Halophenols
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000371876 LUMINOL 25G
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5000455025 TETRADECYLTRIMETHYLA 100G
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5000454560 SALCOMINE 100G
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5000454963 2 4-DIFLUOROPHENOL 100G
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5000454988 TSTU 500G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000446909 MIDAGLIZOLE HYDROCH 10MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000389527 UMBELLIFERONE 25G
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5000460425 2-AMINO-5-FLUOROPHEN 10G
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5000460434 3-ACETYLTHIOPHENE 10G
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Cambridge Isotope Laboratories Parlar 70 (13C10 99%) 10 ug/mL in nonane 1 2 mL
Parlar 70 (13C10 99%) 10 ug/mL in nonane 1 2 mL
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Apexbio Technology LLC Benidipine HCl 91599-74-5 10mM (in 1mL DMSO)
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Benidipine hydrochloride (CAS 91599-74-5) is a dihydropyridine-class small molecule that functions as an inhibitor of voltage-dependent calcium channels thereby modulating calcium influx in vascular smooth muscle and cardiac tissue Additionally benidipine hydrochloride has been shown to suppress mineralocorticoid receptor coactivator (MRC) activation induced by aldosterone This dual inhibitory activity makes it valuable for biomedical research into cardiovascular physiology calcium signaling pathways and the molecular mechanisms underlying mineralocorticoid receptor-associated conditions
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Medchemexpress LLC Jnj-47117096 hydrochloride | 1610536-69-0 | 99.7% | 398.891 g/mol | C21H23ClN4O2 | 25MG
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JNJ-47117096 hydrochloride (MELK-T1 hydrochloride) is the hydrochloride salt of a small-molecule kinase inhibitor selective for MELK and active against FLT3. It is used as a research reagent to probe MELK biology and to evaluate antiproliferative effects in cellular assays.
- Potent MELK inhibition (IC50 23 nM)
- Also inhibits Flt3 (IC50 18 nM)
- Shows cellular antiproliferative activity (Ba/F3 cells IC50 ~1.5 μM without IL-3)
- Provided as a hydrochloride salt to aid solubility in biological assays
- High chemical purity (~99.7%) and documented CAS identifier (1610536-69-0)
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eMolecules DESS-MARTIN PERIODINANE 100G
5000159850 DESS-MARTIN PERIODINANE 100G
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Apexbio Technology LLC TC-H 106 937039-45-7 10mg
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TC-H 106 (CAS 937039-45-7) is a selective inhibitor of class I histone deacetylases (HDACs) targeting HDAC1 HDAC2 HDAC3 and HDAC8 with reported IC50 values of 150 nM 760 nM 370 nM and 5000 nM respectively By inhibiting HDAC activity TC-H 106 interferes with the removal of acetyl groups from histone lysine residues thereby modulating chromatin structure and gene expression In cellular assays TC-H 106 increases histone H3 acetylation in lymphoblastoid cells derived from Friedreich s ataxia (FRDA) patients and enhances frataxin mRNA levels in FRDA mouse models These findings highlight its application in studying epigenetic mechanisms and therapeutic approaches related to HDAC inhibition particularly in neurodegenerative disease models
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000385296 ZIPRASIDONE HYDROCH 5MG
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