Oxazinanes

Aobchem AOBCHEM

5000938848 4-ETHYL-2-METHYLPHENYL BORONI

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eMolecules​ 1225376-02-2 | (R)-2-Phenylmorpholine | ChemScene | MFCD18249849 | 163.220 | C10H13NO | 97.000 | C1CO[C@@H](CN1)c1ccccc1 | 1g | 572305923

(R)-2-Phenylmorpholine | ChemScene | 1225376-02-2 | MFCD18249849 | 163.220 | C10H13NO | 97.000 | C1CO[C@@H](CN1)c1ccccc1 | 1g | 572305923

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eMolecules​ 79323-24-3 | Morpholin-2-ol hydrochloride | Combi-Blocks, Inc. | MFCD14708235 | 139.580 | C4H10ClNO2 | 95.000 | Cl.OC1CNCCO1 | 5g | 603131255

Morpholin-2-ol hydrochloride | Combi-Blocks, Inc. | 79323-24-3 | MFCD14708235 | 139.580 | C4H10ClNO2 | 95.000 | Cl.OC1CNCCO1 | 5g | 603131255

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Aobchem AOBCHEM

5001041309 2R 6S -2 6-DIMETHYLMORPHOLINE

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Aobchem AOBCHEM

5000918261 2-ETHOXY-5-ETHYLPHENYL BORONI

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Medchemexpress LLC tert-Butyl 1S 5R 6S | 5MG

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tert-Butyl 1S 5R 6S | 5MG

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eMolecules​ 163105-90-6 | 2-Methoxypyridine-3-boronic acid | Ambeed | MFCD03411572 | 152.940 | C6H8BNO3 | 98.000 | COc1ncccc1B(O)O | 100g | 570567816

2-Methoxypyridine-3-boronic acid | Ambeed | 163105-90-6 | MFCD03411572 | 152.940 | C6H8BNO3 | 98.000 | COc1ncccc1B(O)O | 100g | 570567816

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eMolecules​ 1225376-02-2 | (R)-2-Phenylmorpholine | J & W PharmLab LLC | MFCD18249849 | 163.220 | C10H13NO | 96.000 | C1CO[C@@H](CN1)c1ccccc1 | 250mg | 517669112

(R)-2-Phenylmorpholine | J & W PharmLab LLC | 1225376-02-2 | MFCD18249849 | 163.220 | C10H13NO | 96.000 | C1CO[C@@H](CN1)c1ccccc1 | 250mg | 517669112

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Medchemexpress LLC Fluphenazine-N-2-chloroethane hydrochloride | 3892-78-2 | 95.5% | 528.89 g/mol | C22H27Cl3F3N3S | 5 MG

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Fluphenazine-N-2-chloroethane hydrochloride is a phenothiazine-derived irreversible calmodulin antagonist used in biochemical and pharmacological research. Supplied as the hydrochloride salt, it is intended for in vitro studies of calmodulin modulation and related signaling pathways.

• Irreversible calmodulin antagonist for biochemical assays.
• Hydrochloride salt form for improved solubility.
• White to off-white solid appearance for convenient handling.
• High purity (95.5%) for reliable experimental results.
• Stable when stored sealed, away from moisture and light.

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Medchemexpress LLC Myristoylcholine chl 50mg

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Myristoylcholine Chloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research

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TARGETMOL CHEMICALS INC UCB7362 hydrochloride 1MG

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Also available in 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. UCB7362 hydrochloride （UCB7362 HCl） is an orally active plasmepsin X (PMX) inhibitor (IC50 7 nM) with antimalarial activity that inhibits parasite growth. Purity 99.1%

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TARGETMOL CHEMICALS INC Besipirdine hydrochloride 1MG

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Also available in 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Besipirdine hydrochloride is a non-receptor-dependent cholinomimetic compound with alpha-adrenergic and cardiovascular activities.Besipirdine hydrochloride inhibits voltage-dependent sodium-potassium channels and inhibits biogenic amine uptake.Besipirdine hydrochloride reduces schedule-induced thirst and enhances cholinergic and adrenergic neurotransmission in the central nervous system in rats. Purity 98.4%

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TARGETMOL CHEMICALS INC ZT 52656A hydrochloride 1MG

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Also available in 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. ZT 52656A is a selective agonist of kappa opioid, and used for the prevention or alleviation of pain in the eye. Purity 99.7%

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TARGETMOL CHEMICALS INC Tiaspirone hydrochloride 1MG

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Also available in 1 mL, 5 mg, 10 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. Tiaspirone hydrochloride (BMY-13859 hydrochloride) exhibits antipsychotic activity. Tiaspirone hydrochloride influences the electrophysiological activity of dopaminergic neurons in the substantia nigra zona compacta (A9 DA cells) and ventral tegmental area (A10 DA cells) in the brain of the rat. Purity 99.98%

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Selleck Chemical LLC Crizotinib hydrochloride S5190-5mg

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Crizotinib (PF-02341066) hydrochloride (Xalkori) inhibits tyrosine phosphorylation of c-Met and nucleophosmin (NPM)-anaplastic lymphoma kinase (ALK) with IC50 of of 11 nM and 24 nM in cell-based assays respectively Crizotinib hydrochloride is also a potent ROS1 inhibitor with Ki less than 0 025 nM Crizotinib induces autophagy through inhibition of the STAT3 pathway in multiple lung cancer cell lines

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