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Benzoic acid, 2-(3-butenyloxy)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141946-22-7

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141946-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141946-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,9,4 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 141946-22:
(8*1)+(7*4)+(6*1)+(5*9)+(4*4)+(3*6)+(2*2)+(1*2)=127
127 % 10 = 7
So 141946-22-7 is a valid CAS Registry Number.

141946-22-7Relevant academic research and scientific papers

Intramolecular Photocycloaddition of 4-Phenoxybut-1-enes: a Convenient Access to the 4-Oxatricyclo3.7>undeca-2,10-diene Skeleton

Al-Qaradawi, Siham Y.,Cosstick, Kevin B.,Gilbert, Andrew

, p. 1145 - 1148 (1992)

The photochemistry of 4-phenoxybut-1-ene is markedly influenced by the presence and position of electron-withdrawing substituents on the benzene ring.A cyano substituent in the 2'-or 4'-position promotes an efficient intramolecular cycloaddition to give g

Development of Macrocyclic Peptides Containing Epoxyketone with Oral Availability as Proteasome Inhibitors

Li, Daqiang,Zhang, Xiaotuan,Ma, Xiaodong,Xu, Lei,Yu, Jianjun,Gao, Lixin,Hu, Xiaobei,Zhang, Jiankang,Dong, Xiaowu,Li, Jia,Liu, Tao,Zhou, Yubo,Hu, Yongzhou

, p. 9177 - 9204 (2018/10/24)

Macrocyclization has been frequently utilized for optimizing peptide or peptidomimetic-based compounds. In an attempt to obtain potent, metabolically stable, and orally available proteasome inhibitors, 30 oprozomib-derived macrocyclic peptides with structural diversity in their N-terminus and linker were successively designed and synthesized for structure-activity relationship (SAR) studies. As a consequence, the macrocyclic peptides with N-methyl-pyrazole (24p, 24x), imidazole (24t), and pyrazole (24v) as their respective N-termini exhibited favorable in vitro activity and metabolic stability, which translated into their potent in vivo proteasome inhibitory activity after oral administration. In particular, compound 24v, as the most distinguished one among this series, displayed excellent chymotrypsin-like (ChT-L, β5) inhibitory potency (IC50 = 16 nM), low nanomolar antiproliferative activity against all three of the tested cell lines, and superior metabolic stability in mouse liver microsome (MLM), as well as favorable inhibition against ChT-L compared to that of oprozomib in BABL/c mice following po administration at a comparatively low dose, thereby representing a promising candidate for further development.

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