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4-phenylbutylmalonic acid monoethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78573-22-5

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78573-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78573-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,7 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78573-22:
(7*7)+(6*8)+(5*5)+(4*7)+(3*3)+(2*2)+(1*2)=165
165 % 10 = 5
So 78573-22-5 is a valid CAS Registry Number.

78573-22-5Relevant academic research and scientific papers

Phosphinic pseudo-tripeptides as potent inhibitors of matrix metalloproteinases: A structure-activity study

Vassiliou, Stamatia,Mucha, Artur,Cuniasse, Philippe,Georgiadis, Dimitris,Lucet-Levannier, Karine,Beau, Fabrice,Kannan, Rama,Murphy, Gillian,Kn?uper, Vera,Rio, Marie-Christine,Basset, Paul,Yiotakis, Athanasios,Dive, Vincent

, p. 2610 - 2620 (2007/10/03)

Several phosphinic pseudo-tripeptides of general formula R-XaaΨ(PO2- CH2)Xaa'-Yaa'-NH2 were synthesized and evaluated for their in vitro activities to inhibit stromelysin-3, gelatinases A and B, membrane type-1 matrix metalloproteinase, collagenases 1 and 2, and matrilysin. With the exception of collagenase-1 and matrilysin, phosphinic pseudo-tripeptides behave as highly potent inhibitors of matrix metalloproteinases, provided they contain in P1' position an unusual long aryl-alkyl substituent. Study of structure-activity relationships regarding the influence of the R and Xaa' substituents in this series may contribute to the design of inhibitors able to block only a few members of the matrix metalloproteinase family.

Synthesis and Hypoglycemic Activity of Phenylalkyloxiranecarboxylic Acid Derivatives

Eistetter, Klaus,Wolf, Horst P. O.

, p. 109 - 113 (2007/10/02)

A series of new 2-(phenylalkyl)oxirane-2-carboxylic acids has been synthesized and studied for its effects on the concentration of blood glucose.Most of the compounds exhibit remarkable blood glucose lowering activities in fasted rats.Structure-activity s

Substituted oxiranecarboxylic acids, their use and medicaments containing them

-

, (2008/06/13)

Substituted oxiranecarboxylic acids of the formula STR1 wherein R1 denotes a hydrogen atom (--H), a halogen atom, a hydroxylroup, a lower alkyl group, a lower alkoxy group or a trifluoromethyl group, R2 has one of the meanings of Rs

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