[CAS NO. 554-57-4]  Methazolamide

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PRODUCTS SPECIFICATIONS [554-57-4]

Catalog
SLK-S4039
Brand
Selleck
CAS
554-57-4

DESCRIPTION [554-57-4]

Overview

MDLMFCD00083416
Molecular Weight236.27
Molecular FormulaC5H8N4O3S2
SMILESN(C(C)=O)=C1SC(S(N)(=O)=O)=NN1C

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM4.2324 mL21.1622 mL42.3245 mL
5 mM0.8465 mL4.2324 mL8.4649 mL
10 mM0.4232 mL2.1162 mL4.2324 mL
50 mM0.0846 mL0.4232 mL0.8465 mL

Description

Methazolamide (CL 8490) is a inhibitor with of 50 nM, 14 nM and 36 nM for hCA I, hCA II and bCA IV isoforms, respectively.

Features

Methazolamide potently inhibits various isoforms of carbonic anhydrase.

Targets

hCAII [1]bCAIV [1]hCAI [1]
14 nM(Ki)36 nM(Ki)50 nM(Ki)

In vitro

Methazolamide is a carbonic anhydrase inhibitor with K of 50 nM, 14 nM and 36 nM for hCA I, hCA II and bCA IV isoforms, respectively. Methazolamide is of strength equal to acetazolamide, another carbonic anhydrase inhibitor used to treat irregular breathing disorders. However, methazolamide differs from acetazolamide in that it fails to activate Ca-dependent potassium channels in skeletal muscles.

In vivo

Methazolamide does not impair respiratory work performance in anesthetized rabbits.


Synonyms

Acetamide, N-[5-(aminosulfonyl)-3-methyl-1,3,4-thiadiazol-2(3H)-ylidene]-
Acetamide, N-(4-methyl-2-sulfamoyl-Δ2-1,3,4-thiadiazolin-5-ylidene)-
N-[5-(Aminosulfonyl)-3-methyl-1,3,4-thiadiazol-2(3H)-ylidene]acetamide
5-Acetylimino-4-methyl-Δ2-1,3,4-thiadiazoline-2-sulfonamide
Methazolamide
Methenamide
N-(4-Methyl-2-sulfamoyl-Δ2-1,3,4-thiadiazolin-5-ylidene)acetamide
Neptazane
Neptazaneat
L 584601