93944-00-4

Upstream product

• 89667-39-0 (E,Z)-7-phenyl-7-(pyridin-3-yl)-6-heptenoic acid 
• 64-17-5 ethanol 
• 93943-87-4 7-phenyl-7-(3-pyridyl)-6-heptenic acid 

Downstream Products

• 163163-82-4 ethyl (E)-7-(3-pyridyl)-7-phenyl-2-(formylmethyl)hept-6-enoate 
• 163163-81-3 ethyl (E)-7-(3-pyridyl)-7-phenyl-2-(prop-2-enyl)hept-6-enoate 
• 93944-01-5 (E)-7-phenyl-7-(3-pyridyl)-6-hepten-1-ol 
• 89667-40-3 isbogrel 

Relevant academic research and scientific papers

N-HYDROXYUREA DERIVATIVES

An N-hydroxyurea derivative or a pharmacologically acceptable salt thereof having the formula (I): wherein, A represents CH, CH-CH2, CH-O, or C=CH, X represents O or S, B represents a C1to C8alkylene, C2to C6alkenylene, m-phenylene, or p-phenylene, R represents a hydrogen atom, halogen atom, C1to C4alkyl which may be substituted with a halogen atom, C1to C4alkoxy which may be substituted with a halogen atom, or nitro, R1represents a hydrogen atom, C1to C4lower alkyl, or phenyl, and R2represents a hydrogen atom, C1to C4alkyl, cycloalkyl, phenyl which may be substituted with a substituent, or methanesulfonyl.

Thromboxane Synthetase Inhibitors (TXSI). Design, Synthesis, and Evaluation of a Novel Series of ω-Pyridylalkenoic Acids

A novel series of ω-pyridylalkenoic acids has been prepared by applying the Wittig reaction.Modifications were made in the ω-aryl moiety, the alkylene chain length, the α-methylene group adjacent to the carbonyl group, and the carboxyl group in the molecu