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N-tert-Butyloxycarbonyl-(S)-1-(4-acetamidophenyl)ethylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

921604-25-3

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921604-25-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 921604-25-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,1,6,0 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 921604-25:
(8*9)+(7*2)+(6*1)+(5*6)+(4*0)+(3*4)+(2*2)+(1*5)=143
143 % 10 = 3
So 921604-25-3 is a valid CAS Registry Number.

921604-25-3Relevant academic research and scientific papers

4-Aminopyrimidines as novel HIV-1 inhibitors

Gadhachanda, Venkat R.,Wu, Baogen,Wang, Zhiwei,Kuhen, Kelli L.,Caldwell, Jeremy,Zondler, Helmut,Walter, Harald,Havenhand, Mark,He, Yun

, p. 260 - 265 (2007/10/03)

A series of 4-aminopyrimidines (1) was identified as novel HIV inhibitors of unknown molecular target. Structural modifications were carried out to establish its SAR and identify the linking site for target identification. A number of analogs were found to possess single digit inhibitory activity for HIV replication. Several analogs with various potential linkers, including a biotinated analog, also exhibited excellent potency, and could serve as tools for the identification of novel anti-HIV targets.

Azetidine, pyrrolidine and piperidine derivatives

-

, (2008/06/13)

A class of substituted azetidine, pyrrolidine and piperidine derivatives are selective agonists of 5-HT1 -like receptors, being potent agonists of the human 5-HT1Dα receptor subtype whilst possessing at least a 10-fold selective affinity for the 5-HT1Dα receptor subtype relative to the 5-HT1Dβ subtype; they are therefore useful in the treatment and/or prevention of clinical conditions, in particular migraine and associated disorders, for which a subtype-selective agonist of 5-HT1D receptors is indicated, whilst eliciting fewer side-effects, notably adverse cardiovascular events, than those associated with non-subtype-selective 5-HT1D receptor agonists.

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