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Filtered Search Results
TARGETMOL CHEMICALS INC Palonosetron hydrochloride
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Also available in 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Palonosetron hydrochloride (RS 25259) is a 5-HT3 antagonist used in the prevention and treatment of chemotherapy-induced nausea and vomiting. Purity 99.97%
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Medchemexpress LLC Dihydro dutasteride | 164656-22-8 | MFCD24386648 | 99.7% | 530.55 g/mol | C27H32F6N2O2 | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Dihydro dutasteride is the active metabolite of dutasteride and acts as a potent inhibitor of 5α-reductase isozymes. Supplied as a high-purity research reference standard, it is intended for use in biochemical studies, metabolite profiling, assay development, and mechanism-of-action experiments.
- High purity suitable for analytical and reference use.
- Molecular weight 530.55 g/mol.
- Chemical formula C27H32F6N2O2.
- Available in small pack sizes for laboratory assays.
- Used as a reference standard in metabolism and enzyme inhibition studies.
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Aobchem AOBCHEM
5000938848 4-ETHYL-2-METHYLPHENYL BORONI
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TARGETMOL CHEMICALS INC Xamoterol hemifumarate 10MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Also available in 1 mg, 5 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Xamoterol hemifumarate is a potent and selective beta1-adrenoceptor agonist.Xamoterol hemifumarate is a potential compound for the study of the relationship between cardiac arrhythmias and beta1-adrenergic stimulation with IKr. Purity 99.79%
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Cayman Chemical CP 24 879 hydrochloride
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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A Δ5/Δ6 desaturase inhibitor; reduces liver arachidonate content by ~50% in mice at 3 mg/kg; increases mead acid content and inhibits leukotriene C4 synthesis in murine mastocytoma cells at 5 µM
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Aobchem AOBCHEM
5000940560 METHYL 4-CHLORO-2-METHYL-2H-IN
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Aobchem AOBCHEM
5001023383 3-BROMO-4-ETHOXYPHENYL BORONI
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Selleck Chemical LLC Ramosetron Hydrochloride S3723-25mg
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Ramosetron Hydrochloride (YM-060) is the hydrochloride salt of ramosetron a selective serotonin (5-HT) receptor antagonist with potential antiemetic activity
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Aobchem AOBCHEM
5001035667 N- 1 1-DIMETHYLETHOXY CARBONY
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eMolecules S S-BN-PYBOX 1G
5000161567 S S-BN-PYBOX 1G
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Medchemexpress LLC 4,7-benzothiazoledione, 5-[[2-(dimethylamino)ethyl]amino]-2-methyl- | 477603-18-2 | 99.1% | 10 MG
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BN-82685 (IRC-083065) is a quinone-based CDC25 phosphatase inhibitor used in cell-cycle and cancer research. Supplied as a brown-to-red solid for laboratory research use only.
- Quinone-based CDC25 phosphatase inhibitor used to modulate cell-cycle checkpoints.
- Molecular formula C12H15N3O2S.
- Molecular weight 265.33 g·mol⁻¹.
- CAS number 477603-18-2.
- Appearance: brown to red solid.
- Available in milligram-scale quantities for research applications.
- For research use only; not for human or clinical use.
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Aobchem AOBCHEM
5000943232 ETHANONE 2-CHLORO-1- 6- METHY
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Cayman Chemical Y27632 hydrochloride
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A potent, ATP-competitive inhibitor of ROCKs including p160ROCK (Ki = 140 nM) and ROCK2 (IC50 = 800 nM); also inhibits PRK2 with an IC50 value of 600 nM
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Cayman Chemical Fingolimod hydrochloride
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An immune modulator and a prodrug form of FTY720 phosphate; decreases the number of circulating lymphocytes in mice at 1 mg/kg; increases skin allograft survival in rats from 0.3-3 mg/kg; prevents disease development in a rat model of EAE; inhibits S1P lyase from 0.3-30 µM
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Cayman Chemical Dimebolin hydrochloride
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A neuroprotective agent; binds to histamine H1 and H2 receptors (IC50s = 3.8 and 287 nM, respectively), as well as α1A-, α1B-, α1D-, and α2A-ARs, imidazoline I2 receptors, and 5-HT2A, 5-HT2C, 5-HT6, and 5-HT7 receptors (Kis = 8-313 nM); inhibits NMDA-evoked currents and voltage-gated calcium channels in mouse primary striatal neurons (IC50s = 10 and 50 μM, respectively); inhibits glutamate-induced apoptosis in primary striatal neurons derived from the YAC128 transgenic mouse model of Huntington’s disease at 50 μM; inhibits cell death induced by amyloid-β (25-35) in cerebellar granule cells at 25 μM; inhibits decreases TWAA acquisition in a rat model of AF64A-induced Alzheimer’s disease at 1 mg/kg
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