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Filtered Search Results
Medchemexpress LLC Triphenyl compound A | 21306-65-0 | 99.8% | 399.53 g/mol | C21H21NO3S2 | 5 MG
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TPh A (Triphenyl Compound A) is a small-molecule research compound that selectively binds the nuclear protein pirin and disrupts the Bcl3-pirin complex. It is supplied as a powder for laboratory use, with high reported purity and analytical characterization suitable for cellular tool compound applications.
- Potent pirin inhibitor with reported Ki ≈ 0.6 μM.
- Disrupts formation of the Bcl3-pirin complex in biochemical assays.
- High purity (99.81%) suitable for research applications.
- Supplied as a powder for straightforward handling and aliquoting.
- Characterized by formula C21H21NO3S2 and molecular weight 399.53 g/mol.
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Enzo Life Sciences Bafilomycin B1 (1mg). CAS: 88899-56-3; 80112-34-1
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Macrolide antibiotic that acts as a specific inhibitor of vacuolar-type H+-ATPase. Purity: ≥95% (HPLC). Solubility: Slightly soluble in methanol or DMSO; insoluble in water. Long Term Storage: -20°C.
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Selleck Chemical LLC Zotarolimus
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Zotarolimus (ABT-578 A 179578) is an analogue of rapamycin and inhibits FKBP-12 binding with IC50 of 2 8 nM
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SLINGSHOT BIOSCIENCES TRUCYTES TM POTENCY CD19 KIT
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NC3824319 TRUCYTES TM POTENCY CD19 KIT
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Enzo Life Sciences Monensin . sodium salt (1g). CAS: 22373-78-0
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Antibiotic that functions as Na+ ionophore. Blocks glycoprotein secretion. Inhibits proliferation of several lymphoma cell lines through cell cycle arrest and apoptosis. Blocks ceramide transport through the Golgi apparatus. Purity: ≥90%. Appearance: White to light yellow powder. Solubility: Soluble in 100% ethanol (25mg/ml), methanol (50mg/ml), chloroform or DMSO (25mg/ml). Slightly soluble in water. Long Term Storage: -20°C.
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Medchemexpress LLC Fosmidomycin sodium salt | 66508-37-0 | 99.7% | 205.08 | 50 MG
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Fosmidomycin sodium salt is a phosphonic acid antibiotic and an antimalarial agent, active against both Gram-negative and Gram-positive bacteria. It has shown effectiveness in in vivo studies, with animals treated intraperitoneally or orally becoming apparently free of parasites. Mice treated for 8 days were totally cured.
- Phosphonic acid antibiotic.
- Antimalarial agent.
- Active against both Gram-negative and Gram-positive bacteria.
- In vivo studies show that animals treated intraperitoneally with dosages >10 mg/kg are apparently free of parasites.
- In vivo studies show that animals treated orally with 50 or 100 mg/kg are apparently free of parasites.
- Mice treated with 30 mg/kg over an 8-day period were totally cured.
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Enzo Life Sciences AS601245 (5mg). CAS: 345987-15-7
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Potent and cell permeable ATP competitive JNK inhibitor (hJNK1: IC50=150nM, hJNK2: IC50=220nM and hJNK3: IC50=70 nM). Displays anti-inflammatory properties and has been shown to reduce TNF-α plasma levels induced by LPS in mice. Alternative name: 1,3-Benzothiazol-2-yl-(2-{[2-(3-pyridinyl)ethyl]amino}-4-pyrimidinyl) acetonitrile, JNK Inhibitor V. Purity: ≥95% (HPLC). Solubility: Soluble in DMSO (10mg/ml). Long Term Storage: -20°C.
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Selleck Chemical LLC Sugammadex
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Sugammadex (ORG-25969) is a selective relaxant binding agent indicated for reversal of neuromuscular blockade induced by rocuronium bromide and vecuronium bromide during surgery in adults
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Medchemexpress LLC HY-B0711 500mg Medchemexpress, Carglumic Acid N-Carbamyl-L-glutamic acid CAS:1188-38-1 Purity:98%
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Medchemexpress,HY-B0711 500mg Carglumic Acid N-Carbamyl-L-glutamic acid CAS:1188-38-1 Formula:C6H10N2O5 Carglumic acid, a functional analogue of N-acetylglutamate (NAG) and a carbamoyl phosphate synthetase 1 (CPS1) activator, is used to treat acute and chronic hyperammonemia associated with NAG synthase (NAGS) deficiency. Purity:98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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AURUM PHARMATECH INC NDIMETHYLAMINOCARBONYL 500MG
NC2395894 NDIMETHYLAMINOCARBONYL 500MG
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TARGETMOL CHEMICALS INC Pregnenolone monosulfate 25MG
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Also available in 1 mL, 5 mg, 10 mg and bulk. Please contact Fisher for quotes. Pregnenolone monosulfate (3beta-Hydroxy-5-pregnen-20-one monosulfate) is a potent nootropic steroid that positively regulates NMDA recordings and is utilized in the study of neuroticism and depression. Purity 99.46%
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Enzo Life Sciences 3,3'-Diindolylmethane (500mg). CAS: 1968-05-4
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Dimer of indole-3-carbinol (ALX-350-347). Anticancer and antineoplastic agent. Induces apoptosis in human cancer cells. Activator of cytochrome P450. Partial agonist of aryl hydrocarbon receptor (AhR). Alternative name: DIM. Purity: ≥98% (HPLC). Appearance: White to light pink powder. Solubility: Soluble in DMSO (200mg/ml); insoluble in water. Long Term Storage: -20°C.
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Medchemexpress LLC 4-amino-2-[4-[1-(benzyloxycarbonyl)-2(S)-[(1,1-dimethylethyl)amino]carbonyl-piperazinyl]-6,7-dimethoxyqu | 189349-50-6 | 99.9% | 522.60 | C27H34N6O5 | 5 MG
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L-765314 is a research reagent: a selective α1B (alpha-1B) adrenergic receptor antagonist used to probe α1B-mediated signaling in pharmacology and neuroscience studies. It is supplied as a solid powder with documented affinity and high reported purity, suitable for in vitro and in vivo experiments.
- High affinity for α1B receptors (human Ki 2.0 nM; rat Ki 5.4 nM).
- High purity suitable for research (reported 99.92%).
- Solid powder form enabling flexible formulation and dosing.
- Molecular weight 522.60 and formula C27H34N6O5 for precise calculations.
- Stable under recommended storage conditions for long-term use.
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Medchemexpress LLC 4-(6-fluoro-3-oxo-3,5-dihydro-2H-pyrazolo[4,3-c]quinolin-2-yl)benzoic acid | 486449-65-4 | 98.0% | 323.28 | C17H10FN3O3 | 10 MG
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CD80-IN-3 is a small-molecule inhibitor of CD80 used in research to disrupt CD80/CD28 signaling. It shows in vitro activity (EC50 630 nM; Kd 125 nM) and is supplied as a solid or as a 10 mM solution in DMSO with manufacturer analytical data available.
- Potent CD80 inhibitor that blocks CD80/CD28 interaction (EC50 630 nM; Kd 125 nM).
- High purity (98.02%).
- Molecular weight 323.28 and formula C17H10FN3O3.
- Solid, light brown to yellow appearance; also available as a 10 mM solution in DMSO.
- Available in small research pack sizes such as 10 mg.
- For research use only; not for human or clinical use.
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Medchemexpress LLC TTA-A2 | 953778-63-7 | 99.33% | 378.39 | 10 MG
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TTA-A2 is a potent, selective, and orally active T-type voltage-gated calcium channel antagonist with reduced pregnane X receptor (PXR) activation. It is equally potent against the Cav3.1 (a1G) and Cav3.2 (a1H) channels. TTA-A2 can be used for the research of a variety of human neurological diseases, including sleep disorders and epilepsy.
- Potent and selective T-type voltage-gated calcium channel antagonist
- Reduced pregnane X receptor activation
- Equally potent against Cav3.1 and Cav3.2 channels
- Useful for research into neurological diseases such as sleep disorders and epilepsy
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