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247233-66-5

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247233-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 247233-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,2,3 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 247233-66:
(8*2)+(7*4)+(6*7)+(5*2)+(4*3)+(3*3)+(2*6)+(1*6)=135
135 % 10 = 5
So 247233-66-5 is a valid CAS Registry Number.

247233-66-5Downstream Products

247233-66-5Relevant academic research and scientific papers

A torsional strain mechanism to tune pitch in supramolecular helices

Li, Liang-Shi,Jiang, Hongzhou,Messmore, Benjamin W.,Bull, Steve R.,Stupp, Samuel I.

, p. 5873 - 5876 (2008/09/16)

(Figure Presented) On the turn: Torsional strain has been used to control the pitch of helical nanostructures in the range of tens to hundreds of nanometers. In this method, sterically induced torsional strain on the primary helices forces the secondary h

Reversal of multiple drug resistance in cholangiocarcinoma by the glutathione S-transferase-π-specific inhibitor O 1-hexadecyl-γ-glutamyl-S-benzylcysteinyl-D-phenylglycine ethylester

Nakajima, Takaharu,Takayama, Tetsuji,Miyanishi, Koji,Nobuoka, Atsushi,Hayashi, Tsuyoshi,Abe, Tomoyuki,Kato, Junji,Sakon, Kiyoyuki,Naniwa, Yoshimitsu,Tanabe, Hirohumi,Niitsu, Yoshiro

, p. 861 - 869 (2007/10/03)

Cholangiocarcinoma is markedly resistant to chemotherapy and has a dismal prognosis, but its mechanism of drug resistance is unknown. This study examines whether glutathione S-transferase-π (GSTP1-1) is involved in resistance to anticancer drugs in cholangiocarcinoma and whether GSTP1-1-specific inhibitors can overcome this resistance. First, immunohistochemical examination disclosed strong staining of all our 17 cholangiocarcinoma specimens for GSTP1-1, irrespective of histological type. Transfection of the GSTP1-1 antisense expression vector into a human cholangiocarcinoma cell line (HuCCT1) apparently decreased its intracellular GSTP1-1 concentration, and the sensitivity of transfectants to adriamycin (ADR), cisplatin, and alkylating agents such as melphalan and 4-hydroxyperoxycyclophosphamide (4-HC) was increased significantly, compared with that of mock transfectants. We next synthesized GSTP1-1-specific inhibitors by elongating the carbon chain of the ethylester at the N-terminal of γ-glutamyl-S-benzylcysteinyl-phenylglycyl diethylester and performed a pharmacokinetic study on them. Of six GSTP1-1 inhibitors tested, O1-hexadecyl-γ-glutamyl-S-benzylcysteinyl-D-phenylglycine ethylester (C16C2) showed the smallest volume of central compartment and smallest volume of distribution at steady state and the second smallest clearance, being the most effective inhibitor in vivo. The IC50 value of ADR or 4-HC for HuCCT1 cells decreased greater by treatment with C16C2 in a dose-dependent manner, paralleling the decrease in GSTP1-1 activity, than that of ADR or 4-HC alone. The antitumor activity of ADR or cyclophosphamide was clearly enhanced by combination therapy with C16C2 in a xenograft model. In conclusion, our results demonstrated that GSTP1-1 is a resistance factor for anticancer drugs in cholangiocarcinoma and that C16C2, a GSTP1-1-specific inhibitor, is a potent agent against the resistance.

Effective gelation of water using a series of bis-urea dicarboxylic acids

Estroff, Lara A.,Hamilton, Andrew D.

, p. 3447 - 3450 (2007/10/03)

At concentrations as low as 0. 3 wt % a novel family of bis-urea dicarboxylic acids gel water (see picture). The aggregation state (vesicles, gel, or fibers) depends on the pH, the ionic strength, and the molecular weight of the gelator. In this way, the gelation properties of an aqueous system are controlled by the molecular design.

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