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4-Thiazolidinecarboxamide, 3-[(2S,3S)-3-amino-2-hydroxy-4-(3-methoxyphenyl)-1-oxobutyl]-N-[(2,6- dimethylphenyl)methyl]-5,5-dimethyl-, (4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

672965-18-3

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672965-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 672965-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,2,9,6 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 672965-18:
(8*6)+(7*7)+(6*2)+(5*9)+(4*6)+(3*5)+(2*1)+(1*8)=203
203 % 10 = 3
So 672965-18-3 is a valid CAS Registry Number.

672965-18-3Downstream Products

672965-18-3Relevant academic research and scientific papers

Structure-activity relationships of novel HIV-1 protease inhibitors containing the 3-amino-2-chlorobenzoyl-allophenylnorstatine structure

Mimoto, Tsutomu,Nojima, Satoshi,Terashima, Keisuke,Takaku, Haruo,Shintani, Makoto,Hayashi, Hideya

, p. 1299 - 1308 (2008/09/19)

A series of peptidomimetic human immunodeficiency virus (HIV) protease inhibitors containing substituted allophenylnorstatine (Apns: (2S,3S)-3-amino-2-hydroxy-4-phenylbutyric acid) were designed and synthesized. From the structure-activity relationship of this series of compounds, SM-309515 was found to have potent antiviral activity against wild-type and resistant HIV-1s and to possess a desirable pharmacokinetic profile in dogs.

Structure-activity and structure-metabolism relationships of HIV protease inhibitors containing the 3-hydroxy-2-methylbenzoyl-allophenylnorstatine structure

Mimoto, Tsutomu,Terashima, Keisuke,Nojima, Satoshi,Takaku, Haruo,Nakayama, Mitsunobu,Shintani, Makoto,Yamaoka, Takashi,Hayashi, Hideya

, p. 281 - 293 (2007/10/03)

A series of peptidomimetic human immunodeficiency virus (HIV) protease inhibitors containing substituted allophenylnorstatine [Apns: (2S,3S)-3-amino-2-hydroxy-4-phenylbutyric acid] were designed and synthesized. From the structure-metabolism relationship of this type of HIV protease inhibitors, the compounds having para substitution of the phenyl ring of Apns and/or 2,6-disubstitution of the P2′ benzylamine were found to be able to avoid the P2 phenol glucuronidation that occurs with SM-319777 (formerly named JE-2147, KNI-764); one of the main metabolic pathways of SM-319777. These new analogues, such as SM-322377, had more desirable pharmacokinetic profiles and more potent antiviral activity against not only wild type HIV-1 but also the multi-drug-resistant HIV-1 than SM-319777.

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