Unsubstituted Phenols
Medchemexpress LLC HY-N0001 100mg , (-)-Epicatechin (-)-Epicatechol;Epicatechin;epi-Catechin CAS:490-46-0 Purity:98%
Medchemexpress, HY-N0001 100mg (-)-Epicatechin (-)-Epicatechol;Epicatechin;epi-Catechin CAS:490-46-0 Formula:C15H14O6 IC50: 3.2 μM (COX-1) Purity:98% (-)-Epicatechin inhibits cyclooxygenase-1 ( COX-1 ) with an IC 50 of 3.2 μM. (-)-Epicatechin inhibits the IL-1β-induced expression of iNOS by blocking the nuclear localization of the p65 subunit of NF-κB. 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.
Sigma Aldrich Fine Chemicals Biosciences Phenol Red powder BioReage25G
PHENOL2 Phenol Red powder BioReage25G
Medchemexpress LLC Honokiol dichloroacetate | 1620160-42-0 | 99.1% | 488.19 g/mol | C22H18Cl4O4 | 25MG
Honokiol DCA (honokiol dichloroacetate) is a dichloroacetate derivative of honokiol supplied as a high-purity research compound. It has been reported to inhibit the growth of human prostate cancer cells in vitro and to suppress androgen receptor protein levels. The material is a colorless to light yellow liquid with molecular formula C22H18Cl4O4 and molecular weight 488.19 g/mol. Recommended storage is solid at -20°C and in solvent at -80°C for longer-term storage.
![Medchemexpress LLC N-[5-amino-1,2,3,4-tetrahydro-1-[4-(trifluoromethyl)phenyl]-3-quinolinyl]-2-propenamide | 2766575-48-6 | MFCD22417285 | 99.8% | 361.36 | C19H18F3N3O | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000285876.png-250.jpg)
Medchemexpress LLC N-[5-amino-1,2,3,4-tetrahydro-1-[4-(trifluoromethyl)phenyl]-3-quinolinyl]-2-propenamide | 2766575-48-6 | MFCD22417285 | 99.8% | 361.36 | C19H18F3N3O | 10 MG
SWTX-143 is a covalent, irreversible inhibitor of the YAP/TAZ-TEAD transcriptional complex developed for research. It binds the palmitoylation pocket of TEAD isoforms and suppresses YAP/TAZ-TEAD transcriptional activity, and has demonstrated oral activity in preclinical studies. The compound is supplied as a high-purity solid intended for biochemical and cell-based research applications.
- Covalent, irreversible inhibitor of YAP/TAZ-TEAD.
- Binds the palmitoylation pocket of TEAD isoforms.
- Inhibits YAP/TAZ-TEAD transcriptional activity.
- Demonstrated oral activity in preclinical studies.
- High reported purity (about 99.8%).
- Supplied as a white to off-white solid.
- Available in milligram-scale packages for laboratory research.
- Suitable for biochemical and cell-based assays.
Medchemexpress LLC (+)-Tyrphostin B44 (Tyrphostin AG 835) | 133550-37-5 | MFCD00209855 | 97.0% | 308.33 g/mol | C18H16N2O3 | 5 MG
(+)-Tyrphostin B44 (Tyrphostin AG 835) is a small-molecule research compound that acts as an epidermal growth factor receptor (EGFR) inhibitor and has reported antitumor activity. It is provided as a high-purity solid intended for in-vitro and preclinical research, with recommended storage conditions for powder and solutions to maintain stability.
- EGFR inhibitor with reported antitumor activity.
- High purity (97.04%) suitable for research applications.
- Solid powder form for accurate weighing and formulation.
- Recommended storage: powder at -20°C for long term or 4°C for short term.
- Molecular weight 308.33 g/mol; formula C18H16N2O3.
![eMolecules Medchem Express / 6-Hydroxymelatonin / 5mg / 482204684 / HY-W011956 / / 2208-41-5 / [null] / 248.282 / C13H16N2O3](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502469158.JPG-250.jpg)
eMolecules Medchem Express / 6-Hydroxymelatonin / 5mg / 482204684 / HY-W011956 / / 2208-41-5 / [null] / 248.282 / C13H16N2O3
Medchem Express / 6-Hydroxymelatonin / 5mg / 482204684 / HY-W011956 / / 2208-41-5 / [null] / 248.282 / C13H16N2O3
eMolecules Medchem Express / Isoquercitrin / 10mg / 446275352 / HY-N0768 / / 21637-25-2 / MFCD29050128 / 464.379 / C21H20O12
Medchem Express / Isoquercitrin / 10mg / 446275352 / HY-N0768 / / 21637-25-2 / MFCD29050128 / 464.379 / C21H20O12
Sigma Aldrich Fine Chemicals Biosciences Salidroside >=95% (LC/MS-ELSD) | 10338-51-9 | MFCD00210553 | 1MG
Salidroside >=95% (LC/MS-ELSD) | Purity: >=95% (LC/MS-ELSD) | Mol Wt: 300.3 | 10338-51-9 | MFCD00210553 | 1MG
STA PHARMACEUTICAL US LLC Fmoc-(S)-3-Amino-4-(2,4-dichloro-phenyl)-butyric acid | 1 g | CAS 270063-49-5 | MDL MFCD01861045
Fmoc-(S)-3-Amino-4-(2,4-dichloro-phenyl)-butyric acid is a Amino Acid reagent (Subcategory: Beta AA) sold by WuXi TIDES. Offered in 1 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 270063-49-5
- MDL: MFCD01861045
- InChIKey: UAGBOWBNDBDJMF-KRWDZBQOSA-N
- Molecular Weight: 470.346
- Molecular Formula: C25H21Cl2NO4
- Purity: ≥95%
- Container Type: 15 mL HDPE
- Pack Size: 1 g
- Net Weight: 1 g
- Gross Weight: 7.8 g
- Commodity Code: 29242970
- Country Of Origin: China
- IUPAC: (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(2,4-dichlorophenyl)butanoic acid
- SMILES: ClC1=CC(Cl)=C(C[C@H](NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)CC(O)=O)C=C1
Medchemexpress LLC Combretastatin A-1 | 109971-63-3 | 97.0% | 25 MG
Combretastatin A-1 is a small-molecule microtubule polymerization inhibitor that binds the colchicine-binding site on tubulin, leading to tubulin depolymerization, AKT deactivation, and inhibition of the Wnt/β-catenin signaling pathway. Supplied for research use only.
- Microtubule polymerization inhibitor that targets the colchicine-binding site on tubulin.
- Inhibits Wnt/β-catenin signaling via tubulin depolymerization-mediated AKT deactivation.
- High purity (97.0%) suitable for research and analytical applications.
- Available as solid and DMSO solution formats, including 25 MG solid pack sizes.
- Molecular formula C18H20O6 and molecular weight 332.35 g·mol⁻1.