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Other Targets

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Cat. No. Product Name Field of Application Chemical Structure
DCAPI1397 Orlistat (Alli, Xenical) Featured Orlistat is a drug designed to treat obesity. Orlistat's primary function is preventing the absorption of fats from the human diet by acting as a lipase inhibitor, thereby reducing caloric intake. Orlistat is intended for use in conjunction with a healthcare provider-supervised reduced-calorie diet.
DC23573 ORM-10962 ORM-10962 is a potent, highly selective sodium-calcium exchanger (NCX) inhibitor, significantly reduces inward/outward NCX currents with IC50 of 55 and 67 nM, respectively.
DCAPI1297 Orotic acid (6-Carboxyuracil) Orotic acid (6-Carboxyuracil)
DC22407 Orvepitant Orvepitant (GW823296) is a potent and selective, brain penetrant NK1 receptor antagonist with pKi of 10.2.
DC23149 Oseltamivir acid Oseltamivir acid (GS 4071, Ro 64-0802, Oseltamivir carboxylate) is a potent inhibitor of influenza neuraminidase (NA) with Ki of <1 nM for both A and B strains,showed potent activity against COVID-19(SARS-COV-2).
DC8554 OSI-420 Featured OSI-420 (Desmethyl Erlotinib,CP-473420) is an active metabolite of erlotinib which is an orally active EGFR tyrosin kinase inhibitor with IC50 of 2 and 20 nM for human EGFR and EGFR autophosphorylation in tumor cells.
DC9974 Isturisa (Osilodrostat) Featured Osilodrostat is an inhibitor of aldosterone synthase and aromatase, for treating Cushing’s disease.
DC11438 Osimertinib analogue Featured Osimertinib analogue (C-005) is a potent EGFR inhibitor, which is 2-5 fold more selective than Osimertinib between above EGFR mutants and wild-type EGFR(A431) cells.
DC21449 OSMI-1 Featured OSMI-1 is a cell-permeable, small molecule O-GlcNAc transferase (OGT) inhibitor with IC50 of 2.7 uM.
DC12453 OSMI-4 OSMI-4 (OGT inhibitor 4b) is a novel potent, selective, cell-active O-linked N-acetylglucosamine transferase (OGT) inhibitor with EC50 of ~3 uM.
DC22304 ILK-IN-2 (CPD 22: OSU-T315 analog) Featured ILK-IN-2 (OSU-T315 analog) is a ILK inhibitor.
DC21450 OSW-1 Featured OSW-1 is a natural anti-enterovirus and anti-cancer compound that targets oxysterol-binding protein (OSBP) with Ki of 26 and 54 nM for OSBP and ORP4L, respectively.
DC9501 Otilonium (bromide) Otilonium Bromide is an antimuscarinic used as a spasmolytic agent.
DC12312 OTX008 (Calixarene 0118; PTX008) Featured OTX008 is a selective inhibitor of galectin-1.
DC7150 Birabresib (OTX015) Featured OTX-015 is a new potent BRD2/3/4 inhibitor with evident anti-proliferative activity in several cell lines representative of mature B-cell tumors.
DC22719 OUP-16 OUP-16 is a potent H4R agonist with a considerable selectivity over H3R..
DC23553 o-vanillin o-vanillin (C29L.
DC21022 OX-14 OX-14 is a highly potent farnesyl pyrophosphate synthase (FPPS) inhibitor with IC50 of 2.46 nM, with significantly lower binding affinity to hydroxyapatite.
DC8676 Oxadiazon Oxadiazon is a preemergent herbicide.
DC10480 Oxamflatin Featured Oxamflatin is a potent inhibitor of histone deacetylases (IC50 = 15.7 nM).
DCAPI1236 Oxfendazole Oxfendazole
DCAPI1110 Oxibendazole Oxibendazole
DC8961 Potassium Oxonate Oxonic acid potassium salt is an inhibitor of uricase, oxonic inhibits the phosphorylation of 5-FU to 5-fluorouridine-5'-monophosphate catalyzed by pyrimidine phosphoribosyl-transferase in a different manner from allopurinol in cell-free extracts and inta
DC10232 Oxybenzone Oxybenzone is a benzophenone derivative used as a sunscreen agent.
DC9112 Oxybutynin HCl Oxybutynin is also a possible treatment of hyperhidrosis (hyper-active sweating) .
DC20489 Oxythiamine chloride hydrochloride Oxythiamine chloride is a small molecule transketolase inhibitor with Kd of 33 nM, shows functional assay of human transketolase inhibition in HCT-116 cells with EC50 of 26 nM.
DC12352 Oxythiamine (Hydroxythiamin) Oxythiamine, an antimetabolite and a vitamin B1 antagonist, is a well-known thiamine antagonist and inhibitor of transketolase.
DCAPI1345 Ozagrel HCl Ozagrel HCl
DC9445 Ozagrel (sodium) Ozagrel(OKY-046) sodium salt is an antiplatelet agent working as a thromboxane A2 synthesis inhibitor.
DC7222 P005091(P5091) Featured P005091(P5091) is a selective and potent inhibitor of ubiquitin-specific protease 7 (USP7) with EC50 of 4.2 μM.

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