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p-tolyl 2,4-di-O-acetyl-1-thio-α-L-rhamnopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

943221-79-2

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943221-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 943221-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,2,2 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 943221-79:
(8*9)+(7*4)+(6*3)+(5*2)+(4*2)+(3*1)+(2*7)+(1*9)=162
162 % 10 = 2
So 943221-79-2 is a valid CAS Registry Number.

943221-79-2Relevant academic research and scientific papers

Synthesis and biological evaluation of acylated oligorhamnoside derivatives structurally related to mezzettiaside-6 with cytotoxic activity

Song, Gaopeng,Li, Sumei,Lei, Zhiwei,Li, Yibin,Li, Junhua,Liao, Yixian,Cui, Zi-Ning

, p. 6691 - 6702 (2016)

Two partially acylated oligorhamnoside derivatives 1 and 2 structurally related to the natural product mezzettiaside-6 were synthesized via a '2 + 1 + 1' convergent strategy. The bioassay results showed that the introduction of the acetyl groups to the 2-position of the terminal l-rhamnose was helpful to improve in vitro cytotoxicity. Compound 1 showed both extensive in vitro cytotoxicity in tumor cell lines and potential antimultidrug resistance capability. Preliminary mechanistic studies demonstrated that compound 1 could inhibit cell growth by inducing apoptosis, arresting cell cycle progression at the S phase in K562 cells.

Total synthesis of cleistetroside-2, partially acetylated dodecanyl tetrarhamnoside derivative isolated from Cleistopholis patens and Cleistopholis glauca

Zhang, Zaihong,Wang, Peng,Ding, Ning,Song, Gaopeng,Li, Yingxia

, p. 1159 - 1168 (2008/02/02)

The total synthesis of a partially acetylated dodecanyl tetrarhamnoside derivative, cleistetroside-2, which was isolated from Cleistopholis patens and Cleistopholis glauca and showed significant in vitro antibacterial activity against the Gram-positive ba

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