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934107-80-9

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934107-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 934107-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,1,0 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 934107-80:
(8*9)+(7*3)+(6*4)+(5*1)+(4*0)+(3*7)+(2*8)+(1*0)=159
159 % 10 = 9
So 934107-80-9 is a valid CAS Registry Number.

934107-80-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methylsulfonylpiperidin-3-amine

1.2 Other means of identification

Product number -
Other names 1-Methanesulfonylpiperidin-3-ylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:934107-80-9 SDS

934107-80-9Downstream Products

934107-80-9Relevant academic research and scientific papers

Development of a Selective Dual Discoidin Domain Receptor (DDR)/p38 Kinase Chemical Probe

R?hm, Sandra,Berger, Benedict-Tilman,Schr?der, Martin,Chatterjee, Deep,Mathea, Sebastian,Joerger, Andreas C.,Pinkas, Daniel M.,Bufton, Joshua C.,Tjaden, Amelie,Kovooru, Lohitesh,Kudolo, Mark,Pohl, Christian,Bullock, Alex N.,Müller, Susanne,Laufer, Stefan,Knapp, Stefan

, p. 13451 - 13474 (2021/09/28)

Discoidin domain receptors 1 and 2 (DDR1/2) play a central role in fibrotic disorders, such as renal and pulmonary fibrosis, atherosclerosis, and various forms of cancer. Potent and selective inhibitors, so-called chemical probe compounds, have been developed to study DDR1/2 kinase signaling. However, these inhibitors showed undesired activity on other kinases such as the tyrosine protein kinase receptor TIE or tropomyosin receptor kinases, which are related to angiogenesis and neuronal toxicity. In this study, we optimized our recently published p38 mitogen-activated protein kinase inhibitor7toward a potent and cell-active dual DDR/p38 chemical probe and developed a structurally related negative control. The structure-guided design approach used provided insights into the P-loop folding process of p38 and how targeting of non-conserved amino acids modulates inhibitor selectivity. The developed and comprehensively characterized DDR/p38 probe,30(SR-302), is a valuable tool for studying the role of DDR kinase in normal physiology and in disease development.

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