17766 Results for: "2,2,3,3,3-Pentafluoropropylamine+hydrochloride"
A first generation tricyclic antidepressant 1 * 5 g
Supplier: Cayman Chemical
A first generation tricyclic antidepressant 1 * 5 g
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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 * 1 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 * 1 mg
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A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 1 g
Supplier: Cayman Chemical
A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 1 g
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An inhibitor of JAK3 (IC50 = 79 nM) 1 * 10 mg
Supplier: Cayman Chemical
An inhibitor of JAK3 (IC50 = 79 nM) 1 * 10 mg
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A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 5 g
Supplier: Cayman Chemical
A tricyclic antidepressant that inhibits the reuptake of serotonin and norepinephrine and acts as an antagonist at histamine, seroto nin, adrenergic, and muscarinic receptors with Ki values in the nanomolar range 1 * 5 g
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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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A potent inhibitor of MELK (IC50 = 0.41 nM) 1 * 5 mg
Supplier: Cayman Chemical
A potent inhibitor of MELK (IC50 = 0.41 nM) 1 * 5 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 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 selective, reversible inhibitor of MAO-B (Ki = 0.091 M) over MAO-A (Ki = 9.06 M) 1 * 500 mg
Supplier: Cayman Chemical
A selective, reversible inhibitor of MAO-B (Ki = 0.091 M) over MAO-A (Ki = 9.06 M) 1 * 500 mg
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A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 50 mg
Supplier: Cayman Chemical
A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 50 mg
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Ulixertinib hydrochloride_50mg pack 1 * 50 mg
Supplier: Apollo Scientific
Ulixertinib hydrochloride_50mg pack 1 * 50 mg
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BMS_582949 hydrochloride_25mg pack 1 * 25 mg
Supplier: Apollo Scientific
BMS_582949 hydrochloride_25mg pack 1 * 25 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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A -adrenergic receptor agonist with potent positive inotropic effects in vivo 1 * 5 mg
Supplier: Cayman Chemical
A -adrenergic receptor agonist with potent positive inotropic effects in vivo 1 * 5 mg
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A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 5 mg
Supplier: Cayman Chemical
A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 5 mg
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Selectively inhibits human NHE-1 with an IC50 value of 14 nM 1 * 1 mg
Supplier: Cayman Chemical
Selectively inhibits human NHE-1 with an IC50 value of 14 nM 1 * 1 mg
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Selectively inhibits human NHE-1 with an IC50 value of 14 nM 1 * 5 mg
Supplier: Cayman Chemical
Selectively inhibits human NHE-1 with an IC50 value of 14 nM 1 * 5 mg
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1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 5 mg
Supplier: Cayman Chemical
1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 5 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 * 250 mg
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 * 250 mg
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2-Amino-5-hydroxypyridine hydrochloride_5g pack 1 * 5 g
Supplier: Apollo Scientific
2-Amino-5-hydroxypyridine hydrochloride_5g pack 1 * 5 g
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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 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 * 5 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 * 5 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 * 25 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 * 25 mg
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An epimer of chlortetracycline 1 * 1 mg
Supplier: Cayman Chemical
An epimer of chlortetracycline 1 * 1 mg
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An active metabolite of proguanil, produced by CYP2C19 1 * 5 mg
Supplier: Cayman Chemical
An active metabolite of proguanil, produced by CYP2C19 1 * 5 mg
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A first generation tricyclic antidepressant 1 * 25 g
Supplier: Cayman Chemical
A first generation tricyclic antidepressant 1 * 25 g
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: GRANT INSTRUMENTS
: BOCHEM
: VWR Collection
: DWK Life Sciences
: Thermo Fisher Scientific
: VWR Collection
: Oxford Nanopore Technologies
: Integra
: Industrial Physics
: AAT Bioquest
: Integra
: Palbam
: VWR Collection
: VWR Collection
: FACELLITATE
: NANOENTEK
: Greiner Bio-One