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Filtered Search Results
Aobchem AOBCHEM
5000862788 1- 2 3-DIFLUOROPHENYL -2 2 2-T
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Aobchem AOBCHEM
5000862796 2 3-DIFLUOROPHENYL TRIMETHYLS
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eMolecules 142266-62-4 | 2,5,6-TRICHLORONICOTINAMIDE | AstaTech | MFCD22493418 | 225.450 | C6H3Cl3N2O | 95.000 | NC(=O)c1cc(Cl)c(Cl)nc1Cl | 0.25g | 347152262
2,5,6-TRICHLORONICOTINAMIDE | AstaTech | 142266-62-4 | MFCD22493418 | 225.450 | C6H3Cl3N2O | 95.000 | NC(=O)c1cc(Cl)c(Cl)nc1Cl | 0.25g | 347152262
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Selleck Chemical LLC GGTI 298 TFA salt
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GGTI 298 is a geranylgeranyltransferase I inhibitor with ability to arrest human tumor cells in the G1 phase of the cell cycle and induce apoptosis
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Medchemexpress LLC [Sar9,Met(O2)11]-Substance P | 110880-55-2 | 99.6% | 1393.66 | 25 MG
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[Sar9,Met(O2)11]-Substance P is a tachykinin NK1 receptor selective agonist.
- Target: NK1 receptor
- Cell line: U-373MG ATCC
- IC50 value: 1.1 x 10-10 M
- Increases mean arterial blood pressure and heart rate
- Increases face washing and sniffing
- Produces grooming
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BIOHIPPO
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5000860685 MET/C-MET/HGFR BIOSIMILAR
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Selleck Chemical LLC AGI-5198
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AGI-5198 (IDH-C35) is the first highly potent and selective inhibitor of IDH1 R132H/R132C mutants with IC50 of 0 07 M/0 16 M
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![Apexbio Technology LLC Cytochrome P450 CYP1B1 (190-198) [Homo sapiens] 1mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000097039.png-250.jpg)
Apexbio Technology LLC Cytochrome P450 CYP1B1 (190-198) [Homo sapiens] 1mg
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Cytochrome P450 CYP1B1 190-198 is a tumor-associated antigen peptide derived from CYP1B1 It is designed to induce HLA-A2-restricted T-cell responses against the CYP1B1(190-198) epitope thereby promoting tumor-specific cytotoxic immune responses Cytochrome P450 CYP1B1 190-198 exerts its biological activity primarily through antigen-specific activation of CD8 T cells In HLA-A2 transgenic mouse models this peptide delivered via plasmid DNA and poly(lactide-co-glycolide) microparticles demonstrates the ability to elicit CYP1B1 peptide-specific T-cell immunity Based on these pharmacological properties Cytochrome P450 CYP1B1 190-198 holds research potential in cancer immunotherapy and studies of tumor-specific cytotoxic T-cell responses
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![Medchemexpress LLC Pyridine, 4-[2-(2-fluorophenyl)-4-(4-fluorophenyl)-1H-imidazol-5-yl]- | 1784751-19-4 | 99.9% | 333.33 | C20H13F2N3 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000215362.png-250.jpg)
Medchemexpress LLC Pyridine, 4-[2-(2-fluorophenyl)-4-(4-fluorophenyl)-1H-imidazol-5-yl]- | 1784751-19-4 | 99.9% | 333.33 | C20H13F2N3 | 5 MG
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TA-02 is a small-molecule inhibitor of p38 MAPK used in research to probe MAPK signaling and cardiogenic pathways. It inhibits phosphorylation of downstream proteins such as MAPKAPK2 and HSP27 and shows activity against TGFBR-2.
- Potent p38 MAPK inhibition (IC50 20 nM).
- High purity suitable for research applications (99.85%).
- Molecular formula C20H13F2N3; molecular weight 333.33.
- Available as small solid quantities and as a 10 mM solution in DMSO.
- Useful for studies of cardiogenesis and TGFBR-2 related signaling.
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Aobchem AOBCHEM
5000862639 1- 2 3-DIFLUOROPHENYL -2 2 2-T
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Medchemexpress LLC 93-O17S | 2227008-67-3 | C44H83N3O4S2 | 25 MG
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93-O17S is an ionizable lipid involved in the construction of Lipid Nanoparticles (LNP) and can achieve mRNA delivery to the spleen. This product is for research use only.
- Ionizable lipid
- Involved in the construction of lipid nanoparticles (LNP)
- Achieves mRNA delivery to the spleen
- Delivers luciferase mRNA to the spleen of mice
- Purity: 98.0%
- Appearance: Oil
- Color: Light yellow to yellow
- Soluble in DMSO and ethanol
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Ambeed AMBEED
5000868498 2-CHLORO-5-METHYLTHIAZOLE- 1GR
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Ambeed AMBEED
5000868497 METHYL-4-BROMOTHIAZOLE-2-C 1GR
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Aobchem AOBCHEM
5000864327 1- 2 3-DIHYDROBENZOFURAN-5-YL
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TARGETMOL CHEMICALS INC VH-298 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. VH-298 is a potent inhibitor of VHL that stabilizes HIF-alpha and elicits a hypoxic response via a different mechanism, that is the blockade of the VHLHIF-alpha protein-protein interaction downstream of HIF-alpha hydroxylation by PHD enzymes. Purity 100%
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