat Dec 16 17:55:09 GMT 2023
Record UNII
38Y76163XT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SORBINICATE
INN   WHO-DD  
INN  
Official Name English
D-GLUCITOL, 1,2,3,4,5,6-HEXA-3-PYRIDINECARBOXYLATE
Common Name English
sorbinicate [INN]
Common Name English
Sorbinicate [WHO-DD]
Common Name English
NICOTINIC ACID, HEXAESTER WITH D-GLUCITOL
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29703
Created by admin on Sat Dec 16 17:55:09 GMT 2023 , Edited by admin on Sat Dec 16 17:55:09 GMT 2023
Code System Code Type Description
INN
3807
Created by admin on Sat Dec 16 17:55:09 GMT 2023 , Edited by admin on Sat Dec 16 17:55:09 GMT 2023
PRIMARY
FDA UNII
38Y76163XT
Created by admin on Sat Dec 16 17:55:09 GMT 2023 , Edited by admin on Sat Dec 16 17:55:09 GMT 2023
PRIMARY
NCI_THESAURUS
C152406
Created by admin on Sat Dec 16 17:55:09 GMT 2023 , Edited by admin on Sat Dec 16 17:55:09 GMT 2023
PRIMARY
ChEMBL
CHEMBL2103972
Created by admin on Sat Dec 16 17:55:09 GMT 2023 , Edited by admin on Sat Dec 16 17:55:09 GMT 2023
PRIMARY
PUBCHEM
3058386
Created by admin on Sat Dec 16 17:55:09 GMT 2023 , Edited by admin on Sat Dec 16 17:55:09 GMT 2023
PRIMARY
SMS_ID
100000083771
Created by admin on Sat Dec 16 17:55:09 GMT 2023 , Edited by admin on Sat Dec 16 17:55:09 GMT 2023
PRIMARY
EVMPD
SUB10595MIG
Created by admin on Sat Dec 16 17:55:09 GMT 2023 , Edited by admin on Sat Dec 16 17:55:09 GMT 2023
PRIMARY
MESH
C015238
Created by admin on Sat Dec 16 17:55:09 GMT 2023 , Edited by admin on Sat Dec 16 17:55:09 GMT 2023
PRIMARY
CAS
6184-06-1
Created by admin on Sat Dec 16 17:55:09 GMT 2023 , Edited by admin on Sat Dec 16 17:55:09 GMT 2023
PRIMARY
DRUG CENTRAL
2460
Created by admin on Sat Dec 16 17:55:09 GMT 2023 , Edited by admin on Sat Dec 16 17:55:09 GMT 2023
PRIMARY