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Filtered Search Results
Medchemexpress LLC MPT0G211 | 2151853-97-1 | 99.8% | 293.32 g/mol | C17H15N3O2 | 50MG
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MPT0G211 is a potent, orally active, and selective histone deacetylase 6 (HDAC6) inhibitor used in preclinical research. It penetrates the blood-brain barrier and has demonstrated neuroprotective effects, reduction of tau phosphorylation, and anticancer/anti-metastatic activity in published models.
- Potent HDAC6 inhibitor (IC50 = 0.291 nM)
- Highly selective for HDAC6 (>1,000-fold vs other HDAC isoforms)
- Orally active and brain-penetrant
- Demonstrated neuroprotective effects and reduced tau phosphorylation in preclinical models
- Shows anticancer and anti-metastatic activity in preclinical studies
- High purity for research use (99.79%)
- Molecular formula C17H15N3O2; molecular weight 293.32 g/mol
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eMolecules 173054-11-0 | Ambeed | (R)-3-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid | 1g | 552688526 | A275618 | MFCD00151888 | 502.567 | C29H30N2O6
Medchem Express | Sincalide | 1mg | 446275846 | HY-P0093 | 25126-32-3 | MFCD00079849 | 1143.270 | C49H62N10O16S3
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![eMolecules 4382-54-1 | 5-Methoxyindole-2-carboxylic acid | Ambeed | MFCD00005614 | 191.186 | C10H9NO3 | 97.000 | COc1ccc2[nH]c(cc2c1)C(O)=O | 250mg | 552628484](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502419512.JPG-250.jpg)
eMolecules 4382-54-1 | 5-Methoxyindole-2-carboxylic acid | Ambeed | MFCD00005614 | 191.186 | C10H9NO3 | 97.000 | COc1ccc2[nH]c(cc2c1)C(O)=O | 250mg | 552628484
5-Methoxyindole-2-carboxylic acid | Ambeed | 4382-54-1 | MFCD00005614 | 191.186 | C10H9NO3 | 97.000 | COc1ccc2[nH]c(cc2c1)C(O)=O | 250mg | 552628484
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Medchemexpress LLC Metronidazole | 443-48-1 | 50 G
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Metronidazole is an orally active nitroimidazole antibiotic that can cross the blood-brain barrier. It is used for the research of anaerobic infections.
- Orally active nitroimidazole antibiotic
- Crosses the blood-brain barrier
- Used for research of anaerobic infections
- Inhibits anaerobic protozoa (Trichomonas vaginalis, Entamoeba histolytica, Giardia lamblia, Balantidium coli)
- Inhibits anaerobic bacteria and demonstrates good bactericidal activity (4-8 μg/mL)
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Medchemexpress LLC Sulfadimethoxine (Standard) | 122-11-2 | 99.86% | 50 MG
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Sulfadimethoxine (Standard) is the analytical standard of Sulfadimethoxine, a sulfonamide antibiotic used to treat various infections. This product is intended solely for research and analytical applications.
- Serves as a reference standard for assays.
- Used in qualitative, quantitative, and methodological research experiments.
- Applicable for techniques such as HPLC, GC, and MS.
- For research use only.
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Medchemexpress LLC N-hydroxy-4-((quinolin-8-ylamino)methyl)benzamide | 2151853-97-1 | 99.8% | 293.32 g·mol-1 | C17H15N3O2 | 10MG
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MPT0G211 is a potent, orally active, and selective HDAC6 inhibitor intended for preclinical research applications. It is used in biochemical and cellular studies to probe HDAC6-related pathways relevant to neurodegeneration and oncology, and is characterized by sub-nanomolar potency and high chemical purity.
- Selective HDAC6 inhibition (IC50 0.291 nM).
- Sub-nanomolar potency suitable for biochemical assays.
- High purity, 99.8%.
- Suitable for in vitro and in vivo preclinical studies.
- Soluble in DMSO for stock solution preparation.
- Available in small research pack sizes for screening and confirmation studies.
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eMolecules 1741-41-9 | Isobutyraldehyde diethyl acetal | MFCD00059384 | 25g
Ambeed | 3-Iodo-5-nitropyridin-2-ol | 5g | 490528038 | A188069 | 25391-58-6 | MFCD06008303 | 265.994 | C5H3IN2O3
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Medchemexpress LLC JAB-3068 hydrochloride | 2169223-49-6 | 98.9% | 50 MG
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JAB-3068 hydrochloride (SHP2-IN-6 hydrochloride) is a potent SHP2 inhibitor with an IC50 of 25.8 nM. It inhibits the proliferation of KYSE-520 cells with an IC50 of 2.17 μM. This compound is a solid with a light yellow to yellow appearance and a molecular weight of 513.00.
- Potent SHP2 inhibitor
- Inhibits proliferation of KYSE-520 cells
- Molecular weight: 513.00
- Chemical formula: C22H27ClF2N6O2S
- Appearance: Solid
- Color: Light yellow to yellow
- Solubility in DMSO: 115 mg/mL (224.17 mM)
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Medchemexpress LLC Cyanidin-3-O-galactoside chloride | 27661-36-5 | 5 MG
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Cyanidin-3-O-galactoside chloride is a component derived from the extract peel of hawthorn fruit (EPHF), demonstrating potent Acetylcholinesterase (AChE) inhibitory activity.
- Exhibits strong antioxidant activity
- Shows potent acetylcholinesterase (AChE) inhibitory activity
- Displays high cytotoxicity against human tumor cell lines MCF-7 and SKOV-3
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eMolecules 926307-97-3 | ChemScene | 5-(Hydroxymethyl)isoindolin-1-one | 25mg | 801476250 | CS-0149655 | MFCD13177814 | 163.176 | C9H9NO2
ChemScene | 5-(Hydroxymethyl)isoindolin-1-one | 25mg | 801476250 | CS-0149655 | 926307-97-3 | MFCD13177814 | 163.176 | C9H9NO2
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eMolecules 683219-94-5 | 4-(9H-Fluoren-9-ylmethoxycarbonylamino)-4-phenyl-butyric acid | J&W PharmLab LLC | MFCD03412511 | 401.462 | C25H23NO4 | 96.000 | OC(=O)CCC(NC(=O)OCC1c2ccccc2-c2ccccc12)c1ccccc1 | 500mg | 773119686
4-(9H-Fluoren-9-ylmethoxycarbonylamino)-4-phenyl-butyric acid | J&W PharmLab LLC | 683219-94-5 | MFCD03412511 | 401.462 | C25H23NO4 | 96.000 | OC(=O)CCC(NC(=O)OCC1c2ccccc2-c2ccccc12)c1ccccc1 | 500mg | 773119686
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eMolecules 154471-65-5 | Ambeed | 1-Methyl-3-(trifluoromethyl)-1H-pyrazole | 1g | 552700633 | A305600 | MFCD00179867 | 150.104 | C5H5F3N2
ChemScene | (4-Morpholinophenyl)methanamine | 250mg | 441661635 | CS-0035444 | 214759-74-7 | MFCD02682050 | 192.262 | C11H16N2O
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Medchemexpress LLC Fenpropimorph | 67564-91-4 | 98.7% | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Fenpropimorph is a fungicide that operates by inhibiting the sterol pathway. It blocks δ8-δ7-sterol isomerase at lower concentrations and δ14-sterol reductase at higher concentrations in yeast, which prevents ergosterol biosynthesis. Fenpropimorph also has an inhibitory effect on sterol synthesis in certain plants and mammalian cells.
- Inhibits the sterol pathway
- Blocks delta8-delta7-sterol isomerase
- Blocks delta14-sterol reductase
- Prevents ergosterol biosynthesis
- Inhibits sterol synthesis in plants
- Inhibits sterol synthesis in mammalian cells
- For research use only
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Medchemexpress LLC Gozanertinib | 1226549-49-0 | 98.4% | 50 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Gozanertinib is an orally active furanopyrimidine-based EGFR inhibitor with IC50s of 15 nM for EGFRWT and 48 nM for EGFRL858R/T790M. It can occupy the ATP-binding site and demonstrates significant antitumor efficacy. This compound is intended for research use only.
- Orally active EGFR inhibitor
- IC50 of 15 nM for EGFRWT
- IC50 of 48 nM for EGFRL858R/T790M
- Occupies ATP-binding site
- Demonstrates significant antitumor efficacy
- Molecular weight: 533.62
- Formula: C32H31N5O3
- Appearance: solid, off-white to light yellow
- Inhibits HCC827, H1975, and A431 cell lines
- Reduces phosphorylated EGFR in a dose-dependent manner
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![Sigma Aldrich Fine Chemicals Biosciences Benzo[a]fluoranthene BCR(R), certified reference material | 203-33-8 | MFCD00215890 | 100MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/501762349.PNG-250.jpg)
Sigma Aldrich Fine Chemicals Biosciences Benzo[a]fluoranthene BCR(R), certified reference material | 203-33-8 | MFCD00215890 | 100MG
Benzo[a]fluoranthene BCR(R), certified reference material | Mol Wt: 252.31 | 203-33-8 | MFCD00215890 | 100MG
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