22289 Results for: "3-(Trifluoromethoxy)pyrrolidine+hydrochloride"
An inhibitor of JAK3 (IC50 = 79 nM) 1 * 1 mg
Supplier: Cayman Chemical
An inhibitor of JAK3 (IC50 = 79 nM) 1 * 1 mg
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A major active metabolite of saxagliptin inhibits DPP-4 (Ki = 2.6 nM for human recombinant enzyme) 1 * 1 mg
Supplier: Cayman Chemical
A major active metabolite of saxagliptin inhibits DPP-4 (Ki = 2.6 nM for human recombinant enzyme) 1 * 1 mg
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A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 10 mg
Supplier: Cayman Chemical
A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 10 mg
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A pan inhibitor PKD (IC50s = 1, 2.5, and 2 nM for PKD1, PKD2, and PKD3, respectively) 1 * 10 mg
Supplier: Cayman Chemical
A pan inhibitor PKD (IC50s = 1, 2.5, and 2 nM for PKD1, PKD2, and PKD3, respectively) 1 * 10 mg
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2-3-(2,3-dichlorophenoxy)propylamino-ethanol, monohydrochloride 1 * 5 mg
Supplier: Cayman Chemical
2-3-(2,3-dichlorophenoxy)propylamino-ethanol, monohydrochloride 1 * 5 mg
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An active metabolite of proguanil, produced by CYP2C19 1 * 10 mg
Supplier: Cayman Chemical
An active metabolite of proguanil, produced by CYP2C19 1 * 10 mg
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A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 500 µG
Supplier: Cayman Chemical
A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 500 µG
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A selective antagonist of GABAB receptors (IC50 = 43 µM) 1 * 5 mg
Supplier: Cayman Chemical
A selective antagonist of GABAB receptors (IC50 = 43 µM) 1 * 5 mg
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A -adrenergic receptor agonist with potent positive inotropic effects in vivo 1 * 100 mg
Supplier: Cayman Chemical
A -adrenergic receptor agonist with potent positive inotropic effects in vivo 1 * 100 mg
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A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 1 mg
Supplier: Cayman Chemical
A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 1 mg
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A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 10 mg
Supplier: Cayman Chemical
A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 10 mg
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1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 50 mg
Supplier: Cayman Chemical
1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 50 mg
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1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 10 mg
Supplier: Cayman Chemical
1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 10 mg
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An inhibitor of PARPs which can be used in cells or in animals 1 * 10 mg
Supplier: Cayman Chemical
An inhibitor of PARPs which can be used in cells or in animals 1 * 10 mg
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An ATP-competitive, pan-Akt kinase inhibitor (IC50s = 2, 13, and 9 nM for Akt1, 2, and 3, respectively) that inhibits proliferation and induces apoptosis in various human tumor cells in vitro and in xenografts in immunocompromised mice 1 * 5 mg
Supplier: Cayman Chemical
An ATP-competitive, pan-Akt kinase inhibitor (IC50s = 2, 13, and 9 nM for Akt1, 2, and 3, respectively) that inhibits proliferation and induces apoptosis in various human tumor cells in vitro and in xenografts in immunocompromised mice 1 * 5 mg
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A cell-permeable inhibitor of Hhat (IC50 = 0.85 µM) 1 * 1 mg
Supplier: Cayman Chemical
A cell-permeable inhibitor of Hhat (IC50 = 0.85 µM) 1 * 1 mg
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1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 10 mg
Supplier: Cayman Chemical
1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 10 mg
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A steroidal alkaloid that suppresses NF-B signaling in LPS-stimulated macrophages, blocking induced expression of iNOS and COX-2 1 * 100 mg
Supplier: Cayman Chemical
A steroidal alkaloid that suppresses NF-B signaling in LPS-stimulated macrophages, blocking induced expression of iNOS and COX-2 1 * 100 mg
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A steroidal alkaloid that suppresses NF-B signaling in LPS-stimulated macrophages, blocking induced expression of iNOS and COX-2 1 * 10 mg
Supplier: Cayman Chemical
A steroidal alkaloid that suppresses NF-B signaling in LPS-stimulated macrophages, blocking induced expression of iNOS and COX-2 1 * 10 mg
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A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 10 mg
Supplier: Cayman Chemical
A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 10 mg
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A potent, cell-permeable inhibitor of SET7/9 (IC50 = 2 nM) that demonstrates greater than 1,000-fold selectivity over a panel of 18 other methyltransferases 1 * 1 mg
Supplier: Cayman Chemical
A potent, cell-permeable inhibitor of SET7/9 (IC50 = 2 nM) that demonstrates greater than 1,000-fold selectivity over a panel of 18 other methyltransferases 1 * 1 mg
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LY2584702 Hydrochloride_5mg pack 1 * 5 mg
Supplier: Apollo Scientific
LY2584702 Hydrochloride_5mg pack 1 * 5 mg
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SB_203580 Hydrochloride_10mg pack 1 * 10 mg
Supplier: Apollo Scientific
SB_203580 Hydrochloride_10mg pack 1 * 10 mg
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A fluoroquinolone antibiotic that displays broad spectrum antibacterial activity by inhibiting the bacterial regulatory enzyme DNA g yrase (IC50 = 0.92 µg/ml) as well as topoisomerase IV (IC50 = 1.62 µg/ml) 1 * 1 g
Supplier: Cayman Chemical
A fluoroquinolone antibiotic that displays broad spectrum antibacterial activity by inhibiting the bacterial regulatory enzyme DNA g yrase (IC50 = 0.92 µg/ml) as well as topoisomerase IV (IC50 = 1.62 µg/ml) 1 * 1 g
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A cell-permeable inhibitor of Hhat (IC50 = 0.85 µM) 1 * 10 mg
Supplier: Cayman Chemical
A cell-permeable inhibitor of Hhat (IC50 = 0.85 µM) 1 * 10 mg
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A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 50 mg
Supplier: Cayman Chemical
A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 50 mg
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A blocker of KCNQ channels that potently inhibits KCNQ1 and 2 homomeric channels (IC50 = 0.75 and 0.71 µM, respectively) as well as KCNQ2+3 heteromultimers (IC50 = 0.6 µM) 1 * 5 mg
Supplier: Cayman Chemical
A blocker of KCNQ channels that potently inhibits KCNQ1 and 2 homomeric channels (IC50 = 0.75 and 0.71 µM, respectively) as well as KCNQ2+3 heteromultimers (IC50 = 0.6 µM) 1 * 5 mg
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BMS_582949 hydrochloride_10mg pack 1 * 10 mg
Supplier: Apollo Scientific
BMS_582949 hydrochloride_10mg pack 1 * 10 mg
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LY2584702 Hydrochloride_25mg pack 1 * 25 mg
Supplier: Apollo Scientific
LY2584702 Hydrochloride_25mg pack 1 * 25 mg
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A potent inhibitor of IB kinases (IKKs), displaying IC50 values of 200, 40, and 70 nM for IKK, IKK, and IKK complex, respectively , in cell-free assays 1 * 50 mg
Supplier: Cayman Chemical
A potent inhibitor of IB kinases (IKKs), displaying IC50 values of 200, 40, and 70 nM for IKK, IKK, and IKK complex, respectively , in cell-free assays 1 * 50 mg
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Supplier: GRANT INSTRUMENTS
Supplier: BOCHEM
Supplier: VWR Collection
Supplier: OMEGA BIO-TEK
Supplier: DWK Life Sciences
Supplier: Thermo Fisher Scientific
Supplier: VWR Collection
Supplier: Oxford Nanopore Technologies
Supplier: Integra
Supplier: Industrial Physics
Supplier: AAT Bioquest
Supplier: Integra
Supplier: Palbam
Supplier: VWR Collection
Supplier: VWR Collection
Supplier: FACELLITATE
Supplier: NANOENTEK
Supplier: Greiner Bio-One