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Filtered Search Results
Aobchem AOBCHEM
5000937794 1 2-DIHYDRO- - 1-METHYLETHYL -
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eMolecules 57260-71-6 | 1-Boc-piperazine | Chem-Impex | MFCD00075265 | 186.255 | C9H18N2O2 | 99.000 | CC(C)(C)OC(=O)N1CCNCC1 | 25g | 386904163
1-Boc-piperazine | Chem-Impex | 57260-71-6 | MFCD00075265 | 186.255 | C9H18N2O2 | 99.000 | CC(C)(C)OC(=O)N1CCNCC1 | 25g | 386904163
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Apexbio Technology LLC Dilazep dihydrochloride 20153-98-4 50mg
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Dilazep dihydrochloride is a small-molecule inhibitor targeting adenosine reuptake It is designed to block the cellular uptake of adenosine thereby increasing extracellular adenosine concentrations and regulating adenosine receptor-mediated pathways Dilazep dihydrochloride exerts its biological activity primarily through inhibition of adenosine reuptake resulting in vasodilation and suppression of platelet aggregation Based on these pharmacological properties Dilazep dihydrochloride holds research potential in studies of coronary blood flow regulation platelet aggregation mechanisms cardiomyocyte metabolism and protective cellular responses during ischemia-reperfusion injury
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Apexbio Technology LLC Y-39983 dihydrochloride 173897-44-4 50mg
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Y-39983 dihydrochloride (CAS 173897-44-4) is a selective inhibitor of Rho-associated coiled-coil containing protein kinase (ROCK) exhibiting an IC50 of 3 6 nM for ROCK inhibition It demonstrates substantially reduced inhibitory activity against protein kinase C (PKC IC50 0 42 M) and Ca2 /calmodulin-dependent protein kinase II (CaMKII IC50 0 81 M) In ex vivo studies Y-39983 dihydrochloride induces relaxation of pre-contracted rabbit ciliary arteries and has been shown to increase optic nerve head blood flow Furthermore dose-dependent reductions in intraocular pressure have been observed in both rabbit and monkey models These properties suggest its value for research on ROCK-related signaling in ocular physiology and vascular tone regulation
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Apexbio Technology LLC SCH 79797 dihydrochloride 5mg
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SCH 79797 dihydrochloride (CAS 1216720-69-2) is a potent and selective non-peptide antagonist of protease-activated receptor 1 (PAR1) It inhibits the binding of thrombin receptor-activating peptide to PAR1 with an IC50 of 70 nM and displays a Ki of 35 nM for receptor modulation SCH 79797 dihydrochloride prevents thrombin-induced platelet aggregation with an IC50 of 3 M and demonstrates antiproliferative and pro-apoptotic effects as well as attenuation of myocardial ischemia/reperfusion injury The compound is utilized in biomedical research to study PAR1-mediated signaling in vascular smooth muscle cells endothelial cells and astrocytes
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Medchemexpress LLC N-(tert-butoxycarbonyl)-N-methyl-D-alanine | 19914-38-6 | MFCD00063137 | 25g
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N-(tert-Butoxycarbonyl)-N-methyl-D-alanine is an alanine derivative[1]
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eMolecules 57260-71-6 | 1-Boc-piperazine | Chem-Impex | MFCD00075265 | 186.255 | C9H18N2O2 | 99.000 | CC(C)(C)OC(=O)N1CCNCC1 | 250g | 386904165
1-Boc-piperazine | Chem-Impex | 57260-71-6 | MFCD00075265 | 186.255 | C9H18N2O2 | 99.000 | CC(C)(C)OC(=O)N1CCNCC1 | 250g | 386904165
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Medchemexpress LLC N4-ACETYLSULFAMETHOX 10MG | 10MG
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N4-ACETYLSULFAMETHOX 10MG | 10MG
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Apexbio Technology LLC KX2-391 dihydrochloride 1038395-65-1 5mg
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KX2-391 dihydrochloride (CAS 1038395-65-1) is an orally bioavailable small molecule that inhibits Src tyrosine kinase through selective interaction with the peptide substrate binding site rather than the ATP-binding site By blocking this non-catalytic domain KX2-391 disrupts Src kinase-mediated signaling pathways involved in tumor cell proliferation and metastatic processes Src kinases are frequently upregulated in various malignancies underscoring their importance in cancer biology KX2-391 is widely utilized in preclinical studies investigating Src-driven mechanisms of oncogenesis and tumor progression
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Medchemexpress LLC N-(tert-Butoxycarbonyl)-O-(tert-butyl)-L-threonyl-L-proline | 1432793-68-4 | 97.05% | 372.46 | 50 MG
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N-(tert-Butoxycarbonyl)-O-(tert-butyl)-L-threonyl-L-proline is a proline derivative. Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances.
- Proline derivative
- Can be used as an ergogenic supplement
- Influences secretion of anabolic hormones
- Supplies fuel during exercise
- Improves mental performance during stress-related tasks
- Prevents exercise-induced muscle damage
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Cambridge Isotope Laboratories Piperazine 2HCl (2 2 3 3 5 5 6 6-D8 98%) 1 g
Piperazine 2HCl (2 2 3 3 5 5 6 6-D8 98%) 1 g
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Apexbio Technology LLC GW 583340 dihydrochloride 10mg
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GW 583340 dihydrochloride (CAS 1173023-85-2) is a small molecule inhibitor targeting the tyrosine kinase activity of both EGFR and ErbB2 exhibiting potent inhibitory effects with IC50 values of 0 01 M and 0 014 M respectively In addition to suppressing these receptor-mediated signaling pathways GW 583340 dihydrochloride has been shown to inhibit ABC transporters including ABCG2 and ABCB1 thereby reversing transporter-associated multidrug resistance This compound is utilized in tumor biology research to investigate the modulation of oncogenic signaling mechanisms underlying drug resistance and to explore potential therapeutic strategies
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Selleck Chemical LLC CRT0066101 dihydrochloride
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CRT0066101 dihydrochloride is a small molecule PKD family specific inhibitor which specifically blocks PKD1/2 activity and does not suppress PKC /PKC /PKC activity in multiple
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TARGETMOL CHEMICALS INC Y-33075 dihydrochloride 10MG
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Also available in 1 mL, 2 mg, 5 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Y-33075 dihydrochloride is a selective inhibitor of ROCK with an IC50 of 3.6 nM. Purity 99.43%
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TARGETMOL CHEMICALS INC Sultosilic acid piperazine
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Also available in 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Sultosilic acid piperazine salt (A-585) is a novel lipid-lowering compound that can be used to study type IIb familial combined hyperlipidemia. Purity 99.1%
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