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| Product | Description | |
|---|---|---|
| Elastin, soluble from human lung | lyophilized powder. Group: Fluorescence/luminescence spectroscopy. |  |
| Elbanizine | Elbanizine is an antihistamine which is used for the treatment of allergic asthma. Synonyms: 1-(2-((2,6-dimethyl-3-nitro-4-pyridyl)amino)ethyl)-4-(diphenylmethyl)piperazine. Grade: >98.0%. CAS No. 110629-41-9. Molecular formula: C26H31N5O2. Mole weight: 445.57. |  |
| Elbasvir | Elbasvir has been found to restrain viral phosphoprotein so that could be used against hepatitis C virus and is currently under Phase II trail. Uses: Elbasvir has been found to restrain viral phosphoprotein so that could be used against hepatitis c virus and is currently under phase ii trail. Synonyms: Elbasvir; MK-8742; UNII-632L571YDK; 632L571YDK; MK8742; MK 8742. Grade: 98%. CAS No. 1370468-36-2. Molecular formula: C49H55N9O7. Mole weight: 882.02. | |
| Elbasvir | Elbasvir (MK-8742) is a hepatitis C virus nonstructural protein 5A ( HCV NS5A ) inhibitor with EC 50 s of 4, 3 and 3 nM against genotype 1a, 1b, and 2a, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-8742. CAS No. 1370468-36-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15789. |  |
| Elcatonin | Elcatonin is a calcitonin derivative used as an anti-parathyroid agent. Synonyms: Elcatonin Acetate. Grade: 98%. CAS No. 60731-46-6. Molecular formula: C148H244N42O47. Mole weight: 3363.82. | |
| Elcatonin (Ser-Asn-Leu-Ser-Thr-Asu-Val-Leu-Gly-Lys-Leu-Ser-Gln-Glu-Leu-His-Lys-Leu-Gln-Thr-Tyr-Pro- Arg-Thr-Asn-Val-Gly-Ala-Gly-Thr-Pro-NH2) | Elcatonin is a Calcitonin derivative which is transformed from eel ?s calcitonin by changing the S-S bond into the stable C-N bond. It inhibits the absorption and autolysis of bones, thus leads to blood calcium descending. In addition, it inhibits the bone salts dissolving and transferring and promotes the excretion of calcium and phosphorus in urine. Meanwhile, it inhibits renal tubules reabsorbing calcium, phosphorus and sodium and keeps blood calcium at normal level. It is mainly used for remitting or eliminating the pain caused by Osteoporosis. Elcatonin synthetic is a single, non-glycosylated polypeptide chain containing 31aa. Group: Biochemicals. Grades: Highly Purified. CAS No. 60731-46-6. Pack Sizes: 200ug. US Biological Life Sciences. |  Worldwide |
| Elcubragistat | Elcubragistat (ABX-1431) is a highly potent, selective, and orally available, CNS-penetrant monoacylglycerol lipase (MAGL) inhibitor with an IC50 of 14 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABX-1431. CAS No. 1446817-84-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-117632. | |
| Eldacimibe | Eldacimibe is a Sterol O-acyltransferase inhibitor originated by Wyeth. No development was reported for Atherosclerosis and Hypercholesterolaemia in USA. Uses: Atherosclerosis; hypercholesterolaemia. Synonyms: ACA 147; ANA 147; WAY 125147; WAY ACA 147; 1,3-Dioxane-4,6-dione, 5-(((3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl)amino)(((4-(2,2-dimethylpropyl)phenyl)-methyl)hexylamino)methylene-2,2-dimethyl. Grade: 98%. CAS No. 141993-70-6. Molecular formula: C39H58N2O5. Mole weight: 634.89. | |
| Eldecalcitol | Eldecalcitol, a vitamin D analog, has strong effects to reduce calcium reabsorption into the body from bones, therefore increasing bone mineral density, and to increase calcium absorption in intestines. Synonyms: Edirol; ED-71; 2-(3-Hydroxypropoxy)-1,25-dihydroxyvitamin D3; 2-(3-Hydroxypropoxy)calcitriol; 1alpha,25-dihydroxy-2beta-(3-hydroxypropoxy)vitamin D3. Grade: >98%. CAS No. 104121-92-8. Molecular formula: C30H50O5. Mole weight: 490.72. | |
| Eldecalcitol | Eldecalcitol (ED-71) is an orally active vitamin D3 analogue, inhibits bone resorption and increases bone mineral density. Eldecalcitol (ED-71) displays anti-tumor effect and inhibits cell proliferation, migration and induces apoptosis by suppressing GPx-1 [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ED-71; 2-(3-hydroxypropoxy)-1,25-dihydroxyvitamin D3. CAS No. 104121-92-8. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-A0020. | |
| Eldecalcitol | Eldecalcitol. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (1R,2R,3R,Z)-5-((E)-2-((1R,3aS,7aR)-1-((R)-6-hydroxy-6-methylheptan-2-yl)-7a-methylhexahydro-1H-inden-4(2H)-ylidene)ethylidene)-2-(3-hydroxypropoxy)-4-methylenecyclohexane-1,3-diol. CAS No. 104121-92-8. Molecular formula: C30H50O5. Mole weight: 490.72. Catalog: APB104121928. | |
| Eldecalcitol Intermediate A | Eldecalcitol Intermediate A is an intermediate of eldecalcitol, a vitamin D3 analogue for the treatment of osteoporosis. Eldecalcitol is more active in bone resorption inhibition in comparison with alfacalcidol. Synonyms: 3-[(1R,2R,4Z,6R)-2,6-bis[[tert-butyl(dimethyl)silyl]oxy]-4-(2-diphenylphosphorylethylidene)-3-methylidenecyclohexyl]oxypropoxy-tert-butyl-dimethylsilane. CAS No. 200636-54-0. Molecular formula: C42H71O5PSi3. Mole weight: 771.25. | |
| Eldecalcitol Intermediate CD | Eldecalcitol Intermediate CD is a vital component used in the compound industry. Specifically designed for pharmaceutical applications, this intermediate plays a crucial role in the synthesis of Eldecalcitol, a drug used for the research of osteoporosand other bone-related disorders. Synonyms: ED71-CD ring; 25-[(triethylsilyl)oxy]de-A,B-cholestan-8-one; (1R,3aR,7aR)-7a-Methyl-1-((R)-6-methyl-6-((triethylsilyl)oxy)heptan-2-yl)hexahydro-1H-inden-4(2H)-one. CAS No. 144848-24-8. Molecular formula: C24H46O2Si. Mole weight: 394.71. | |
| Eldelumab | Eldelumab is a humanized anti-CXCL10 (IP-10) monoclonal antibody that binds to CXCL10 and blocks CXCL10-induced calcium flux and cell migration. Eldelumab has been use for the treatment of ulcerative colitis. Synonyms: BMS-936557; MDX-1100. CAS No. 946414-98-8. | |
| Eldelumab | Eldelumab (BMS-936557) is a human anti-CXCL10 (IP-10) monoclonal antibody (IgG1 type). Eldelumab selectively binds to CXCL10 and blocks CXCL10-induced calcium flux and cell migration. Eldelumab can be used in studies of autoimmune and auto-inflammatory diseases such as rheumatoid arthritis, ulcerative colitis and crohn's disease[1][2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: BMS-936557; MDX-1100. CAS No. 946414-98-8. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P99190. | |
| Elderberry Extract (Ratio) | Elderberry Extract (Ratio). Group: Others. Purity: 4:1~20:1. Elderberry Extract (Ratio). Cat No: EXTW-061. |  |
| Elderberry Fruit Freeze Dried Powder | Elderberry Fruit Freeze Dried Powder. |  CA, FL & NJ |
| Elderberry P.E. 10:1 | Elderberry P.E. 10:1. | CA, FL & NJ |
| Elecampane Root Powder | Elecampane Root Powder. | CA, FL & NJ |
| Eleclazine | Eleclazine is a selective Sodium channel antagonist. Eleclazin showed a shortening of the QTc interval (the time interval between the start of the Q-wave and end of the T-wave in the heart's electrical cycle) in patients with long QT-3 (LQT3) syndrome. Phase III clinical trilas for the treatment of Long QT syndrome, Phase II/III clinical trilas for the treatment of Hypertrophic cardiomyopathy and Phase II clinical trilas for the treatment of Ventricular arrhythmias are on-going. Uses: Long qt syndrome;hypertrophic cardiomyopathy;ventricular arrhythmias. Synonyms: GS-6615; GS 6615; GS6615; Eleclazine. 4-[(pyrimidin-2-yl)methyl]-7-[4-(trifluoromethoxy)phenyl]- 3,4-dihydro-1,4-benzoxazepin-5(2H)-one. Grade: 95%. CAS No. 1443211-72-0. Molecular formula: C21H16F3N3O3. Mole weight: 415.37. | |
| Eleclazine HCl | Eleclazine HCl is a novel late Na+ current inhibitor. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Eleclazine Hydrochloride; Eleclazine HCl; GS-6615; GS 6615; GS6615. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 1448754-43-5. Molecular formula: C21H17ClF3N3O3. Mole weight: 451.83. Purity: >98%. IUPACName: 4-(pyrimidin-2-ylmethyl)-7-(4-(trifluoromethoxy)phenyl)-3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-one hydrochloride. Canonical SMILES: O=C1N(CC2=NC=CC=N2)CCOC3=CC=C(C4=CC=C(OC(F)(F)F)C=C4)C=C13.[H]Cl. Product ID: ACM1448754435. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Eleclazine hydrochloride | Eleclazine (GS 6615) hydrochloride is a selective cardiac late sodium current inhibitor and a weak inhibitor of potassium current with IC 50 value of <1 μM and approximately 14.2 μM, respectively. Eleclazine hydrochloride shows concurrent protection against autonomically induced atrial premature beats, repolarization alternans and heterogeneity, and atrial fibrillation in porcine model. Eleclazine hydrochloride can be used to research cardiac arrhythmias [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS 6615 hydrochloride. CAS No. 1448754-43-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-16738A. | |
| Electreoless NICKEL SULPHATE | Electreoless NICKEL SULPHATE. CAS No. 10101-98-1. Molecular Formula NiSO4 * 6H2O. Electroless Electroplating Chemicals |  Cater Chemicals Corp. Illinois IL |
| Electrical Conductivity Carbon Nanotubes (SWCNTs) | Electrical Conductivity Carbon Nanotubes (SWCNTs). Group: Single wall cnt. CAS No. 308068-56-6. >98% (SWNT) Electric current density >10-2S/cm. |  |
| Electric Heating Reduce Graphene Oxide Powder | Carbon black oil appears as a dark colored liquid with a petroleum-like odor. Less dense than water and insoluble in water. Vapors heavier than air.;Carbon, activated is a black grains that have been treated to improve absorptive ability. May heat spontaneously if not properly cooled after manufacture.;Carbon, animal or vegetable origin appears as a black powder or granular mixed with a tar or starch and water binder pressed into regular lumps or briquettes. Heats slowly and ignites in air especially if wet.;Graphite (natural) appears as a mineral form of the element carbon. Hexagonal crystals or thin leaf-like layers. Steel-gray to black with a metallic luster and a greasy feel. An electrical conductor. Used for high-temperature crucibles, as a lubricant and in "lead" pencils.;DryPowder; DryPowder, Liquid; DryPowder, PelletsLargeCrystals; DryPowder, PelletsLargeCrystals, WetSolid, OtherSolid, Liquid; DryPowder, WetSolid, Liquid; Liquid; OtherSolid; OtherSolid, GasVapor, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid, Liquid; WetSolid; WetSolid, Liquid;OtherSolid; PelletsLargeCrystals;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; DryPowder, WetSolid; Liquid; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, O | |
| Electrode pole pieces | Electrode pole pieces. Uses: Designed for use in research and industrial production. Product Category: Mesoporous Carbon and Carbon Nanomaterials. CAS No. 7440-44-0. Product ID: ACM7440440-167. Alfa Chemistry ISO 9001:2015 Certified. Categories: methane. | |
| Electroless nickel plating solution | Electroless nickel plating solution. Group: Electronic materials. | |
| Electroless nickel plating strike | Electroless nickel plating strike. Group: Electronic materials. | |
| Electroless silver plating solution | Electroless silver plating solution. Group: Electronic materials. | |
| ELECTROLYTICALLY REFINED LEAD (trace elements) | certified Reference Material, chips. Group: Certified reference materials (crms)metal alloys. | |
| Electrolytic Copper with added Impurities | Electrolytic Copper with added Impurities. Uses: For analytical and research use. Group: Physical properties; metal alloys; physical properties. Catalog: APS007775. Format: Neat. Shipping: Room Temperature. | |
| Electronic Magnet Pole Identifier | Electronic Magnet Pole Identifier. Group: Magnetic nanoparticles. | |
| electron-transferring-flavoprotein dehydrogenase | An iron-sulfur flavoprotein, forming part of the mitochondrial electron-transfer system. Group: Enzymes. Synonyms: ETF-QO; ETF:ubiquinone oxidoreductase; electron transfer flavoprotein dehydrogenase; electron transfer flavoprotein Q oxidoreductase; electron transfer flavoprotein-ubiquinone oxidoreductase; electron transfer flavoprotein reductase. Enzyme Commission Number: EC 1.5.5.1. CAS No. 86551-03-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1556; electron-transferring-flavoprotein dehydrogenase; EC 1.5.5.1; 86551-03-3; ETF-QO; ETF:ubiquinone oxidoreductase; electron transfer flavoprotein dehydrogenase; electron transfer flavoprotein Q oxidoreductase; electron transfer flavoprotein-ubiquinone oxidoreductase; electron transfer flavoprotein reductase. Cat No: EXWM-1556. | |
| Eledoisin | Eledoisin. Group: Biochemicals. Grades: Purified. CAS No. 69-25-0. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Eledoisin | Eledoisin (Eledone peptide) is a specific agonist of NK2 and NK3 receptors. Uses: Scientific research. Group: Peptides. Alternative Names: Eledone peptide. CAS No. 69-25-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P0006. | |
| Eledoisin | Eledoisin is an undecapeptide of mollusk origin and it belongs to the tachykinin family of neuropeptides. It was first isolated from the posterior salivary glands of two mollusk species Eledone muschata and Eledone aldovandi. Eledoisin has the amino acid sequence pGlu-Pro-Ser-Lys-Asp-Ala-Phe-Ile-Gly-Leu-Met-NH2. It is the Potent natural tachykinin receptor ligand. Uses: Neurotransmitter agents. Synonyms: Eledone peptide; Eledoisinum; 5-oxo-L-prolyl-L-prolyl-L-seryl-L-lysyl-L-α-aspartyl-L-alanyl-L-phenylalanyl-L-isoleucylglycyl-L-leucyl-L-methioninamide. Grade: >98%. CAS No. 69-25-0. Molecular formula: C54H85N13O15S. Mole weight: 1188.41. | |
| Eledoisin Related Peptide | Eledoisin-Related Peptide, a substance P analogue, is a tachykinin receptor ligand. Synonyms: Eledoisin-Related Peptide; Eledoisin RP; H-Lys-Phe-Ile-Gly-Leu-Met-NH2; L-lysyl-L-phenylalanyl-L-isoleucyl-glycyl-L-leucyl-L-methioninamide; (S)-2,6-diamino-N-((5S,8S,14S,17S)-14-sec-butyl-5-carbamoyl-8-isobutyl-7,10,13,16-tetraoxo-18-phenyl-2-thia-6,9,12,15-tetraazaoctadecan-17-yl)hexanamide; Lpiglm. Grade: ≥95%. CAS No. 2990-43-4. Molecular formula: C34H58N8O6S. Mole weight: 706.94. | |
| Eledoisin-Related Peptide | Eledoisin-Related Peptide. Group: Biochemicals. Grades: Purified. CAS No. 2990-43-4. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Eledoisin Related Peptide 2TFA | Eledoisin Related Peptide 2TFA, a substance P analogue, is a tachykinin receptor ligand. Synonyms: H-Lys-Phe-Ile-Gly-Leu-Met-NH2.2TFA; L-lysyl-L-phenylalanyl-L-isoleucyl-glycyl-L-leucyl-L-methioninamide trifluoroacetic acid. Grade: ≥95%. CAS No. 2918768-25-7. Molecular formula: C34H58N8O6S.2C2HF3O2. Mole weight: 934.99. | |
| Eledoisin trifluoroacetate | Eledoisin was first isolated from the posterior salivary glands of two mollusk species Eledone muschata and Eledone aldovandi. It is a potent natural tachykinin receptor ligand, and a potent vasodilator that increases capillary permeability. Synonyms: H-Pyr-Pro-Ser-Lys-Asp-Ala-Phe-Ile-Gly-Leu-Met-NH2.TFA; L-pyroglutamyl-L-prolyl-L-seryl-L-lysyl-L-alpha-aspartyl-L-alanyl-L-phenylalanyl-L-isoleucyl-glycyl-L-leucyl-L-methioninamide trifluoroacetic acid; Eledoisin, mono(trifluoroacetate) (salt); 5-Oxo-L-prolyl-L-prolyl-L-seryl-L-lysyl-L-aspartyl-L-alanyl-L-phenylalanyl-L-isoleucylglycyl-L-leucyl-L-methioninamide trifluoroacetate; Eledoisin, trifluoroacetate (1:1). Grade: ≥95%. CAS No. 10129-92-7. Molecular formula: C54H85N13O15S.C2HF3O2. Mole weight: 1302.42. | |
| Elemene Liposome | Elemene is a mixture of sesquiterpene alkenes, dominated by β-elemene, with broad-spectrum antitumor effects. This product is a pre-formulated liposome with elemene. It is only for research purposes. Group: Drug-loaded liposome. Categories: liposomes, niosomes, ethosomes, and transfersomes. |  |
| Elemi | Elemi. Group: Polymers. CAS No. 9000-75-3. Mole weight: CAS: 9000-75-3. soft. | |
| Elemicin | Elemicin is an orally active alkenylbenzene widely distributed in many herbs and spices. Elemicin inhibits Stearoyl-CoA Desaturase 1 (SCD1) by metabolic activation. Elemicin has anti-influenza activities, antimicrobial , antioxidant, and antiviral activities. Elemicin and its reactive metabolite of 1-Hydroxyelemicin can induce hepatotoxicity [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 487-11-6. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N6807. | |
| Elemicin | A constituent of the essential oil of nutmeg and is responsible for the psychoactive effects of nutmeg. Also a minor constituent of the oleoresin and essential oil of Manila elemi (Canarium luzonicum). Exhibits anticholinergic-like effects in humans. Group: Biochemicals. Alternative Names: 1,2,3-Trimethoxy-5-(2-propen-1-yl)-benzene; 5-Allyl-1,2,3-trimethoxybenzene; 1-(3,4,5-Trimethoxyphenyl)-2-propene; 3, 4, 5-Trimethoxyallyl Benzene ; 5-(Prop-2-enyl)-1,2,3-trimethoxybenzene; 5-Allyl-1,2,3-trimethoxybenzene. Grades: Highly Purified. CAS No. 487-11-6. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Elemicin | Elemicin is a alkenylbenzene widely distributed in many herbs and spices. Elemicin inhibits Stearoyl-CoA Desaturase 1 (SCD1) by metabolic activation. Elemicin is one of the main components in aromatic food and has antimicrobial, antioxidant, and antiviral activities. Elemicin possesses genotoxicity and carcinogenicity. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,2,3-TRIMETHOXY-5-(2-PROPENYL)BENZENE;5-ALLYL-1,2,3-TRIMETHOXYBENZENE;ELEMICIN;1,2,3-trimethoxy-5-(2-propenyl)-benzen;1,2,3-trimethoxy-5-allylbenzene (elemicin);3,4,5-Trimethoxyallylbenzene;4-allyl-1,2,6-trimethoxybenzene;5-allyl-1,2,3-trimethoxy-benzen. Product Category: Inhibitors. Appearance: Oil. CAS No. 487-11-6. Molecular formula: C12H16O3. Mole weight: 208.3. Purity: 0.98. IUPACName: 1,2,3-trimethoxy-5-prop-2-enylbenzene. Canonical SMILES: COC1=CC(=CC(=C1OC)OC)CC=C. Density: 1.011 g/cm³. Product ID: ACM487116. Alfa Chemistry ISO 9001:2015 Certified. | |
| Elenbecestat | Elenbecestat (E2609) is a potent, orally bioavailable and CNS-penetrant BACE-1 inhibitor. Elenbecestat has the potential for Alzheimer's disease (AD) research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: E2609. CAS No. 1388651-30-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109055. | |
| Elenbecestat | Elenbecestat is a novel, potent and orally bioavailable BACE1 inhibitor for the treatment of Alzheimer's disease (AD), which demonstrates prolonged reductions in plasma beta-amyloid levels after single dosing. Synonyms: E2609; N-[3-[(4aS,5R,7aS)-2-amino-5-methyl-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]thiazin-7a-yl]-4-fluorophenyl]-5-(difluoromethyl)pyrazine-2-carboxamide. Grade: ≥98%. CAS No. 1388651-30-6. Molecular formula: C19H18F3N5O2S. Mole weight: 437.44. | |
| Elenestinib | Elenestinib is a next-generation KIT D816V inhibitor. Elenestinib exhibits potent inhibition of KIT D816V and an evolved pre-clinical profile with limited central nervous system penetration. Synonyms: BLU-263. CAS No. 2505078-08-8. Molecular formula: C27H29FN10O. Mole weight: 528.6. | |
| Elenestinib | Elenestinib (BLU-263) is an orally active inhibitor of Tyrosine kinase with an IC 50 value of 6 nM for KIT D816V. Elenestinib minimally penetrates the blood-brain barrier. Elenestinib can be used in the study of systemic mastocytosis [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BLU-263. CAS No. 2505078-08-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-152839. | |
| Elesclomol | Elesclomol (STA-4783) is a potent copper ionophore and promotes copper-dependent cell death (cuproptosis). Elesclomol specifically binds ferredoxin 1 (FDX1) ?2/?3 helices and ?5 strand. Elesclomol inhibits FDX1-mediated Fe-S cluster biosynthesis. Elesclomol is an oxidative stress inducer that induces cancer cell apoptosis. Elesclomol is a reactive oxygen species (ROS) inducer. Elesclomol can be used for Menkes and associated disorders of hereditary copper deficiency research[1][2][3][4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: STA-4783. CAS No. 488832-69-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-12040. | |
| Elesclomol | Elesclomol is a HSP-90 Inhibitor, and is a small-molecule bis(thio-hydrazide amide) with oxidative stress induction, pro-apoptotic, and potential antineoplastic activities. Elesclomol induces oxidative stress, creating high levels of reactive oxygen species (ROS), such as hydrogen peroxide, in both cancer cells and normal cells. Because tumor cells have elevated levels of ROS compared to normal cells, the increase in oxidative stress beyond baseline levels elevates ROS beyond sustainable levels, exhausting tumor cell antioxidant capacity, which may result in the induction of the mitochondrial apoptosis pathway. Normal cells are spared because the increase in the level of oxidative stress induced by this agent is below the threshold at which apoptosis is induced. Elesclomol is currently developed by Synta Pharmaceuticals Corp. Synonyms: STA4783; STA-4783; STA 4783, Elesclomol. CAS No. 488832-69-5. Molecular formula: C19H20N4O2S2. Mole weight: 400.52. | |
| Eletriptan | Eletriptan is Serotonin 1D receptor agonist originated by Pfizer. It is a second generation triptan drug. It is used as an abortive medication, blocking a migraine attack which is already in progress. Eletriptan was approved by the FDA for the acute treatment of migraine with or without aura in adults in 2002. Uses: Menstrual migraine; migraine. Synonyms: 3-[[(2R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole; (R)-5-[2-(Benzenesulfonyl)ethyl]-3-[(N-methylpyrrolidin-2-yl)methyl]-1H-indole; Eletriptan; UK 116044; UK-116,044; UK-116,044-04 [as hydrobromide]; UNII-22QOO9B8KI; Relpax free amine. Grade: 98%. CAS No. 143322-58-1. Molecular formula: C22H26N2O2S. Mole weight: 382.52. | |
| Eletriptan-[d3] | Eletriptan-[d3], is the labelled analogue of Eletriptan, which is a serotonin 5-HTIB/ID receptor agonist. Eletriptan is a second generation triptan medication intended for treatment of migraine headaches. Synonyms: Eletriptan-d3; 3-[[(2R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole-d3; 3-{[(2R)-1-(2H3)Methyl-2-pyrrolidinyl]methyl}-5-[2-(phenylsulfonyl)ethyl]-1H-indole. Grade: 95% by HPLC; 95% atom D. CAS No. 1287040-94-1. Molecular formula: C22H23D3N2O2S. Mole weight: 385.54. | |
| Eletriptan-d3 hydrobromide | Eletriptan-d3 is used as an internal standard for the quantification of eletriptan by GC- or LC-MS. Eletriptan is an agonist of the serotonin (5-HT) receptor types 5-HT1B and 5-HT1D. Synonyms: UK 116044-d3; 3-[[(2R)-1-methyl-d3-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole, monohydrobromide. Grade: ≥99% atom D. Molecular formula: C22H23D3N2O2S·HBr. Mole weight: 466.45. | |
| Eletriptan HBr | Eletriptan induces concentration-dependent contractions of meningeal artery, coronary artery, and saphenous vein. The potency of Eletriptan is higher in meningeal artery than in coronary artery (86-fold) or saphenous vein (66-fold). Synonyms: Eletriptan Hydrobromide; CHEBI:61176; M41W832TA3; UNII-M41W832TA3; eletriptan hydrobromide; Relpax; UK 166,044; UK 166044; UK-166,044; UK-166044. Grade: >98%. CAS No. 177834-92-3. Molecular formula: C22H26N2O2S.HBr. Mole weight: 463.43. | |
| Eletriptan hydrobromide | Eletriptan hydrobromide (Eletriptan HBr) is a 5-HT 1B and 5-HT 1D receptor agonist with antimigraine activity, with K i of 0.92 nM and 3.14 nM, respectively [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Eletriptan HBr; UK-116044 hydrobromide. CAS No. 177834-92-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0010. | |
| Eletriptan hydrobromide | Eletriptan hydrobromide. Group: Biochemicals. Grades: Highly Purified. CAS No. 177834-92-3. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
| Eletriptan Hydrobromide | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Eletriptan Hydrobromide | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopyapi standardspharmaceutical toxicology. Alternative Names: (R)-5-[2-(Benzenesulfonyl)ethyl]-3-[(N-methylpyrrolidin-2-yl)methyl]-1H-indole hydrobromide, Relpax, Relert,3-[[(2R)-1-methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-Indole hydrobromide (1:1), 1H-Indole, 3-[[(2R)-1-methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-, monohydrobromide (9CI), UK 116044-04, 1H-Indole, 3-[(1-methyl-2-pyrrolidinyl)methyl]-5-[2-(phenylsulfonyl)ethyl]-, monohydrobromide, (R)-, Eletriptan hydrobromide. | |
| Eletriptan Impuirty 1 | Eletriptan Impuirty 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 153525-55-4. Molecular formula: C21H24N2O2S. Mole weight: 368.5. Catalog: APB153525554. | |
| Eletriptan N-oxide | An impurity of Eletriptan. Synonyms: 3-[[(2R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole N Oxide. Grade: > 95%. CAS No. 1217641-89-8. Molecular formula: C22H26N2O3S. Mole weight: 398.53. | |
| Eletriptan N-Oxide | An impurity of Eletriptan. Group: Biochemicals. Alternative Names: 3-[[(2R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole N Oxide. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Eletriptan (UK-116044, Relpax, 3-[[(2R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole) | A serotonin 5-HTIB/ID receptor agonist. Group: Biochemicals. Alternative Names: UK-116044, Relpax, 3-[[(2R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Eleutherobin | Eleutherobin can be isolated from a marine soft coral. Uses: Designed for use in research and industrial production. Additional or Alternative Names: β-D-Arabinopyranoside, [(4R,4aS,5Z,7R,10S,11S,12aR)-3,4,4a,7,10,11,12,12a-octahydro-7-methoxy-1,10-dimethyl-4-(1-methylethyl)-11-[[(2E)-3-(1-methyl-1H-imidazol-4-yl)-1-oxo-2-propen-1-yl]oxy]-7,10-epoxybenzocyclodecen-6-yl]methyl, 2-acetate. Product Category: Inhibitors. CAS No. 174545-76-7. Molecular formula: C35H48N2O10. Mole weight: 656.8. Purity: 95%+. IUPACName: [(1S,2S,4R,8R,9S,10Z,12R)-11-[[(2R,3S,4R,5R)-3-Acetyloxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-12-methoxy-1,5-dimethyl-8-propan-2-yl-15-oxatricyclo[10.2.1.04,9]pentadeca-5,10,13-trien-2-yl] (E)-3-(1-methylimidazol-4-yl)prop-2-enoate. Canonical SMILES: CO[C@@]12/C(CO[C@H]3[C@H]([C@@H]([C@@H](CO3)O)O)OC(C)=O)=C\[C@@]4([H])[C@@](C(C)=CC[C@@H]4C(C)C)([H])C[C@@H]([C@@](O1)(C=C2)C)OC(/C=C/C5=CN(C)C=N5)=O. Product ID: ACM174545767. Alfa Chemistry ISO 9001:2015 Certified. | |
| Eleutherococcus Senticosus Liquid Extract | Eleutherococcus Senticosus Liquid Extract. | CA, FL & NJ |
| Eleuthero Extract | Eleuthero Root Extract (also known as siberian ginseng root extract ) is prepared from the root of the plant Siberian Ginseng, it has been traditionally used to negate stress and fatigue. The active ingredients of eleuthero root extract, also known as acanthopanax senticosus extract is eleutherosides. Siberian ginseng root extract is used to increase stamina and to stimulate the immune system and used for conditions of the heart and blood vessels such as high blood pressure, low blood pressure, and atherosclerosis. Group: Others. Mole weight: 742.72. Eleuthero Extract; Eleutherococcus Sentisosus. Cat No: EXTC-042. | |
| Eleutheroside A | Eleutheroside A. Group: Biochemicals. Alternative Names: Daucosterol; Alexandrin; Daucosterin; Sitogluside. Grades: Plant Grade. CAS No. 474-58-8. Pack Sizes: 20mg. Molecular Formula: C35H60O6, Molecular Weight: 576.847. US Biological Life Sciences. | Worldwide |
| Eleutheroside A | Daucosterol can be used as an efficient and inexpensive neuroprotectant, to which the IGF1-like activity of Daucosterol contributes. Daucosterol could be potentially developed as a medicine for ischemic stroke treatment. Uses: Analgesic. Synonyms: Daucosterol; Sitogluside; Alexandrin; beta-Sitosterol glucoside; Daucosterin; Coriandrinol. Grade: >98%. CAS No. 474-58-8. Molecular formula: C35H60O6. Mole weight: 576.85. | |
| Eleutheroside B | Eleutheroside B. Group: Biochemicals. Alternative Names: Syringin; Lilacin; Methoxyconiferin; Magnolenin A; Alyposide; Syringoside; Ligustrin; Ilexanthin A. Grades: Plant Grade. CAS No. 118-34-3. Pack Sizes: 20mg. Molecular Formula: C17H24O9, Molecular Weight: 372.367. US Biological Life Sciences. | Worldwide |
| Eleutheroside B1 | Eleutheroside B1, a coumarin compound, has a wide spectrum of anti-human influenza virus efficacy, with an IC50 value of 64-125 μg/ml. Eleutheroside B1 mediates its anti-influenza activity through POLR2A and N-glycosylation. Eleutheroside B1 inhibits the mRNA expression of several chemokine genes and the influenza nucleoprotein (NP) gene, and exhibits low cytotoxicity. Antiviral and anti-inflammatory activities. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Solid. CAS No. 16845-16-2. Molecular formula: C17H20O10. Mole weight: 384.33. Purity: 0.98. Canonical SMILES: O=C1C=CC2=CC(OC)=C(O[C@@H]3[C@@H]([C@H]([C@@H]([C@@H](CO)O3)O)O)O)C(OC)=C2O1. Product ID: ACM16845162. Alfa Chemistry ISO 9001:2015 Certified. Categories: Eleutheroside B4. | |
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