Thiophenes
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Filtered Search Results
Aobchem AOBCHEM
5001005315 2-CHLORO-5-PHENYLTHIOPHENE 1G
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Aobchem AOBCHEM
5001005553 3-FLUOROPHENYL THIOPHEN-2-YL
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Aobchem AOBCHEM
5001005857 ETHYL 2- 4-CYANOPHENYL THIO B
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Aobchem AOBCHEM
5001005909 ETHYL 2- 4-CYANOPHENYL THIO B
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Aobchem AOBCHEM
5001009831 6-BROMO-4-FLUOROBENZO B THIOPH
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Aobchem AOBCHEM
5001047098 4-METHYLTHIOPHENE-2-CARBOXALDE
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Aobchem AOBCHEM
5001047199 N- 1 1-DIMETHYLETHYL -2-THIOPH
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Aobchem AOBCHEM
5001047438 N- 1 1-DIMETHYLETHYL -2-THIOPH
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Aobchem AOBCHEM
5001047525 THIOPHENE-2-CARBOXYLIC ACID ME
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eMolecules 6164-79-0 | Methyl 2-Pyrazinecarboxylate | AA Blocks LLC | MFCD00014611 | 138.126 | C6H6N2O2 | 0.000 | COC(=O)c1cnccn1 | 5g | 410181915
Methyl 2-Pyrazinecarboxylate | AA Blocks LLC | 6164-79-0 | MFCD00014611 | 138.126 | C6H6N2O2 | 0.000 | COC(=O)c1cnccn1 | 5g | 410181915
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Apexbio Technology LLC Canertinib dihydrochloride 289499-45-2 100mg
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Canertinib dihydrochloride (CAS 289499-45-2) is a small-molecule inhibitor targeting the pan-ErbB family of receptor tyrosine kinases It is designed to irreversibly inhibit ErbB receptors thereby disrupting Akt and MAPK signaling pathways Canertinib dihydrochloride exerts its biological activity primarily through irreversible binding to ErbB receptor family members In cell-based studies Canertinib dihydrochloride demonstrates apoptotic induction and reduced cell viability with an IC50 value of 3 5 nM Apoptosis induction was observed in BT474 (ErbB2-overexpressing breast cancer) and SK-N-SH (neuroblastoma) cell lines Based on these pharmacological properties Canertinib dihydrochloride holds research potential in oncology specifically for investigating ErbB signaling pathways and evaluating anti-tumor effects in cancer models
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Medchemexpress LLC Lubeluzole dihydrochloride | 144665-09-8 | 99.0% | 506.44 | C22H27Cl2F2N3O2S | 1 MG
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Lubeluzole dihydrochloride is the dihydrochloride salt of lubeluzole, a neuroprotective research reagent that modulates neuronal voltage-gated sodium and calcium channels. It is provided as a high-purity solid intended for in vitro and preclinical pharmacology studies.
- 99.0% HPLC purity.
- White to off-white solid appearance.
- Molecular weight 506.44 g/mol.
- Molecular formula C22H27Cl2F2N3O2S.
- Storage: -20°C (sealed); in solution store at -80°C for long-term.
- Suitable for neuroscience and pharmacology research applications.
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Apexbio Technology LLC H 89 2HCl 130964-39-5 50mg
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H 89 2HCl (CAS 130964-39-5) is a small-molecule inhibitor targeting cyclic AMP-dependent protein kinase (PKA) It exhibits a Ki of approximately 48 nM toward PKA and demonstrates substantial selectivity compared to related kinases such as PKG (about 10-fold) PKC MLCK calmodulin kinase II and casein kinases (approximately 500-fold) In PC12D cells H 89 at micromolar concentrations suppresses forskolin-induced phosphorylation events and neurite outgrowth without altering intracellular cAMP levels Due to its selective inhibitory profile H 89 is widely utilized in cell signaling studies examining cAMP-dependent pathways
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Medchemexpress LLC 2-Amino-2- thiophen- | 1G
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2-Amino-2- thiophen- | 1G
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Medchemexpress LLC Lomerizine dihydrochloride | 101477-54-7 | 99.95% | 1 ML
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Lomerizine dihydrochloride, also known as KB-2796, is a potent antagonist of L- and T-type voltage-gated calcium channels. This chemical is supplied at a concentration of 10mM in 1mL of DMSO. It is crucial for researchers studying calcium channel modulation and related neurological processes.
- Antagonist of L-type voltage-gated calcium channels
- Antagonist of T-type voltage-gated calcium channels
- Packaged as a 10mM solution in DMSO
- Recommended storage at 4°C, sealed, away from moisture
- Stable in solvent for 6 months at -80°C or 1 month at -20°C
- Suitable for shipping at room temperature for durations less than 2 weeks
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