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phosphoric acid dibenzyl ester 8-methoxy-1-methyl-1H-benzo[de][1,6]naphthyridin-9-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

680615-39-8

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680615-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 680615-39-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,0,6,1 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 680615-39:
(8*6)+(7*8)+(6*0)+(5*6)+(4*1)+(3*5)+(2*3)+(1*9)=168
168 % 10 = 8
So 680615-39-8 is a valid CAS Registry Number.

680615-39-8Downstream Products

680615-39-8Relevant academic research and scientific papers

Antineoplastic Agents. 380. Isolation and X-ray Crystal Structure Determination of Isoaaptamine from the Republic of Singapore Hymeniacidon sp. and Conversion to the Phosphate Prodrug Hystatin 1

Pettit, George R.,Hoffmann, Holger,McNulty, James,Higgs, Kerianne C.,Murphy, Alison,Molloy, David J.,Herald, Delbert L.,Williams, Michael D.,Pettit, Robin K.,Doubek, Dennis L.,Hooper, John N. A.,Albright, Leslie,Schmidt, Jean M.,Chapuis, Jean-Charles,Tackettt, Larry P.

, p. 506 - 509 (2004)

By use of bioassay (murine P388 lymphocytic leukemia cell line) guided isolation procedures, extracts of the Republic of Singapore marine sponge Hymeniacidon sp. were found to contain demethyl-oxyaaptamine (1) and aaptamine (3) as prominent cancer cell growth inhibitory constituents accompanied by the trace, albeit more active, component isoaaptamine (4). The isolation, X-ray structure elucidation, and antineoplastic and antimicrobial activities of isoaaptamine (4) have been summarized. Because of instability, isoaaptamine (4) was converted to a stable sodium phosphate prodrug designated hystatin 1 (7).

Aaptamine and isoaaptamine and structural modifications thereof

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Page/Page column 5; 7, (2010/02/13)

Disclosed herein is the isolation and elucidation of the structure of isoaptamine (2), and its conversion to numerous novel related compounds, which appear to have antimicrobial and/or cancer fighting properties. Also disclosed is the conversion of isoaaptamine (2) to the phosphate prodrug hystatin 1 (11), as well as the conversion of aaptamine to numerous compounds, including but not limited to: 9-demethyloxyaaptamine (3); 4-methylaaptamine (4); 1,4-dimethylaaptamine iodide (5); 4-N-methyl-8,9-dihydroxy-4H benzo[de][1,6]naphthyridine (7); 4-N-methyl-8 methoxy-9 hydroxy-4H benzo[de][1,6]naphthyridine (8); 1-H-Benzo[de][1-6]naphthyridinium salts (9a-c); hystatin 2 (10a); and others.

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