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Details

Stereochemistry ACHIRAL
Molecular Formula C17H23NO4
Molecular Weight 305.3688
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CETRAXATE

SMILES

NC[C@H]1CC[C@@H](CC1)C(=O)OC2=CC=C(CCC(O)=O)C=C2

InChI

InChIKey=FHRSHSOEWXUORL-HDJSIYSDSA-N
InChI=1S/C17H23NO4/c18-11-13-1-6-14(7-2-13)17(21)22-15-8-3-12(4-9-15)5-10-16(19)20/h3-4,8-9,13-14H,1-2,5-7,10-11,18H2,(H,19,20)/t13-,14-

HIDE SMILES / InChI

Molecular Formula C17H23NO4
Molecular Weight 305.3688
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including: http://www.229877.com/article/2016/0303/article_36173.html | https://www.ncbi.nlm.nih.gov/pubmed/4261023

Cetraxate is an oral gastrointestinal medication, mucosal protectant. Cetraxate might indirectly stimulate capsaicin-sensitive afferent nerves and increase mucosal blood flow, and that this may be a key mechanism underlying its gastroprotective action. Cetraxate prevents gastric mucosal blood flow decrease in H. pylori-infected patients. It is usually used to improve gastric mucosal lesion in acute gastritis or acute exacerbation of chronic gastritis and to treat gastric ulcer. The most commonly reported adverse reactions include constipation, rash, nausea, vomiting, dry mouth and diarrhea.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Neuer

Approved Use

It is usually used to improve gastric mucosal lesion in acute gastritis or acute exacerbation of chronic gastritis and to treat gastric ulcer.
Primary
Neuer

Approved Use

It is usually used to improve gastric mucosal lesion in acute gastritis or acute exacerbation of chronic gastritis and to treat gastric ulcer.
PubMed

PubMed

TitleDatePubMed
Comparison of cetraxate-based and pantoprazole-based triple therapies in the treatment of Helicobacter pylori infection.
2004 Apr
Cetraxate raises levels of calcitonin gene-related peptide and substance P in human plasma.
2004 Apr
DA-9601 for erosive gastritis: results of a double-blind placebo-controlled phase III clinical trial.
2004 Aug 15
Efficacy of triple therapy plus cetraxate for the Helicobacter pylori eradication in partial gastrectomy patients.
2005 May
[Eradication therapy for the remnant stomach infected with Helicobacter pylori ].
2005 Nov
[Cetraxate hydrochloride (Neuer) induces the effectiveness of new triple therapy in H. pylori eradication].
2005 Nov
Comparison of the effects of cytoprotective drugs on human plasma adrenocorticotropic hormone and cortisol levels with continual stress exposure.
2005 Nov
15th anniversary of rebamipide: looking ahead to the new mechanisms and new applications.
2005 Oct
Are gastroprotective drugs useful for gastric ulcer healing: re-evaluation using current ICH E9 guidelines.
2007 Feb
[Side effects of gastric muco-protective agents].
2007 Oct 28
Gastroduodenal mucosal injury in patients taking low-dose aspirin and the role of gastric mucoprotective drugs: possible effect of rebamipide.
2010 Jul
Rebamipide: a gastrointestinal protective drug with pleiotropic activities.
2010 Jun
Patents

Sample Use Guides

200 mg 3-4 times per day
Route of Administration: Oral
In Vitro Use Guide
The amounts of Cetraxate to prolong the recalcification time of citrated plasma to 2 times were approximately 50 ug in the ordinary glass tube and 25 ug in the siliconized tube.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:12:29 GMT 2023
Edited
by admin
on Fri Dec 15 16:12:29 GMT 2023
Record UNII
5VPA8CPF0N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CETRAXATE
INN   MI   WHO-DD  
INN  
Official Name English
BENZENEPROPANOIC ACID, 4-(((4-(AMINOMETHYL)CYCLOHEXYL)CARBONYL)OXY)-, TRANS-
Common Name English
cetraxate [INN]
Common Name English
BENZENEPROPANOIC ACID, 4-(((TRANS-4-(AMINOMETHYL)CYCLOHEXYL)CARBONYL)OXY)-
Common Name English
P-HYDROXYHYDROCINNAMIC ACID TRANS-4-(AMINOMETHYL)CYCLOHEXANECARBOXYLATE
Common Name English
CETRAXATE [MI]
Common Name English
Cetraxate [WHO-DD]
Common Name English
CETRAXATE [JAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28197
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
Code System Code Type Description
DRUG CENTRAL
582
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY
CHEBI
17340
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY
ChEMBL
CHEMBL1187445
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY
INN
4091
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY
SMS_ID
100000081516
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID2040658
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY
CAS
34675-84-8
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
PRIMARY
MERCK INDEX
m3293
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY Merck Index
MESH
C000665
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY
NCI_THESAURUS
C79885
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY
FDA UNII
5VPA8CPF0N
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY
CHEBI
58112
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY
EVMPD
SUB07457MIG
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY
WIKIPEDIA
Cetraxate
Created by admin on Fri Dec 15 16:12:30 GMT 2023 , Edited by admin on Fri Dec 15 16:12:30 GMT 2023
PRIMARY
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SALT/SOLVATE -> PARENT
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ACTIVE MOIETY