890087-03-3

Basic information

• Product Name: 4-Chloro-2-cyclohexyl-1H-iMidazo[4,5-c]quinoline
• Synonyms: 1H-IMidazo[4,5-c]quinoline, 4-chloro-2-cyclohexyl-;4-Chloro-2-cyclohexyl-1H-iMidazo[4,5-c]quinoline;4-Chloro-2-Cyclohexyl-3H-Imidazo[4,5-C]Quinoline
• CAS NO: 890087-03-3
• Molecular Formula: C₁₆H₁₆ClN₃
• Molecular Weight: 285.77134
• Mol File: 890087-03-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 245-250 °C
• Boiling Point: 542.0±30.0 °C(Predicted)
• Appearance: /
• Density: 1.325±0.06 g/cm3(Predicted)
• PKA: 10.38±0.40(Predicted)
• CAS DataBase Reference: 4-Chloro-2-cyclohexyl-1H-iMidazo[4,5-c]quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chloro-2-cyclohexyl-1H-iMidazo[4,5-c]quinoline(890087-03-3)
• EPA Substance Registry System: 4-Chloro-2-cyclohexyl-1H-iMidazo[4,5-c]quinoline(890087-03-3)

Safety Data

• Hazardous Substances Data: 890087-03-3(Hazardous Substances Data)

Upstream product

• 87751-33-5 quinoline-3,4-diamine 
• 2099-63-0 anthranilic acid hydrochloride 
• 121845-92-9 2-<2-nitroethylideneamino>benzoic acid 
• 39061-97-7 4-chloro-3-nitroquinoline 
• 50332-66-6 3-nitro-quinolin-4-ol 
• 42606-33-7 3-nitro-4-aminoquinoline 
• 890086-92-7 2-cyclohexyl-1H-imidazo[4,5-c]quinoline 
• 890086-97-2 2-cyclohexyl-1H-imidazo[4,5-c]quinoline 5-oxide 

Downstream Products

• 1141444-55-4 2-cyclohexyl-N-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-4-amine 
• 1141444-48-5 2-cyclohexyl-N-(3,5-difluorophenyl)-1H-imidazo[4,5-c]quinolin-4-amine 
• 1141444-52-1 4-(2-cyclohexyl-1H-imidazo[4,5-c]quinolin-4-ylamino)phthalonitrile 
• 1141444-44-1 2-cyclohexyl-N-(2,4-dichlorophenyl)-1H-imidazo[4,5-c]quinolin-4-amine 
• 1141444-54-3 N-(benzo[d][1,3]dioxol-5-yl)-2-cyclohexyl-1H-imidazo[4,5-c]quinolin-4-amine 
• 1141444-39-4 N-(3-chlorophenyl)-2-cyclohexyl-1H-imidazo[4,5-c]quinolin-4-amine 
• 1141444-42-9 2-cyclohexyl-N-(3,5-dichlorophenyl)-1H-imidazo[4,5-c]quinolin-4-amine 
• 1141444-50-9 N-(3,5-bis(trifluoromethyl)phenyl)-2-cyclohexyl-1H-imidazo[4,5-c]quinolin-4-amine 
• 1141444-53-2 2-cyclohexyl-N-(3,4-dimethoxyphenyl)-1H-imidazo[4,5-c]quinolin-4-amine 
• 1141444-46-3 2-cyclohexyl-N-(3,4-difluorophenyl)-1H-imidazo[4,5-c]quinolin-4-amine 

Relevant articles and documents

Novel 2-and 4-Substituted 1H-Imidazo[4,5-c]quinolin-4-amine derivatives as allosteric modulators of the A3 adenosine receptor

4-Arylamino and 2- cycloalkyl (including amino substitution) modifications were made in a series of 1Himidazo[ 4,5-c]quinolin-4-amine derivatives as allosteric modulators of the human A3 adenosine receptor (AR). In addition to allosteric modula

Structure-activity relationships of new 1H-imidazo[4,5-c]quinolin-4-amine derivatives as allosteric enhancers of the A3 adenosine receptor

1H-Imidazo[4,5-c]quinolin-4-amine derivatives have been synthesized as allosteric modulators of the human A3 adenosine receptor (AR). Structural modifications were made at the 4-amino and 2 positions. The compounds were tested in both binding and functional assays, and many were found to be allosteric enhancers of the action of A3AR agonists by several different criteria. First, a potentiation of the maximum efficacy of the agonist C1-IB-MECA was observed for numerous derivatives. Also, a number of these compounds decreased the rate of dissociation of the agonist [ 125I]I-AB-MECA from the A3AR. Most prominently, compound 43 (LUF6000) was found to enhance agonist efficacy in a functional assay by 45% and decrease dissociation rate similarly without influencing agonist potency. The structural requirements for allosteric enhancement at the A3AR were distinct from the requirements to inhibit equilibrium binding. Thus, we have prepared allosteric enhancers of the human A3AR that have an improved allosteric effect in comparison to the inhibition of equilibrium binding at the orthosteric site.