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Details

Stereochemistry ACHIRAL
Molecular Formula C28H31N3O6
Molecular Weight 505.5622
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HEPRONICATE

SMILES

CCCCCCC(COC(=O)C1=CN=CC=C1)(COC(=O)C2=CN=CC=C2)COC(=O)C3=CN=CC=C3

InChI

InChIKey=GUIBJJJLGSYNKE-UHFFFAOYSA-N
InChI=1S/C28H31N3O6/c1-2-3-4-5-12-28(19-35-25(32)22-9-6-13-29-16-22,20-36-26(33)23-10-7-14-30-17-23)21-37-27(34)24-11-8-15-31-18-24/h6-11,13-18H,2-5,12,19-21H2,1H3

HIDE SMILES / InChI

Molecular Formula C28H31N3O6
Molecular Weight 505.5622
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Hepronicate is a nicotinic acid derivative, developed and used in Japan under the name Megrin for the treatment of peripheral circulatory disorders. The therapeutic effect of the drug is explained by its vasodilation properties.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
MEGRIN

Approved Use

Peripheral circulatory disorders such as Raynaud's disease, Buerger's disease, arteriosclerosis obliterans; chilblains, frostbite.

Launch Date

1971
Palliative
MEGRIN

Approved Use

Peripheral circulatory disorders such as Raynaud's disease, Buerger's disease, arteriosclerosis obliterans; chilblains, frostbite.

Launch Date

1971
Palliative
MEGRIN

Approved Use

Peripheral circulatory disorders such as Raynaud's disease, Buerger's disease, arteriosclerosis obliterans; chilblains, frostbite.

Launch Date

1971
Curative
MEGRIN

Approved Use

Peripheral circulatory disorders such as Raynaud's disease, Buerger's disease, arteriosclerosis obliterans; chilblains, frostbite.

Launch Date

1971
Curative
MEGRIN

Approved Use

Peripheral circulatory disorders such as Raynaud's disease, Buerger's disease, arteriosclerosis obliterans; chilblains, frostbite.

Launch Date

1971
Patents

Patents

Sample Use Guides

The recommended adult dose is 300-600 mg (3-6 tablets) administered orally three times/day after food.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:34:21 GMT 2023
Edited
by admin
on Fri Dec 15 15:34:21 GMT 2023
Record UNII
E4RK86FAVR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HEPRONICATE
INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
HEPRONICATE [MI]
Common Name English
2-HEXYL-2-(HYDROXYMETHYL)-1,3-PROPANEDIOL TRINICOTINATE
Systematic Name English
hepronicate [INN]
Common Name English
HEPRONICATE [JAN]
Common Name English
HEPRONICATE [MART.]
Common Name English
Hepronicate [WHO-DD]
Common Name English
MEGRIN
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C471
Created by admin on Fri Dec 15 15:34:21 GMT 2023 , Edited by admin on Fri Dec 15 15:34:21 GMT 2023
Code System Code Type Description
PUBCHEM
3588
Created by admin on Fri Dec 15 15:34:21 GMT 2023 , Edited by admin on Fri Dec 15 15:34:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID60222680
Created by admin on Fri Dec 15 15:34:21 GMT 2023 , Edited by admin on Fri Dec 15 15:34:21 GMT 2023
PRIMARY
NCI_THESAURUS
C65843
Created by admin on Fri Dec 15 15:34:21 GMT 2023 , Edited by admin on Fri Dec 15 15:34:21 GMT 2023
PRIMARY
DRUG CENTRAL
1359
Created by admin on Fri Dec 15 15:34:21 GMT 2023 , Edited by admin on Fri Dec 15 15:34:21 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106360
Created by admin on Fri Dec 15 15:34:21 GMT 2023 , Edited by admin on Fri Dec 15 15:34:21 GMT 2023
PRIMARY
MERCK INDEX
m757
Created by admin on Fri Dec 15 15:34:21 GMT 2023 , Edited by admin on Fri Dec 15 15:34:21 GMT 2023
PRIMARY Merck Index
EVMPD
SUB08014MIG
Created by admin on Fri Dec 15 15:34:21 GMT 2023 , Edited by admin on Fri Dec 15 15:34:21 GMT 2023
PRIMARY
SMS_ID
100000083948
Created by admin on Fri Dec 15 15:34:21 GMT 2023 , Edited by admin on Fri Dec 15 15:34:21 GMT 2023
PRIMARY
CAS
7237-81-2
Created by admin on Fri Dec 15 15:34:21 GMT 2023 , Edited by admin on Fri Dec 15 15:34:21 GMT 2023
PRIMARY
INN
2733
Created by admin on Fri Dec 15 15:34:21 GMT 2023 , Edited by admin on Fri Dec 15 15:34:21 GMT 2023
PRIMARY
FDA UNII
E4RK86FAVR
Created by admin on Fri Dec 15 15:34:21 GMT 2023 , Edited by admin on Fri Dec 15 15:34:21 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY