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methyl 5-[4-(α-D-mannopyranosyloxy)phenyl]pyridine-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1295649-64-7

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1295649-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1295649-64-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,5,6,4 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1295649-64:
(9*1)+(8*2)+(7*9)+(6*5)+(5*6)+(4*4)+(3*9)+(2*6)+(1*4)=207
207 % 10 = 7
So 1295649-64-7 is a valid CAS Registry Number.

1295649-64-7Downstream Products

1295649-64-7Relevant academic research and scientific papers

MANNOSIDE COMPOUNDS AND METHODS OF USE THEREOF

-

, (2012/08/28)

The present invention encompasses compounds and methods for treating urinary tract infections.

Lead optimization studies on FimH antagonists: Discovery of potent and orally bioavailable ortho-substituted biphenyl mannosides

Han, Zhenfu,Pinkner, Jerome S.,Ford, Bradley,Chorell, Erik,Crowley, Jan M.,Cusumano, Corinne K.,Campbell, Scott,Henderson, Jeffrey P.,Hultgren, Scott J.,Janetka, James W.

, p. 3945 - 3959 (2012/07/16)

Herein, we describe the X-ray structure-based design and optimization of biaryl mannoside FimH inhibitors. Diverse modifications to the biaryl ring to improve druglike physical and pharmacokinetic properties of mannosides were assessed for FimH binding affinity based on their effects on hemagglutination and biofilm formation along with direct FimH binding assays. Substitution on the mannoside phenyl ring ortho to the glycosidic bond results in large potency enhancements several-fold higher than those of corresponding unsubstituted matched pairs and can be rationalized from increased hydrophobic interactions with the FimH hydrophobic ridge (Ile13) or "tyrosine gate" (Tyr137 and Tyr48) also lined by Ile52. The lead mannosides have increased metabolic stability and oral bioavailability as determined from in vitro PAMPA predictive model of cellular permeability and in vivo pharmacokinetic studies in mice, thereby representing advanced preclinical candidates with promising potential as novel therapeutics for the clinical treatment and prevention of recurring urinary tract infections.

COMPOUNDS AND METHODS FOR TREATING BACTERIAL INFECTIONS

-

, (2011/05/06)

The present invention encompasses compounds and methods for treating urinary tract infections.

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