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Details

Stereochemistry ACHIRAL
Molecular Formula C17H11N6O3.Na.H2O
Molecular Weight 388.3127
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of QUINOTOLAST SODIUM MONOHYDRATE

SMILES

O.[Na+].O=C(NC1=NN=N[N-]1)C2=CC(OC3=CC=CC=C3)=C4C=CC=CN4C2=O

InChI

InChIKey=DNKDMMYDHNPYGV-UHFFFAOYSA-M
InChI=1S/C17H12N6O3.Na.H2O/c24-15(18-17-19-21-22-20-17)12-10-14(26-11-6-2-1-3-7-11)13-8-4-5-9-23(13)16(12)25;;/h1-10H,(H2,18,19,20,21,22,24);;1H2/q;+1;/p-1

HIDE SMILES / InChI

Molecular Formula HO
Molecular Weight 17.0073
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C17H12N6O3
Molecular Weight 348.3156
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Quinotolast (also known as FK021) is an orally active mast cell stabilizer which has a cytoprotective effect on the gastric mucosa. Quinotolast was patented in 1985 by Japanese pharmaceutical company Fujisawa Pharmaceutical Co., Ltd. as an antiallergic and antiulcer agent. In preclinical models, Quinotolast potently inhibited such type I allergic reactions as passive cutaneous anaphylaxis (PCA) and anaphylactic bronchoconstriction in rats by both intravenous and oral dosing. Quinotolast inhibited histamine release from rat peritoneal cells, but it had no antagonistic effect on histamine-, serotonin-, platelet activating factor- or bradykinin-induced cutaneous reactions in rats. Moreover, it was clearly demonstrated that quinotolast and DSCG had a cross tachyphylaxis to inhibit PCA in rats, suggesting that these drugs, at least in part, share the same mechanism of action. Quinotolast caused a significant increase in the mucociliary transport rate in quails. Quinotolast significantly depressed the cough reflex induced by citric acid in normal and bronchitic guinea pigs.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Effects of a novel orally-active antiallergic drug, quinotolast (FK021), on airway clearance].
1994 Oct
Patents

Sample Use Guides

guinea pig: 10 mg/kg,
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:59:22 GMT 2023
Edited
by admin
on Sat Dec 16 10:59:22 GMT 2023
Record UNII
S9D69QXP6B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
QUINOTOLAST SODIUM MONOHYDRATE
Common Name English
FK-021
Code English
4H-QUINOLIZINE-3-CARBOXAMIDE, 4-OXO-1-PHENOXY-N-2H-TETRAZOL-5-YL-, SODIUM SALT, HYDRATE (1:1:1)
Systematic Name English
4H-QUINOLIZINE-3-CARBOXAMIDE, 4-OXO-1-PHENOXY-N-1H-TETRAZOL-5-YL-, MONOSODIUM SALT, MONOHYDRATE
Common Name English
Code System Code Type Description
FDA UNII
S9D69QXP6B
Created by admin on Sat Dec 16 10:59:22 GMT 2023 , Edited by admin on Sat Dec 16 10:59:22 GMT 2023
PRIMARY
CAS
121191-32-0
Created by admin on Sat Dec 16 10:59:22 GMT 2023 , Edited by admin on Sat Dec 16 10:59:22 GMT 2023
PRIMARY
PUBCHEM
23663988
Created by admin on Sat Dec 16 10:59:22 GMT 2023 , Edited by admin on Sat Dec 16 10:59:22 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ANHYDROUS->SOLVATE
Related Record Type Details
ACTIVE MOIETY