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Filtered Search Results
MEDCHEMEXPRESS LLC AZELIRAGON 5MG
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501873864 AZELIRAGON 5MG
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GRAINGER INC IMIDAZOLE-4-CARBOXALDEHYDE 1G
502781136 IMIDAZOLE-4-CARBOXALDEHYDE 1G
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Medchemexpress LLC Aftin-4 | 866893-90-5 | 98.4% | 368.48 | 1 ML
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Aftin-4 is an Amyloid-β42 (Aβ42) inducer. It selectively and potently increases Aβ1-42 in N2a cells, primary neurons, and brain lysates, with an EC50 value around 30 μM. It also increases Aβ1-42 levels in vivo in mice and can provoke sustained toxicity reminiscent of Alzheimer's disease (AD).
- Amyloid-β42 (Aβ42) inducer
- Selectively and potently increases Aβ1-42 in N2a cells, primary neurons, and brain lysates
- Increases Aβ1-42 levels in vivo in mice
- Available in various quantities from 2 mg to 100 mg for in-stock options
- Purity: 98.44%
- Solid appearance, white to off-white color
- Recommended storage for powder: -20°C for 3 years, 4°C for 2 years
- Recommended storage for in solvent: -80°C for 2 years, -20°C for 1 year
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Medchemexpress LLC NS-638 | 150493-34-8 | 99.8% | 325.72 g/mol | C15H11ClF3N3 | 2 MG
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NS-638 is a small nonpeptide research compound that acts as a Ca2+-channel blocker. It inhibits K+-stimulated intracellular Ca2+ elevation with an IC50 of 3.4 μM and is supplied as a solid or as DMSO solutions for laboratory use.
- Potent Ca2+ channel blocker with IC50 3.4 μM.
- High supplied purity (reported 99.84%).
- Available as solid and 10 mM DMSO solution formats.
- Molecular weight 325.72 g/mol.
- Powder storage: -20°C (3 years) or 4°C (2 years); in solvent: -80°C (2 years) or -20°C (1 year).
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Matrix Scientific (1-METHYL-1H-IMIDAZOL-2-YL)-5G
(1-Methyl-1H-imidazol-2-yl)methanol, >95%; 5g,C5H8N2O, MFCD00964673, mw 112.13, [17334-08-6]
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Medchemexpress LLC 2'3'-c-di-AM(PS)2 (Rp,Rp) enantiomer (ammonium salt) | 98.9% | 10 MG
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2'3'-c-di-AM(PS)2 (Rp,Rp) enantiomer ammonium salt is the less active enantiomer of 2'3'-c-di-AM(PS)2 (Rp,Rp), an activator of stimulator of interferon genes (STING). This chemical is intended for laboratory research and manufacture of substances.
- Appearance: Solid
- Color: White to off-white
- Molecular weight: 724.60
- Formula: C20H30N12O10P2S2
- Purity: 98.9%
- Solubility in water: ≥ 100 mg/mL
- Solubility in DMSO: 50 mg/mL
- Recommended storage for solid: -20°C, sealed, away from moisture and light.
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eMolecules 497223-28-6 | Medchem Express | Cenicriviroc Mesylate | 1mg | 446264726 | HY-14882A | 793.05 | C42H56N4O7S2
Pharmablock | N-(2-methoxyethyl)but-3-en-1-amineoxalic acid | 50mg | 778477023 | PBT5193-3 | 219.237 | C9H17NO5
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Medchemexpress LLC 4-(2-(4-amino-1,2,5-oxadiazol-3-yl)-1-ethyl-7-((3S)-3-piperidinylmethyl)oxy)-2-methyl-3-butyn-2-ol | 937174-76-0 | MFCD14105605 | 98.5% | 425.48 g/mol | C21H27N7O3 | 25 MG
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GSK-690693 is a small-molecule, ATP-competitive pan-Akt inhibitor used for biochemical and cell-based research into PI3K/Akt signaling. It inhibits Akt1, Akt2, and Akt3 with low nanomolar potency (IC50s: 2 nM, 13 nM, 9 nM). The compound has molecular formula C21H27N7O3 and a molecular weight of 425.48 g/mol, and is supplied as a high-purity solid for laboratory research.
- Inhibits Akt1, Akt2, and Akt3 with low nanomolar potency.
- ATP-competitive mechanism of action.
- Suitable for biochemical and cell-based assays.
- Supplied as a high-purity solid (~98.5%).
- Molecular formula C21H27N7O3; molecular weight 425.48 g/mol.
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Aobchem 1-Methylbenzimidazole, AOBCHEM USA 28423-25G. 1632-83-3. MFCD00192275
1-Methylbenzimidazole, AOBCHEM USA 28423-25G. 1632-83-3. MFCD00192275
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eMolecules 65039-05-6 | 1-Butyl-3-methylimidazolium iodide | MFCD08276307 | 25g
Ambeed | 1-Butyl-3-methylimidazolium iodide | 25g | 552640159 | A199824 | 65039-05-6 | MFCD08276307 | 266.126 | C8H15IN2
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Medchemexpress LLC NH-3 | 447415-26-1 | 99.4% | C28H27NO6 | 100 MG
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NH-3 is an orally active, reversible thyroid hormone receptor (THR) antagonist with an IC50 of 55 nM. It is derived from the selective thyromimetic GC-1 and inhibits the binding of thyroid hormones to their receptor and also inhibits cofactor recruitment. NH-3 also functions as a click chemistry reagent, featuring an Alkyne group that can participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Orally active, reversible thyroid hormone receptor antagonist
- Inhibits thyroid hormone binding to its receptor and cofactor recruitment
- Functions as a click chemistry reagent
- Contains an alkyne group for copper-catalyzed azide-alkyne cycloaddition
- Modestly decreases heart rate in vivo
- Inhibits tachycardic and TSH suppressant effects in vivo
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eMolecules 929095-18-1 | Medchem Express | GSK461364 | 5mg | 446271172 | HY-50877 | MFCD12755419 | 543.61 | C27H28F3N5O2S
Medchem Express | GSK461364 | 5mg | 446271172 | HY-50877 | 929095-18-1 | MFCD12755419 | 543.610 | C27H28F3N5O2S
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Medchemexpress LLC Olmesartan | 144689-24-7 | 99.9% | 446.50 | 50 MG
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Olmesartan, also known as RNH-6270, is an angiotensin II receptor (AT1R) antagonist that is utilized in the treatment of high blood pressure. It is intended for research use only.
- It is an angiotensin II receptor (AT1R) antagonist.
- It is used to treat high blood pressure.
- It inhibits the growth of HeLa cells in a concentration- and time-dependent manner.
- Repeated dosing decreases mean arterial blood pressure without significantly influencing body weight or food intake.
- Treatment inhibits cardiac hypertrophy.
- Treatment reverses decreased gene expressions of ACE2 and Mas receptor, and inhibits enhanced NADPH oxidase (Nox)4 expression and reactive oxygen species.
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Medchemexpress LLC Leu-AMS R enantiomer | 459.48 | 10 MG
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Leu-AMS R enantiomer is the R enantiomer of Leu-AMS. Leu-AMS is a potent inhibitor of leucyl-tRNA synthetase (LRS) and inhibits the growth of bacteria. For research use only.
- Potent inhibitor of leucyl-tRNA synthetase (LRS).
- Inhibits the growth of bacteria.
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eMolecules 1257426-19-9 | Medchem Express | TBA-354 | 5mg | 446261354 | HY-12485 | MFCD28009369 | 436.347 | C19H15F3N4O5
Medchem Express | GSK2983559 active metabolite | 5mg | 446270296 | HY-19764 | 1423186-80-4 | MFCD30489727 | 458.550 | C21H22N4O4S2
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