21863 Results for: "Benzyl+thioacetimidate+hydrochloride"
A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 1 mg
Supplier: Cayman Chemical
A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 1 mg
Expand 1 Items
SB_203580 Hydrochloride_100mg pack 1 * 100 mg
Supplier: Apollo Scientific
SB_203580 Hydrochloride_100mg pack 1 * 100 mg
Expand 1 Items
1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 1 mg
Supplier: Cayman Chemical
1-2-(4-methoxyphenyl)-2-3-(4-methoxyphenyl)propoxyethyl-1H-i midazole,monohydrochloride 1 * 1 mg
Expand 1 Items
An active metabolite of proguanil, produced by CYP2C19 1 * 50 mg
Supplier: Cayman Chemical
An active metabolite of proguanil, produced by CYP2C19 1 * 50 mg
Expand 1 Items
A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 5 mg
Supplier: Cayman Chemical
A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 5 mg
Expand 1 Items
A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 5 mg
Supplier: Cayman Chemical
A potent, selective antagonist of the serotonin (5-HT) receptor 5-HT3 (pKi = 10.4 in rat cortex) 1 * 5 mg
Expand 1 Items
An antibiotic that can inhibit cell wall synthesis in plant-pathogenic oomycetes (MIC = 25 µg/ml for P. medicaginis M2913) and certa in fungi as well as some bacterial species (MIC = 400 µg/ml for S. aureus) 1 * 1 mg
Supplier: Cayman Chemical
An antibiotic that can inhibit cell wall synthesis in plant-pathogenic oomycetes (MIC = 25 µg/ml for P. medicaginis M2913) and certa in fungi as well as some bacterial species (MIC = 400 µg/ml for S. aureus) 1 * 1 mg
Expand 1 Items
2-Amino-5-hydroxypyridine hydrochloride_5g pack 1 * 5 g
Supplier: Apollo Scientific
2-Amino-5-hydroxypyridine hydrochloride_5g pack 1 * 5 g
Expand 1 Items
A first generation tricyclic antidepressant 1 * 25 g
Supplier: Cayman Chemical
A first generation tricyclic antidepressant 1 * 25 g
Expand 1 Items
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
Expand 1 Items
1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 100 mg
Supplier: Cayman Chemical
1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl) -1-phenanthrenemethanamine, monohydrochloride 1 * 100 mg
Expand 1 Items
A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 5 mg
Supplier: Cayman Chemical
A slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of AP-A (glutamyl AP 1 * 5 mg
Expand 1 Items
A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 10 mg
Supplier: Cayman Chemical
A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 1 * 10 mg
Expand 1 Items
A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 5 mg
Supplier: Cayman Chemical
A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 5 mg
Expand 1 Items
A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 10 mg
Supplier: Cayman Chemical
A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 10 mg
Expand 1 Items
A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 50 mg
Supplier: Cayman Chemical
A benzazepine derivative that antagonizes the binding of AVP to vasopressin V2 receptors (IC50 = 14 nM) 1 * 50 mg
Expand 1 Items
A selective antagonist of GABAB receptors (IC50 = 43 µM) 1 * 10 mg
Supplier: Cayman Chemical
A selective antagonist of GABAB receptors (IC50 = 43 µM) 1 * 10 mg
Expand 1 Items
An orally active, selective inhibitor of Cdk4 (IC50 = 11 nM) and Cdk6 (IC50 = 16 nM) with antiproliferative activity against retinob lastoma-positive tumor cells, blocking retinoblastoma phosphorylation and inducing G1 arrest 1 * 1 mg
Supplier: Cayman Chemical
An orally active, selective inhibitor of Cdk4 (IC50 = 11 nM) and Cdk6 (IC50 = 16 nM) with antiproliferative activity against retinob lastoma-positive tumor cells, blocking retinoblastoma phosphorylation and inducing G1 arrest 1 * 1 mg
Expand 1 Items
An antibiotic that can inhibit cell wall synthesis in plant-pathogenic oomycetes (MIC = 25 µg/ml for P. medicaginis M2913) and certa in fungi as well as some bacterial species (MIC = 400 µg/ml for S. aureus) 1 * 25 mg
Supplier: Cayman Chemical
An antibiotic that can inhibit cell wall synthesis in plant-pathogenic oomycetes (MIC = 25 µg/ml for P. medicaginis M2913) and certa in fungi as well as some bacterial species (MIC = 400 µg/ml for S. aureus) 1 * 25 mg
Expand 1 Items
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
Expand 1 Items
A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme (IC50s for both enzymes 0.5 nM) 1 * 5 mg
Supplier: Cayman Chemical
A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme (IC50s for both enzymes 0.5 nM) 1 * 5 mg
Expand 1 Items
A steroidal alkaloid that suppresses NF-B signaling in LPS-stimulated macrophages, blocking induced expression of iNOS and COX-2 1 * 50 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 * 50 mg
Expand 1 Items
GDC_0994 hydrochloride_1mg pack 1 * 1 mg
Supplier: Apollo Scientific
GDC_0994 hydrochloride_1mg pack 1 * 1 mg
Expand 1 Items
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
Expand 1 Items
A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 100 mg
Supplier: Cayman Chemical
A broad-spectrum, indole-based antiviral compound that blocks viral fusion with target membranes, prohibiting viral entry into cells 1 * 100 mg
Expand 1 Items
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
Expand 1 Items
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
Expand 1 Items
A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme (IC50s for both enzymes 0.5 nM) 1 * 10 mg
Supplier: Cayman Chemical
A potent inhibitor of JAK2 that also inhibits the JAK2V617F mutant enzyme (IC50s for both enzymes 0.5 nM) 1 * 10 mg
Expand 1 Items
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 * 5 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 * 5 mg
Expand 1 Items
A conventional antipsychotic drug that potently activates several neuroreceptors, including serotonin (Kis = 10, 60, and 57 nM for 5 -HT2A, 5-HT2C, and 5-HT6, respectively), dopamine D2 (Ki = 11 nM), and adrenergic 1A (Ki = 5 nM) receptors 1 * 1 g
Supplier: Cayman Chemical
A conventional antipsychotic drug that potently activates several neuroreceptors, including serotonin (Kis = 10, 60, and 57 nM for 5 -HT2A, 5-HT2C, and 5-HT6, respectively), dopamine D2 (Ki = 11 nM), and adrenergic 1A (Ki = 5 nM) receptors 1 * 1 g