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Benzamide, N-(2-aminophenyl)-4-(hexahydro-4-methyl-1H-1,4-diazepin-1-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

766497-44-3

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766497-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 766497-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,6,4,9 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 766497-44:
(8*7)+(7*6)+(6*6)+(5*4)+(4*9)+(3*7)+(2*4)+(1*4)=223
223 % 10 = 3
So 766497-44-3 is a valid CAS Registry Number.

766497-44-3Relevant academic research and scientific papers

Discovery of N-[2-hydroxy-6-(4-methoxybenzamido)phenyl]-4- (4-methyl-1,4-diazepan-1-yl)benzamide (darexaban, YM150) as a potent and orally available factor Xa inhibitor

Hirayama, Fukushi,Koshio, Hiroyuki,Ishihara, Tsukasa,Hachiya, Shunichiro,Sugasawa, Keizo,Koga, Yuji,Seki, Norio,Shiraki, Ryouta,Shigenaga, Takeshi,Iwatsuki, Yoshiyuki,Moritani, Yumiko,Mori, Kenichi,Kadokura, Takeshi,Kawasaki, Tomihisa,Matsumoto, Yuzo,Sakamoto, Shuichi,Tsukamoto, Shin-Ichi

scheme or table, p. 8051 - 8065 (2012/03/08)

Inhibitors of factor Xa (FXa), a crucial serine protease in the coagulation cascade, have attracted a great deal of attention as a target for developing antithrombotic agents. We previously reported findings from our optimization study of a high-throughpu

Synthesis and biological activity of novel 1,2-disubstituted benzene derivatives as factor Xa inhibitors

Koshio, Hiroyuki,Hirayama, Fukushi,Ishihara, Tsukasa,Shiraki, Ryouta,Shigenaga, Takeshi,Taniuchi, Yuta,Sato, Kazuo,Moritani, Yumiko,Iwatsuki, Yoshiyuki,Kaku, Seiji,Katayama, Naoko,Kawasaki, Tomihisa,Matsumoto, Yuzo,Sakamoto, Shuichi,Tsukamoto, Shin-Ichi

, p. 1305 - 1323 (2007/10/03)

Factor Xa (fXa) is a serine protease that plays a pivotal role in the coagulation cascade. High-throughput screening of the Yamanouchi compound library yielded lead compound 1 with the ability to inhibit fXa at micromolar concentrations. To improve its fX

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