127574-36-1 Usage
Description
1H-Imidazole-4-carboxamide, 5-amino-1-(diphenylmethyl)is a chemical compound belonging to the imidazole class. It features a five-membered ring composed of three carbon atoms and two nitrogen atoms, along with a carboxamide group, an amino group, and a diphenylmethyl substituent. 1H-Imidazole-4-carboxamide, 5-amino-1-(diphenylmethyl)holds potential in pharmaceuticals and drug development due to its unique structural properties, which may confer biological activity as an enzyme inhibitor or receptor modulator. Research on 1H-Imidazole-4-carboxamide, 5-amino-1-(diphenylmethyl)could pave the way for the creation of new drugs and therapies to address a range of medical conditions.
Uses
Used in Pharmaceutical Development:
1H-Imidazole-4-carboxamide, 5-amino-1-(diphenylmethyl)is utilized as a key component in the development of pharmaceuticals, leveraging its structural properties to act as an enzyme inhibitor or receptor modulator. Its potential applications in this field are vast, as it may contribute to the treatment of various medical conditions by interacting with specific biological targets.
Used in Drug Discovery:
In the realm of drug discovery, 1H-Imidazole-4-carboxamide, 5-amino-1-(diphenylmethyl)serves as a valuable chemical entity. Its unique structure positions it as a candidate for further research and development, with the aim of identifying and optimizing its interactions with biological targets. This process is crucial for the advancement of novel therapeutic agents that can address unmet medical needs.
Used in Enzyme Inhibition:
1H-Imidazole-4-carboxamide, 5-amino-1-(diphenylmethyl)is employed as an enzyme inhibitor, capitalizing on its ability to bind to and modulate the activity of specific enzymes. This application is significant in the context of various diseases and conditions where enzyme dysregulation plays a critical role, offering a potential therapeutic strategy to restore normal enzyme function.
Used in Receptor Modulation:
As a receptor modulator, 1H-Imidazole-4-carboxamide, 5-amino-1-(diphenylmethyl)is applied to influence the activity of cellular receptors, which are often implicated in numerous physiological and pathological processes. By modulating receptor function, this compound may contribute to the regulation of cellular signaling pathways, providing a means to treat diseases associated with receptor dysregulation.
Check Digit Verification of cas no
The CAS Registry Mumber 127574-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,7 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127574-36:
(8*1)+(7*2)+(6*7)+(5*5)+(4*7)+(3*4)+(2*3)+(1*6)=141
141 % 10 = 1
So 127574-36-1 is a valid CAS Registry Number.
127574-36-1Relevant articles and documents
Synthetic studies on compounds related to aminoimidazolecarboxamide: Synthesis of angularly fused purine derivatives and a solid phase ring transformation (ANRORC) to imidazo [1,5-a] pyrazine
Chattopadhyay, Gautam,Ray, Parlha Sinha
, p. 546 - 552 (2013/06/26)
l-Benzyl-5-aminoimidazole-4-carboxamide la has been used as a convenient precursor for the synthesis of new triazolo [3,4-i] purines 6 and the corresponding tetrazolo analogue 7. A mesoionic isomer 8 seems to exist along with 7. Interesting heteroaryl-purine motifs have also been prepared via suitably substituted 9-benzyIpurines. Imidazo |I,5-a| pyrazine derivative has been prepared in a solid phase exploitation of suitable imidazolium salt via ANRORC.
Studies on the effect of alkali on the compounds related to aminoimidazoliumcarboxamides
Chatiopadhyay
, p. 509 - 511 (2007/10/02)
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