Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H6N8 |
| Molecular Weight | 238.2082 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N1N=NN=C1C2=CC3=C(C=CC=C3)N4N=NN=C24
InChI
InChIKey=LIRHINFDFZWXPL-UHFFFAOYSA-N
InChI=1S/C10H6N8/c1-2-4-8-6(3-1)5-7(9-11-14-15-12-9)10-13-16-17-18(8)10/h1-5H,(H,11,12,14,15)
| Molecular Formula | C10H6N8 |
| Molecular Weight | 238.2082 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/2801334
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2801334
Tetrazolast (also known as MDL 26,024GO) is a tetrazoloquinoline derivative patented by Merrell Dow Pharmaceuticals, Inc. as an antiallergic and antiasthmatic agent. Tetrazolast was shown to be an orally absorbed mediator release inhibitor in the rat passive cutaneous anaphylaxis and passive peritoneal anaphylaxis tests. In addition, the compound was shown to both elicit and inhibit elicitation of the Bezold-Jarisch reflex in the dog. Tetrazolast also significantly reduced Ascaris-induced changes in pulmonary mechanics in cynomolgus monkeys. The compound inhibited both early and late phase antigen induced-changes in Ascaris-sensitive sheep, as well as the increased airway hyperreactivity which normally follows antigen challenge.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:26:41 GMT 2025
by
admin
on
Mon Mar 31 19:26:41 GMT 2025
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| Record UNII |
X015V3LF01
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| Record Status |
Validated (UNII)
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Official Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English |
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NCI_THESAURUS |
C29712
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SUB10947MIG
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95104-27-1
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100000082719
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ACTIVE MOIETY |