48200 Results for: "TET-dT+Phosphoramidite&pageNo=8"
AdipoRon ≥98% (by HPLC)
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Novel and orally active adiponectin receptor agonist for AdipoR1 and AdipoR2.
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DiBAC₄(3) ≥98% (by HPLC), Ultrapure membrane stain, for histology
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Membrane Potential Detector
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Zinquin free acid ≥98% (by HPLC), Ultrapure fluorescent indicator, for the determination of zinc
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Zinc dye
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GSK-3β inhibitor XVIII ≥98% (by HPLC)
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Cell-permeable, potent and selective GSK-3β inhibitor.
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Diphenylboric acid-2-aminoethyl ester (2-APB) ≥98% (by HPLC)
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Cell permeable modulator of Ins(1,4,5)-P3-induced Ca²⁺ release. A prototype drug for a group of structurally related calcium channel blockers in human platelets. Has been shown, in the absence of other stimuli, to activate TRPV1, V2 and V3, but not TRPV4, V5 and V6 expressed in HEK 293 cells. Potentiates the effect of capsaicin, protons and heat on TRPV1. It was originally introduced as an IP3 receptor blocker and subsequently as an inhibitor of store-operated Ca²⁺ entry (75µM).
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DEA NONOate ≥98% (by NMR), white to off-white solid
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DEA NONOate is used as a nitric oxide donor.
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Necrostatin-7 ≥98% (by HPLC, TLC)
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Necroptosis inhibitor
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Procaspase-3-activator (PAC-1) ≥98% (by HPLC), white to off-white solid
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Caspase-3 activator
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8-Bromoadenosine-3',5'-cyclic monophosphothioate, Sp-isomer sodium salt ≥98% (by HPLC)
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PKA activator.
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5-Aza-2'-deoxycytidine ≥98% (by HPLC)
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DNA methyltransferase inhibitor
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8-Hydroxyguanosine ≥98% (by HPLC)
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Oxidised form of the nucleoside guanosine.
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5,5-Dimethyl-1-pyrroline-N-oxide ≥98% (by ELSD)
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Spin trapping reagent
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DIPPMPO ≥98% (by TLC, 1H-NMR, 13C-NMR)
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Most efficient spin trap for the in vitro and in vivo detection of O-, N-, S-, and C-centered free radicals.
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DAF-FM diacetate 2,5 mg/ml ≥98% (by HPLC)
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Fluorescent probe for NO detection. Cell permeable.
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DAF-2 diacetate 5 mM in DMSO ≥98% (by HPLC)
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Fluorescent probe for NO detection. Cell permeable.
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6-Cyano-7-nitroquinoxaline-2,3-dione disodium salt, disodium salt ≥98% (by TLC)
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AMPA/kainate receptor antagonist
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3,5-Dimethyl-1-adamantanamine hydrochloride ≥98% (by argentometric titration)
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NMDA receptor antagonist.
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Dimethyl-W84 dibromide ≥98% (by HPLC)
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M2 receptor modulator.
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PNU-120596 ≥98% (by HPLC)
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Nicotinic acetylcholine receptor activator.
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5-(N-Ethyl-N-isopropyl)amiloride ≥98% (by TLC)
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Selective inhibitor of the Na /H antiporter.
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Aconitine ≥98% (by HPLC)
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Na⁺ channel activator.
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L-α-Phosphatidylinositol-3,4,5-P3 ·7Na ≥98% (by TLC)
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PKC substrate.
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U-46619 ≥98%
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Prostaglandin H₂/thromboxane A₂ receptor agonist; stable analog of thromboxane A₂. Induces platelet aggregation at 32 nM and activates p38 MAPK.
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Anti-Proteasome 20S beta5t subunit Mouse Monoclonal Antibody [clone: b8-17]
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Anti-Proteasome 20S beta5t subunit Mouse Monoclonal Antibody [clone: b8-17]
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Farnesyl thiotriazole ≥98% (by TLC)
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PKC activator.
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PROTEASOME 19S RPN10/S5A SUBUNIT MONOCLONAL ANTIBODY (S5A-18) 1 * 100 µl
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PROTEASOME 19S RPN10/S5A SUBUNIT MONOCLONAL ANTIBODY (S5A-18) 1 * 100 µl
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RK-682 ≥98% (by HPLC)
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RK-682 is a novel tyrosine phosphatase inhibitor isolated from Streptomyces sp. It inhibits the dual specificity VHR phosphatase (IC50=2.0µM) selectively over CD45 (IC50=54µM), Cdc25B and PTP1B (IC50~42µM). RK-682 inhibits cell cycle progression of Ball-1 cells at the G1/S transition and enhances ATP-induced long-term potentiation in guinea pig hippocampal CA1 neurons. Shows potent activity against HIV-1 protease.