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2-Amino-3-(4-chlorobenzoyl)-6-benzyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132861-88-2

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132861-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132861-88-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,6 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132861-88:
(8*1)+(7*3)+(6*2)+(5*8)+(4*6)+(3*1)+(2*8)+(1*8)=132
132 % 10 = 2
So 132861-88-2 is a valid CAS Registry Number.

132861-88-2Downstream Products

132861-88-2Relevant academic research and scientific papers

THIOPHENES USEFUL FOR MODULATING THE ADENOSINE RECEPTOR

-

, (2008/06/13)

The present invention relates to compounds of formulas (IA), (IB), and (IC): STR1 the preparation thereof, pharmaceutical formulations thereof, and their use in medicine as allosteric adenosine receptor modulators for uses including protection against hypoxia and ischemia induced injury and treatment of adenosine-sensitive cardiac arrhythmias.

Allosteric modulation of the adenosine A1 receptor. Synthesis and biological evaluation of novel 2-amino-3-benzoylthiophenes as allosteric enhancers of agonist binding

Van Der Klein, Pieter A. M.,Kourounakis, Angeliki P.,IJzerman, Ad P.

, p. 3629 - 3635 (2007/10/03)

Novel allosteric enhancers of agonist binding to the rat adenosine A1 receptor are described. The lead compound for the new series was PD 81,723 ((2-amino-4,5-dimethyl-3-thienyl)[3-(trifluoromethyl)phenyl]methanone), a compound previously reported by Bruns and co-workers (Mol. Pharmacol. 1990, 38, 950-958). The 4,5-dimethyl group and the benzoyl moiety were targets for further modifications, leading to series of 4,5-dialkyl (12a-g), of tetrahydrobenzo (12h-u), and of tetrahydropyridine (13a-g) derivatives. A number of compounds, in particular 12b, 12e, 12j, 12n, and 12u, proved superior to PD 81,723. Their EC50 values for enhancing the binding of the adenosine A1 receptor agonist N6-cyclopentyladenosine to the receptor were lower, and/or their antagonistic activity on the adenosine A1 receptor was shown to be diminished.

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