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Name Description Size Catalog # Supplier  
Alprostadil Prostaglandin with some selectivity for EP3 and EP4 receptors (Ki values are 1.1, 2.1, 36, 10 and 33 nM for mouse EP3, EP4, EP1, EP2 and IP receptors respectively). Inhibits platelet aggregation and is a vasodilator in vivo. Purity > 98% 10mg 1620 TOCRIS BIOSCIENCE More Info
Alprostadil Prostaglandin with some selectivity for EP3 and EP4 receptors (Ki values are 1.1, 2.1, 36, 10 and 33 nM for mouse EP3, EP4, EP1, EP2 and IP receptors respectively). Inhibits platelet aggregation and is a vasodilator in vivo. Purity > 98% 50mg 1620 TOCRIS BIOSCIENCE More Info
Alrestatin Specific inhibitor of aldose reductase (IC50 = 148 µM). Attenuates glucose-induced angiotensin II production in rat vascular smooth muscle in vitro. Purity > 98% 10mg 0485 TOCRIS BIOSCIENCE More Info
Alrestatin Specific inhibitor of aldose reductase (IC50 = 148 µM). Attenuates glucose-induced angiotensin II production in rat vascular smooth muscle in vitro. Purity > 98% 50mg 0485 TOCRIS BIOSCIENCE More Info
Alsterpaullone A cell-permeable, potent, reversible, and ATP competitive inhibitor of GSK-3β (IC50 = 4 nM) and Cdk1/cyclin B (IC50 = 35 nM). Displays remarkable in vitro antitumor activity. Inhibits Tau phosphorylation at sites that are typically phosphoryl... n/a 126870 CALBIOCHEM/EMD BIOSCIENCES More Info
Alytesin Purity: > 95% 1 mg 06-271-83060 GENWAY BIOTECH INC. More Info
Alytesin Purity: > 95% 5 mg 06-271-83060 GENWAY BIOTECH INC. More Info
Alytesin Amphibian bombesin-like peptide. In vivo, stimulates gastric acid secretion, intestinal contraction, rat uterine contraction and hypertension in the dog. Also modulates thermoregulation following central administration in vivo. Purity > 98% 1mg 1893 TOCRIS BIOSCIENCE More Info
AM1172 n/a n/a n/a CAYMAN CHEMICAL CO. More Info
AM404 n/a n/a n/a CAYMAN CHEMICAL CO. More Info
AM 251 CB1 receptor antagonist / inverse agonist 10mg Asc-088-10mg ASCENT SCIENTIFIC LTD. More Info
AM 251 CB1 receptor antagonist / inverse agonist 50mg Asc-088-50mg ASCENT SCIENTIFIC LTD. More Info
AM404 Anandamide transport inhibitor 10mg Asc-095-10mg ASCENT SCIENTIFIC LTD. More Info
AM404 Anandamide transport inhibitor 50mg Asc-095-50mg ASCENT SCIENTIFIC LTD. More Info
AM 114 Inhibitor of the chymotrypsin-like activity of the 20S proteasome (IC50 ~ 1 µM). Displays anticancer activity; inhibits cell growth in human colon cancer HCT116 p53+/+ cells (IC50 = 1.49 µM). Purity > 98% 10mg 2564 TOCRIS BIOSCIENCE More Info
AM 114 Inhibitor of the chymotrypsin-like activity of the 20S proteasome (IC50 ~ 1 µM). Displays anticancer activity; inhibits cell growth in human colon cancer HCT116 p53+/+ cells (IC50 = 1.49 µM). Purity > 98% 50mg 2564 TOCRIS BIOSCIENCE More Info
AM 1172 Metabolically stable anandamide uptake inhibitor (IC50 = 2.1 - 2.5 µM) and fatty acid amide hydrolase (FAAH) inhibitor (Ki = 3.18 µM). Inhibits N-arachidonylethanolamine (AEA) accumulation (IC50 = 24 µM) and hydrolysis (Ki = 3 &m... 10mg 3381 TOCRIS BIOSCIENCE More Info
AM 251 Potent CB1 receptor antagonist (IC50 = 8 nM, Ki = 7.49 nM) that displays 306-fold selectivity over CB2 receptors. Also potent GPR55 agonist (EC50 = 39 nM). Also available as part of the Cannabinoid CB1 Receptor Tocrisettm. Purity > 99% 10mg 1117 TOCRIS BIOSCIENCE More Info
AM 251 Potent CB1 receptor antagonist (IC50 = 8 nM, Ki = 7.49 nM) that displays 306-fold selectivity over CB2 receptors. Also potent GPR55 agonist (EC50 = 39 nM). Also available as part of the Cannabinoid CB1 Receptor Tocrisettm. Purity > 99% 50mg 1117 TOCRIS BIOSCIENCE More Info
AM 251 Potent CB1 receptor antagonist (IC50 = 8 nM, Ki = 7.49 nM) that displays 306-fold selectivity over CB2 receptors. Also potent GPR55 agonist (EC50 = 39 nM). Also available as part of the Cannabinoid CB1 Receptor Tocrisettm. Purity > 99% 1mg 1117 TOCRIS BIOSCIENCE More Info
AM 281 Potent, selective CB1 cannabinoid receptor antagonist/inverse agonist (Ki values are 12 and 4200 nM for CB1 and CB2 receptors respectively). Increases locomotor activity following systemic administration in vivo. Analog of SR141716A (Ki = 14 nM). ... 10mg 1115 TOCRIS BIOSCIENCE More Info
AM 281 Potent, selective CB1 cannabinoid receptor antagonist/inverse agonist (Ki values are 12 and 4200 nM for CB1 and CB2 receptors respectively). Increases locomotor activity following systemic administration in vivo. Analog of SR141716A (Ki = 14 nM). ... 50mg 1115 TOCRIS BIOSCIENCE More Info
AM 404 Competitive and selective inhibitor of carrier-mediated anandamide transport (IC50 = 1 µM). Does not activate CB1 receptors or inhibit anandamide hydrolysis but has been shown to activate native and cloned vanilloid receptors (pEC50 = 7.4). ... 10mg 1116 TOCRIS BIOSCIENCE More Info
AM 404 Competitive and selective inhibitor of carrier-mediated anandamide transport (IC50 = 1 µM). Does not activate CB1 receptors or inhibit anandamide hydrolysis but has been shown to activate native and cloned vanilloid receptors (pEC50 = 7.4). ... 50mg 1116 TOCRIS BIOSCIENCE More Info
AM 580 An analog of retinoic acid that acts as a selective RARalpha agonist (EC50 values are 0.3, 8.6 and 13 nM for RARalpha, RARbeta and RARgamma respectively). Significantly induces IL-4, IL-5 and IL-13 and inhibits IL-12 and IFNgamma synthesis, and in... 10mg 0760 TOCRIS BIOSCIENCE More Info
AM 580 An analog of retinoic acid that acts as a selective RARalpha agonist (EC50 values are 0.3, 8.6 and 13 nM for RARalpha, RARbeta and RARgamma respectively). Significantly induces IL-4, IL-5 and IL-13 and inhibits IL-12 and IFNgamma synthesis, and in... 50mg 0760 TOCRIS BIOSCIENCE More Info
AM 630 CB2 antagonist/inverse agonist (Ki = 31.2 nM) that displays 165-fold selectivity over CB1 receptors. Behaves as a weak partial/inverse agonist at CB1 receptors. Purity > 98% 10mg 1120 TOCRIS BIOSCIENCE More Info
AM 630 CB2 antagonist/inverse agonist (Ki = 31.2 nM) that displays 165-fold selectivity over CB1 receptors. Behaves as a weak partial/inverse agonist at CB1 receptors. Purity > 98% 50mg 1120 TOCRIS BIOSCIENCE More Info
AM 80 Retinoic acid receptor alpha (RARalpha) agonist that induces differentiation (ED50 = 0.79 nM) and apoptosis of HL-60 cells in vitro. Exhibits antiproliferative effects against a variety of human tumor cells lines (mean values of 35, 40 and 60% gro... 10mg 3507 TOCRIS BIOSCIENCE More Info
AM 80 Retinoic acid receptor alpha (RARalpha) agonist that induces differentiation (ED50 = 0.79 nM) and apoptosis of HL-60 cells in vitro. Exhibits antiproliferative effects against a variety of human tumor cells lines (mean values of 35, 40 and 60% gro... 50mg 3507 TOCRIS BIOSCIENCE More Info
Amanitin 1 mg; from Amanita phalloides. Formula: C39H54N10O14SLD50: approximately 0.1 mg/kg (oral, man)Molecular weight: Mr = 919. Bicyclic octapeptide that inhibits the RNA polymerase of eukaryotic cells. n/a 10161284001 ROCHE APPLIED SCIENCE More Info
AMD1 The RP-38903 AMD1 protein is a full length bacterially expressed recombinant protein.RP-38903 is suitable for use as a control in ELISA and Western blot applications.The RP-38903 amino acid sequence corresponds to the NCBI accession number NP_0016... 10 µg purified protein (100µg/ml) in 50mM Tris-Acetate, pH7.5, 1mM EDTA and 20% Glycerol. RP-38903 THERMO SCIENTIFIC PIERCE PROTEIN RESEARCH PRODUCTS More Info
AMG 9810 Potent and selective, competitive vanilloid TRPV1 receptor antagonist (IC50 = 17 nM). Inhibits capsaicin-, proton-, heat- and endogenous ligand-induced activation of human and rat recombinant TRPV1 receptors. Displays antihyperalgesic properties i... 10mg 2316 TOCRIS BIOSCIENCE More Info
AMG 9810 Potent and selective, competitive vanilloid TRPV1 receptor antagonist (IC50 = 17 nM). Inhibits capsaicin-, proton-, heat- and endogenous ligand-induced activation of human and rat recombinant TRPV1 receptors. Displays antihyperalgesic properties i... 50mg 2316 TOCRIS BIOSCIENCE More Info
AMI-193 Selective 5-HT antagonist, which binds to 5-HT2 sites as potently as spiperone but has lower affinity for 5-HT2C receptors. Also a high affinity D2 receptor antagonist (Ki = 3 nM). Lacks the disruptive effect of spiperone on animal behavior. Purit... 10mg 0524 TOCRIS BIOSCIENCE More Info
AMI-193 Selective 5-HT antagonist, which binds to 5-HT2 sites as potently as spiperone but has lower affinity for 5-HT2C receptors. Also a high affinity D2 receptor antagonist (Ki = 3 nM). Lacks the disruptive effect of spiperone on animal behavior. Purit... 50mg 0524 TOCRIS BIOSCIENCE More Info
Amidotrizoic acid World Health Organization (WHO) International Chemical Reference Substance 100 mg ICRS0206 EUROPEAN DIRECTORATE FOR THE QUALITY OF MEDICINES & HEALTHCARE More Info
AMIKACIN n/a n/a n/a NAT'L. INSTITUTE FOR BIOLOGICAL More Info
Amiloride eNaC blocker 100mg Asc-281-100mg ASCENT SCIENTIFIC LTD. More Info
Aminoacylase-1 Purity: 0.95 0.05 mg 10-288-22335F GENWAY BIOTECH INC. More Info
Aminoacylase-1 Purity: 0.95 0.1 mg 10-288-22335F GENWAY BIOTECH INC. More Info
8-Aminoadenosine Melting Point: 180-185?C dec.Storage and Stability:May be stored at RT for short-term only. Long-term storage is recommended at -20?C. For maximum recovery of product, centrifuge the original vial prior to removing the cap. 25mg A1374-07A UNITED STATES BIOLOGICAL More Info
2-Aminoadenosine Storage and Stability:May be stored at RT for short-term only. Long-term storage is recommended at -20?C. For maximum recovery of product, centrifuge the original vial and prior to removing the cap. 25mg A1374-07 UNITED STATES BIOLOGICAL More Info
3-Aminobenzamide An inhibitor of poly(ADP-ribose) polymerase, which protects cells from UV-B-induced apoptosis via influence on the cytoskeleton. Purity > 98% 100mg 0788 TOCRIS BIOSCIENCE More Info
3-Aminobiphenyl Solubility: Chloroform, Dichloromethane, Ethyl Acetate, MethanolStorage and Stability:May be stored at RT for short-term only. Long-term storage is recommended at -20?C. For maximum recovery of product, centrifuge the original vial prior to removi... 100mg A1375-72 UNITED STATES BIOLOGICAL More Info
5-Aminoindole Melting Point: 122-124?CSolubility: DMSO, MethanolStorage and Stability:May be stored at RT for short-term only. Long-term storage is recommended at -20?C. For maximum recovery of product, centrifuge the original vial prior to removing the cap. 100mg A1378-28 UNITED STATES BIOLOGICAL More Info
5-Aminoisoquinoline Melting Point: 125-127?CSolubility: Chloroform, Ethyl Acetate, MethanolStorage and Stability:May be stored at RT for short-term only. Long-term storage is recommended at -20?C. For maximum recovery of product, centrifuge the original vial prior to... 250mg A1378-36 UNITED STATES BIOLOGICAL More Info
Aminolevulinic Acid n/a 1.0 mg AG055 CELL SCIENCES INC. More Info
Aminopeptidase Recombinant Aeromonas Aminopeptidase 100U/250U/500U ENZ- 275 PROSPEC-TANY TECHNOGENE LTD. More Info
Aminopeptidase Purity: > 98.0% as determined by:(a) Analysis by RP-HPLC.(b) Analysis by SDS-PAGE. 100 units 10-663-45301 GENWAY BIOTECH INC. More Info
Page 7 of 3,739
Records 301 - 350 of 186,906
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