2180127-82-4

Basic information

• Product Name: 2-(4-(2-(3,4-dimethoxyphenyl)-3-isopropyl-1H-indol-5-yl)piperidin-1-yl)-N-methylethan-1-amine
• CAS NO: 2180127-82-4
• Molecular Weight: 435.61
• Mol File: 2180127-82-4.mol

Chemical Properties

• CAS DataBase Reference: 2-(4-(2-(3,4-dimethoxyphenyl)-3-isopropyl-1H-indol-5-yl)piperidin-1-yl)-N-methylethan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-(2-(3,4-dimethoxyphenyl)-3-isopropyl-1H-indol-5-yl)piperidin-1-yl)-N-methylethan-1-amine(2180127-82-4)
• EPA Substance Registry System: 2-(4-(2-(3,4-dimethoxyphenyl)-3-isopropyl-1H-indol-5-yl)piperidin-1-yl)-N-methylethan-1-amine(2180127-82-4)

Safety Data

• Hazardous Substances Data: 2180127-82-4(Hazardous Substances Data)

Usage

Molecular structure

Complex with a long and detailed structure

Family

Indole derivatives

Contains

A piperidine group

Field of application

Medicinal chemistry (research and development)

Potential applications

Pharmacology and drug discovery

Further studies needed

Specific interactions, properties, and potential biological activities require investigation through additional studies and experiments.

Upstream product

• 439612-51-8 5-bromo-3-isopropyl-1H-indole 
• 10075-50-0 5-bromo-1H-indole 

Relevant articles and documents

Discovery of Potent and Orally Bioavailable Small Molecule Antagonists of Toll-like Receptors 7/8/9 (TLR7/8/9)

The toll-like receptor (TLR) family is an evolutionarily conserved component of the innate immune system, responsible for the early detection of foreign or endogenous threat signals. In the context of autoimmunity, the unintended recognition of self-motifs as foreign promotes initiation or propagation of disease. Overactivation of TLR7 and TLR9 have been implicated as factors contributing to autoimmune disorders such as psoriasis, arthritis, and lupus. In our search for small molecule antagonists of TLR7/9, 7f was identified as possessing excellent on-target potency for human TLR7/9 as well as for TLR8, with selectivity against other representative TLR family members. Good pharmacokinetic properties and a relatively balanced potency against TLR7 and TLR9 in mouse systems (systems which lack functional TLR8) made this an excellent in vivo tool compound, and efficacy from oral dosing in preclinical models of autoimmune disease was demonstrated.