94231 Results for: "3-Bromo-5-(trifluoromethoxy)benzyl+bromide&pageNo=9"
Rocaglamide ≥98% (by HPLC)
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NF-kappaB inhibitor
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20-Hydroxyecdysone ≥95% (by 1H-NMR), white powder
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Ecdysteroid.
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Sinefungin ≥95% (by HPLC)
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Methyltransferase inhibitor
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Piericidin A (from Streptomyces sp. MST-AS5364) ≥95% (by HPLC)
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Antibiotic. Specific and potent inhibitor of NADH-ubiquinone oxidoreductase (complex I) that binds to ubiquinone binding site(s). Inhibits both mitochondrial and bacterial NADH ubiquinone oxidoreductase. Anticancer agent that prevents up-regulation of GRP78, and exhibits cytotoxic activity for etoposide resistant cancer cells under glucose-deprived conditions.
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Carbenicillin disodium salt ≥92%
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Inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacterial cell membrane. Effective against Gram-positive and Gram-negative bacteria and Pseudomonas.
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Prodigiosin ≥95% (by HPLC)
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NADPH oxidase inhibitor
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Myricetin ≥90% (by HPLC)
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Chemopreventive agent
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HAT activator, CTPB ≥97% (by 1H-NMR)
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p300 HAT activator.
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YC-1 ≥98% (by HPLC)
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Guanylyl cyclase activator
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Busulphan ≥98% DNA alkylating agent
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Busulfan is antineoplastic bifunctional, DNA alkylating agent that causes DNA damage by cross-linking DNA and proteins.
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Zinc protoporphyrin ≥95% (by TLC)
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Potent and selective inhibitor of heme oxygenase (Ki=3nM), the enzyme that generates carbon monoxide (CO). Inhibits soluble guanylyl cyclase. Produces a time- and concentration-dependent inactivation of all three isoforms of nitric oxide synthase (IC50=0.8µM, 4.0µM, and 5.0µM for nNOS (NOS I), iNOS (NOS II) and eNOS (NOS III), respectively). Does not cross the blood-brain barrier. An useful tool to elucidate the role of CO in signal transduction and as a neurotransmitter.
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Calcium pantothenate ≥98% (by HPLC)
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Precursor for coenzyme A biosynthesis.
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Adenosine-3’,5’-cyclic Monophosphothioate, Rp-Isomer sodium salt ≥99% (by HPLC)
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Competitive inhibitor of cyclic AMP-dependent protein kinase I and II.Metabolic stability towards mammalian cyclic nucleotide- responsive phosphodiesterases.
Discriminates between protein kinase A (antagonist) and some other cyclic AMP receptors, e.g. channels or CAP 3 (agonist).Membrane-permeant for several systems (for improved permeability more lipophilic analogues e.g. Rp-8-Br-cAMPS are recommended).
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Ac-WEHD-pNA ≥98% (by HPLC)
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Colorimetric caspase substrate for caspase-1, -4, -5 and -14.
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MMP-3 inhibitor ≥95% (by HPLC)
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Inhibitor of matrix metalloproteinase 3 (MMP-3) (IC50=5µM).
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Tyrphostin AG 1295 ≥98%
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Selective inhibitor of tyrosine kinase in platelet-derived growth factor (PDGF) receptor.
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Bisindolylmaleimide II ≥97% (by 1H-NMR)
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PKC inhibitor
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Tyrphostin AG 1478 ≥98% (by HPLC)
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EGFR inhibitor
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Pifithrin-α (cyclic) hydrobromide ≥95% (by HPLC)
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p53 inhibitor
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Ubiquinone-5 ≥95% (by HPLC)
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Ubiquinone-5 ≥95% (by HPLC)
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Sibutramine hydrochloride monohydrate ≥98% (by HPLC)
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Anti-obesity agent.