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Details

Stereochemistry MIXED
Molecular Formula C24H33NO3
Molecular Weight 383.5237
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NAFTIDROFURYL

SMILES

CCN(CC)CCOC(=O)C(CC1CCCO1)CC2=CC=CC3=CC=CC=C23

InChI

InChIKey=KBAFPSLPKGSANY-UHFFFAOYSA-N
InChI=1S/C24H33NO3/c1-3-25(4-2)14-16-28-24(26)21(18-22-12-8-15-27-22)17-20-11-7-10-19-9-5-6-13-23(19)20/h5-7,9-11,13,21-22H,3-4,8,12,14-18H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C24H33NO3
Molecular Weight 383.5237
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/1369714

Naftidrofuryl (INN), also known as nafronyl or as the oxalate salt naftidrofuryl oxalate or nafronyl oxalate, is a vasodilator used in the management of peripheral and cerebral vascular disorders. The drug act as a selective antagonist of 5-HT2 receptors. Naftidrofuryl is marketed under a variety of trade names, including Artocoron, Azunaftil, Di-Actane, Dusodril, Enelbin, Frilix, Gevatran, Iridus, Iridux, Luctor, Nafti, Naftoling, Naftodril, Nafoxal, Praxilene, Sodipryl retard, and Vascuprax. Praxilene belongs to a group of medicines known as ‘metabolic activators’. These are used to treat different types of blood circulation problems. Praxilene allows the body to make better use of the oxygen in your blood. Praxilene is used to treat the following symptoms: cramp-like pains; cramps in legs at night; severe pain in r legs when people are resting (rest pain); pale or blue fingers or toes which get worse when it is cold; numbness, tingling or burning feelings in the fingers or toes (Raynaud’s syndrome or acrocyanosis); open sores on the legs or feet (trophic ulcers); poor circulation caused by diabetes (diabetic arteriopathy).

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.06 µM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Praxilene

Approved Use

Unknown

Launch Date

2016
PubMed

PubMed

TitleDatePubMed
New treatment options in intermittent claudication: the US experience.
2001 Apr
Naftidrofuryl in quality of life (NIQOL). A Belgian study.
2001 Dec
[Intermittent claudication. Walking plus vasoactive drug treatment].
2001 Jul 5
Inhibition of purified pig and human liver retinyl ester hydrolase by pharmacologic agents.
2001 May
Effect of naftidrofuryl on intramuscular partial oxygen pressure (pO2) prior to, during and after physical load on the treadmill in apparently healthy subjects.
2002
Findings of the Naftidrofuryl in Quality of Life (NIQOL) European study program.
2002 Mar
Naftidrofuryl-induced liver injury.
2003 Jun
Naftidrofuryl: a review of its use in the treatment of intermittent claudication.
2005
[Inpatient infusion treatment for acute tinnitus with and without adjuvant psychotherapeutic intervention. A comparison of psychological effectiveness].
2006 Oct
Assessment of binding affinity to 5-hydroxytryptamine 2A (5-HT2A) receptor and inverse agonist activity of naftidrofuryl: comparison with those of sarpogrelate.
2009 Aug
Naftidrofuryl for intermittent claudication: meta-analysis based on individual patient data.
2009 Mar 10
Pharmacologic therapy for intermittent claudication.
2009 May
Vasodilators and vasoactive substances for idiopathic sudden sensorineural hearing loss.
2009 Oct 7
Fatal intoxication with naftidrofuryl.
2009 Sep
Screening of a chemical library reveals novel PXR-activating pharmacologic compounds.
2015 Jan 5
Patents

Patents

Sample Use Guides

The recommended dose is one or two capsules (100 mg naftidrofuryl oxalate) three times a day, for a minimum of three months
Route of Administration: Oral
In Vitro Use Guide
After culture in a rat serum enriched with naftidrofuryl at concentration of 20 uM, we observed a protective effect of this drug toward the disruption of axonal microtubules by vinka alkaloids
Substance Class Chemical
Created
by admin
on Sat Dec 16 15:48:37 GMT 2023
Edited
by admin
on Sat Dec 16 15:48:37 GMT 2023
Record UNII
42H8PQ0NMJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NAFTIDROFURYL
INN   WHO-DD  
INN  
Official Name English
NAFRONYL [MI]
Common Name English
2-(DIETHYLAMINO)ETHYL TETRAHYDRO-.ALPHA.-(1-NAPHTHYLMETHYL)-2-FURANPROPIONATE
Systematic Name English
2-FURANPROPANOIC ACID, TETRAHYDRO-A-(1-NAPHTHALENYLMETHYL)-, 2-(DIETHYLAMINO)ETHYL ESTER
Common Name English
Naftidrofuryl [WHO-DD]
Common Name English
DROSUNAL
Brand Name English
TETRAHYDRO-.ALPHA.-(1-NAPHTHALENYLMETHYL)-2-FURANPROPANOIC ACID 2-(DIETHYLAMINO)ETHYL ESTER
Systematic Name English
3-(1-NAPHTHYL)-2-TETRAHYDROFURFURYLPROPIONIC ACID 2-(DIETHYLAMINO)ETHYL ESTER
Systematic Name English
DUBIMAX
Brand Name English
NAFRONYL
MI  
Common Name English
TETRAHYDRO-.ALPHA.-(1-NAPHTHYLMETHYL)-2-FURANPROPIONIC ACID 2-(DIETHYLAMINO)ETHYL ESTER
Systematic Name English
GEVATRAN
Brand Name English
naftidrofuryl [INN]
Common Name English
Classification Tree Code System Code
WHO-ATC C04AX21
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
NCI_THESAURUS C29707
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
NCI_THESAURUS C66885
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
WHO-VATC QC04AX21
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
Code System Code Type Description
FDA UNII
42H8PQ0NMJ
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
MERCK INDEX
m7707
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY Merck Index
DRUG BANK
DB13588
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
WIKIPEDIA
Naftidrofuryl
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
EVMPD
SUB09130MIG
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
PUBCHEM
4417
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
ECHA (EC/EINECS)
250-572-2
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
INN
2177
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
MESH
D009257
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
ChEMBL
CHEMBL1620794
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
EPA CompTox
DTXSID3023344
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
CAS
31329-57-4
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
DRUG CENTRAL
1870
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
SMS_ID
100000084457
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
NCI_THESAURUS
C87212
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY
RXCUI
7236
Created by admin on Sat Dec 16 15:48:38 GMT 2023 , Edited by admin on Sat Dec 16 15:48:38 GMT 2023
PRIMARY RxNorm
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SALT/SOLVATE -> PARENT
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ACTIVE MOIETY