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Nicofuranose

HCID 25495
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
12041-87-1
Standard SMILES
O=C(OC[C@H]1O[C@](O)(COC(=O)c2cccnc2)[C@@H](OC(=O)c2cccnc2)[C@@H]1OC(=O)c1cccnc1)c1cccnc1
InChIKey
FUWFSXZKBMCSKF-ZASNTINBSA-N
Molecular formula
C30H24N4O10
Average molar mass
600.5 g/mol
Monoisotopic mass
600.14924298

Overview

Nicofuranose is an organooxygen compound. It is functionally related to a tetracarboxylic acid.

Names & identifiers

Preferred name
Nicofuranose
IUPAC
[(2R,3R,4S,5R)-5-hydroxy-3,4-bis(pyridine-3-carbonyloxy)-5-(pyridine-3-carbonyloxymethyl)oxolan-2-yl]methyl pyridine-3-carboxylate
English name
NICOFURANOSE
Molecular formula
C30H24N4O10
Molecular weight
600.53

Names & synonyms

NICOFURANOSE15351-13-0BradilanNicofuranosaNicofuranosoNicofuranosumTetranicotinoylfructoseES 304DTXSID6023365ES-304D-Fructofuranose 1,3,4,6-tetranicotinateGF99P6327K
Show more names
Vasperdilá-d-fructofuranose tetranicotinateBETA-D-FRUCTOFURANOSE TETRANICOTINATEβ-D-Fructofuranose, 1,3,4,6-tetra-3-pyridinecarboxylate1,3,4,6-Tetrakis-O-(3-pyridinylcarbonyl)hex-2-ulofuranoseβ-D-Fructofuranose 1,3,4,6-tetrakis(3-pyridinecarboxylate)
DTXCID703365[(2R,3R,4S,5R)-5-hydroxy-3,4-bis(pyridine-3-carbonyloxy)-5-(pyridine-3-carbonyloxymethyl)oxolan-2-yl]methyl pyridine-3-carboxylatenicofurazone((2R,3R,4S,5R)-5-hydroxy-3,4-bis(pyridine-3-carbonyloxy)-5-(pyridine-3-carbonyloxymethyl)oxolan-2-yl)methyl pyridine-3-carboxylateRefChem:854092C10AD031,3,4,6-tetranicotinoyl fructose1,3,4,6-tetranicotinoyl fructofuranose

Database identifiers

CAS
12041-87-1、15351-13-0

Properties

Computed structural properties

XLogP
1.3
Topological polar surface area
186 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
14
Rotatable bonds
14
Heavy atoms
44
Formal charge
0
Complexity
1,020

Experimental & physicochemical properties

DrugsPharmaceuticals -> Antilipidemics

Physicochemical properties

Melting point
133 · 133-136°C
alpha
18 · D18 -8.5° (after 4-6 hours in CHCl3)
Boiling point
756 · 756.0±60.0 °C(Predicted)
Density
1.5 · 1.50±0.1 g/cm3(Predicted)
pka
9.53 · 9.53±0.70(Predicted)
CAS DataBase Reference
15351 · 15351-13-0
FDA UNII
99 P6327K · GF99P6327K
ATC code
10 AD03 · C10AD03
Risk Statements
20 · 20/21/22
Safety Statements
22 · 22-36/37/39

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Safety data

risk_code
20/21/22
safety_code
22-36/37/39

Chemistry & industry

Pharmacology

ATC Code · 2 items

C - Cardiovascular system

QC - Cardiovascular system

MeSH Pharmacological ClassificationDrugs used to cause dilation of the blood vessels.

Applications

UsesNicofuranose is used as a vasodilator, and a hypolipidemic agent that is used to treat lipid metabolism disorders.

Suppliers13 total

陕西缔都新材料有限公司029-63373950 17392216152 · [email protected]
LGM Pharma1-(800)-881-8210 · [email protected]
上海迈瑞尔生化科技有限公司4006356688 18621169109 · [email protected]
阿法埃莎(中国)化学有限公司400-6106006 · [email protected]
安耐吉化学&3A(安徽泽升科技股份有限公司)400-0056266 · [email protected]
杭州璟皓生物科技有限公司(原河南辛迪加生物)17513242016 · [email protected]
天津希恩思生化科技有限公司400 638 7771 · [email protected]
Shaanxi Didu New Materials Co. Ltd+86-86-17392712779 +86-13289823923 · [email protected]
江苏艾康生物医药研发有限公司025-58859352 15955137747 · [email protected]

Related reactions

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
PubChem CID
25495
DTXSID
DTXSID6023365
ChEMBL
CHEMBL1697844
ChEBI
CHEBI:135846
UNII
GF99P6327K
EC Number
239-385-7
Nikkaji
J8.561H
天津希恩思生化科技有限公司400-6387771-6039 18920764717 · [email protected]
XIAMEN AMITY INDUSTRY AND TRADE CO., LTD.+8618950047208 · [email protected]
上海一飞生物科技有限公司021-65675885 18964387627 · [email protected]
DAYANG CHEM (HANGZHOU) CO.,LTD+86-88938639 +86-17705817739 · [email protected]

Additional notes

DefinitionChEBI: Nicofuranose is an organooxygen compound. It is functionally related to a tetracarboxylic acid.