BP15182
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Quercimeritrin
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Quercimeritrin has antibacterial activity, it shows promising activity against Staphylococcus aureus.
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BP15183
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Riamilovir
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Riamilovir is a broad-spectrum antiviral drug candidate.
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BP15184
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Riboflavin Tetrabutyrate
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Riboflavin Tetrabutyrate is a lipophilic flavin derivative. Riboflavin Tetrabutyrate has antioxidative and lipid peroxide-removing activity.
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BP15185
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RO2959 Hydrochloride
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RO2959 hydrochloride is a potent and selective inhibitor of CRAC channel(IC50: 402 nM). It is also a potent inhibitor of human IL-2.
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BP15186
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Rofecoxib
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Rofecoxib binds to and inhibits the enzyme cyclooxygenase-2 (COX-2), resulting in an inhibition of the conversion of arachidonic acid to prostaglandins. Rofecoxib is a synthetic, nonsteroidal derivative of phenyl-furanone with anti-inflammatory, antipyretic and analgesic properties and potential antineoplastic properties. COX-related metabolic pathways may represent key regulators of cell proliferation and neo-angiogenesis. Some epithelial tumor cell types overexpress pro-angiogenic COX-2.
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BP15187
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RS 504393
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RS 504393 is a highly selective CCR2 chemokine receptor antagonist (IC50s: 89 nM and > 100 μM for human recombinant CCR2 and CCR1).
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BP15188
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Rutaevin
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Rutaevin shows the inhibitory activity on nitric oxide (NO) production in lipopolysaccharide-activated RAW264.7 macrophages, it may be as a valuable anti-inflammatory agent.
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BP15189
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RWJ 63556
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RWJ 63556 is an orally active inhibitor of COX-2 selective/5-lipoxygenase, shows anti-inflammatory activities.
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BP15190
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Salicylamide
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Salicylamide is an over-the-counter drug with analgesic and antipyretic properties, which has similar medicinal properties to aspirin. In the over-the-counter pain remedies, Salicylamide is used in combination with both aspirin and caffeine.
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BP15191
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Sanggenon D
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Sanggenone D represents a new scaffold of positive GABAA receptor modulators, it also inhibits COX-2 activity (IC 50 = 73-100 μM). Sanggenone D has anti-inflammatory activity, it can inhibit NO production from lipopolysaccharide (LPS)-induced RAW 264.7 cells at > 10 uM; inhibition of nitric oxide production was mediated by suppression of iNOS enzyme induction but not by direct inhibition of iNOS enzyme activity.
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BP15192
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SB297006
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SB 297006 is an antagonist of C-C chemokine receptor 3 (CCR3; IC50 = 39 nM), which normally is activated by eotaxin, eotaxin-3, MCP-3, MCP-4, RANTES, and MIP-1δ. It is at least 250-fold selective for CCR3 over a panel of other chemokine receptors. SB 297006 blocks CCR3-mediated calcium mobilization induced by eotaxin, eotaxin-2, and MCP-4 in transfected cells. It suppresses antigen-induced accumulation of Th2 lymphocytes and eosinophils in lungs of mice when delivered subcutaneously (100 mg/kg).
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BP15193
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SC57666
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SC57666 is a selective inhibitor of COX2(IC50 of 26 nM).
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BP15194
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SC58451
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SC58451 is a potent and selective inhibitor of Cox-2.
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BP15195
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Secologanic acid
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Secologanic acid is a plant growth inhibitor, it shows inhibition of nitric oxide production in lipopolysaccharide-activated macrophages.
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BP15196
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Sikokianin C
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Sikokianin C shows antimalarial activity against the chloroquine-resistant strain of Plasmodium falciparum, with the IC (50) value of 0.56 microg/mL.
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BP15197
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S-Methylisothiourea sulfate
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S-Methylisothiourea sulfate is a potent and selective inhibitor of iNOS and exerts beneficial effects in rodent models of septic shock.
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BP15198
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S-MTC
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S-MTC is a selective inhibitor of type I nitric oxide synthase.
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BP15199
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S-Nitroso-N-acetyl-DL-penicillamine
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S-Nitroso-N-acetyl-DL-penicillamine acts as a stable inhibitor of platelet aggregation, is a nitric oxide donor and.
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BP15200
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StemRegenin 1
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StemRegenin 1 is an aryl hydrocarbon receptor (AhR) inhibitor.
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BP15201
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Stylopine hydrochloride
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Stylopine is a protoberberine-type alkaloid that has potential biological activities, including anti-inflammatory activity.
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