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3-(2-chlorophenylamino)-1-methylquinolinium iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1268525-91-2

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1268525-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268525-91-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,5,2 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1268525-91:
(9*1)+(8*2)+(7*6)+(6*8)+(5*5)+(4*2)+(3*5)+(2*9)+(1*1)=182
182 % 10 = 2
So 1268525-91-2 is a valid CAS Registry Number.

1268525-91-2Downstream Products

1268525-91-2Relevant academic research and scientific papers

3-SUBSTITUTED QUINOLINIUM AND 7H-INDOLO[2,3-c]QUINOLINIUM SALTS AS NEW ANTIINFECTIVES

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Page/Page column 7, (2012/07/13)

The present invention relates to quinolinium antiinfective agents in which the qunolinium nucleus is fused to an indole ring or the qunolinium nucleus is linked to a cyclic structure through an opened indole or a benzothiophene or benzofuran ring. The compound is further substituted with various substituent groups. The compounds are represented by formula (I), (II) and (III): Pharmaceutical compositions and methods of use are also included.

Identification of 3-phenylaminoquinolinium and 3-phenylaminopyridinium salts as new agents against opportunistic fungal pathogens

Mazu, Tryphon K.,Etukala, Jagan R.,Zhu, Xue Y.,Jacob, Melissa R.,Khan, Shabana I.,Walker, Larry A.,Ablordeppey, Seth Y.

experimental part, p. 524 - 533 (2011/02/28)

Previous studies on the indoloquinoline alkaloid, cryptolepine (2), revealed that it has antii-nfective properties among other activities. Using Structure-activity relationship (SAR) techniques, several ring-opened analogs of cryptolepine (3-phenylaminopyridinium and 3-phenylaminoquinolinium derivatives) were designed to improve the potency and lower the cytotoxicity shown by several of the precursor agents. Results indicate that these ring-opened analogs constitute new anti-infective agents with over a 100-fold potency and several fold lower cytotoxicity than cryptolepine from which they are derived.

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