59290-37-8

Upstream product

• 1378825-44-5 4-methyl-3-nitropicolinonitrile 
• 23056-45-3 2-bromo-3-nitro-4-methyl pyridine 
• 21901-18-8 4-Methyl-3-nitro-2-pyridone 
• 6635-86-5 2-amino-4-methyl-3-nitropyridine 

Downstream Products

• 1612242-37-1 4-[(S)-1-(4-chloro-3-trifluoromethyl-phenyl)-2-methylamino-ethylamino]-pyrido[3,2-d]pyrimidine-8-carboxylic acid amide 
• 1612242-38-2 4-[(S)-2-azetidin-1-yl-1-(3-chloro-4-trifluoromethoxy-phenyl)-ethylamino]-pyrido[3,2-d]pyrimidine-8-carboxylamide 
• 1612242-58-6 C₂₄H₁₉F₄N₇O₅S 
• 1612242-74-6 C₂₅H₂₀ClF₃N₆O₆S 
• 1612242-76-8 C₂₄H₁₉ClF₃N₇O₅S 
• 1612241-91-4 4-[(S)-1-(3-fluoro-4-trifluoromethyl-phenyl)-2-methylamino-ethylamino]-pyrido[3,2-d]pyrimidine-8-carboxylic acid amide 

Relevant academic research and scientific papers

AZAQUINAZOLINE CARBOXAMIDE DERIVATIVES

Novel azaquinazoline carboxamide derivatives of formula (I) wherein W1, W2, W3, W4, R1, R2, R3 and m which are defined above, are p70S6K inhibitor, and can be employed, inter alia, for the treatment of hyperproliferative disorders.

Compositions and methods for the treatment of coccidiosis

Anticoccidial compositions which comprise as active ingredient pyridine derivatives having the formula STR1 wherein R1 is hydrogen atom, a halomethyl group or methyl group; R2 is hydrogen atom or an alkyl group of 1-3 carbon atoms; R3 is hydrogen atom, an alkyl group of 1-3 carbon atoms, allyl group, an alkyl group having 2 or 3 carbon atoms and alkoxy of 1 or 2 carbon atoms as a substituent, an alkyl group having 1-3 carbon atoms and hydroxy as a substituent, an alkanoyl group of 1-18 carbon atoms, a haloacetyl group, an alkenoyl group of 3-11 carbon atoms, an aromatic acyl group, a heterocyclic acyl group, an N-alkylcarbamoyl group of 1-4 carbon atoms in the alkyl moiety or hydroxy group; Provided that when R2 is said alkyl group of 1-3 carbon atoms, R3 is said alkyl group of 1-3 carbon atoms and inorganic acid addition salts thereof.