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product name Methazolamide


Description: Methazolamide (also known as CL 8490) is a highly potent and selective  inhibitor of carbonic anhydrase with Ki of 50 nM, 14 nM and 36 nM for hCA I, hCA II and bCA IV isoforms, respectively. Methazolamide is used as a diuretic for the treatment of glaucoma. Methazolamide inhibits tumor-associated carbonic anhydrase IX (CAIX), which may result in increased cell death in hypoxic tumors. 

References: Bioorg Med Chem Lett. 2003;13(5):841-5; Am J Physiol Regul Integr Comp Physiol. 2009;297(3):R648-54.



Molecular Weight (MW)

236.27
Formula

C5H8N4O3S2
CAS No.

554-57-4
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: 47 mg/mL (198.9 mM)
Water: < 1 mg/mL
Ethanol: 3 mg/mL (12.7 mM)
Solubility (In vivo)

 
Synonyms

CL 8490

other peoduct :References PubMed ID::http://www.ncbi.nlm.nih.gov/pubmed/19404645

In Vitro

In vitro activity: Methazolamide is a carbonic anhydrase inhibitor with Ki 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 Ca2+-dependent potassium channels in skeletal muscles.


Kinase Assay:


Cell Assay

In Vivo Methazolamide does not impair respiratory work performance in anesthetized rabbits. 
Animal model  
Formulation & Dosage  
References Bioorg Med Chem Lett. 2003 Mar 10;13(5):841-5; Am J Physiol Regul Integr Comp Physiol. 2009 Sep;297(3):R648-54.

SMND-309

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Author: Sodium channel

Share this post on:

product name Methazolamide


Description: Methazolamide (also known as CL 8490) is a highly potent and selective  inhibitor of carbonic anhydrase with Ki of 50 nM, 14 nM and 36 nM for hCA I, hCA II and bCA IV isoforms, respectively. Methazolamide is used as a diuretic for the treatment of glaucoma. Methazolamide inhibits tumor-associated carbonic anhydrase IX (CAIX), which may result in increased cell death in hypoxic tumors. 

References: Bioorg Med Chem Lett. 2003;13(5):841-5; Am J Physiol Regul Integr Comp Physiol. 2009;297(3):R648-54.



Molecular Weight (MW)

236.27
Formula

C5H8N4O3S2
CAS No.

554-57-4
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: 47 mg/mL (198.9 mM)
Water: < 1 mg/mL
Ethanol: 3 mg/mL (12.7 mM)
Solubility (In vivo)

 
Synonyms

CL 8490

other peoduct :References PubMed ID::http://www.ncbi.nlm.nih.gov/pubmed/19404645

In Vitro

In vitro activity: Methazolamide is a carbonic anhydrase inhibitor with Ki 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 Ca2+-dependent potassium channels in skeletal muscles.


Kinase Assay:


Cell Assay

In Vivo Methazolamide does not impair respiratory work performance in anesthetized rabbits. 
Animal model  
Formulation & Dosage  
References Bioorg Med Chem Lett. 2003 Mar 10;13(5):841-5; Am J Physiol Regul Integr Comp Physiol. 2009 Sep;297(3):R648-54.

SMND-309

Share this post on:

Author: Sodium channel