Selleck Chemicals supplies over 3,000 inhibitors used in the study of cell signaling pathways. We actively tracks the latest science so our customers can rely on us to be the leading supplier of the newest inhibitors.
Company WebsiteArenobufagin is a natural bufadienolide from toad venom and induces apoptosis and autophagy in human hepatocellular carcinoma cells through inhibition of PI3K/Akt/mTOR pathway.
More Information Supplier PageArformoterol Tartrate is the tartrate salt of arformoterol, a long-acting beta-2 adrenergic agonist with bronchodilator activity.
More Information Supplier PageArformoterol Tartrate is the tartrate salt of arformoterol, a long-acting beta-2 adrenergic agonist with bronchodilator activity.
More Information Supplier PageArgatroban (MCI-9038) is a potent and selective synthetic thrombin inhibitor with Ki ranging from 5 nM to 39 nM, used as an anticoagulant.
More Information Supplier PageArgatroban (MCI-9038) is a potent and selective synthetic thrombin inhibitor with Ki ranging from 5 nM to 39 nM, used as an anticoagulant.
More Information Supplier PageArgatroban (Argatroban hydrate, Argipidine,MCI-9038 Monohydrate) is a direct, selective thrombin inhibitor with anticoagulant effects.
More Information Supplier PageArgpressin Acetate is a neurohypophysial hormone found in most mammals. It acts as a neurotransmitter at synapses in the brain, increases [Ca2+]i in cultured rat hippocampal neurons.
More Information Supplier PageArgireline is an innovative neuropeptide widely applied topically on the skin.
More Information Supplier PageAripiprazole (OPC-14597) is a novel atypical antipsychotic drug that is reported to be a high-affinity 5-HT receptor partial agonist.
More Information Supplier PageAripiprazole (OPC-14597) is a novel atypical antipsychotic drug that is reported to be a high-affinity 5-HT receptor partial agonist.
More Information Supplier PageAristolochic acid A (Aristolochic Acid I, Aristolochin, Aristolochine, TR 1736) is a carcinogenic, mutagenic, and nephrotoxic agent extracted from the flowering plant family Aristolochiaceae.Aristolochic acid A significantly reduces both activator protein 1 (AP-1) and nuclear factor-κB (NF-κB) activities.
More Information Supplier PageAristolochic acid A (Aristolochic Acid I, Aristolochin, Aristolochine, TR 1736) is a carcinogenic, mutagenic, and nephrotoxic agent extracted from the flowering plant family Aristolochiaceae.Aristolochic acid A significantly reduces both activator protein 1 (AP-1) and nuclear factor-κB (NF-κB) activities.
More Information Supplier PageAristolone, which could be extracted from essential oil of Elyonurus hensii, is likely to induce an antalgic activity.
More Information Supplier PageARN19702 is an orally active, reversible N-Acylethanolamine acid amidase(NAAA) inhibitor (IC50 on human NAAA = 230 nM) that produces remarkable protective effects against multiple sclerosis in mice.
More Information Supplier PageARN-3236 is a potent, orally available and selective inhibitor of salt-inducible kinase 2 (SIK2) with IC50 of
More Information Supplier PageARN-3236 is a potent, orally available and selective inhibitor of salt-inducible kinase 2 (SIK2) with IC50 of
More Information Supplier PageArnica Montana Extract is extracted from the flowers of Arnica montana L. (Asteraceae). Arnica montana possesses anti-inflammatory, immune-modulatory, anti-sclerotic, analgesic, antifungal, antioxidant, antibacterial, and anticancer bioactivities.
More Information Supplier PageARP 100 (MMP-2 Inhibitor III, Compound 10a) is a potent and selective inhibitor of MMP-2 with an IC50 of 12 nM and displays less inhibitory activity at MMP-9, MMP-3, MMP-1 and MMP-7 with IC50s of 200 nM, 4500 nM, >50,000 nM and >50,000 nM respectively.
More Information Supplier PageARP 100 (MMP-2 Inhibitor III, Compound 10a) is a potent and selective inhibitor of MMP-2 with an IC50 of 12 nM and displays less inhibitory activity at MMP-9, MMP-3, MMP-1 and MMP-7 with IC50s of 200 nM, 4500 nM, >50,000 nM and >50,000 nM respectively.
More Information Supplier PageARQ 621 is an allosteric, and selective Eg5 mitotic motor protein inhibitor. Phase 1.
More Information Supplier PageARQ 621 is an allosteric, and selective Eg5 mitotic motor protein inhibitor. Phase 1.
More Information Supplier PageArrhenatherum Elatius Extract is extracted from Arrhenatherum elatius (L.) Pressl.. Arrhenatherum elatius has ability to remove heavy metals from soil.
More Information Supplier PageARRY-382 is a highly selective, oral inhibitor of the CSF1R with an IC50 of 9 nM.
More Information Supplier PageARRY-382 is a highly selective, oral inhibitor of the CSF1R with an IC50 of 9 nM.
More Information Supplier PageARRY-382 is a highly selective, oral inhibitor of the CSF1R with an IC50 of 9 nM.
More Information Supplier PageARS-1620 is a potent, orally bioavailable covalent inhibitor of KRASG12C and could achieve rapid and sustained in vivo target occupancy to induce tumor regression.
More Information Supplier PageARS-1620 is a potent, orally bioavailable covalent inhibitor of KRASG12C and could achieve rapid and sustained in vivo target occupancy to induce tumor regression.
More Information Supplier PageARS-1620 is a potent, orally bioavailable covalent inhibitor of KRASG12C and could achieve rapid and sustained in vivo target occupancy to induce tumor regression.
More Information Supplier PageARS-1620 is a potent, orally bioavailable covalent inhibitor of KRASG12C and could achieve rapid and sustained in vivo target occupancy to induce tumor regression.
More Information Supplier PageARS-1620 is a potent, orally bioavailable covalent inhibitor of KRASG12C and could achieve rapid and sustained in vivo target occupancy to induce tumor regression.
More Information Supplier PageARS-1620 is a potent, orally bioavailable covalent inhibitor of KRASG12C and could achieve rapid and sustained in vivo target occupancy to induce tumor regression.
More Information Supplier PageARS-853 is a selective, covalent KRAS(G12C) inhibitor that inhibits mutant KRAS-driven signaling by binding to the GDP-bound oncoprotein and preventing activation. ARS-853 also induces apoptosis.
More Information Supplier PageARS-853 is a selective, covalent KRAS(G12C) inhibitor that inhibits mutant KRAS-driven signaling by binding to the GDP-bound oncoprotein and preventing activation. ARS-853 also induces apoptosis.
More Information Supplier PageARS-853 is a selective, covalent KRAS(G12C) inhibitor that inhibits mutant KRAS-driven signaling by binding to the GDP-bound oncoprotein and preventing activation. ARS-853 also induces apoptosis.
More Information Supplier PageART558 is a potent, selective, low molecular weight, allosteric inhibitor of DNA Polθ with an IC50 of 7.9 nM.
More Information Supplier PageART558 is a potent, selective, low molecular weight, allosteric inhibitor of DNA Polθ with an IC50 of 7.9 nM.
More Information Supplier PageART558 is a potent, selective, low molecular weight, allosteric inhibitor of DNA Polθ with an IC50 of 7.9 nM.
More Information Supplier PageART558 is a potent, selective, low molecular weight, allosteric inhibitor of DNA Polθ with an IC50 of 7.9 nM.
More Information Supplier PageART812 is an orally active DNA polymerase Polθ inhibitor with an IC50 value of 7.6 nM.
More Information Supplier PageART812 is an orally active DNA polymerase Polθ inhibitor with an IC50 value of 7.6 nM.
More Information Supplier PageART812 is an orally active DNA polymerase Polθ inhibitor with an IC50 value of 7.6 nM.
More Information Supplier PageART812 is an orally active DNA polymerase Polθ inhibitor with an IC50 value of 7.6 nM.
More Information Supplier PageART812 is an orally active DNA polymerase Polθ inhibitor with an IC50 value of 7.6 nM.
More Information Supplier PageArteether is a well-known antimalarial drug which acts by producing free radicals within the malarial parasite.
More Information Supplier PageArtemether (SM-224, CGP 56696) is an antimalarial for the treatment of resistant strains of falciparum malaria.
More Information Supplier PageArtemisia Annua Extract is extracted from Artemisia Annua, which has antimalarial and anticancer effects.
More Information Supplier PageArtemisic acid (Artemisinic acid), an amorphane sesquiterpene isolated from Artemisia annua L., has a variety of pharmacological activity, such as antimalarial activity, anti-tumor activity, antipyretic effect, antibacterial activity, allelopathy effect and anti-adipogenesis effect.
More Information Supplier PageArtemisinin is a sesquiterpene endoperoxide which is a potent antimalarial agent.
More Information Supplier PageArtemisinin is a sesquiterpene endoperoxide which is a potent antimalarial agent.
More Information Supplier PageArtemisinin is a sesquiterpene endoperoxide which is a potent antimalarial agent.
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