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Z-D-Phe-L-Leu is a synthetic peptide consisting of the amino acids Z-D-phenylalanine and L-leucine. Z-D-Phe-L-Leu is characterized by its unique structure and properties, which make it a valuable asset in research and pharmaceutical applications. Its potential in various medical fields, such as cancer therapy and drug development, is attributed to its ability to interact with specific receptors and enzymes in the body. Z-D-Phe-L-Leu is a promising compound in the realm of chemical and biomedical research, offering versatility and effectiveness in studying biological processes and developing new treatments.

4313-72-8

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4313-72-8 Usage

Uses

Used in Pharmaceutical Research and Development:
Z-D-Phe-L-Leu is used as a research tool for studying biological processes and developing new treatments. Its unique structure and properties allow it to interact with specific receptors and enzymes in the body, making it a valuable asset in understanding and manipulating these processes.
Used in Cancer Therapy:
Z-D-Phe-L-Leu is used as a potential therapeutic agent in cancer treatment. Its ability to interact with specific biological targets makes it a promising candidate for the development of new cancer therapies.
Used in Drug Development:
Z-D-Phe-L-Leu is used as a compound in the development of new drugs. Its unique properties and interactions with biological targets make it a valuable component in the creation of novel pharmaceuticals with potential therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 4313-72-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,1 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4313-72:
(6*4)+(5*3)+(4*1)+(3*3)+(2*7)+(1*2)=68
68 % 10 = 8
So 4313-72-8 is a valid CAS Registry Number.

4313-72-8Downstream Products

4313-72-8Relevant academic research and scientific papers

Diastereoselective specificity for the hydrolysis of dipeptide esters in aqueous media

Ueoka, Ryuichi,Goto, Kouichi,Tanoue, Osamu,Miki, Atsushi,Yoshimitsu, Shinya,Imamura, Chikara,Ihara, Yasuji,Murakami, Yukito

, p. 73 - 74 (2007/10/03)

The diastereoselectivity for the hydrolysis of p-methoxycarbonylphenyl N-(benzyloxycarbonyl)-D(L)-phenylalanyl-L-leucinate in aqueous solution was inverted by changing concentrations of the substrates or the reaction temperature. The monomer-aggregate transition operated on the LL-substrate, which was suggested by the spectroscopic measurements, seems to be responsible for such behavior.

Efficient 1,4-Asymetric Induction Utilizing Electrostatic Interaction between Ligand and Substrate in the Asymmetric Hydrogenation of Didehydrodipeptides

Yamagishi, Takamichi,Ikeda, Satoru,Yatagai, Masanobu,Yamaguchi, Motowo,Hida, Mitsuhiko

, p. 1787 - 1790 (2007/10/02)

Electrostatic interaction between the amino group of the achiral 3-dimethylaminopropylidenebismethylenebis(diphenylphosphine) (1) and the carboxy group of the substrate enable an effective 1,4-asymmetric induction in the RhI-catalysed hydrogenation of didehydrodipeptides, to give (S,S)-or (R,R)-products selectively.The selectivity reached up to 94percent diastereoisomeric excess with acetyl didehydrodipeptides and 92percent with benzyloxycarbonyl substrates.

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