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1407510-82-0

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1407510-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1407510-82-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,7,5,1 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1407510-82:
(9*1)+(8*4)+(7*0)+(6*7)+(5*5)+(4*1)+(3*0)+(2*8)+(1*2)=130
130 % 10 = 0
So 1407510-82-0 is a valid CAS Registry Number.

1407510-82-0Downstream Products

1407510-82-0Relevant articles and documents

Synthesis of ciprofloxacin dimers for evaluation of bacterial permeability in atypical chemical space

Ross, Audrey G.,Benton, Bret M.,Chin, Donovan,De Pascale, Gianfranco,Fuller, John,Leeds, Jennifer A.,Reck, Folkert,Richie, Daryl L.,Vo, Jason,LaMarche, Matthew J.

, p. 3468 - 3475 (2015)

Abstract We describe the synthesis and evaluation of a library of variably-linked ciprofloxacin dimers. These structures unify and expand on the use of fluoroquinolones as probes throughout the antibiotic literature. A dimeric analog (19) showed enhanced inhibition of its intracellular target (DNA gyrase), and translation to antibacterial activity in whole cells was demonstrated. Overall, cell permeation was governed by physicochemical properties and bacterial type. A principal component analysis demonstrated that the dimers occupy a unique and privileged region of chemical space most similar to the macrolide class of antibiotics.

Siderophore-mediated cargo delivery to the cytoplasm of escherichia coli and pseudomonas aeruginosa: Syntheses of monofunctionalized enterobactin scaffolds and evaluation of enterobactin-cargo conjugate uptake

Zheng, Tengfei,Bullock, Justin L.,Nolan, Elizabeth M.

, p. 18388 - 18400 (2013/01/15)

The design and syntheses of monofunctionalized enterobactin (Ent, l- and d-isomers) scaffolds where one catecholate moiety of enterobactin houses an alkene, aldehyde, or carboxylic acid at the C5 position are described. These molecules are key precursors to a family of 10 enterobactin-cargo conjugates presented in this work, which were designed to probe the extent to which the Gram-negative ferric enterobactin uptake and processing machinery recognizes, transports, and utilizes derivatized enterobactin scaffolds. A series of growth recovery assays employing enterobactin-deficient E. coli ATCC 33475 (ent-) revealed that six conjugates based on l-Ent having relatively small cargos promoted E. coli growth under iron-limiting conditions whereas negligible-to-no growth recovery was observed for four conjugates with relatively large cargos. No growth recovery was observed for the enterobactin receptor-deficient strain of E. coli H1187 (fepA-) or the enterobactin esterase-deficient derivative of E. coli K-12 JW0576 (fes-), or when the d-isomer of enterobactin was employed. These results demonstrate that the E. coli ferric enterobactin transport machinery identifies and delivers select cargo-modified scaffolds to the E. coli cytoplasm. Pseudomonas aeruginosa PAO1 K648 (pvd-, pch-) exhibited greater promiscuity than that of E. coli for the uptake and utilization of the enterobactin-cargo conjugates, and growth promotion was observed for eight conjugates under iron-limiting conditions. Enterobactin may be utilized for delivering molecular cargos via its transport machinery to the cytoplasm of E. coli and P. aeruginosa thereby providing a means to overcome the Gram-negative outer membrane permeability barrier.

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