80443-18-1 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 16 carbon (C) atoms, 14 hydrogen (H) atoms, and 4 nitrogen (N) atoms.
Explanation
The compound has a core structure consisting of an imidazo-pyridine ring system, which is further modified by the attachment of a phenylmethyl (benzyl) group.
Explanation
It is classified as an organic compound because it contains carbon and hydrogen atoms, along with other elements like nitrogen.
Explanation
The compound is used in the synthesis and development of pharmaceutical drugs, indicating its potential applications in the field of medicinal chemistry.
Explanation
Studies have shown that the compound has potential therapeutic properties, including the ability to act as an antiviral and anti-inflammatory agent.
Explanation
Due to its structural and functional properties, the compound may have applications in the treatment of certain neurological and psychiatric disorders.
Explanation
The compound's potential to be used in different pharmacological applications is attributed to its unique structure and functional properties.
Chemical Structure
Imidazo-pyridine core with a phenylmethyl substituent
Classification
Organic compound
Applications
Medicinal chemistry
Therapeutic Properties
Antiviral and anti-inflammatory agent
Potential Applications
Treatment of neurological and psychiatric disorders
Pharmacological Applications
Various uses
Check Digit Verification of cas no
The CAS Registry Mumber 80443-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,4 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80443-18:
(7*8)+(6*0)+(5*4)+(4*4)+(3*3)+(2*1)+(1*8)=111
111 % 10 = 1
So 80443-18-1 is a valid CAS Registry Number.
80443-18-1Relevant articles and documents
Design and synthesis of purine analogues as highly specific ligands for FcyB, a ubiquitous fungal nucleobase transporter
Lougiakis, Nikolaos,Gavriil, Efthymios-Spyridon,Kairis, Markelos,Sioupouli, Georgia,Lambrinidis, George,Benaki, Dimitra,Krypotou, Emilia,Mikros, Emmanuel,Marakos, Panagiotis,Pouli, Nicole,Diallinas, George
, p. 5941 - 5952 (2016/11/09)
In the course of our study on fungal purine transporters, a number of new 3-deazapurine analogues have been rationally designed, based on the interaction of purine substrates with the Aspergillus nidulans FcyB carrier, and synthesized following an effective synthetic procedure. Certain derivatives have been found to specifically inhibit FcyB-mediated [3H]-adenine uptake. Molecular simulations have been performed, suggesting that all active compounds interact with FcyB through the formation of hydrogen bonds with Asn163, while the insertion of hydrophobic fragments at position 9 and N6 of 3-deazaadenine enhanced the inhibition.
Anti-inflammatory deoxyribosides
-
, (2008/06/13)
The novel compounds 3-deaza-2'-deoxyadenosine and certain of its derivatives and their pharmaceutically acceptable salts have anti-inflammatory activity as well as immune response suppression activity. 3-Deaza-2'-deoxyadenosine and certain of its intermed
