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Filtered Search Results
eMolecules METHYL PROPIOLATE 10G
5000224593 METHYL PROPIOLATE 10G
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Selleck Chemical LLC Dimethindene maleate-E1796-5MG
Dimethindene maleate is a selective antagonist of histamine H1 and exhibits antihistamine effects It suppresses the cromakalim-induced/glibenclamide-sensitive K currents in a concentration-dependent and reversible manner
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Medchemexpress LLC L-methionine N-(5-(imidazol-5-ylmethylamino)methyl-2'-methylbiphenyl) methyl ester | 344900-92-1 | 99.8% | 466.60 g/mol | C25H30N4O3S | 10MG
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FTI-2153 is a potent, highly selective farnesyltransferase inhibitor used as a research reagent to study protein prenylation, Ras processing, and cellular responses to FTase inhibition. The compound is provided with solubility and storage guidance to support preparation of DMSO stocks and in vitro or in vivo formulation workflows.
- Potent FTase inhibition, IC50 1.4 nM.
- Selective inhibition of H-Ras processing in cellular assays.
- Available in small-mass vials and ready-to-use DMSO stock solutions.
- Molecular weight 466.60 g/mol and formula C25H30N4O3S.
- Storage recommended at -20°C under nitrogen; in solvent: -80°C (6 months) or -20°C (1 month).
- Soluble in DMSO (up to ~90 mg/mL); datasheet provides stock preparation volumes and in vivo formulation options.
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eMolecules Ambeed / Ethyl 4-ethoxybenzoate / 25g / 624120658 / A217486 / / 23676-09-7 / MFCD00009116 / 194.230 / C11H14O3
Ambeed / Ethyl 4-ethoxybenzoate / 25g / 624120658 / A217486 / / 23676-09-7 / MFCD00009116 / 194.230 / C11H14O3
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Selleck Chemical LLC Dimethindene maleate-25MG
Dimethindene maleate is a selective antagonist of histamine H1 and exhibits antihistamine effects It suppresses the cromakalim-induced/glibenclamide-sensitive K currents in a concentration-dependent and reversible manner
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Medchemexpress LLC Cipralisant maleate | 223420-20-0 | 99.8% | 332.39 g/mol | C18H24N2O4 | 25 MG
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Cipralisant maleate is a potent, selective histamine H3 receptor ligand used in neuroscience research. It functions as a full antagonist in vivo and shows agonist activity in vitro, with high receptor affinity; it is provided as a solid research chemical for pharmacological and behavioral studies involving wakefulness and attention mechanisms.
- High affinity for histamine H3 receptor.
- Potent antagonist activity in vivo.
- Agonist activity observed in vitro.
- High purity suitable for research applications.
- Available in small-scale quantities with storage recommendations for stability.
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![eMolecules Medchem Express / TRPM8 antagonist 2 / 5mg / 437899175 / HY-112430 / / 259674-19-6 / [null] / 398.506 / C26H26N2O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502454827.PNG-250.jpg)
eMolecules Medchem Express / TRPM8 antagonist 2 / 5mg / 437899175 / HY-112430 / / 259674-19-6 / [null] / 398.506 / C26H26N2O2
Medchem Express / TRPM8 antagonist 2 / 5mg / 437899175 / HY-112430 / / 259674-19-6 / [null] / 398.506 / C26H26N2O2
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Medchemexpress LLC 11beta-Hydroxyprogesterone | 600-57-7 | 5 MG
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11beta-Hydroxyprogesterone is a potent inhibitor of 11β-Hydroxysteroid dehydrogenase. It activates the human mineralocorticoid receptor in COS-7 cells (ED50 of 10 nM) and exhibits agonist mineralocorticoid activity by activating the transiently expressed human mineralocorticoid receptor (hMR) in COS-7 cells. Its agonist activity is linked to contacts between its 11β-hydroxyl group and Asn770 within the hMR-ligand-binding domain.
- Potent inhibitor of 11β-Hydroxysteroid dehydrogenase.
- Activates human mineralocorticoid receptor in COS-7 cells with an ED50 of 10 nM.
- Displays agonist mineralocorticoid activity.
- Exhibits hypertensinogenic activity in rats, dependent on an intact adrenal and mineralocorticoid receptor activation.
- Classified as an endogenous metabolite and a steroid.
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TARGETMOL CHEMICALS INC Prochlorperazine Maleate 200MG
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Also available in 1 mL, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Prochlorperazine Maleate (Capazine) is a phenothiazine antipsychotic used principally in the treatment of NAUSEA; VOMITING; and VERTIGO. It is more likely than CHLORPROMAZINE to cause EXTRAPYRAMIDAL DISORDERS. Purity 99.99%
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TARGETMOL CHEMICALS INC Trimipramine maleate 500MG
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Also available in 1 mL, 50 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. Trimipramine maleate (Surmontil maleate) appears to inhibit serotonin transport and norepinephrine uptake by nerve terminals. This increases available norepinephrine or serotonin and prolongs its action. Trimipramine Maleate is the maleate salt form of trimipramine, a tricyclic secondary amine of the dibenzazepine class, with an antidepressant property. Purity 98.02%
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Chemscene ChemScene | Methyl 4-bromo-1H-pyrrole-2-carboxylate | 25G | CS-W007392 | 0.98 | 934-05-4| MFCD00832855 | 204.023
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ChemScene | Methyl 4-bromo-1H-pyrrole-2-carboxylate | 25G | CS-W007392 | 0.98 | 934-05-4| MFCD00832855 | 204.023
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Medchemexpress LLC Cinepazide Maleate | 26328-04-1 | C26H35N3O9 | 100 MG
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Cinepazide Maleate is a piperazine derivative that acts as a weak calcium channel blocker and a potent vasodilator. It is used for the research of cerebrovascular diseases, including ischemic stroke and brain infarct. The salt form offers enhanced water solubility and stability, making it suitable for various research applications. This product is for research use only and not intended for patient use.
- Piperazine derivative
- Weak calcium channel blocker
- Potent vasodilator
- Used for cerebrovascular disease research
- Enhanced water solubility and stability
- For research use only
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eMolecules ChemScene / Methyl 5-hexenoate / 5g / 447993418 / CS-0015919 / 0.000 / 2396-80-7 / MFCD00671538 / 128.171 / C7H12O2
ChemScene / Methyl 5-hexenoate / 5g / 447993418 / CS-0015919 / 0.000 / 2396-80-7 / MFCD00671538 / 128.171 / C7H12O2
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Cayman Chemical BetulIn 3 28-dIacetate 25mg
A triterpene with antiviral and hepatoprotective activities; inhibits SFV replication in virus-infected Huh7 cells (IC50 = 9.1 µM); improves hepatic function in various rat models of hepatitis at 20 mg/kg
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MEDCHEMEXPRESS LLC UNC3866 5MG
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501871766 UNC3866 5MG
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