1027483-26-6

Basic information

• Product Name: (3-Methoxy-phenyl)-pyridin-3-yl-methanol
• CAS NO: 1027483-26-6
• Molecular Weight: 215.252
• Mol File: 1027483-26-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3-Methoxy-phenyl)-pyridin-3-yl-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (3-Methoxy-phenyl)-pyridin-3-yl-methanol(1027483-26-6)
• EPA Substance Registry System: (3-Methoxy-phenyl)-pyridin-3-yl-methanol(1027483-26-6)

Safety Data

• Hazardous Substances Data: 1027483-26-6(Hazardous Substances Data)

Upstream product

• 500-22-1 3-pyridinecarboxaldehyde 
• 36282-40-3 (3-methoxyphenyl)magnesium bromide 

Downstream Products

• 1384458-29-0 C₂₃H₁₉NOS 
• 1025879-17-7 (E)-7-[3-(4-Diethoxymethyl-benzyloxy)-phenyl]-7-pyridin-3-yl-hept-6-enoic acid ethyl ester 
• 163164-13-4 ethyl (E)-7-<3-<(4-formylphenyl)methoxy>phenyl>-7-(3-pyridyl)hept-6-enoate 
• 163164-12-3 ethyl (E)-7-(3-hydroxyphenyl)-7-(3-pyridyl)hept-6-enoate 
• 1026858-27-4 (E)-7-(3-Methoxy-phenyl)-7-pyridin-3-yl-hept-6-enoic acid 
• 1026377-03-6 (E)-7-(3-Hydroxy-phenyl)-7-pyridin-3-yl-hept-6-enoic acid 
• 260417-55-8 (3-methoxyphenyl)-(3-pyridinyl)methanone 

Relevant articles and documents

Aryl aryl methyl thio arenes prevent multidrug-resistant malaria in mouse by promoting oxidative stress in parasites

We have synthesized a new series of aryl aryl methyl thio arenes (AAMTAs) and evaluated antimalarial activity in vitro and in vivo against drug-resistant malaria. These compounds interact with free heme, inhibit hemozoin formation, and prevent Plasmodium falciparum growth in vitro in a concentration-dependent manner. These compounds concentration dependently promote oxidative stress in Plasmodium falciparum as evident from the generation of intraparasitic oxidants, protein carbonyls, and lipid peroxidation products. Furthermore, AAMTAs deplete intraparasite GSH levels, which is essential for antioxidant defense and survival during intraerythrocytic stages. These compounds displayed potent antimalarial activity not only in vitro but also in vivo against multidrug-resistant Plasmodium yoelii dose dependently in a mouse model. The mixtures of enantiomers of AAMTAs containing 3-pyridyl rings were found to be more efficient in providing antimalarial activity. Efforts have been made to synthesize achiral AAMTAs 17-23 and among them, compound 18 showed significant antimalarial activity in vivo