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| Product | Description | |
|---|---|---|
| Ethyl eosin | Ethyl eosin is a fluorescent dye with an absorption peak at 527 nm and an absorption shoulder at 487 nm [1]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 6359-5-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-D1489. |  |
| Ethyl Eosin certified | Ethyl Eosin certified. Group: Biochemicals. Alternative Names: Solvent Red 45; CI 45386; 2',4',5',7'-Tetrabromoeosin ethyl ester potassium salt. Grades: Highly Purified. CAS No. 6359-3-5. Pack Sizes: 10g, 25g, 50g, 100g. US Biological Life Sciences. |  Worldwide |
| Ethyl Eosin, Certified (Solvent Red 45) | Ethyl Eosin, Certified (Solvent Red 45). Group: Biochemicals. Alternative Names: C.I. 45386. Grades: Certified Dye. Pack Sizes: 5g, 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| Fenoterol Hydrobromide | A β2-adrenergic agonist. Bronchodilator; tocolytic. Fenoterol hydrobromide is a sympathomimetic drug. It is used to treat asthma, bronchitis and emphysema.[1] Fenoterol administration might be linked to liver damage.[2] It has anti-inflammatory effects on eosinophil function.[3] Fenoterol hydrobromide has been used in chromatography-tandem mass spectrometry (LC&-MS-MS) for specific and sensitive detection of β-agonists (BAG).[4]. Group: Biochemicals. Alternative Names: 2-(3,5-Dihydroxyphenyl)-2-hydroxy-2?-(4-hydroxyphenyl)-1?-methyldiethylamine hydrobromide; 5- [1-Hydroxy-2- [ [2- (4-hydroxyphenyl) -1-methylethyl] amino] ethyl] -1, 3-benzenediol Hydrobromide; 1- (3, 5-Dihydroxyphenyl) -2-[2- (3-p-hydroxyphenyl) propylamino]ethanol Hydrobromide; Airum; Berotec; Dosberotec; Fenoterol Bromide; Partusisten; Phenoterol Hydrobromide; Th 1165a. Grades: Highly Purified. CAS No. 1944-12-3. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C??H??BrNO?, Molecular Weight: 384.26. US Biological Life Sciences. | Worldwide |
| Imetit dihydrobromide | Imetit dihydrobromide is a potent and high affinity agonist at histamine H3 and H4 receptors (Ki = 0.3 and 2.7 nM, respectively). It induces an eosinophil shape change (EC50 = 25 nM). Synonyms: 5-[2-(Imidazol-4-yl)ethyl]isothiourea dihydrobromide. Grades: ≥98% by HPLC. CAS No. 32385-58-3. Molecular formula: C6H10N4S.2HBr. Mole weight: 332.06. |  |
| LY255283 | This active molecular is a competitive leukotriene B4 receptor antagonist and IC50 value is about 100 nM. LY 255283 is selective for the BLT2 receptor, since IC50 values at the BLT1 receptor are >10 μM. LY255283 inhibits eosinophil chemotaxis by 80% at a concentration of 10 μM. It also inhibits the binding of radiolabeled LTB4 to eosinophil membranes and IC50 value is 260 nM. LY255283 reduces airway obstruction in animal models of asthma. However, clinical trials for asthma had been discontinued. Uses: Asthma. Synonyms: LY 255283; LY255283; LY-255283; (1-(5-Ethyl-2-hydroxy-4-(6-methyl-6-(1H-tetrazol-5-yl)heptyloxy)phenyl)ethanone). Grades: 98%. CAS No. 117690-79-6. Molecular formula: C19H28N4O3. Mole weight: 360.45. | |
| LY 255283 | LY255283, a competitive leukotriene B4 receptor antagonist, is used in leukotriene receptor research along with other selective leukotriene receptor agonists and antagonist to identify and differentiate the physiological and cell signaling effects of the leukotriene B4 receptor on processes such as paclitaxel resistance in MCF-7/DOX breast cancer cells, monocyte-derived dendritic cell chemotaxis, and 5-lipoxygenase activity and interleukin-8 production in human neutrophils. LY255283 may be used to help verify that an observed process or cell event is leukotriene B4 receptor-dependent.Antagonists of the chemotactic and inflammatory lipoxygenase product leukotriene B4 (LTB4) have been potential drug development targets for several years.1,2 The tetrazole LY255283 is a competitive antagonist of the BLT2 receptor. It displaces radiolabeled LTB4 from guinea pig lung membrane, with an IC50 of about 100nM.3 LY255283 exhibits IC50 values of ~950nM and >10uM at human recombinant BLT2 and BLT1 receptors, respectively.4 LY255283 inhibits eosinophil chemotaxis by 80% at a concentration of 10uM, and inhibits the binding of radiolabeled LTB4 to eosinophil membranes with an IC50 of 260nM.1. Group: Biochemicals. Alternative Names: 1-[5-ethyl-2-hydroxy-4-[[6-methyl-6-(1H-tetrazol-5-yl)heptyl]oxy]phenyl]-ethanone. Grades: Highly Purified. CAS No. 117690-79-6. Pack Sizes: 10mg, 25mg. Molecular Formula: C19H28N4O3, Molecular Weight: 360.5. US Biological Life Sciences. | Worldwide |
| SCH 336 | SCH 336 is a potent and selective CB2 receptor inverse agonist (Ki = 1.8 nM, EC50 = 2 nM) with 100-fold selectivity over CB1. SCH 336 has been shown to increase forskolin stimulated cAMP accumulation in CHO cells expressing human CB2 receptors. It inhibits leukocyte migration in a murine model of delayed-type hypersensitivity and suppresses antigen-induced lung eosinophilia in a mouse allergy model. Synonyms: SCH-336; SCH 336; SCH336. N- [ (1S) -1- [4- [ [4-Methoxy-2- [ (4-methoxyphenyl) sulfonyl] phenyl] sulfonyl] phenyl] ethyl] methanesulfonamide. Grades: ≥98% by HPLC. CAS No. 447459-51-0. Molecular formula: C23H25NO8S3. Mole weight: 539.64. | |
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