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ethyl 2-(2-amino-4-methylpentanamido)-6-diazo-5-oxohex-anoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1998725-11-3

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1998725-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1998725-11-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,9,9,8,7,2 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1998725-11:
(9*1)+(8*9)+(7*9)+(6*8)+(5*7)+(4*2)+(3*5)+(2*1)+(1*1)=253
253 % 10 = 3
So 1998725-11-3 is a valid CAS Registry Number.

1998725-11-3Downstream Products

1998725-11-3Relevant academic research and scientific papers

PRODRUGS OF GLUTAMINE ANALOGS

-

, (2017/02/28)

Prodrugs of glutamine analogs, such as prodrugs of aza-serine, and 6-diazo-5-oxo-norleucine (DON), and 5-diazo-4-oxo-L-norvaline (L-DONV) are disclosed.

Discovery of 6-Diazo-5-oxo- l -norleucine (DON) Prodrugs with Enhanced CSF Delivery in Monkeys: A Potential Treatment for Glioblastoma

Rais, Rana,Jan?a?ík, Andrej,Tenora, Luká?,Nedelcovych, Michael,Alt, Jesse,Englert, Judson,Rojas, Camilo,Le, Anne,Elgogary, Amira,Tan, Jessica,Monincová, Lenka,Pate, Kelly,Adams, Robert,Ferraris, Dana,Powell, Jonathan,Majer, Pavel,Slusher, Barbara S.

, p. 8621 - 8633 (2016/10/03)

The glutamine antagonist 6-diazo-5-oxo-l-norleucine (DON, 1) has shown robust anticancer efficacy in preclinical and clinical studies, but its development was halted due to marked systemic toxicities. Herein we demonstrate that DON inhibits glutamine metabolism and provides antitumor efficacy in a murine model of glioblastoma, although toxicity was observed. To enhance DON's therapeutic index, we utilized a prodrug strategy to increase its brain delivery and limit systemic exposure. Unexpectedly, simple alkyl ester-based prodrugs were ineffective due to chemical instability cyclizing to form a unique diazo-imine. However, masking both DON's amine and carboxylate functionalities imparted sufficient chemical stability for biological testing. While these dual moiety prodrugs exhibited rapid metabolism in mouse plasma, several provided excellent stability in monkey and human plasma. The most stable compound (5c, methyl-POM-DON-isopropyl-ester) was evaluated in monkeys, where it achieved 10-fold enhanced cerebrospinal fluid to plasma ratio versus DON. This strategy may provide a path to DON utilization in glioblastoma multiforme patients.

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