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82989-25-1

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82989-25-1 Usage

Description

Tazanolast is an orally active antiallergic agent that is effective in treating bronchial asthma and nasal allergy. It works by inhibiting IgG and IgE-mediated antigen-antibody reactions.

Uses

Used in Pharmaceutical Industry:
Tazanolast is used as a therapeutic agent for the treatment of bronchial asthma and nasal allergy. Its ability to inhibit IgG and IgE-mediated antigen-antibody reactions makes it a valuable drug for managing allergic reactions and improving the quality of life for patients suffering from these conditions.

Originator

Wakamoto (Japan)

Check Digit Verification of cas no

The CAS Registry Mumber 82989-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,8 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82989-25:
(7*8)+(6*2)+(5*9)+(4*8)+(3*9)+(2*2)+(1*5)=181
181 % 10 = 1
So 82989-25-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H15N5O3/c1-2-3-7-21-13(20)12(19)14-10-6-4-5-9(8-10)11-15-17-18-16-11/h4-6,8H,2-3,7H2,1H3,(H,14,19)(H,15,16,17,18)

82989-25-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Tazanolast

1.2 Other means of identification

Product number -
Other names WP-833

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:82989-25-1 SDS

82989-25-1Downstream Products

82989-25-1Relevant articles and documents

TETRAZOLE DERIVATIVES AND ALDOSE REDUCTASE INHIBITION THEREWITH

-

, (2008/06/13)

The present invention relates to an aldose reductase inhibitor having the following formula: R1 is a hydrogen atom or --A--COOR5 (A is an alkylene group having 1 to 4 carbon atoms and R5 is a hydrogen atom or a lower alkyl group), and R2, R3 and R4 are the same as or different from each other and selected from the group consisting of a hydrogen atom, a hydroxy group, a halogen atom, a carboxyl group, an alkyl group, an amide group, an amino group, an alkoxy group, an aryl group, an aryloxy group, an alkylthio group, an alkylsulfinyl group, an alkylsulfonyl group, a nitro group, --NHCOCOOR6 (R6 is a hydrogen atom or a lower alkyl group), a mono or dialkylaminosulfonyl group, and a residual group having the following formula: (A and R5 are the same as in the above). The compounds defined in the above are excellent in aldose reductase inhibitory activity and low in toxicity. Therefore, those compounds are useful as a preventive agent and/or a remedy for diabetic complications such as neuropathy, retinopathy, nephropathy, cataracts and keratopathy

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