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330685-48-8

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330685-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 330685-48-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,6,8 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 330685-48:
(8*3)+(7*3)+(6*0)+(5*6)+(4*8)+(3*5)+(2*4)+(1*8)=138
138 % 10 = 8
So 330685-48-8 is a valid CAS Registry Number.

330685-48-8Downstream Products

330685-48-8Relevant academic research and scientific papers

Synthesis and biological evaluation of RON-neoglycosides as tumor cytotoxins

Langenhan, Joseph M.,Endo, Matthew M.,Engle, Jeffrey M.,Fukumoto, Liane L.,Rogalsky, Derek R.,Slevin, Lauren K.,Fay, Lindsay R.,Lucker, Ryan W.,Rohlfing, James R.,Smith, Kyle R.,Tjaden, Anja E.,Werner, Halina M.

, p. 2663 - 2676 (2012/01/07)

Cardenolides such as digitoxin have been shown to inhibit cancer cell growth, to reduce cancer metastasis, and to induce apoptosis in tumor cells. Among the most potent digitoxin-based cytotoxins identified to date are MeON-neoglycosides generated via oxyamine neoglycosylation. Here, we report our studies of oxyamine neoglycosylation aimed at facilitating the elucidation of linkage-diversified digitoxin neoglycoside structure-activity relationships. We identified conditions suitable for the convenient synthesis of digitoxin neoglycosides and found that sugar structure, rather than RON-glycosidic linkage, exerts the strongest influence on neoglycoside yield and stereochemistry. We synthesized a library of digitoxin neoglycosides and assessed their cytotoxicity against eight human cancer cell lines. Consistent with previous findings, our data show that the structure of RON-neoglycosidic linkages influences both the potency and selectivity of digitoxin neoglycosides.

HIV Integrase inhibitors

-

, (2008/06/13)

The present invention relates to the inhibition of HIV integrase, and to the treatment of AIDS or ARC by administering compounds of the following formula, or a tautomer of said compound, or a pharmaceutically acceptable salt, solvate or prodrug thereof: wherein R1, R2 and B1 are as defined herein.

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