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212912-12-4

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212912-12-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 212912-12-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,9,1 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 212912-12:
(8*2)+(7*1)+(6*2)+(5*9)+(4*1)+(3*2)+(2*1)+(1*2)=94
94 % 10 = 4
So 212912-12-4 is a valid CAS Registry Number.

212912-12-4Downstream Products

212912-12-4Relevant articles and documents

New anti-HIV derivatives: Synthesis and antiviral evaluation

De Michelis,Rocheblave,Priem,Chermann,Kraus

, p. 1253 - 1262 (2007/10/03)

A small focused library of 18 compounds incorporating the motif 1,3-(N,N'-dibenzyl)diamino-2-propanol has been synthesized, using adapted synthetic methodologies. These series of compounds were evaluated for their in vitro anti-HIV activity on infected MT4 cells (syncytium formation observation). Some of the new synthesized compounds show potent anti-HIV activities. EC50 values for compounds (31, 40, 34, 37 and 46Scheme 3(i) Na2SO4, CH2Cl2, rt; (ii) NaBH4, EtOH, 0°C; (iii) Boc2O, CH2Cl2, 0°C; (iv) DMSO, TFAA, Et3N, CH2Cl2, -60°C; (v) TFA, CH2Cl2, rt; (vi) BOP, RCOOH, Et3N, CH2Cl2, rt.) range from 0.1 to 1μM. In order to determine at which level these new derivatives interfere with the HIV replicative cycle, inhibition assays on recombinant HIV protease and HIV integrase have been performed. None of the compounds were found active on these two enzymatic targets. Experiments are in progress in order to identify their biological target within the HIV replicative cycle. Copyright (C) 2000 Elsevier Science Ltd.

Synthesis and anti-HIV activities of symmetrical N1,N3-dibenzyl-2- hydroxy-propane derivatives

Medou,Bouygues,Rocheblave,Chermann,Kraus

, p. 1861 - 1866 (2007/10/03)

We report the synthesis and the anti-HIV activities of new C2- symmetrical and achiral N1,N3-dibenzyl-2-hydroxy-propane isosteres. Some of them showed significant inhibitory activity with respect to HIV-infected MT4 cells

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