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ethyl N-[[(3R,5S)-7-chloro-5-(2,3-dimethoxyphenyl)-1-(3-hydroxy-2,2-dimethylpropyl)-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepin-3-yl]acetyl]-L-alaninate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

383662-10-0

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  • ethyl N-[[(3R,5S)-7-chloro-5-(2,3-dimethoxyphenyl)-1-(3-hydroxy-2,2-dimethylpropyl)-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepin-3-yl]acetyl]-L-alaninate

    Cas No: 383662-10-0

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383662-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 383662-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,3,6,6 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 383662-10:
(8*3)+(7*8)+(6*3)+(5*6)+(4*6)+(3*2)+(2*1)+(1*0)=160
160 % 10 = 0
So 383662-10-0 is a valid CAS Registry Number.

383662-10-0Relevant articles and documents

Benzoxazepinones and their use as squalene synthase inhibitors

-

, (2008/06/13)

There is disclosed a compound represented by the formula [I]: wherein R1 is optionally substituted 1-carboxyethyl group, optionally substituted alkyl-sulfonyl group, optionally substituted (carboxy-cycloalkyl)-alkyl group, -X1-X2-Ar-X3-X4-COOH (wherein X1 and X4 are a bond or alkylene group, X2 and X3 are a bond, -O-, -S-, Ar is divalent aromatic group etc.), R2 is alkyl group optionally substituted with alkanoyloxy group and/or hydroxy group, R3 is alkyl group, and W is halogen atom, etc., or a salt thereof. The compound has the cholesterol lowering activity and the triglyceride lowering activity and is useful for preventing and/or treating hyperlipidemia.

Synthesis of novel 4,1-benzoxazepine derivatives as squalene synthase inhibitors and their inhibition of cholesterol synthesis

Miki, Takashi,Kori, Masakuni,Mabuchi, Hiroshi,Tozawa, Ryu-ichi,Nishimoto, Tomoyuki,Sugiyama, Yasuo,Teshima, Koichiro,Yukimasa, Hidefumi

, p. 4571 - 4580 (2007/10/03)

Modification of the carboxyl group at the 3-position and introduction of protective groups to the hydroxy group of the 4,1-benzoxazepine derivative 2 (metabolite of 1) were carried out, and the inhibitory activity for squalene synthase and cholesterol syn

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