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Filtered Search Results
Aobchem (3-Isopropoxy-4-methoxyphenyl)(methyl)sulfane | 95% | C11H16O2S | 1g
(3-Isopropoxy-4-methoxyphenyl)(methyl)sulfane | 95% | C11H16O2S | 1g
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Aobchem 5-(3 5-Dimethylphenyl)oxazole | 95% | CAS 2006648-43-5 | C11H11NO | 5g
5-(3 5-Dimethylphenyl)oxazole | 95% | CAS 2006648-43-5 | C11H11NO | 5g
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Aobchem 4-(Oxazol-5-yl)benzamide | 95% | CAS 672324-90-2 | C10H8N2O2 | 250mg
4-(Oxazol-5-yl)benzamide | 95% | CAS 672324-90-2 | C10H8N2O2 | 250mg
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Aobchem 2-(2-Bromo-4 5-difluorophenoxy)propane | ≥97% | CAS 1266253-67-1 | C9H9BrF2O | 500mg
2-(2-Bromo-4 5-difluorophenoxy)propane | ≥97% | CAS 1266253-67-1 | C9H9BrF2O | 500mg
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Aobchem AOBCHEM
5001080750 2- 4-METHOXYPHENYL -2-METHYL-2
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Aobchem AOBCHEM
5001080751 2- 4-METHOXYPHENYL -2-METHYL-2
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Aobchem AOBCHEM
5001082191 2-ETHOXY-3-METHOXYPHENYL ETH
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Aobchem (2-Isopropoxy-4-methoxyphenyl)boronic acid | 95% | CAS 2898529-85-4 | C10H15BO4 | 1g
(2-Isopropoxy-4-methoxyphenyl)boronic acid | 95% | CAS 2898529-85-4 | C10H15BO4 | 1g
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Aobchem 2-Chloro-4-(chloromethyl)-1-methylbenzene | 95% | CAS 2719-40-6 | C8H8Cl2 | 5g
2-Chloro-4-(chloromethyl)-1-methylbenzene | 95% | CAS 2719-40-6 | C8H8Cl2 | 5g
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Aobchem 5-(3-Methoxyphenyl)-6-methyl-2-pyridinamine | 95% | CAS 1368241-16-0 | C13H14N2O | 500mg
5-(3-Methoxyphenyl)-6-methyl-2-pyridinamine | 95% | CAS 1368241-16-0 | C13H14N2O | 500mg
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Aobchem 2-(Chloromethyl)-1 4-diethylbenzene | 95% | CAS 56140-53-5 | C11H15Cl | 1g
2-(Chloromethyl)-1 4-diethylbenzene | 95% | CAS 56140-53-5 | C11H15Cl | 1g
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Aobchem 1-(5-Ethyl-2-methoxyphenyl)ethanol | 95% | CAS 1367821-88-2 | C11H16O2 | 500mg
1-(5-Ethyl-2-methoxyphenyl)ethanol | 95% | CAS 1367821-88-2 | C11H16O2 | 500mg
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Medchemexpress LLC Trans-4-((R)-1-aminoethyl)-N-(pyridin-4-yl)cyclohexanecarboxamide dihydrochloride | 129830-38-2 | MFCD03490488 | 99.9% | 320.26 | C14H23Cl2N3O | 100 MG
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Y-27632 dihydrochloride is an ATP-competitive inhibitor of Rho-associated kinases used as a research reagent to probe ROCK signaling pathways. Provided as the dihydrochloride salt, it has reported Ki values for ROCK-I and ROCK-II and is suitable for biochemical and cell-based assays investigating neuronal differentiation, epilepsy models, and fibrosis.
- ATP-competitive ROCK inhibitor with defined Ki values for ROCK-I and ROCK-II.
- High reported purity for reliable assay performance.
- Available in multiple pack sizes, including 100 mg, for flexible experimental use.
- Applicable in biochemical and cell-based assays, including neuronal differentiation studies.
- Stable when stored sealed at 4°C according to handling recommendations.
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Medchemexpress LLC Y-27632 dihydrochloride | 129830-38-2 | MFCD03490488 | 99.9% | 320.26 g/mol | C14H23Cl2N3O | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Y-27632 dihydrochloride is an ATP-competitive inhibitor of Rho-associated protein kinases (ROCK) used in research to modulate cytoskeletal dynamics, cell morphology, and motility in vitro and in vivo. It is supplied as a high-purity, white to off-white solid suitable for laboratory assays and preclinical studies.
- ATP-competitive ROCK inhibitor (ROCK-I Ki = 220 nM; ROCK-II Ki = 300 nM).
- Orally active; applicable to in vivo and in vitro studies.
- High purity (≈99.9%) for reproducible experimental results.
- Molecular weight 320.26 g/mol for stoichiometric calculations.
- White to off-white solid; convenient handling and storage.
- Available in small research quantities suitable for assay development.
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Medchemexpress LLC Y-27632 dihydrochloride | 129830-38-2 | MFCD03490488 | 99.9% | 320.26 g/mol | C14H23Cl2N3O | 25 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Y-27632 dihydrochloride is an orally active, ATP-competitive inhibitor of Rho-associated kinases (ROCK) used in research to alter cytoskeletal dynamics, cell survival, and differentiation. It selectively inhibits ROCK-I and ROCK-II and has reported antiepileptic effects and applications in stem cell and neurobiology studies.
- ATP-competitive ROCK inhibitor with Ki values for ROCK-I (220 nM) and ROCK-II (300 nM).
- Orally active compound applicable in both in vitro and in vivo research.
- Reported antiepileptic effects in preclinical studies.
- Modulates apoptosis and promotes mesendodermal differentiation in stem cell models.
- White to off-white solid with molecular weight 320.26 g/mol and formula C14H23Cl2N3O.
- High purity suitable for analytical and experimental use.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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