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12,13-dihydro-2,10-dibenzyloxy-6-N-(1-benzyloxymethyl-2-benzyloxyethylamino)-13-(β-D-2,3,4,6-tetra-O-benzylglucopyranosyl)-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

357401-16-2

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357401-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 357401-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,4,0 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 357401-16:
(8*3)+(7*5)+(6*7)+(5*4)+(4*0)+(3*1)+(2*1)+(1*6)=132
132 % 10 = 2
So 357401-16-2 is a valid CAS Registry Number.

357401-16-2Downstream Products

357401-16-2Relevant academic research and scientific papers

PROCESS FOR PRODUCING INDOLOPYRROLOCARBAZOLE DERIVATIVE

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Page/Page column 27-28, (2008/06/13)

The present invention relates to an industrially preferable process for producing an indolopyrrolocarbazole derivative represented by the formula (I): or a pharmaceutically acceptable salt thereof, which is useful as an anti-cancer agent. The above proce

Practical synthesis of a potent indolocarbazole-based, DNA topoisomerase inhibitor

Akao, Atsushi,Hiraga, Shouichi,Iida, Takehiko,Kamatani, Asayuki,Kawasaki, Masashi,Mase, Toshiaki,Nemoto, Takayuki,Satake, Nobuya,Weissman, Steven A,Tschaen, David M,Rossen, Kai,Petrillo, Daniel,Reamer, Robert A,Volante

, p. 8917 - 8923 (2007/10/03)

DNA topoisomerase I inhibitors are currently under investigation as cancer chemotherapy agents of which indolocarbazole glycoside (1) has been identified as a promising candidate. A practical, scalable synthesis of 1 that limits the isolation of cytotoxic compounds to only that of the final product is described. The convergent process features a novel phase transfer-promoted glycosylation of aglycone core (4); subsequent hydrolysis provides anhydride (8). The hydrazine fragment (3), which is coupled with 8, is synthesized via a modification of existing procedures. The coupled product (2) is subsequently hydrogenated to provide 1 in excellent purity via direct crystallization (>99.3 A%).

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