Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H7N5O3 |
| Molecular Weight | 233.1836 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C(=O)NC1=CC=CC(=C1)C2=NN=NN2
InChI
InChIKey=VWQZJJZGISNFOE-UHFFFAOYSA-N
InChI=1S/C9H7N5O3/c15-8(9(16)17)10-6-3-1-2-5(4-6)7-11-13-14-12-7/h1-4H,(H,10,15)(H,16,17)(H,11,12,13,14)
| Molecular Formula | C9H7N5O3 |
| Molecular Weight | 233.1836 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: http://www.dcchemicals.com/products_Show.asp?id=4171http://meds.qlifepro.com/detail/620006023/tazanolastCurator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/9150859
Sources: http://www.dcchemicals.com/products_Show.asp?id=4171http://meds.qlifepro.com/detail/620006023/tazanolast
Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/9150859
Tazanolast, an anti-allergic and anti-asthmatic agent with selective mast-cell stabilising effects, was developed jointly by Wakamoto and Torii Pharmaceuticals.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: GO:0002553 Sources: http://www.ncbi.nlm.nih.gov/pubmed/9150859 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Palliative | Unknown Approved UseUnknown |
|||
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
1.18 μg/mL |
75 mg single, oral dose: 75 mg route of administration: Oral experiment type: SINGLE co-administered: |
ACITAZANOLAST plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
2.18 μg × h/mL |
75 mg single, oral dose: 75 mg route of administration: Oral experiment type: SINGLE co-administered: |
ACITAZANOLAST plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
2.48 h |
75 mg single, oral dose: 75 mg route of administration: Oral experiment type: SINGLE co-administered: |
ACITAZANOLAST plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
Funbound
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
4% |
ACITAZANOLAST plasma | Homo sapiens |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2382790
0.01 and 0.033% aerosol inhalation.
Route of Administration:
Respiratory
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/9150859
WP-871 (Acitazanolast) may inhibit histamine release mainly by preventing the increase in intracellular Ca2+ concentration
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:04:51 GMT 2025
by
admin
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Mon Mar 31 18:04:51 GMT 2025
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| Record UNII |
99Y8VJ356G
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C29712
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2006
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C74133
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DTXSID3048732
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77
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100000084603
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CHEMBL2104654
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7216
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114607-46-4
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99Y8VJ356G
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C065288
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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SOLVATE->ANHYDROUS | |||
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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PRODRUG -> METABOLITE ACTIVE |
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |