U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C30H24N4O10
Molecular Weight 600.5324
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NICOFURANOSE

SMILES

O[C@]2(COC(=O)C1=CN=CC=C1)O[C@H](COC(=O)C3=CN=CC=C3)[C@@H](OC(=O)C4=CN=CC=C4)[C@@H]2OC(=O)C5=CN=CC=C5

InChI

InChIKey=FUWFSXZKBMCSKF-ZASNTINBSA-N
InChI=1S/C30H24N4O10/c35-26(19-5-1-9-31-13-19)40-17-23-24(42-28(37)21-7-3-11-33-15-21)25(43-29(38)22-8-4-12-34-16-22)30(39,44-23)18-41-27(36)20-6-2-10-32-14-20/h1-16,23-25,39H,17-18H2/t23-,24-,25+,30-/m1/s1

HIDE SMILES / InChI

Molecular Formula C30H24N4O10
Molecular Weight 600.5324
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Nicofuranose is a niacin derivative used as a hypolipidemic agent. The Nicofuranose administration leads to inhibition of free fatty acid turnover and consequently a marked reduction in triglyceride turnover. Nicofuranose, unlike clofibrate, did not affect the mechanisms responsible for the clearance of plasma triglycerides.

Approval Year

PubMed

PubMed

TitleDatePubMed
The mechanism of action of clofibrate and tetranicotinoylfructose (Bradilan) on the kinetics of plasma free fatty acid and triglyceride transport in type IV and type V hypertriglyceridaemia.
1974-06
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:54:40 GMT 2025
Edited
by admin
on Mon Mar 31 17:54:40 GMT 2025
Record UNII
GF99P6327K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ES 304
Preferred Name English
NICOFURANOSE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
NICOFURANOSE [MART.]
Common Name English
ES-304
Code English
D-FRUCTOFURANOSE 1,3,4,6-TETRANICOTINATE
Common Name English
NICOFURANOSE [MI]
Common Name English
nicofuranose [INN]
Common Name English
Nicofuranose [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-VATC QC10AD03
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
WHO-ATC C10AD03
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
NCI_THESAURUS C98151
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
NCI_THESAURUS C29707
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C83921
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
WIKIPEDIA
NICOFURANOSE
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
FDA UNII
GF99P6327K
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
ECHA (EC/EINECS)
239-385-7
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
RXCUI
104486
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY RxNorm
EVMPD
SUB09237MIG
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
INN
1565
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
CAS
15351-13-0
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
PUBCHEM
25495
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
DRUG BANK
DB13422
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
DRUG CENTRAL
1916
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
ChEMBL
CHEMBL1697844
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
MERCK INDEX
m843
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY Merck Index
SMS_ID
100000084395
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
EPA CompTox
DTXSID6023365
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
MESH
C100123
Created by admin on Mon Mar 31 17:54:40 GMT 2025 , Edited by admin on Mon Mar 31 17:54:40 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY