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2-(acetyl-carboxymethyl-amino)-4-chloro-benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

914221-22-0

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914221-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 914221-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,2,2 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 914221-22:
(8*9)+(7*1)+(6*4)+(5*2)+(4*2)+(3*1)+(2*2)+(1*2)=130
130 % 10 = 0
So 914221-22-0 is a valid CAS Registry Number.

914221-22-0Relevant academic research and scientific papers

Synthesis of some cryptolepine analogues, assessment of their antimalarial and cytotoxic activities, and consideration of their antimalarial mode of action

Onyeibor, Onyeka,Croft, Simon L.,Dodson, Hilary I.,Feiz-Haddad, Mohammad,Kendrick, Howard,Millington, Nicola J.,Parapini, Silvia,Phillips, Roger M.,Seville, Scott,Shnyder, Steven D.,Taramelli, Donatella,Wright, Colin W.

, p. 2701 - 2709 (2007/10/03)

A series of analogues of cryptolepine (1) have been synthesized and evaluated for their in vitro antiplasmodial and cytotoxic properties. The IC50 values of several compounds (11a, 11k-m, 11o, 13) against Plasmodium falciparum (strain K1) were 90% at doses of 25 mg kg-1 day -1 with no apparent toxicity to the mice. 2,7-Dibromocryptolepine (15) was evaluated at several dose levels, and a dose-dependent suppression of parasitemia was seen (ED90 = 21.6 mg kg-1 day -1). The antimalarial mode of action of 1 appears to be similar to that of chloroquine and involves the inhibition of hemozoin formation. A number of analogues were assessed for their effects on the inhibition of β-hematin (hemozoin) formation, and the results were compared with their antiplasmodial activities having taken account of their predicted accumulation into the acidic parasite food vacuole. No correlation was seen (r2 = 0.0781) suggesting that the potent antimalarial activity of compounds such as 15 involves other mechanisms in addition to the inhibition of hemozoin formation.

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