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Ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(5-cyano-2-benzothiazolyl)-2-ethoxycarbonylpropionate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

150611-03-3

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150611-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150611-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,6,1 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 150611-03:
(8*1)+(7*5)+(6*0)+(5*6)+(4*1)+(3*1)+(2*0)+(1*3)=83
83 % 10 = 3
So 150611-03-3 is a valid CAS Registry Number.

150611-03-3Downstream Products

150611-03-3Relevant academic research and scientific papers

Design, synthesis and biological activity of amidinobicyclic compounds (derivatives of DX-9065a) as factor Xa inhibitors: SAR study of S1 and aryl binding sites

Komoriya, Satoshi,Kanaya, Naoaki,Nagahara, Takayasu,Yokoyama, Asako,Inamura, Kazue,Yokoyama, Yukio,Katakura, Shin-Ichi,Hara, Tsuyoshi

, p. 2099 - 2114 (2007/10/03)

Since factor Xa (fXa) plays a pivotal role in the blood coagulation cascade, inhibition of fXa is thought to be an effective treatment for a variety of thrombotic events. (2S)-2-[4-[[(3S)-1-Acetimidoyl-3-pyrrolidinyl]oxy]phenyl] -3-(7-amidino-2-naphthyl)p

AROMATIC AMIDINE DERIVATIVES AND SALTS THEREOF

-

, (2008/06/13)

An anticoagulant agent which comprises, as an active ingredient, an aromatic amidine derivative represented by the following general formula (1) or a salt thereof: STR1 wherein the group represented by STR2 is a group selected from indolyl, benzofuranyl, benzothienyl, benzimidazolyl, benzoxazolyl, benzothiazolyl, naphthyl, tetrahydronaphthyl and indanyl; X is a single bond, an oxygen atom, a sulfur atom or a carbonyl group; and Y is a saturated or unsaturated 5-or 6-membered heterocyclic moiety or cyclic hydrocarbon moiety optionally having a substituent group, an amino group optionally having a substituent group or an aminoalkyl group optionally having a substituent group.The inventive compound has a high anticoagulant capacity based on its excellent FXa inhibition activity.

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