667940-67-2

Upstream product

• 1000819-09-9 C₃₂H₄₃N₃O₃S 
• 27514-07-4 7-azabicyclo[2.2.1]heptane hydrochloride 
• 50910-54-8 trans-4-aminocyclohexanol hydrochloride 
• 666852-65-9 ethyl 2-{5-[(tert-butoxycarbonyl)amino]-2-thienyl}-2-methylpropanoate 
• 666852-64-8 ethyl 2-methyl-2-(5-nitro-2-thienyl)propanoate 
• 666852-63-7 ethyl 2-methyl-2-(2-thienyl)propanoate 
• 667940-71-8 C₃₅H₃₇N₃O₃S 

Downstream Products

• 1000819-28-2 C₃₀H₃₈N₄O₃S₂ 
• 1000819-37-3 C₃₄H₃₈N₄O₅S 
• 863561-73-3 C₃₁H₄₆N₄O 
• 863561-58-4 3-[3,3-dimethyl-4-oxo-4-(7-azabicyclo[2.2.1]heptan-7-yl)butyl]-4-[(1S)-1-methyl-2-{1-benzyl-pyrrolidin-3-ylamino}ethyl]-5-(3,5-dimethylphenyl)-1H-pyrrole 
• 863561-76-6 C₃₃H₃₇N₅O₇S₂ 
• 863561-74-4 C₃₈H₄₈N₄OS 
• 667940-58-1 2-(1,1-dimethyl-2-oxo-2-(7-azabicyclo[2.2.1]heptan-7-yl)ethyl)-4-[(1S)-1-methyl-2-(4-{pyridin-4-yl}piperidin-1-yl)carbonylamino-ethyl]-5-(3,5-dimethylphenyl)-6H-thieno[2,3-b]pyrrole 
• 667940-66-1 C₃₂H₄₂N₄O₃S₂ 

Relevant academic research and scientific papers

Synthesis and structure-activity relationships of thieno[2,3-b]pyrroles as antagonists of the GnRH receptor

A new class of small-molecule GnRH antagonists, the thieno[2,3-b]pyrroles, was designed. Herein, the synthesis and structure-activity relationships are described. Substitution at the C4 position was investigated; during this study, it was observed that in

PYRROLE DERIVATIVES AS GONADOTROPIN RELEASING HORMONE (GNRH) ANTAGONISTS

The invention relates to a group of novel thieno-pyrrole compounds of formula (I) wherein: R1,R2, R3, R4 M, and R5 are as defined in the specification, as inter alia, gonadotrophin releasing hor

THIENO-PYRROLE COMPOUNDS AS ANTAGONISTS OF GONADOTROPIN RELEASING HORMONE

The invention relates to a group of novel thieno-pyrrole compounds of Formula (I), wherein: R1, R2, R4, R5, R6, R6a, R7, R8, A and B are as defined in the specificatio