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8-[(3-trifluoromethyl)benzyloxy]caffeine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1220521-27-6

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1220521-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1220521-27-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,0,5,2 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1220521-27:
(9*1)+(8*2)+(7*2)+(6*0)+(5*5)+(4*2)+(3*1)+(2*2)+(1*7)=86
86 % 10 = 6
So 1220521-27-6 is a valid CAS Registry Number.

1220521-27-6Downstream Products

1220521-27-6Relevant academic research and scientific papers

Inhibition of monoamine oxidase by 8-benzyloxycaffeine analogues

Strydom, Belinda,Malan, Sarel F.,Castagnoli Jr., Neal,Bergh, Jacobus J.,Petzer, Jacobus P.

experimental part, p. 1018 - 1028 (2010/04/26)

Based on recent reports that several (E)-8-styrylcaffeinyl analogues are potent reversible inhibitors of monoamine oxidase B (MAO-B), a series of 8-benzyloxycaffeinyl analogues were synthesized and evaluated as inhibitors of baboon liver MAO-B and recombinant human MAO-A and -B. The 8-benzyloxycaffeinyl analogues were found to inhibit reversibly both MAO isoforms with enzyme-inhibitor dissociation constants (Ki values) ranging from 0.14 to 1.30 μM for the inhibition of human MAO-A, and 0.023-0.59 μM for the inhibition of human MAO-B. The most potent MAO-A inhibitor was 8-(3-methylbenzyloxy)caffeine while 8-(3-bromobenzyloxy)caffeine was the most potent MAO-B inhibitor. The analogues inhibited human and baboon MAO-B with similar potencies. A quantitative structure-activity relationship (QSAR) study indicated that the MAO-B inhibition potencies of the 8-benzyloxycaffeinyl analogues are dependent on the Hansch lipophilicity (π) and Hammett electronic (σ) constants of the substituents at C-3 of the benzyloxy ring. Electron-withdrawing substituents with a high degree of lipophilicity enhance inhibition potency. These results are discussed with reference to possible binding orientations of the inhibitors within the active site cavities of MAO-A and -B.

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