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Filtered Search Results
Medchemexpress LLC Urea, N-[3-(1,1-dimethylethyl)-1-(4-methylphenyl)-1H-pyrazol-5-yl]-N' | 1166393-85-6 | 98.6% | 445.52 | 50 MG
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PF-4618433 is a potent and selective PYK2 inhibitor, with an IC50 of 637 nM. It may be suitable for the research of osteoporosis, craniofacial and appendicular skeletal defects, and for targeted bone regeneration.
- Potent and selective PYK2 inhibitor with an IC50 of 637 nM.
- Promotes osteogenesis of hMSC cultures, increasing alkaline phosphatase (ALP) activity and mineralization.
- Enhances osteoblast proliferation.
- Enhances calcium deposition.
- Increases cell proliferation activity in murine bone marrow-derived mesenchymal stem cells (BMSC).
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Medchemexpress LLC Cadrofloxacin 10mg | 153808-85-6 | 411.38 g·mol^-1 | C19H20F3N3O4 | 10 MG
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Cadrofloxacin is a fluoroquinolone antibiotic research compound supplied as a white to off-white solid for laboratory use. It is intended for antibacterial and anti-infection research and is provided with supporting documentation for safe handling and characterization.
- Fluoroquinolone antibiotic used for antibacterial research.
- High purity suitable for analytical and experimental work.
- White to off-white solid powder, convenient for dissolution or formulation.
- Stable when stored frozen as recommended for long-term storage.
- Available with data sheet, certificate of analysis, and safety data sheet.
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Medchemexpress LLC EPQpYEEIPIYL | 147612-86-0 | 99.5% | 1473.52 | 5 MG
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EPQpYEEIPIYL, a phosphopeptide, is a Src homology 2 (SH2) domain ligand. It activates Src family members (e.g. Lck, Hck, Fyn) by binding to SH2 domains.
- Phosphopeptide and Src homology 2 (SH2) domain ligand
- Activates Src family members (e.g., Lck, Hck, Fyn)
- Binds to SH2 domains
- Exhibits highest affinity binding to GST fusion proteins of Lck SH2 domain and Src SH2 domain
- Target: Src
- Pathway: Protein Tyrosine Kinase/RTK
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Medchemexpress LLC HY-B2187 100mg Medchemexpress, Diacetazotol CAS:83-63-6 Purity:>98%
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Medchemexpress, HY-B2187 100mg Diacetazotol CAS:83-63-6 Diacetazotol inhibits dioxin-induced ethoxyresorufin-O-deethylase ( EROD ) activity with IC 50 of 75±4 nM. Diacetazotol extracts from patent US20070032458, compound 3. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC 2-(3-oxo-1-phenyl-3-(4-(trifluoromethyl)phenyl)propyl)malonic acid | 1221962-86-2 | 98.0% | 100 MG
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PS210 is a selective small-molecule activator of 3-phosphoinositide-dependent protein kinase-1 (PDK1), reported to bind the PIF-binding pocket with a Kd of approximately 3 μM. It is supplied as a high-purity research reagent available as solid packs and as a 10 mM solution in DMSO.
- Selective activation of PDK1, reported Kd ≈ 3 μM.
- High purity suitable for biochemical and cellular research.
- Available as solids (1 mg-500 mg) and 10 mM solution in DMSO.
- Stable as powder at -20°C for up to 3 years.
- Molecular formula C19H15F3O5, molecular weight 380.31 g/mol.
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Medchemexpress LLC FzM1.8 | 322.3 g/mol | C18H14N2O4 | 10MG
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FzM1 8 derives from FzM1 is an allosteric agonist of FZD4 with pEC50 of 6 4 FzM1 8 binds to FZD4 and activates the WNT/ -catenin pathway by promoting TCF/LEF transcriptional activity in the absence of any WNT ligand FzM1 8 stabilizes FZD4 with an increased affinity for heterotrimeric G protein and stimulates the release of the G subunit that in turn activates PI3K[1]
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Medchemexpress LLC D5D-IN-326 | 1236767-85-3 | 99.9% | 473.27 | C17H11F8N3O4 | 10 MG
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D5D-IN-326 is a selective, orally active delta-5 desaturase (D5D) inhibitor used in preclinical research. It demonstrates low-nanomolar potency in enzymatic and cell-based assays and has been reported to improve metabolic parameters in diet-induced obese mice. Documentation typically includes a product datasheet, certificate of analysis, and safety data sheet.
- Selective delta-5 desaturase inhibition with low-nanomolar potency.
- Demonstrated activity in enzymatic and cell-based assays.
- Reduces insulin resistance and body weight in preclinical mouse models.
- High purity (99.9% by LC-MS) confirmed by certificate of analysis.
- Supplied as a small-molecule research reagent with supporting documentation for reproducibility.
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Medchemexpress LLC Cadrofloxacin 5mg | 153808-85-6 | 411.38 g·mol⁻1 | C19H20F3N3O4 | 5 MG
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Cadrofloxacin is a fluoroquinolone antibiotic supplied for research use. It is provided as a solid for experimental assays, with manufacturer guidance for solubilization and storage to preserve activity.
- Purity 98.21% as reported by the manufacturer.
- Molecular weight 411.38 g·mol⁻1.
- Soluble in DMSO at about 10 mg/mL with warming and pH adjustment.
- Store powder at -20°C for long-term stability; aliquot solutions to avoid freeze-thaw cycles.
- Suitable for in vitro antibacterial research and assay development.
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eMolecules 2184-85-2 | Ambeed | 2-(2-Chlorophenyl)propanoic acid | 250mg | 552668940 | A239275 | MFCD06658208 | 184.62 | C9H9ClO2
Medchem Express | Daucosterol | 5mg | 446275027 | HY-N0410 | 474-58-8 | MFCD01683621 | 576.859 | C35H60O6
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eMolecules ChemScene / 1-(2-Isopropoxypyridin-3-yl)ethanone / 100mg / 582634293 / CS-0042760 / 0.000 / 1551553-85-5 / MFCD27974420 / 179.219 / C10H13NO2
ChemScene / 1-(2-Isopropoxypyridin-3-yl)ethanone / 100mg / 582634293 / CS-0042760 / 0.000 / 1551553-85-5 / MFCD27974420 / 179.219 / C10H13NO2
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eMolecules 22047-86-5 | Ambeed | 46-Dimethylnicotinic acid | 250mg | 552576485 | A140498 | MFCD00234424 | 151.165 | C8H9NO2
Medchem Express | 734-Trihydroxyisoflavone | 25mg | 761506235 | HY-124953 | 485-63-2 | MFCD00143002 | 270.240 | C15H10O5
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Medchemexpress LLC 2-([1,4'-bipiperidin]-1'-yl)-N-cycloheptyl-6,7-dimethoxyquinazolin-4-amine | 864289-85-0 | 100.0% | 467.65 g/mol | C27H41N5O2 | 100 MG
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C-021 is a small-molecule CCR4 antagonist developed for research applications in immunology and receptor pharmacology. It is provided as a solid powder with high purity and is used in biochemical assays and functional chemotaxis studies.
- Potent CCR4 antagonist with nanomolar activity.
- High purity suitable for biochemical and cellular assays.
- Supplied as a solid powder for flexible formulation.
- Stable when stored under recommended conditions.
- Appropriate for in vitro and in vivo pharmacology studies.
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Sigma Aldrich Fine Chemicals Biosciences Chrysoidine G for microscopy (Bact., Bot., Vit.) | 532-82-1 | MFCD00012976 | 25G
Chrysoidine G for microscopy (Bact., Bot., Vit.) | Mol Wt: 248.71 | 532-82-1 | MFCD00012976 | 25G
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eMolecules ChemScene / 4-Nitropiperidine hydrochloride / 100mg / 603128780 / CS-0162514 / 0.000 / 1881295-85-7 / MFCD29043359 / 166.610 / C5H11ClN2O2
ChemScene / 4-Nitropiperidine hydrochloride / 100mg / 603128780 / CS-0162514 / 0.000 / 1881295-85-7 / MFCD29043359 / 166.610 / C5H11ClN2O2
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eMolecules 104691-86-3 | Medchem Express | Lupiwighteone | 5mg | 705861611 | HY-N3354 | MFCD06796683 | 338.359 | C20H18O5
Ambeed | 5-(Bromomethyl)-2-(trifluoromethyl)pyridine | 250mg | 602852497 | A793147 | 108274-33-5 | MFCD10697684 | 240.023 | C7H5BrF3N
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