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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T36036 | CAY10786 | GPR52 antagonist-1 | GPR |
CAY10786 (GPR52 antagonist-1) is an antagonist of G protein-coupled receptor 52 (GPR52, IC50 = 0.63 μM). | |||
T0719 | Tetrabenazine | Xenazine,Ro 1-9569 | Others , Dopamine Receptor , Monoamine Transporter |
Tetrabenazine (Ro 1-9569) is a drug formerly used as an antipsychotic and treatment of various movement disorders. Tetrabenazine blocks neurotransmitter uptake into adrenergic storage vesicles and has been used as a high... | |||
T39479 | Rovanersen | WVE-120101,Rovanersen | |
Rovanersen (WVE-120101) is an antisense oligonucleotide that can be used for huntington’s disease research. | |||
T26878 | BN-82451 HCl | BN 82451B,BN 82451,BN-82451,BN82451B,BN-82451B,BN82451 | |
BN-82451, a cyclooxygenase inhibitor, is used potentially for the treatment of Huntington’s disease. | |||
T39166 | Tominersen | IONIS-HTTRx,RG6042 | |
Tominersen (RG6042) is a second-generation 2′-O-(2-methoxyethyl) antisense oligonucleotide that targets huntingtin protein (HTT) mRNA and potently suppresses HTT production. Tominersen can be used for the research of Hun... | |||
T60824 | Dyrk1A-IN-3 | ||
Dyrk1A-IN-3 (Compound 8b) is a highly selective inhibitor of dual-specificity tyrosine-regulated kinase 1A (DYRK1A). Dyrk1A-IN-3 has high binding affinity of DYRK1A with an IC 50 of 76 nM. Dyrk1A-IN-3 can be used in neur... | |||
T74881 | FITC-labeled Tominersen | ||
FITC-labeled Tominersen is Tominersen labeled with FITC. Tominersen (RG6042) is a second-generation 2′-O-(2-methoxyethyl) antisense oligonucleotide that targets huntingtin protein (HTT) mRNA and potently suppresses HTT p... | |||
T73683 | AC-VEID-CHO TFA | ||
AC-VEID-CHO (TFA) is a peptide-derived inhibitor targeting Caspases-6, -3, and -7, exhibiting IC50 values of 16.2 nM, 13.6 nM, and 162.1 nM, respectively. This compound demonstrates significant inhibitory potency and is ... | |||
T61063 | SEN177 | ||
SEN177 shows the potential in the research of Huntington’s disease that is a potent inhibitor of glutaminyl cyclase (QPCT) with an IC 50 of 0.013μM for glutaminyl-peptide cyclotransferase-like (QPCTL). The Ki value of SE... | |||
T37791 | A-971432 | ||
A-971432 is a sphingosine-1-phosphate receptor 5 (S1P5) agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.006, 0.362, and >10 µM, respectively). It inhibits forskolin-induced cAMP production in CHO cel... | |||
T83669 | PMX-53 TFA | AcPhe-[Orn-Pro-D-Cyclohexylalanine-Trp-Arg],AcF-[OPdChaWR],3D53 | |
PMX-53, a macrocyclic complement 5a (C5a) peptidomimetic and C5a receptor antagonist (IC50 = 0.3 µM), effectively inhibits the C5a-induced secretion of myeloperoxidase (MPO) in isolated human polymorphonuclear leukocytes... |