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(2S)-2-methyl-N-((S)-1-phenylethyl)octanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128342-66-5

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128342-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128342-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,4 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128342-66:
(8*1)+(7*2)+(6*8)+(5*3)+(4*4)+(3*2)+(2*6)+(1*6)=125
125 % 10 = 5
So 128342-66-5 is a valid CAS Registry Number.

128342-66-5Downstream Products

128342-66-5Relevant academic research and scientific papers

Further novel anti-parasitic compounds

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Page/Page column 15-16, (2016/05/19)

A novel structural class of highly N-methylated linear lipopeptide compounds useful for the treatment of parasitic disease.

NOVEL ANTI-PARASITIC COMPOUNDS

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, (2012/05/07)

A novel structural class of highly N-methylated linear lipopeptide compounds useful for the treatment of parasitic disease.

Almiramides A-C: Discovery and development of a new class of leishmaniasis lead compounds

Sanchez, Laura M.,Lopez, Dioxelis,Vesely, Brian A.,Della Togna, Gina,Gerwick, William H.,Kyle, Dennis E.,Linington, Roger G.

experimental part, p. 4187 - 4197 (2010/08/19)

Leishmaniasis is a debilitating disease caused by protozoan parasites of the genus Leishmania, which affects an estimated 12 million people worldwide. The discovery of new lead compounds for leishmaniasis is therefore a pressing concern for global health programs. The organic extract of a Panamanian collection of the marine cyanobacterium Lyngbya majuscula showed strong in vitro activity in two complementary screens against the tropical parasite Leishmania donovani, the causative agent of visceral leishmaniasis. Chromatographic separation of this complex mixture led to the isolation of the highly N-methylated linear lipopeptides, almiramides A-C (1-3). Comparison with the biological activities of a number of related metabolites and semisynthetic derivatives revealed key features required for activity and afforded one new compound (11) with superior in vitro activity. Subsequent synthesis of a library of simplified analogues led to the discovery of several compounds with improved therapeutic indices to the natural products.

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