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(4-METHYL-PIPERAZIN-1-YL)-PIPERIDIN-2-YL-METHANONE, also known as MPMPM, is a synthetic chemical compound with a molecular formula C15H26N4O. It is a piperazine derivative that is widely used in pharmaceutical research and development as a building block for the synthesis of various drug candidates. MPMPM's structure and properties make it a versatile and valuable compound for medicinal chemistry research.

1008091-05-1

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1008091-05-1 Usage

Uses

Used in Pharmaceutical Research and Development:
MPMPM is used as a building block in the synthesis of various drug candidates for the development of new therapeutic agents for various medical conditions. Its potential pharmacological activities have been investigated, making it a promising candidate for the creation of innovative treatments.
Used in Medicinal Chemistry Research:
MPMPM's versatile structure and properties make it a valuable compound for medicinal chemistry research. It can be utilized to explore and understand the mechanisms of action, efficacy, and safety of new drug candidates, contributing to the advancement of pharmaceutical sciences.

Check Digit Verification of cas no

The CAS Registry Mumber 1008091-05-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,8,0,9 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1008091-05:
(9*1)+(8*0)+(7*0)+(6*8)+(5*0)+(4*9)+(3*1)+(2*0)+(1*5)=101
101 % 10 = 1
So 1008091-05-1 is a valid CAS Registry Number.

1008091-05-1Upstream product

1008091-05-1Relevant articles and documents

2-Aminomethyl piperidines as novel urotensin-II receptor antagonists

Jin, Jian,Wang, Yonghui,Wang, Feng,Shi, Dongchuan,Erhard, Karl F.,Wu, Zining,Guida, Brian F.,Lawrence, Sarah K.,Behm, David J.,Disa, Jyoti,Vaidya, Kalindi S.,Evans, Christopher,McMillan, Lynette J.,Rivero, Ralph A.,Neeb, Michael J.,Douglas, Stephen A.

, p. 2860 - 2864 (2008/12/22)

A series of 2-aminomethyl piperidines has been discovered as novel urotensin-II receptor antagonists. The synthesis, initial structure-activity relationships, and optimization of the initial hit that resulted in the identification of potent, cross-species active, and functional urotensin-II receptor antagonists such as 1a and 11a are described.

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