136423-95-5

Basic information

• Product Name: 3-(4-methylbenzyloxy)-2-pyridinecarboxaldehyde guanylhydrazone sulphate
• Synonyms: 3-(4-methylbenzyloxy)-2-pyridinecarboxaldehyde guanylhydrazone sulphate
• CAS NO: 136423-95-5
• Molecular Weight: 381.412
• Mol File: 136423-95-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(4-methylbenzyloxy)-2-pyridinecarboxaldehyde guanylhydrazone sulphate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-methylbenzyloxy)-2-pyridinecarboxaldehyde guanylhydrazone sulphate(136423-95-5)
• EPA Substance Registry System: 3-(4-methylbenzyloxy)-2-pyridinecarboxaldehyde guanylhydrazone sulphate(136423-95-5)

Safety Data

• Hazardous Substances Data: 136423-95-5(Hazardous Substances Data)

Upstream product

• 104-81-4 4-Methylbenzyl bromide 
• 136423-83-1 3-(4-methylbenzyloxy)-2-pyridinemethanol 
• 14173-30-9 3-hydroxy-2-hydroxymethylpyridine hydrochloride 
• 2834-84-6 aminoguanidine sulphate 
• 136423-86-4 3-(4-methylbenzyloxy)-2-pyridinecarboxaldehyde 

Relevant articles and documents

Guanylhydrazones of 3-substituted 2-pyridinecarboxaldehyde and of (2-substituted 3-pyridinyloxy) acetaldehyde as prostanoid biosynthesis and platelet aggregation inhibitors

Some guanylhydrazones of (3-benzyloxy)-2-pyridinecarboxaldehyde and of (2-substituted 3-pyridinyloxy)acetaldehyde were prepared in order to evaluate their possible activity as inhibitors of prostanoid biosynthesis in human serum.Only those products of the second group without the carboxylic function reduced prostanoid generation in vitro at the highest concentration; they also inhibited platelet aggregation induced by arachidonic acid and U-46619.The results suggest that these compounds are both inhibitors of cyclooxygenase and cyclic endoperoxides/TxA2 platelet receptor antagonists.