Phenoxy compounds
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Filtered Search Results
Medchemexpress LLC Ipriflavone | 35212-22-7 | MFCD00221719 | >98.0% | 280.32 | 500 MG
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Ipriflavone is a synthetic isoflavone derivative used to suppress bone resorption. It is intended for research and analytical applications.
- Targets cytochrome P450.
- Relevant to research in metabolic disease.
- Relevant to research in cancer.
- Functions to suppress bone resorption.
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Aobchem 1-Fluoro-2 3-dimethoxybenzene | ≥97% | CAS 394-64-9 | C8H9FO2 | 5g
1-Fluoro-2 3-dimethoxybenzene | ≥97% | CAS 394-64-9 | C8H9FO2 | 5g
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eMolecules 852443-66-4 | ChemScene | 5-(Cyclopropylmethoxy)-1H-pyrazol-3-amine | 100mg | 632319307 | CS-0119828 | MFCD20724093 | 153.185 | C7H11N3O
ChemScene | 5-(Cyclopropylmethoxy)-1H-pyrazol-3-amine | 100mg | 632319307 | CS-0119828 | 852443-66-4 | MFCD20724093 | 153.185 | C7H11N3O
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Aobchem AOBCHEM
5000927182 3- 4- METHYLTHIO PHENOXY TETRA
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Aobchem 1-Fluoro-2 3-dimethoxybenzene | ≥97% | CAS 394-64-9 | C8H9FO2 | 25g
1-Fluoro-2 3-dimethoxybenzene | ≥97% | CAS 394-64-9 | C8H9FO2 | 25g
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000379010 MAO-B-IN-2 100MG
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Medchemexpress LLC GB-110 hydrochloride | 99.86% | 645.23 | 50 MG
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GB-110 hydrochloride is a potent, orally active, and nonpeptidic protease activated receptor 2 (PAR2) agonist. It selectively induces PAR2-mediated intracellular Ca2+ release in HT29 cells with an EC50 of 0.28 μM.
- Potent
- Orally active
- Nonpeptidic protease activated receptor 2 (PAR2) agonist
- Selectively induces PAR2-mediated intracellular Ca2+ release in HT29 cells with an EC50 of 0.28 μM
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Medchemexpress LLC Betaxolol (hydrochloride) | 63659-19-8 | 98.1% | 100 MG
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Betaxolol hydrochloride is a selective beta1 adrenergic receptor blocker used in research for conditions such as hypertension and glaucoma. It functions by selectively blocking beta-1 adrenergic receptors, which primarily affect the heart and kidney, leading to reduced heart rate and blood pressure. Research suggests it may also attenuate anxiety-like behavior during cocaine withdrawal. It is noted to have less systemic beta2- and potentially beta1-adrenergic receptor blockade compared to other similar agents.
- Selective beta1 adrenergic receptor blockade.
- Applicable in hypertension and glaucoma research.
- May be safer for patients with reactive airway disease than some other agents.
- Can attenuate anxiety-like behavior in certain contexts.
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eMolecules 101975-10-4 | Medchem Express | Zardaverine | 5mg | 446265785 | HY-15485 | MFCD00867059 | 268.22 | C12H10F2N2O3
Medchem Express | UNC3230 | 5mg | 533802283 | HY-110150 | 1031602-63-7 | MFCD15031190 | 344.430 | C17H20N4O2S
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U.S. Pharmacopeia TRIMETHOBENZAMIDE HYDROCHLORID
Trimethobenzamide Hydrochloride (200 mg)
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Apexbio Technology LLC LY2874455(Synonyms: LY-2874455, LY 2874455, FGFR inhibitor LY2874455, Fibroblast growth factor receptor inhibitor LY2874455), 5mg, CAS: 1254473-64-7.
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LY2874455 (CAS 1254473-64-7) is a small molecule inhibitor targeting fibroblast growth factor receptors (FGFRs) proteins functioning through ligand-induced receptor dimerization and tyrosine kinase activation By blocking FGFR phosphorylation and downstream signaling pathways LY2874455 inhibits proliferation and migration in FGFR-dependent cancer cell models LY2874455 shows inhibition of FGFR phosphorylation in FGFR1- FGFR2- and FGFR3-expressing cancer cell lines and xenografts demonstrating antitumor efficacy across various FGFR-driven tumor types It serves as a valuable tool molecule in oncology research investigating FGFR-mediated cancers
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Apexbio Technology LLC JW 55 664993-53-7 10mg
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JW 55 (CAS 664993-53-7) is a small-molecule inhibitor that targets the poly(ADP-ribose) polymerase (PARP) domains of tankyrase 1 and tankyrase 2 (TNKS1/2) with reported IC50 values of 1 9 M and 0 83 M respectively By inhibiting TNKS1/2 activity JW 55 stabilizes AXIN2 a component of the -catenin destruction complex leading to enhanced degradation of -catenin and suppression of canonical Wnt/ -catenin signaling In vitro JW 55 suppresses Wnt pathway activity in colorectal cancer cells harboring APC or -catenin mutations In vivo it reduces Wnt-driven phenotypes in Xenopus embryos and diminishes polyp formation in APC-mutant mice supporting its utility as a research tool in Wnt/ -catenin signaling and cancer biology
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Aobchem AOBCHEM
5001019625 2- 2- METHYLTHIO PHENOXY PYRID
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Medchemexpress LLC Flecainide | 54143-55-4 | 100.0% | 414.34 | 100 MG
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Flecainide is an orally active antiarrhythmic agent that blocks sodium channels and inhibits calcium ion release mediated by the cardiac ryanodine receptor (RyR2). It is used in research for diseases such as catecholaminergic polymorphic ventricular tachycardia (CPVT).
- Orally active antiarrhythmic agent.
- Blocks sodium channels.
- Inhibits calcium ion release mediated by the cardiac ryanodine receptor (RyR2).
- Used in research for diseases such as catecholaminergic ventricular tachycardia (CPVT).
- In vitro studies show it significantly reduces irregular Ca2+ release in single cardiomyocytes.
- Under investigation for premature ventricular beats, premature ventricular complexes, and various ventricular arrhythmias.
- Clinical trials are exploring its use for atrial fibrillation and supraventricular tachycardia.
- Has been studied for pain management.
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eMolecules 81069-02-5 | 3,3'-Dithiobis(sulphosuccinimidyl propionate) | Apollo Scientific | MFCD01861949 | 564.520 | C14H16N2O14S4 | 0.000 | OS(=O)(=O)C1CC(=O)N(OC(=O)CCSSCCC(=O)ON2C(=O)CC(C2=O)S(O)(=O)=O)C1=O | 100mg | 562466622
3,3'-Dithiobis(sulphosuccinimidyl propionate) | Apollo Scientific | 81069-02-5 | MFCD01861949 | 564.520 | C14H16N2O14S4 | 0.000 | OS(=O)(=O)C1CC(=O)N(OC(=O)CCSSCCC(=O)ON2C(=O)CC(C2=O)S(O)(=O)=O)C1=O | 100mg | 562466622
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