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938443-21-1

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938443-21-1 Usage

General Description

4-(2,7-dichloropyrido[2,3-d]pyrimidin-4-yl)morpholine is a chemical compound that belongs to the class of pyrimidine derivatives. It consists of a dichloropyrido[2,3-d]pyrimidin-4-yl group attached to a morpholine ring. 4-(2,7-dichloropyrido[2,3-d]pyrimidin-4-yl)morpholine is commonly used in pharmaceutical research as a potential drug candidate due to its diverse biological activities. It has been studied for its potential antineoplastic and antihypertensive properties, as well as its ability to inhibit protein kinases. Additionally, 4-(2,7-dichloropyrido[2,3-d]pyrimidin-4-yl)morpholine has been investigated for its potential role in the treatment of various diseases and conditions, making it an important target for further research and synthesis of related compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 938443-21-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,8,4,4 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 938443-21:
(8*9)+(7*3)+(6*8)+(5*4)+(4*4)+(3*3)+(2*2)+(1*1)=191
191 % 10 = 1
So 938443-21-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H10Cl2N4O/c12-8-2-1-7-9(14-8)15-11(13)16-10(7)17-3-5-18-6-4-17/h1-2H,3-6H2

938443-21-1Relevant articles and documents

Pyridine and miazines mTOR inhibitors

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, (2016/10/17)

The invention belongs to the technical field of medicines, and particularly relates to a pyridopyrimidine mammalian target of rapamycin (mTOR) inhibitor which is shown as a general formula (I), pharmaceutically acceptable salts and stereoisomers thereof, and deuterated pyridopyrimidine mammalian mTOR inhibitors, wherein Z, Z, Z, R, R, R, X and W are defined in the specifications. The invention also relates to preparation methods for the compounds, medicinal inhibitors and medicinal compositions which contain the compounds, and the application of the compounds to preparation of medicines for treating and/or preventing post-transplant lymphoproliferative diseases which have response to inhibition of mTOR activity.

The discovery and optimisation of pyrido[2,3-d]pyrimidine-2,4-diamines as potent and selective inhibitors of mTOR kinase

Malagu, Karine,Duggan, Heather,Menear, Keith,Hummersone, Marc,Gomez, Sylvie,Bailey, Christine,Edwards, Peter,Drzewiecki, Jan,Leroux, Frederic,Quesada, Mar Jimenez,Hermann, Gesine,Maine, Stephanie,Molyneaux, Carrie-Anne,Le Gall, Armelle,Pullen, James,Hickson, Ian,Smith, Lisa,Maguire, Sharon,Martin, Niall,Smith, Graeme,Pass, Martin

scheme or table, p. 5950 - 5953 (2010/07/05)

We describe a novel series of potent inhibitors of the kinase activity of mTOR. The compounds display good selectivity relative to other PI3K-related kinase family members and, in cellular assays, inhibit both mTORC1 and mTORC2 complexes and exhibit good antiproliferative activity.

PYRIDO-,PYRAZO- AND PYRIMIDO-PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS

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Page/Page column 57; 59, (2008/06/13)

There is provided compounds of formula (I), which are suitable for the treatment of cancer.

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