BP10580
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Omaveloxolone
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Omaveloxolone (RTA-408) is a synthetic triterpenoid that activates the cytoprotective transcription factor Nrf2 and inhibits NF-κB signaling. Phase 2.
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BP10476
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ON 146040
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ON 146040 is an effective inhibitor of PI3K isoforms with IC50s of 14 and 20 nM for PI3Kα and PI3Kδ, respectively.
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BP10360
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ON1231320
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ON1231320 is a Polo-like kinase 2 (PLK2) inhibitor.
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BP10414
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ON123300
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ON123300 is a potent and multi-targeted kinase inhibitor for CDK4/Ark5/PDGFRβ/FGFR1/RET/Fyn (IC50: 3.9/5/26/26/9.2/11 nM).
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BP10265
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Onatasertib
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CC-223 is an orally available mTOR inhibitor with potential antitumor activity. CC-223 inhibits the activity of mTOR, which may result in the induction of tumor cell apoptosis and a decrease in tumor cell proliferation. CC-223 is a potent mTOR kinase inhibitor (IC50: 16 nM), with >150-fold sensitivity than the related lipid kinase PI3Kα (IC50: 4 μM).
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BP10806
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ONC212
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ONC212, a fluorinated-ONC201 analogue, is a selective agonist of GPR132.
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BP10404
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ONO-4059 analog
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ONO-4059 analogue is an analogue of ONO-4059, which is a highly potent and selective oral BTK inhibitor with IC50 of 23.9 nM. Phase 1.
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BP10056
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Onvansertib
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NMS-P937 (NMS1286937), an oral, specific Polo-like Kinase 1 (PLK1) inhibitor, is with IC50 of 2 nM. The specificity of NMS-P937 forPLK1 is 5000-fold higher over PLK2/PLK3.
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BP10716
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Orelabrutinib
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Orelabrutinib is an orally active and irreversible inhibitor of Bruton's tyrosine kinase (BTK).
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BP10936
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Oritinib
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Oritinib is an inhibitor of EGFR with IC50s of 18, 0.7, 4, 0.1, 1.4 and 0.89 nM for EGFR (wt), EGFR (L858R), EGFR (L861Q), EGFR (L858R/T790M), EGFR (d746-750), EGFR (d746-750/T790M), respectively. Oritinib can be used in studies about the treatment of non-small cell lung cancer.
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BP10173
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Oroxin B
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Oroxin B has antioxidant activity.
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BP10496
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Osimertinib
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Osimertinib is a small molecule tyrosine kinase receptor inhibitor and antineoplastic agent that is used in the therapy of selected forms of advanced non-small cell lung cancer (NSCLC).
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BP10957
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Osimertinib dimesylate
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Osimertinib dimesylate is an irreversible and mutant selective EGFR inhibitor (IC50s: 12 and 1 nM against EGFR L858R and EGFR L858R/T790M).
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BP10497
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Osimertinib mesylate
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Osimertinib (AZD-9291) is an irreversible and mutant selective EGFR inhibitor (IC50s: 12/1 nM for EGFR(L858R) and EGFR(L858R/T790M)).
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BP10959
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OSU-T315
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OSU-T315 (1,5-regioisomer) is a ILK inhibitor.
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BP10260
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Otenaproxesul
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ATB-346 is a novel hydrogen sulphide-releasing derivative of naproxen with markedly reduced toxicity.
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BP10390
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OTS514
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OTS514 is a potent TOPK inhibitor. OTS514 exhibits a growth-suppressive effect on small cell lung cancer. OTS514 effectively suppressed the growth of SCLC cell lines (IC50: 0.4 ~ 42.6 nM). Treatment with OTS514 suppressed forkhead box protein M1 (FOXM1) activity. OTS514 treatment reduced CD90-positive SCLC cells and showed a higher cytotoxic effect against lung sphere-derived CSC-like SCLC cells.
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BP10391
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OTS964 hydrochloride
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OTS964 is a potent and selective TOPK inhibitor with potential anticancer activity.
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BP10950
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Oxibendazole
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Oxibendazole is a benzimidazole drug that interferes with metabolic pathways, used to protect against roundworms, strongyles, threadworms, pinworms and lungworm infestations in horses and some domestic pets.
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BP10367
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Oxybenzone
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Oxybenzone is an organic compound used in sunscreens. It is a derivative of benzophenone.
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