Halophenols
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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000377220 COSDOSIRAN SODIUM 1MG
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eMolecules ASL8052 100G
5000165532 ASL8052 100G
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eMolecules PENTAFLUOROPHENOL 100G
5000165455 PENTAFLUOROPHENOL 100G
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Accela Chembio Inc 3-bromo-4-fluorophenol | 25g | 27407-11-0 | MFCD03425884 | 95+% | Shelf Life: 1260 Days | Light Sensitive
3-bromo-4-fluorophenol | 25g | 27407-11-0 | MFCD03425884 | 95+% | Shelf Life: 1260 Days | Light Sensitive
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eMolecules 2 2 2-TRICHLOROACETIMIDIC 100G
5000163779 2 2 2-TRICHLOROACETIMIDIC 100G
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eMolecules SODIUM BENZENESULFINATE 500G
5000163668 SODIUM BENZENESULFINATE 500G
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eMolecules PALLADIUM 0 TETRAKISTRI 25G
5000163386 PALLADIUM 0 TETRAKISTRI 25G
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eMolecules 2-BROMO-3-HYDROXYBENZONITR 10G
5000170631 2-BROMO-3-HYDROXYBENZONITR 10G
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eMolecules 3-BROMOMETHYLPYRIDINE HY 100G
5000170511 3-BROMOMETHYLPYRIDINE HY 100G
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Pfaltz & Bauer Tetrachlorobisphenol A 500G | 79-95-8
Tetrachlorobisphenol A 500G | 79-95-8
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Medchemexpress LLC Levomedetomidine hydrochloride | 190000-46-5 | MFCD12912677 | 99.4% | 236.74 | C13H17ClN2 | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Levomedetomidine hydrochloride is the levorotatory enantiomer of medetomidine, described as a cardioprotective agent with sedative and analgesic effects. Supplied as a white to off-white solid for research use only, it is used in preclinical pharmacology and biochemical studies involving α2-adrenergic receptor activity.
- Enantiomer of medetomidine with levorotatory configuration.
- Cardioprotective agent with sedative and analgesic activity.
- High purity suitable for analytical and preclinical research.
- Solid, white to off-white physical form for easy handling.
- Supplied in small pack sizes appropriate for reference studies.
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eMolecules PHENYLSULFONYLACETONE 100G
5000164731 PHENYLSULFONYLACETONE 100G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000377402 MARTINOSTAT HYDROCH 100MG
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Apexbio Technology LLC AS-605240 648450-29-7 10mM (in 1mL DMSO)
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AS-605240 (CAS 648450-29-7) is a cell-permeable small molecule inhibitor selectively targeting class I phosphoinositide 3-kinases (PI3Ks) with pronounced potency against the PI3K isoform (IC50 0 008 M) and lower activity for PI3K / / (IC50 0 06 0 27 and 0 3 M respectively) Structural studies show that AS-605240 binds to PI3K via interactions with Lys-833 and Val-882 It impairs PI3K/Akt signaling as evidenced by inhibition of C5a-induced PKB phosphorylation in RAW264 macrophages In vivo AS-605240 reduces leukocyte migration and suppresses joint inflammation in mouse models of peritonitis and collagen-induced arthritis highlighting its value for investigating PI3K -mediated immune pathways and inflammatory processes
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eMolecules SODIUM BISTRIMETHYLSILYL 25G
5000164621 SODIUM BISTRIMETHYLSILYL 25G
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