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Benzyl 7-(methoxymethoxy)-8-methyl-2-oxo-2H-chromen-3-ylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1239437-76-3

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1239437-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1239437-76-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,9,4,3 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1239437-76:
(9*1)+(8*2)+(7*3)+(6*9)+(5*4)+(4*3)+(3*7)+(2*7)+(1*6)=173
173 % 10 = 3
So 1239437-76-3 is a valid CAS Registry Number.

1239437-76-3Relevant academic research and scientific papers

NOVOBIOCIN ANALOGUES AND TREATMENT OF POLYCYSTIC KIDNEY DISEASE

-

, (2011/04/24)

Novobiocin analogues are useful in methods of treating, inhibiting, and/or preventing cyst formation in autosomal dominant polycystic kidney disease (ADPKD) in a subject. The disclosure provides methods of treating ADPKD comprising administering a therapeutically effective amount of a coumarin-3-carboxamide novobiocin analogue. Accordingly, the method can include administering a novobiocin analogue in a therapeutically effective amount for reducing levels of mTOR pathway phosphoproteins P-mTOR, P-Akt and P-S6K, or combinations thereof. Further, the method can include administering a novobiocin analogue in a therapeutically effective amount for reducing levels of Hsp-90 client proteins CFTR, ErbB2, c-Raf and Cdk4, or combinations thereof.

Synthesis and evaluation of noviose replacements on novobiocin that manifest antiproliferative activity

Zhao, Huiping,Reddy Kusuma, Bhaskar,Blagg, Brian S. J.

scheme or table, p. 311 - 315 (2010/11/18)

Structural modifications to the coumarin core and benzamide side chain of novobiocin have successfully transformed the natural product from a selective DNA gyrase inhibitor into a potent inhibitor of the Hsp90 C-terminus. However, no structure-activity relationship studies have been conducted on the noviose appendage, which represents the rate-limiting synthon in the preparation of analogues. Therefore, a series of sugar mimics and nonsugar derivatives were synthesized and evaluated to identify simplified compounds that exhibit Hsp90 inhibition. Evaluation against two breast cancer cell lines demonstrated that replacement of the stereochemical complex noviose with simplified alkyl amines increased antiproliferative activity, resulting in novobiocin analogues that manifest IC50 values in the midnanomolar range.

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