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LDN-0064229 is a chemical compound that belongs to the class of phosphodiesterase 2A (PDE2A) inhibitors. It is being studied for its potential therapeutic applications in various central nervous system disorders, including schizophrenia, bipolar disorder, and neuroinflammatory conditions. By inhibiting PDE2A, LDN-0064229 is believed to modulate neurotransmission and improve cognitive function, potentially offering a novel approach for treating these disorders. Preclinical studies have shown promising results in animal models, demonstrating the compound's ability to enhance memory and cognitive function. Further research is needed to fully understand the therapeutic effects and safety profile of LDN-0064229 in humans.

38371-84-5

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38371-84-5 Usage

Uses

Used in Pharmaceutical Industry:
LDN-0064229 is used as a PDE2A inhibitor for its potential therapeutic applications in treating central nervous system disorders such as schizophrenia, bipolar disorder, and neuroinflammatory conditions. Its ability to modulate neurotransmission and improve cognitive function makes it a promising candidate for novel treatment approaches in these areas.
Used in Research and Development:
LDN-0064229 is used as a research tool in preclinical studies to investigate its effects on memory and cognitive function in animal models. This helps in understanding the compound's therapeutic potential and safety profile, paving the way for further development and clinical trials in humans.

Check Digit Verification of cas no

The CAS Registry Mumber 38371-84-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,7 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38371-84:
(7*3)+(6*8)+(5*3)+(4*7)+(3*1)+(2*8)+(1*4)=135
135 % 10 = 5
So 38371-84-5 is a valid CAS Registry Number.

38371-84-5Downstream Products

38371-84-5Relevant academic research and scientific papers

Synthesis and molluscicidal activity of new derivatives of 1-(hydroxy/substituted phenyl)-3-arylpropenones

Nawwar,Haggag,Swellam

, p. 831 - 836 (2007/10/02)

Several 1-(hydroxy/substituted phenyl)propenones were tested as molluscicidal agents among which the 1-(2-hydroxy/substituted phenyl)-3-(2-furyl)propenones 1a-c show the most promising results. In an attempt to improve their activity, new dihydropyrazolo[

Synthesis and Reactions of 1-(2'-Furyl)-3-(substituted-2''-hydroxyphenyl)propanediones

Nair, S. B.,Wadodkar, K. N.

, p. 573 - 574 (2007/10/02)

The title compounds (III) have been synthesised by the base-catalysed Baker-Venkataraman transformation of furoyl esters (II) of substituted 2-hydroxyacetophenones.These propanediones (III) on acid cyclization, bromination, treatment with SO2Cl2, and cond

Synthesis and Antimicrobial Activity of Hydroxyarylpyrazoles

Sharma, T. C.,Bokadia, M. M.,Reddy, N. J.

, p. 228 - 229 (2007/10/02)

Hydroxyarylpyrazolines (III) and Pyrazoles (IV) have been synthesized.Compounds IVa and IVd exhibit marked antifungal activity against A. niger, C. albicans, C. neoformans, T. mentagraphytes and M. canis whereas compound IVc shows activity against the last three fungi.None of the compounds shows any noteworthy antibacterial activity against Staphy. aureus, Staphi. typhi and Esch. coli even at 100 μg/ml.

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