126149-54-0

Upstream product

• 126167-36-0 1-phenyl-6,7-dihydro[1,4]diazepino[6,7,1-hi]indole-3,4-dione 3-oxime 
• 100-47-0 benzonitrile 
• 129042-20-2 (3RS)-3,4,6,7-tetrahydro-3-hydroxy-4-oxo-1-phenylpyrrolo[3,2,1-jk][1,4]benzodiazepine 
• 129042-15-5 Acetic acid 4-oxo-1-phenyl-3,4,6,7-tetrahydro-[1,4]diazepino[6,7,1-hi]indol-3-yl ester 
• 129042-12-2 2-Oxy-1-phenyl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one 
• 33244-57-4 7-benzoyl-1H-indoline 
• 29813-79-4 7-benzoyl-1-bromoacetyl-2,3-dihydro-indole 
• 496-15-1 1-indoline 
• 27158-79-8 1-phenyl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one 
• 1026903-25-2 Methanesulfonic acid 4-oxo-1-phenyl-3,4,6,7-tetrahydro-[1,4]diazepino[6,7,1-hi]indol-3-yl ester 

Downstream Products

• 197895-08-2 (R)-3,9-diamino-1-phenyl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one 
• 197895-07-1 (R)-3-amino-9-nitro-1-phenyl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one 
• 197895-13-9 (R)-3-amino-1-phenyl-9-pyrrolidin-1-yl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one 
• 197895-11-7 (9-amino-4-oxo-1-phenyl-3,4,6,7-tetrahydro-[1,4]diazepino[6,7,1-hi]indol-3-yl)-carbamic acid tert-butyl ester 
• 197894-84-1 (R)-N-[9-amino-3,4,6,7-tetrahydro-4-oxo-1-phenyl-pyrrolo[3.2.1-j,k][1,4]benzodiazepin-3-yl]-3-pyridinecarboxamide 
• 197895-10-6 (9-nitro-4-oxo-1-phenyl-3,4,6,7-tetrahydro-[1,4]diazepino[6,7,1-hi]indol-3-yl)-carbamic acid tert-butyl ester 
• 197895-12-8 (4-oxo-1-phenyl-9-pyrrolidin-1-yl-3,4,6,7-tetrahydro-[1,4]diazepino[6,7,1-hi]indol-3-yl)-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Synthesis, structure-activity relationships, and pharmacological profile of 9-amino-4-oxo-1-phenyl-3,4,6,7-tetrahydro[1,4]diazepino[6,7,1-hi]indoles: Discovery of potent, selective phosphodiesterase type 4 inhibitors

The synthesis, structure-activity relationships, and biological properties of a novel series of potent and selective phosphodiesterase type 4 (PDE4) inhibitors are described. These new aminodiazepinoindoles displayed in vitro PDE4 activity with submicromo

Studies on a novel, potent and orally effective cholecystokinin A antagonist, FK-480. Synthesis and structure-activity relationships of FK-480 and related compounds

We prepared various novel tricyclic 1,4-benzodiazepine derivatives as cholecystokinin (CCK) A antagonists, which were evaluated preliminarily for inhibition of 125I-CCK-8 binding to rat pancreatic membranes in vitro and inhibiting effect on CCK

Tricyclic compounds

Tricyclo benzodiazepines are cholecystokinin antagonists.