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(2S)-tert-(butoxycarbonyl)amino-3,3-dimethyl-N-[(1S)-2-methoxy-1-phenylethyl]butanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

401512-42-3

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401512-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 401512-42-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,1,5,1 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 401512-42:
(8*4)+(7*0)+(6*1)+(5*5)+(4*1)+(3*2)+(2*4)+(1*2)=83
83 % 10 = 3
So 401512-42-3 is a valid CAS Registry Number.

401512-42-3Relevant academic research and scientific papers

A potent, selective inhibitor of matrix metalloproteinase-3 for the topical treatment of chronic dermal ulcers

Fray, M. Jonathan,Dickinson, Roger P.,Huggins, John P.,Occleston, Nicholas L.

, p. 3514 - 3525 (2003)

The pathology of chronic dermal ulcers is characterized by excessive proteolytic activity which degrades extracellular matrix (required for cell migration) and growth factors and their receptors. The overexpression of MMP-3 (stromelysin-1) and MMP-13 (col

Asymmetric synthesis of an MMP-3 inhibitor incorporating a 2-alkyl succinate motif

Ashcroft, Christopher P.,Challenger, Stephen,Derrick, Andrew M.,Storey, Richard,Thomson, Nicholas M.

, p. 362 - 368 (2013/09/06)

An efficient and practical synthesis is presented of the pharmaceutically active MMP-3 inhibitor UK-370,106 (1) via an olefination/catalytic asymmetric hydrogenation sequence. Commercially available 5-bromo-2-iodotoluene was converted in two steps to the

Matrix metalloprotease inhibitors

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Example 32, (2012/04/23)

Compounds of formula (I): or pharmaceutically acceptable salts thereof, or solvates of either entity, wherein the substituents have the values described herein, are useful as matrix metalloprotease (MMP) inhibitors

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