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Orsellinic acid, a natural product isolated and purified from the Chaetomium globosum endophytic, can block platelet activating factor (PAF)-mediated neuronal apoptosis without affecting G-protein coupled receptor (PAFR)-mediated neuroprotection, it can effectively attenuate PAFR-independent neuronal apoptosis.
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Orsellinic acid, a natural product isolated and purified from the Chaetomium globosum endophytic, can block platelet activating factor (PAF)-mediated neuronal apoptosis without affecting G-protein coupled receptor (PAFR)-mediated neuroprotection, it can effectively attenuate PAFR-independent neuronal apoptosis.
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Osalmid can target ribonucleotide reductase small subunit M2 (RRM2) with IC50 of 8.23 μM. It is used for cholecystitis and bile duct inflammation.
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Osalmid can target ribonucleotide reductase small subunit M2 (RRM2) with IC50 of 8.23 μM. It is used for cholecystitis and bile duct inflammation.
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CSNpharm
Ospemifene is a non-hormonal estrogen receptor modulator (SERM) with IC50 values of 827 nM and 1633 nM for ERα and ERβ. Ospemifene is one of the active metabolites of toremifene.
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Ospemifene is a non-hormonal estrogen receptor modulator (SERM) with IC50 values of 827 nM and 1633 nM for ERα and ERβ. Ospemifene is one of the active metabolites of toremifene.
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CSNpharm
Ospemifene is a non-hormonal estrogen receptor modulator (SERM) with IC50 values of 827 nM and 1633 nM for ERα and ERβ. Ospemifene is one of the active metabolites of toremifene.
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CSNpharm
Ospemifene is a non-hormonal estrogen receptor modulator (SERM) with IC50 values of 827 nM and 1633 nM for ERα and ERβ. Ospemifene is one of the active metabolites of toremifene.
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CSNpharm
Ospemifene is a non-hormonal estrogen receptor modulator (SERM) with IC50 values of 827 nM and 1633 nM for ERα and ERβ. Ospemifene is one of the active metabolites of toremifene.
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CSNpharm
OSS_128167 is a potent selective sirtuin 6 (SIRT6) inhibitor with IC50s of 89 μM, 1578 μM and 751 μM for SIRT6, SIRT1 and SIRT2, respectively. OSS_128167 has anti-HBV activity that inhibits HBV transcription and replication. OSS_128167 has anti-cancer, anti-inflammation and anti-viral effects[1][2].
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CSNpharm
OSS_128167 is a potent selective sirtuin 6 (SIRT6) inhibitor with IC50s of 89 μM, 1578 μM and 751 μM for SIRT6, SIRT1 and SIRT2, respectively. OSS_128167 has anti-HBV activity that inhibits HBV transcription and replication. OSS_128167 has anti-cancer, anti-inflammation and anti-viral effects[1][2].
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CSNpharm
OSS_128167 is a potent selective sirtuin 6 (SIRT6) inhibitor with IC50s of 89 μM, 1578 μM and 751 μM for SIRT6, SIRT1 and SIRT2, respectively. OSS_128167 has anti-HBV activity that inhibits HBV transcription and replication. OSS_128167 has anti-cancer, anti-inflammation and anti-viral effects[1][2].
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CSNpharm
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CSNpharm
Osthole, an O-methylated coumarin, is a histamine H1 receptor inhibitior. It exhibits immunomodulatory, antioxidative and anti-inflammatory activities.
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OTX-015 is a potent BET bromodomain inhibitor with EC50 ranging from 10 to 19 nM for BRD2, BRD3, and BRD4 in cell-free assays.
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OTX-015 is a potent BET bromodomain inhibitor with EC50 ranging from 10 to 19 nM for BRD2, BRD3, and BRD4 in cell-free assays.
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CSNpharm
OTX-015 is a potent BET bromodomain inhibitor with EC50 ranging from 10 to 19 nM for BRD2, BRD3, and BRD4 in cell-free assays.
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CSNpharm
OTX-015 is a potent BET bromodomain inhibitor with EC50 ranging from 10 to 19 nM for BRD2, BRD3, and BRD4 in cell-free assays.
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CSNpharm
OTX-015 is a potent BET bromodomain inhibitor with EC50 ranging from 10 to 19 nM for BRD2, BRD3, and BRD4 in cell-free assays.
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Oxaloacetic Acid substrate for malate dehydrogenase and oxaloacetate decarboxylase. Oxaloacetic Acid is an inhibitor of SDH.
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Oxaprozin is a COX inhibitor with IC50s of 2.2 μM and 36 μM for human platelet COX-1 and IL-1-stimulated human synovial cell COX-2, it’s a NSAID used to relieve the inflammation, swelling, stiffness, and joint pain associated with osteoarthritis and rheumatoid arthritis.
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Oxaprozin is a COX inhibitor with IC50s of 2.2 μM and 36 μM for human platelet COX-1 and IL-1-stimulated human synovial cell COX-2, it’s a NSAID used to relieve the inflammation, swelling, stiffness, and joint pain associated with osteoarthritis and rheumatoid arthritis.
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Oxaprozin is a COX inhibitor with IC50s of 2.2 μM and 36 μM for human platelet COX-1 and IL-1-stimulated human synovial cell COX-2, it’s a NSAID used to relieve the inflammation, swelling, stiffness, and joint pain associated with osteoarthritis and rheumatoid arthritis.
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Oxcarbazepine is a voltage-gated sodium channel blocker with IC50 of 160 μM and it is used for the treatment of partial seizure.
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Oxcarbazepine is a voltage-gated sodium channel blocker with IC50 of 160 μM and it is used for the treatment of partial seizure.
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CSNpharm
Oxcarbazepine is a voltage-gated sodium channel blocker with IC50 of 160 μM and it is used for the treatment of partial seizure.
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CSNpharm
Oxcarbazepine is a voltage-gated sodium channel blocker with IC50 of 160 μM and it is used for the treatment of partial seizure.
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CSNpharm
Oxeladin citrate is a cough suppressant, is a highly potent and effective drug used to treat all types of cough of various etiologies.
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CSNpharm
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