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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000431832 S -N-GLYCIDYLPHTHAL 100G
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Ambeed AMBEED
5000867409 1-METHYLCYCLOBUTANAMINE HY 5GR
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Medchemexpress LLC Epoprostenol sodium | 61849-14-7 | 98.03% | C20H31NaO5 | 1 MG
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Epoprostenol sodium (Prostaglandin I2) sodium salt is the synthetic form of the natural prostaglandin derivative prostacyclin (prostaglandin I2). It is registered worldwide for the treatment of Pulmonary arterial hypertension (PAH) and is used in pulmonary hypertension and transplantation as a potent inhibitor of platelet aggregation.
- Registered worldwide for the treatment of pulmonary arterial hypertension (PAH).
- Used in pulmonary hypertension and transplantation.
- Potent inhibitor of platelet aggregation.
- Induces apoptosis in PAH-PASMCs by upregulating the expression of IP receptor and Fas ligand (FasL).
- Storage at -20°C, sealed, away from moisture.
- Compound is unstable in solutions; freshly prepared solutions are recommended.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000431216 VARI FLUOR 568 SE 1MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000431084 3-BENZYL-6-BROMO-2-M 25G
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Cell Signaling Technology CELL SIGNALING TECHNOLOGY INC
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5000588141 NEUROLIGIN PAN F1H7H RABBIT MO
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000430651 LENTIVIRUS TRANSFECT 5ML
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Apexbio Technology LLC Maprotiline HCl 10347-81-6 10mM (in 1mL DMSO)
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Maprotiline HCl (CAS 10347-81-6) is an orally administered selective norepinephrine reuptake inhibitor primarily investigated for its antidepressant properties Mechanistically Maprotiline modulates the extracellular signal-regulated kinase (ERK) pathway and interacts with cellular retinoic acid binding protein 1 (CRABP1) promoting apoptotic processes in cancer cells In preclinical studies Maprotiline has demonstrated the ability to induce cell death via these signaling mechanisms Additionally due to its effects on neuropathic pain modulation Maprotiline is utilized in research exploring chronic pain pathways and investigating pharmacological interventions for pain management
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Apexbio Technology LLC 8-Bromo-cGMP, sodium salt 51116-01-9 25mg
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8-Bromo-cGMP sodium salt (CAS 51116-01-9) is a membrane-permeable analog of cyclic GMP that functions as an activator of protein kinase G (PKG) By mimicking endogenous cGMP it modulates intracellular signaling pathways notably influencing Ca2 channel activity Studies indicate that 8-Bromo-cGMP sodium salt can suppress macroscopic ionic currents and reduce insulin secretion under high K stimulation Due to its role in signal transduction and vascular function this compound is frequently employed in research addressing nociceptive modulation and vascular biology
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000431488 AGAROSE WITH TAE POW 20POUCHES
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eMolecules 883195-40-2 | Ambeed | 3-Amino-5-chlorophenol | 1g | 490495798 | A114197 | MFCD16999375 | 143.57 | C6H6ClNO
Ambeed | 3-Amino-5-chlorophenol | 1g | 490495798 | A114197 | 883195-40-2 | MFCD16999375 | 143.570 | C6H6ClNO
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eMolecules N N-DICYCLOHEXYLCARBODIIMI 5G
5000159047 N N-DICYCLOHEXYLCARBODIIMI 5G
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Aobchem AOBCHEM
5000864771 4-BROMO-1-ISOPROPOXY-2-METHOXY
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Medchemexpress LLC 5-Bromo-3-methylpyridin-2-amine | 3430-21-5 | ≥98.0% | C6H7BrN2 | 500 G
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5-Bromo-3-methylpyridin-2-amine is a biochemical reagent used as a biological material or organic compound for life science related research. It is intended for research use only and not for sale to patients.
- Solid appearance
- Light yellow to brown color
- Purity of ≥98.0%
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Apexbio Technology LLC Rose Bengal 632-69-9 25g
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Rose Bengal (CAS 632-69-9) is a small-molecule inhibitor targeting vesicular glutamate transporter (VGlut) and vesicular monoamine transporter (VMAT) It is designed to inhibit the uptake and storage of glutamate into synaptic vesicles thereby modulating neurotransmitter storage and release Rose Bengal exerts its biological activity primarily through inhibition of glutamate uptake into vesicles without affecting H -ATPase pump activity In vitro experiments demonstrate inhibitory activity with reported Ki values of approximately 19 nM for VGlut and 64 nM for VMAT in isolated synaptic terminals Based on these pharmacological properties Rose Bengal holds research potential in neurobiochemical studies exploring neurotransmitter release and synaptic vesicle trafficking
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