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220741-33-3

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220741-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220741-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,7,4 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 220741-33:
(8*2)+(7*2)+(6*0)+(5*7)+(4*4)+(3*1)+(2*3)+(1*3)=93
93 % 10 = 3
So 220741-33-3 is a valid CAS Registry Number.

220741-33-3Relevant articles and documents

TRIAZOLE DERIVATIVES WITH ANTIFUNGAL ACTIVITY

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Paragraph 00294, (2021/08/14)

Disclosed are compounds of the formula (I) and pharmaceutically acceptable salts thereof, wherein R1, R2, Q2, L1 and n are as defined herein. The compounds have antifungal properties and are useful in the treatment of fungal infections, including infections that are resistant to conventions anti-fungal agents. Q1 is selected from: (Formulae Ia, Ib, Ic, Id, Ie, If, Ig, Ih, Ii, Ij and Ik) wherein * indicates the point of attachment to L1.

Heterocyclic substituted aniline calcium channel blockers

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, (2008/06/13)

The present invention provides compounds that block calcium channels having the Formula I shown below. STR1The present invention also provides methods of using the compounds of Formula I to treat stroke, cerebral ischemia, head trauma, epilepsy, asthma, amyotrophic lateral sclerosis, or pain and to pharmaceutical compositions that contain the compounds of Formula I.

Synthesis of a series of 4-benzyloxyaniline analogues as neuronal N-type calcium channel blockers with improved anticonvulsant and analgesic properties

Hu, Lain-Yen,Ryder, Todd R.,Rafferty, Michael F.,Feng, M. Rose,Lotarski, Susan M.,Rock, David M.,Sinz, Michael,Stoehr, Sally J.,Taylor, Charles P.,Weber, Mark L.,Bowersox, S. Scott,Miljanich, George P.,Millerman, Elizabeth,Wang, Yong-Xiang,Szoke, Balazs G.

, p. 4239 - 4249 (2007/10/03)

In this article, the rationale for the design, synthesis, and biological evaluation of a series of N-type voltage-sensitive calcium channel (VSCC) blockers is described. N-Type VSCC blockers, such as ziconotide, have shown utility in several models of str

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