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134807-37-7

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134807-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134807-37-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,0 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134807-37:
(8*1)+(7*3)+(6*4)+(5*8)+(4*0)+(3*7)+(2*3)+(1*7)=127
127 % 10 = 7
So 134807-37-7 is a valid CAS Registry Number.

134807-37-7Downstream Products

134807-37-7Relevant articles and documents

Structure-based drug design of novel and highly potent pyruvate dehydrogenase kinase inhibitors

Bessho, Yuki,Akaki, Tatsuo,Hara, Yoshinori,Yamakawa, Maki,Obika, Shingo,Mori, Genki,Ubukata, Minoru,Yasue, Katsutaka,Nakane, Yoshitomi,Terasako, Yasuo,Orita, Takuya,Doi, Satoki,Iwanaga, Tomoko,Fujishima, Ayumi,Adachi, Tsuyoshi,Ueno, Hiroshi,Motomura, Takahisa

, (2021/11/23)

Pyruvate dehydrogenase kinases (PDHKs) are fascinating drug targets for numerous diseases, including diabetes and cancers. In this report, we describe the result of our structure-based drug design from tricyclic lead compounds that led to the discovery of highly potent PDHK2 and PDHK4 dual inhibitors in enzymatic assay. The C3-position of the tricyclic core was explored, and the PDHK2 X-ray structure with a representative compound revealed a novel ATP lid conformation in which the phenyl ring of Phe326 mediated the interaction of the Arg258 sidechain and the compound. Compounds with amide linkers were designed to release the ATP lid by forming an intramolecular pi-pi interaction, and these compounds showed single-digit nM IC50 values in an enzymatic assay. We also explored the C4-position of the tricyclic core to reproduce the interaction observed with the C3-position substitution, and the pyrrolidine compound showed the same level of IC50 values. By optimizing an interaction with the Asn255 sidechain through a docking simulation, compounds with 2-carboxy pyrrole moiety also showed single-digit nM IC50 values without having a cation-pi interaction with the Arg258 sidechain.

Total synthesis and absolute stereochemistry of the proteasome inhibitors cystargolides A and B

Tello-Aburto, Rodolfo,Hallada, Liam P.,Niroula, Doleshwar,Rogelj, Snezna

supporting information, p. 10127 - 10130 (2015/10/28)

The absolute stereochemistry of the cystargolides was determined by total synthesis. Evaluation of synthetic cystargolides and derivatives showed that the natural (2S,3R) stereochemistry is essential for activity. Moreover, benzyl esters (-)-10 and (-)-15

PROCESS FOR PRODUCING ALISKIREN

-

, (2011/12/14)

A new route of synthesis of the compound Aliskiren of formula (I), used in the treatment of hypertension, is described.

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