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 About 9 results found for searched term "54-80-8" (0.068 seconds)

Cat.No.  Name Target
M1942 Alectinib ALK
CH5424802; AF802
Alectinib (CH5424802) is a highly selective, orally active and potent ALK inhibitor with IC50 of 1.9 nM. Alectinib (CH5424802) also inhibits ALK F1174L and ALK R1275Q with IC50s of 1 nM and 3.5 nM, respectively. Alectinib demonstrates effective central nervous system (CNS) penetration.
M9175 Vacquinol-1 JNK
NSC13316
Vacquinol-1 is an MKK4 activator, which rapidly and selectively induces glioma cell death.
M10848 LP-922761 Others
LP-922761 is a potent, selective, orally active AAK1 inhibitor in enzymatic and cell analysis IC50 4.8 nM and 7.6 nM, respectively. LP-922761 also inhibits BMP-2-induced protein kinase (BIKE),IC50 24 nM. LP-922761 has no significant activity against cell GAK, opioids, epinephrine alpha2, or GABAa receptors.
M16573 5-Hydroxy-7-acetoxy-8-methoxyflavone Flavonoids
5-Hydroxy-7-acetoxy-8-methoxyflavone
M19917 Midecamycin Antibiotic
Espinomycin A; Medecamycin A1; Platenomycin B1; Rubimycin; Turimycin P3; SF-837
Midecamycin is a naturally occuring macrolide antibiotic that acts by inhibiting bacterial protein synthesis.
M21275 ONO-8430506 PDE
ONO-8430506 is a potent autotaxin phosphodiesterase inhibitor with significant oral exposure and low clearance in higher species.
M28055 JNJ-46281222  GluR
JNJ-46281222 is an metabotropic glutamate (mGlu) 2-selective, highly potent PAM (positive allosteric modulator) with nanomolar affinity (Kd = 1.7 nM) and a high modulatory potency (pEC50 = 7.71).
M30282 Pronethalol Adrenergic Receptor
(±)-Pronethalo
Pronethalol ((±)-Pronethalo) is a non-selective β-adrenergic antagonist. Pronethalol is a potent inhibitor of Sox2 expression. Pronethalol protects against and to reverse Digitalis-induced ventricular arrhythmias and limits the cerebral arteriovenous malformation (AVMs).
M53893 DfTat Others
DfTat is a dimer of the prototypical cell-penetrating peptide TAT.



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