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Filtered Search Results
Apexbio Technology LLC GW 583340 dihydrochloride 10mg
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
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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Selleck Chemical LLC E6446 dihydrochloride
E6446 dihydrochloride is a specific Toll-like receptor 9 inhibitor
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TARGETMOL CHEMICALS INC Y-33075 dihydrochloride 10MG
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
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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TARGETMOL CHEMICALS INC Vofopitant dihydrochloride 1MG
Also available in 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Vofopitant dihydrochloride (GR 205171A) is an orally available, selective tachykinin NK1 receptor antagonist that inhibits [3H]SP binding to NK1 with pKi values of 9.5 and 10.6, respectively. It is a potential compound for the treatment of pathological vomiting. Purity 98.99%
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TARGETMOL CHEMICALS INC PF429242 dihydrochloride 10MG
Also available in 1 mL, 1 mg, 5 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. PF429242 dihydrochloride is a reversible and competitive inhibitor of S1P, with an IC50 of 175 nM. Purity 98.67%
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Selleck Chemical LLC H-1152 dihydrochloride
H-1152 dihydrochloride (2HCl) is a membrane-permeable and selective inhibitor of Rho-associated protein kinase (ROCK) H-1152 inhibits ROCK2 PKA PKC PKG AuroraA and CaMK2 with IC50 of 0 0120 M 3 03 M 5 68 M 0 360 M 0 745 M and 0 180 M respectively
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Accela Chembio Inc 1-boc-4-(4-cyanophenyl)piperazine | 5g | 186650-98-6 | MFCD03791198 | 97+% | Shelf Life: 1980 Days | Light Sensitive
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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1-boc-4-(4-cyanophenyl)piperazine | 5g | 186650-98-6 | MFCD03791198 | 97+% | Shelf Life: 1980 Days | Light Sensitive
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eMolecules 29767-97-3 | 4-(2-Pyridyl)-2-methyl-3-butyn-2-ol | Oakwood Chemical | MFCD00168867 | 161.204 | C10H11NO | 98.000 | CC(C)(O)C#Cc1ccccn1 | 250mg | 537709921
4-(2-Pyridyl)-2-methyl-3-butyn-2-ol | Oakwood Chemical | 29767-97-3 | MFCD00168867 | 161.204 | C10H11NO | 98.000 | CC(C)(O)C#Cc1ccccn1 | 250mg | 537709921
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Selleck Chemical LLC Piperazine Erastin-E1063-25MG
Piperazine Erastin is an analog of Erastin which can induces ferroptosis in cancer cells an iron-dependent form of nonapoptotic cell death
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Selleck Chemical LLC JTE-607 Dihydrochloride
JTE-607 Dihydrochloride is a prodrug compound that is converted to an active form by ester hydrolysis JTE-607 is a multiple cytokine production inhibitor that targets CPSF3 and inhibits pre-mRNA processing JTE-607 inhibits tumor necrosis factor (TNF)-alpha interleukin (IL)-1beta IL-6 IL-8 and IL-10 from LPS-stimulated human PBMCs with IC50 values of 11 nM 5 9 nM 8 8 nM 7 3 nM and 9 1 nM respectively
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TARGETMOL CHEMICALS INC Indinavir sulfate 25MG
Also available in 1 mL, 2 mg, 5 mg, 10 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Indinavir sulfate (L735524 sulfate) is a HIV protease inhibitor.It inhibits the HIV-1 protease with an IC50 value of 0.41 nM and Ki value of 0.24 nM.
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Medchemexpress LLC Indinavir | 150378-17-9 | 100.0% | 613.79 g/mol | C36H47N5O4 | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Indinavir is an orally active HIV-1 protease inhibitor provided as a high-purity research reagent for in vitro and preclinical studies. It is intended for laboratory research use only and not for human or clinical applications.
- High purity compound suitable for biochemical and cell-based assays.
- Well-defined molecular formula and molecular weight for identification.
- Supplied in small research quantities appropriate for screening and pilot studies.
- Includes datasheet, certificate of analysis, and safety data sheet for verification and safe handling.
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eMolecules 72086-72-7 | (S)-4-((tert-Butoxycarbonyl)amino)-5-methoxy-5-oxopentanoic acid | ChemScene | MFCD00076931 | 261.274 | C11H19NO6 | 95.000 | COC(=O)[C@H](CCC(O)=O)NC(=O)OC(C)(C)C | 25g | 536847141
(S)-4-((tert-Butoxycarbonyl)amino)-5-methoxy-5-oxopentanoic acid | ChemScene | 72086-72-7 | MFCD00076931 | 261.274 | C11H19NO6 | 95.000 | COC(=O)[C@H](CCC(O)=O)NC(=O)OC(C)(C)C | 25g | 536847141
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