Details
Stereochemistry | ACHIRAL |
Molecular Formula | C17H23NO4.ClH |
Molecular Weight | 341.83 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.NC[C@H]1CC[C@@H](CC1)C(=O)OC2=CC=C(CCC(O)=O)C=C2
InChI
InChIKey=USROQQUKEBHOFF-SKKCDYJJSA-N
InChI=1S/C17H23NO4.ClH/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);1H/t13-,14-;
DescriptionCurator'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
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
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2095204 Sources: https://www.ncbi.nlm.nih.gov/pubmed/4261023 |
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Target ID: UDP-galactosyltransferase (rat) Sources: https://www.ncbi.nlm.nih.gov/pubmed/9359921 |
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Target ID: WP1111 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | Neuer Approved UseIt is usually used to improve gastric mucosal lesion in acute gastritis or acute exacerbation of chronic gastritis and to treat gastric ulcer. |
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Primary | Neuer Approved UseIt is usually used to improve gastric mucosal lesion in acute gastritis or acute exacerbation of chronic gastritis and to treat gastric ulcer. |
PubMed
Title | Date | PubMed |
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Biocatalytic deprotection of a cetraxate ester by Microbacterium sp. strain 7-1W cells. | 2003 Jan |
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Comparison of cetraxate-based and pantoprazole-based triple therapies in the treatment of Helicobacter pylori infection. | 2004 Apr |
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DA-9601 for erosive gastritis: results of a double-blind placebo-controlled phase III clinical trial. | 2004 Aug 15 |
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Efficacy of triple therapy plus cetraxate for the Helicobacter pylori eradication in partial gastrectomy patients. | 2005 May |
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15th anniversary of rebamipide: looking ahead to the new mechanisms and new applications. | 2005 Oct |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4261023
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.
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NCI_THESAURUS |
C28197
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C84661
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27724-96-5
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DTXSID3046459
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m3293
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100000084687
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08IT6P8VHY
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SUB01172MIG
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CHEMBL1187445
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T-84
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ACTIVE MOIETY
SUBSTANCE RECORD