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tert-butyl N-(diphenylmethylene)-2-methoxy-6-nitro-L-phenylalaninate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1258544-86-3

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1258544-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1258544-86-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,5,4 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1258544-86:
(9*1)+(8*2)+(7*5)+(6*8)+(5*5)+(4*4)+(3*4)+(2*8)+(1*6)=183
183 % 10 = 3
So 1258544-86-3 is a valid CAS Registry Number.

1258544-86-3Relevant academic research and scientific papers

Discovery of brain-penetrant, irreversible kynurenine aminotransferase ii inhibitors for schizophrenia

Dounay, Amy B.,Anderson, Marie,Bechle, Bruce M.,Campbell, Brian M.,Claffey, Michelle M.,Evdokimov, Artem,Evrard, Edelweiss,Fonseca, Kari R.,Gan, Xinmin,Ghosh, Somraj,Hayward, Matthew M.,Horner, Weldon,Kim, Ji-Young,McAllister, Laura A.,Pandit, Jayvardhan,Paradis, Vanessa,Parikh, Vinod D.,Reese, Matthew R.,Rong, Suobao,Salafia, Michelle A.,Schuyten, Katherine,Strick, Christine A.,Tuttle, Jamison B.,Valentine, James,Wang, Hong,Zawadzke, Laura E.,Verhoest, Patrick R.

supporting information; experimental part, p. 187 - 192 (2012/04/23)

Kynurenine aminotransferase (KAT) II has been identified as a potential new target for the treatment of cognitive impairment associated with schizophrenia and other psychiatric disorders. Following a high-throughput screen, cyclic hydroxamic acid PF-04859989 was identified as a potent and selective inhibitor of human and rat KAT II. An X-ray crystal structure and 13C NMR studies of PF-04859989 bound to KAT II have demonstrated that this compound forms a covalent adduct with the enzyme cofactor, pyridoxal phosphate (PLP), in the active site. In vivo pharmacokinetic and efficacy studies in rat show that PF-04859989 is a brain-penetrant, irreversible inhibitor and is capable of reducing brain kynurenic acid by 50% at a dose of 10 mg/kg (sc). Preliminary structurea€"activity relationship investigations have been completed and have identified the positions on this scaffold best suited to modification for further optimization of this novel series of KAT II inhibitors.

Bicyclic And Tricyclic Compounds As KAT II Inhibitors

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Page/Page column 35, (2010/12/31)

Compounds of Formula X: wherein A, X, Y, Z, R5, R6a, and R6b are as defined herein, and pharmaceutically acceptable salts thereof, are described as useful for the treatment of cognitive deficits associated with schizophrenia and other neurodegenerative and/or neurological disorders in mammals, including humans.

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