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Filtered Search Results
Cayman Chemical N-acetyl-2-AmInophenol 25g
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A derivative of acetaminophen; inhibits ADP- or arachidonic acid-induced platelet aggregation in isolated human platelet-rich plasma at 50 µM; decreases disease severity and prevents increases in paw volume in a rat model of collagen-induced arthritis at 1 mg/kg; has been used as a synthetic intermediate in the synthesis of compounds with antimalarial activity; a potential impurity in commercial preparations of acetaminophen
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Cayman Chemical Acetaminophen Inhibitors
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An analgesic and antipyretic compound; an inhibitor of COX-2 that is selective over COX-1 (IC50s = 113.7 and 25.8 µM, respectively, in human blood ex vivo); induces ferroptotic cell death in primary mouse hepatocytes; has a metabolite that depletes glutathione reserves in the liver
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Medchemexpress LLC Bis(2-cyanoethyl) diisopropylphosphoramidite | 102690-88-0 | 95.0% | 271.30 | 5 G
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Bis(2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite monomer used in the synthesis of oligonucleotides. It is for research use only and not sold to patients.
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Cambridge Isotope Laboratories Acetaminophen (ring-13C6 98%) 1 mg
Acetaminophen (ring-13C6 98%) 1 mg
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000702279 OTS964 HYDROCHLORID 10MM/1ML
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000703493 BMS-202 HYDROCHLORI 100MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000701972 U92016A HYDROCHLORI 1MG
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Medchemexpress LLC 3-methyl-5-[(2S)-1-methyl-2-pyrrolidinyl]isoxazole hydrochloride | 147388-83-8 | MFCD11045960 | 99.4% | 202.68 g·mol⁻¹ | C9H15ClN2O | 1 ML
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ABT-418 hydrochloride is a potent, selective agonist of neuronal nicotinic acetylcholine receptors (nAChRs) used in preclinical research to investigate cholinergic signaling, cognition, and anxiolytic mechanisms. It is supplied as a solid and as a ready-to-use 10 mM solution for laboratory applications. CAS 147388-83-8; molecular weight 202.68 g·mol⁻¹. For research use only.
- Potent, selective agonist of neuronal nicotinic acetylcholine receptors.
- Available as solid and as 10 mM solution ready for use.
- High purity suitable for analytical and biological studies.
- Stable under recommended storage conditions.
- Intended for laboratory research use only.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000745187 KT-474 HYDROCHLORID 100MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000664154 IUB0271 HYDROCHLORI 5MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000664418 IUB0271 HYDROCHLORI 25MG
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Medchemexpress LLC Mepazine hydrochloride | 2975-36-2 | >98.0% | 10MM 1ML
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Mepazine hydrochloride | 2975-36-2 | >98.0% | 10MM 1ML
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000746992 GNF2133 HYDROCHLORI 10MG
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Medchemexpress LLC CSRM617 hydrochloride | 1353749-74-2 | 100.0% | 100 MG
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CSRM617 hydrochloride is the hydrochloride salt of a selective small-molecule inhibitor of the transcription factor ONECUT2, supplied as a white to off-white solid for research use.
- Selective inhibitor of ONECUT2 transcription factor.
- Hydrochloride salt, white to off-white solid.
- Purity 99.97%.
- Molecular weight 291.69 g/mol.
- Soluble in DMSO (100 mg/mL; ultrasonic assistance recommended).
- Store sealed, away from moisture; in solvent: -80°C (6 months), -20°C (1 month).
- For research use only; not for human use.
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Medchemexpress LLC BI-9627 hydrochloride | 1422252-46-7 | 98.0% | 392.80 | 25 MG
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BI-9627 hydrochloride is a potent and selective sodium-hydrogen exchanger isoform 1 (NHE1) inhibitor, with IC50 values of 6 nM and 31 nM. It demonstrates high selectivity over other NHE isoforms and has shown effects on autophagy, pH regulation, and Ca2+ recovery in various cell types. This compound exhibits favorable pharmacokinetic properties and cardioprotective activity. For research use only.
- Potent sodium-hydrogen exchanger isoform 1 (NHE1) inhibitor (IC50 = 6 and 31 nM).
- High selectivity (>30-fold) against NHE2; no activity against NHE3.
- Decreases autophagy in HTR-8/SVneo cells.
- Reduces pHi of human sperm and partially reverses DMA effect.
- Prolongs Ca2+ recovery time in KO hiPSC-CMs.
- Low drug-drug interaction (DDI) potential.
- Excellent pharmacokinetics in rat and dog.
- Potent activity in isolated heart model of ischemia-reperfusion injury.
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