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1-isopropyl-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)piperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1373010-41-3

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1373010-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373010-41-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,0,1 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1373010-41:
(9*1)+(8*3)+(7*7)+(6*3)+(5*0)+(4*1)+(3*0)+(2*4)+(1*1)=113
113 % 10 = 3
So 1373010-41-3 is a valid CAS Registry Number.

1373010-41-3Downstream Products

1373010-41-3Relevant academic research and scientific papers

Method of preparing Quinoline-5,8-dione derivatives for TGase 2 inhibitor

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, (2020/04/28)

I Is -5,8- of the quinoline, dione derivative compound. of Formula I, or a stereoisomer or a pharmaceutically acceptable salt thereof, wherein the compound of Formula, TGase 2 has, inhibitory effects TGase 2, and thus the pharmaceutical composition may be useful for preventing or treating disorders or diseases mediated by TGase 2 or inhibiting. (by machine translation)

Quinoline-5,8-dione derivatives for TGase 2 inhibitor, and the pharmaceutical composition comprising the same

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, (2019/10/29)

The present invention relates to a quinolin-5,8-dione derivative compound represented by chemical formula I, an optical isomer thereof or a pharmaceutically acceptable salt thereof. The compound represented by chemical formula I of the present invention has a TGase 2 inhibitory effect, and the pharmaceutical composition comprising the same can be usefully used for preventing or treating disorders or diseases mediated by TGase 2 or response to TGase 2 inhibition.COPYRIGHT KIPO 2020

INDAZOLE COMPOUNDS AS KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME

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Page/Page column 68; 72; 73, (2013/04/25)

The present teaching provide indazole compounds represented by Structural Formulae (I) or (I') or a pharmaceutically acceptable salt thereof. Also described are pharmaceutical compositions and methods of use thereof as protein kinase inhibitors, such as T

PLK-4 INHIBITORS AND METHOD OF TREATING CANCER WITH SAME

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, (2012/05/04)

The invention is directed to a compound represented by the following Structural Formula (I) and (II) and pharmaceutically acceptable salts thereof: (Formula (I)); (Formula (IV)). Compounds represented by this structural formula are kinase inhibitors and are, therefore, disclosed herein for the treatment of cancer. Definitions for the variables in the structural formula are provided herein.

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