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3-fluoro-4,4',5-trimethoxy-3'-O-tert-butyldiphenylsilyl-(Z)-stilbene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

861995-10-0

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861995-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 861995-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,9,9 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 861995-10:
(8*8)+(7*6)+(6*1)+(5*9)+(4*9)+(3*5)+(2*1)+(1*0)=210
210 % 10 = 0
So 861995-10-0 is a valid CAS Registry Number.

861995-10-0Downstream Products

861995-10-0Relevant academic research and scientific papers

Antineoplastic agents. 509. Synthesis of fluorcombstatin phosphate and related 3-halostilbenes

Pettit, George R.,Minardi, Mathew D.,Rosenberg, Heidi J.,Hamel, Ernest,Bibby, Michael C.,Martin, Sandie W.,Jung, M. Katherine,Pettit, Robin K.,Cuthbertson, Timothy J.,Chapuis, Jean-Charles

, p. 1450 - 1458 (2008/12/22)

The present SAR study of combretastatin A-3 (3a) focused on replacement of the 3-hydroxyl group by a series of halogens. That approach with Z-stilbenes resulted in greatly enhanced (> 10-100-fold) cancer cell growth inhibition against a panel of human cancer cell lines and the murine P388 lymphocytic leukemia cell line. Synthesis of the 3-fluoro-Z-stilbene designated fluorcombstatin (11a) and its potassium 3′-O-phosphate derivative (16c) by the route 7 → 8a → 11a → 14 → 16c illustrates the general synthetic pathway. The 3′-O-phosphoric acid ester (15) of 3-bromo-Z-stilbene 13a was also converted to representative cation salts to evaluate the potential for improved aqueous solubility, and the potassium salt (16 mg/mL in water) proved most useful. The fluoro (11a), chloro (12a), and bromo (13a) halocombstatins were nearly equivalent to combretastatin A-4 (1a) as inhibitors of tubulin polymerization and of the binding of colchicine to tubulin. The tubulin binding in cell-free systems was also retained in human umbilical vein endothelial cells. All three halocombstatins retained the powerful human cancer cell line inhibitory activity of combretastatin A-4 (1a) and proved superior to combretastatin A-3 (3a). In addition, the halocombstatins targeted Gram-positive bacteria and Cryptococcus neoformans.

Halocombstatins and methods of synthesis thereof

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Page/Page column 4, (2008/06/13)

The invention relates to novel compounds denominated halocombstatins. The halocombstatins are derivatives of combretastatin A-3, and include compounds that exhibit cancer growth cell inhibition against a panel of human cancer cell lines and the murine P38

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