Halophenols
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000445744 2-BROMO-2 -FLUOROACE 1G
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Medchemexpress LLC 2 4 6-TRIIODOPHENOL 5MG
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5000210339 2 4 6-TRIIODOPHENOL 5MG
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Cambridge Isotope Laboratories PCB Mixture (34 72 100 209) (unlabeled) 400 ug/mL in isooctane 1 2 mL
PCB Mixture (34 72 100 209) (unlabeled) 400 ug/mL in isooctane 1 2 mL
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eMolecules BROMO-PEG3-T-BUTYL ESTER 25G
5000210996 BROMO-PEG3-T-BUTYL ESTER 25G
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5000431577 CHELATING AGAROSE I 5ML
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5000450004 3-CHLORO-2-PYRAZINAM 250G
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eMolecules DIHYDROXYBORANYLBORONIC A 5G
5000164309 DIHYDROXYBORANYLBORONIC A 5G
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eMolecules METHOXYMETHYLTRIPHENYLPH 25G
5000164018 METHOXYMETHYLTRIPHENYLPH 25G
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5000380463 USP7 USP47 INHIBITOR 10MM 1ML
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eMolecules N N-DICYCLOHEXYLCARBODIIMI 5G
5000164807 N N-DICYCLOHEXYLCARBODIIMI 5G
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eMolecules 4-Ethoxy-3-methoxyphenol | 65383-58-6 | MFCD19301270 | 1g
Combi-Blocks | 4-Ethoxy-3-methoxyphenol | 1g | 296402175 | YF-6720 | 95.000 | 65383-58-6 | MFCD19301270 | 168.192 | C9H12O3
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Biotium BIOTIUM INC
5000501537 VIATAG 595-615 1000X 30 UL
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Medchemexpress LLC Slingshot inhibitor D3 | 1715076-35-9 | 99.5% | 461.55 g·mol⁻¹ | C25H19NO4S2 | 10MM 1ML
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Slingshot inhibitor D3 is a potent, selective, reversible, and competitive inhibitor of Slingshot phosphatases (SSH family) used in biochemical and cell-based assays to probe SSH function. It is supplied as a ready-to-use 10 mM solution in DMSO and is intended for inhibition studies, mechanistic assays, and compound screening.
- Potent inhibition of Slingshot 1 (IC50 = 3 μM) and activity against Slingshot 2 (Ki = 3.9 μM).
- Supplied as a 10 mM solution in DMSO, 1 mL vial ready for use.
- High purity (~99.5%) suitable for research applications.
- Molecular weight 461.55 g·mol⁻¹ and formula C25H19NO4S2.
- Useful for biochemical and cell-based assays to study Slingshot-mediated dephosphorylation pathways.
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Apexbio Technology LLC Tolperisone HCl 3644-61-9 10mM (in 1mL DMSO)
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Tolperisone HCl (CAS 3644-61-9) is a small-molecule inhibitor targeting voltage-gated sodium channels It is designed to inhibit sodium ion influx thereby modulating neuronal excitability and suppressing neuromuscular transmission Tolperisone HCl exerts its biological activity primarily through the inhibition of voltage-gated sodium channels interfering with neuronal signal propagation and affecting muscle tone and contraction Based on these pharmacological properties Tolperisone HCl holds research potential in studies of muscle spasticity neuromuscular disorders and the physiological basis of muscle relaxation and neuromuscular modulation
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Apexbio Technology LLC Nafcillin Sodium 7177-50-6 10mM (in 1mL DMSO)
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Nafcillin Sodium (7177-50-6) is a small-molecule inhibitor targeting -lactamase It is designed to reversibly inhibit -lactamase thereby preventing bacterial resistance mediated by hydrolysis of -lactam antibiotics Nafcillin Sodium exerts its biological activity primarily through reversible inhibition of -lactamase In in vitro studies Nafcillin Sodium demonstrates inhibitory activity with an IC50 value of approximately 33 mM Based on these pharmacological properties Nafcillin Sodium holds research potential in investigating -lactamase-mediated antibiotic resistance mechanisms evaluating therapeutic combination strategies and studying bacterial susceptibility profiles
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