6 Results for "

arenes

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "arenes" in MCE Product Catalog:

Cat. No.: HY-I0101
CAS No.: 60705-62-6
Synonyms: Tetra-tert-butyl(tetrahydroxy)calix[4]arene
Target:  

Drug Intermediate

Research Areas:  

Others

4-tert-Butylcalix[4]arene (Tetra-tert-butyl(tetrahydroxy)calix[4]arene) is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-19094
CAS No.: 124750-95-4
Target:  

Angiotensin Receptor

Research Areas:  

Cardiovascular Disease

DuP-532 is an angiotensin type 1 receptor antagonist with potential activity in the suppression of hypertension and heart failure. DuP-532 can react with a range of aryl and heteroaryl halides to form perfluoroalkyl(hetero)arenes in moderate to high yields. Computational studies of DuP-532 suggest that coordination of a second phenyl ring ligand may lower the energy barrier for decarboxylation of perfluorocarboxylates, thereby promoting the perfluoroalkylation reaction .
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Cat. No.: HY-W440555
CAS No.: 112269-92-8
Synonyms: para-Sulfonatocalix[n]arene
Target:  

Amyloid-β

Research Areas:  

Neurological Disease

4-Sulfocalix[4]arene (para-Sulfonatocalix[n]arene) is a amyloid-beta 42 binder with a Kd of 5.39 M. 4-Sulfocalix[4]arene can inhibit amyloid β-peptide fibrillation and reduce amyloid cytotoxicity .
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Cat. No.: HY-W440556
CAS No.: 137407-62-6
Synonyms: 4-Sulfocalix[8]arene
Target:  

Amyloid-β

Research Areas:  

Neurological Disease

GL-522 (4-Sulfocalix[8]arene) is a Aβ42 inhibitor. GL-522 bind to Aβ42 through nonspecific and multipoint hydrophobic interactions with a Kd of 276  μM. GL-522 effectively inhibits Aβ42 fibrillation and reduces amyloid cytotoxicity. GL-522 can be used for Alzheimer's disease research .
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Cat. No.: HY-12491
CAS No.: 691388-62-2
Target:  

PI3K Apoptosis

Research Areas:  

Cancer

PIK-C98 is a potent and selective PI3K inhibitor, with IC50s of 0.59, 1.64, 3.65, and 0.74 μM for α, β, δ, and γ isoforms, respectively. PIK-C98 inhibits all class I PI3Ks but has no effects on AKT or mTOR activity. PIK-C98 interferes with the ATP-binding pockets of PI3Ks by forming H-bonds and arene-H interactions with specific amino acid residues. PIK-C98 induces apoptosis by inhibiting PI3K. PIK-C98 can be used for the research of multiple myeloma .
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Cat. No.: HY-189131
CAS No.: 1628717-55-4
Synonyms: CTT-1057
Target:  

PSMA Bacterial

Research Areas:  

Infection Cancer

Vidoflufolastat (CTT-1057) is a PSMA inhibitor with an IC50 of 0.4 nM. Vidoflufolastat binds irreversibly to the active-site zinc ion through its phosphoramidate core, while its distal fluorobenzoyl ring interacts with the arene-binding site. Vidoflufolastat can be used in research on prostate cancer and Pseudomonas aeruginosa infection .
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