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2-(4-METHYLPIPERAZINO)-3-PYRIDINAMINE is a chemical compound characterized by a piperazine ring with a methyl group and a pyridinamine group attached. It is widely recognized in medicinal chemistry for its role as a building block in the synthesis of various pharmaceutical drugs. 2-(4-METHYLPIPERAZINO)-3-PYRIDINAMINE has demonstrated antitumor and antifungal activities, positioning it as a potentially valuable asset in drug development. Its adaptable structure and diverse pharmacological properties render it a promising candidate for the creation of innovative therapeutics.

5028-17-1

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5028-17-1 Usage

Uses

Used in Pharmaceutical Development:
2-(4-METHYLPIPERAZINO)-3-PYRIDINAMINE is utilized as a key component in the synthesis of pharmaceutical drugs due to its versatile chemical structure and pharmacological properties. It serves as a fundamental building block, contributing to the development of new medications with potential applications in various therapeutic areas.
Used in Antitumor Applications:
In the field of oncology, 2-(4-METHYLPIPERAZINO)-3-PYRIDINAMINE is employed as an antitumor agent. Its reported antitumor activities make it a valuable compound for the development of drugs aimed at treating cancer. 2-(4-METHYLPIPERAZINO)-3-PYRIDINAMINE's ability to target and inhibit the growth of tumor cells could lead to the creation of novel cancer therapies.
Used in Antifungal Applications:
2-(4-METHYLPIPERAZINO)-3-PYRIDINAMINE also finds use in antifungal applications. Its demonstrated antifungal properties suggest that it could be instrumental in developing new treatments for fungal infections, offering an alternative or adjunct to existing antifungal medications.
Used in Medicinal Chemistry Research:
In the realm of medicinal chemistry research, 2-(4-METHYLPIPERAZINO)-3-PYRIDINAMINE is used as a subject of study for understanding its structure-activity relationships and exploring its potential in the development of new drugs. Researchers leverage its chemical and biological characteristics to design and synthesize novel compounds with improved therapeutic profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 5028-17-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,2 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5028-17:
(6*5)+(5*0)+(4*2)+(3*8)+(2*1)+(1*7)=71
71 % 10 = 1
So 5028-17-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H16N4/c1-13-5-7-14(8-6-13)10-9(11)3-2-4-12-10/h2-4H,5-8,11H2,1H3

5028-17-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methylpiperazin-1-yl)pyridin-3-amine

1.2 Other means of identification

Product number -
Other names 1-(3-Amino-2-pyridyl)-4-methylpiperazine

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:5028-17-1 SDS

5028-17-1Downstream Products

5028-17-1Relevant academic research and scientific papers

METHODS OF USING INDAZOLE-3-CARBOXAMIDES AND THEIR USE AS WNT/B-CATENIN SIGNALING PATHWAY INHIBITORS

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Paragraph 0335; 0337, (2018/05/16)

This disclosure features the use of one or more indazole-3-carboxamide compounds or salts or analogs thereof, in the treatment of one or more diseases or conditions independently selected from the group consisting of a tendinopathy, dermatitis, psoriasis, morphea, ichthyosis, Raynaud's syndrome, and Darier's disease; and/or for promoting wound healing. The methods include administering to a subject (e.g., a subject in need thereof) a therapeutically effective amount of one or more indazole-3-carboxamide compounds or salts or analogs thereof as described anywhere herein.

INDAZOLE-3-CARBOXAMIDES AND THEIR USE AS WNT/B-CATENIN SIGNALING PATHWAY INHIBITORS

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Paragraph 00304, (2013/03/28)

lndazole-3-carboxamide compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of an indazole-3- carboxamide compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as genetic diseases and neurological conditions/disorders/diseases due to mutations or dysregulation of the Wnt pathway and/or of one or more of Wnt signaling components. Also provided are methods for treating Wnt-related disease states.

PIPERAZINYLPHENALKYL LACTAM/AMINE LIGANDS FOR THE 5HT1B RECEPTOR

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Page/Page column 72-73, (2010/11/30)

The present invention relates to novel derivatives, that are compounds of Formula (I), wherein R1, R2, R3, R14, X, Y, n and m are defined herein, their pharmaceutically acceptable salts, pharmaceutical compositions and methods using said compounds in treating or preventing depression, anxiety, obsessive compulsive disorder (OCD) and other disorders for which selective antagonists, inverse agonists and partial agonists of serotonin 1 (5-HT1) receptors, specifically, antagonists of 5-HT1B are useful.

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