Phenoxy compounds
2-Chlorophenyl Trifluoromethanesulfonate 97.0+%, TCI America™
CAS: 66107-36-6 Molecular Formula: C7H4ClF3O3S Molecular Weight (g/mol): 260.611 MDL Number: MFCD07784322 InChI Key: KTLNEJOQAOFUTO-UHFFFAOYSA-N Synonym: Trifluoromethanesulfonic Acid 2-Chlorophenyl Ester, 2-Chlorophenyl Triflate PubChem CID: 581421 IUPAC Name: (2-chlorophenyl) trifluoromethanesulfonate SMILES: C1=CC=C(C(=C1)OS(=O)(=O)C(F)(F)F)Cl
Medchemexpress LLC Emvododstat (PTC299) | 1256565-36-2 | 99.9% | 467.34 g/mol | C25H20Cl2N2O3 | 50MG
PTC299 (emvododstat) is an orally active small-molecule inhibitor that selectively suppresses VEGFA mRNA translation and inhibits dihydroorotate dehydrogenase (DHODH). Provided for research use, it is supplied as solid samples and DMSO solutions and is used in studies of VEGF regulation, pyrimidine biosynthesis, and oncology and immunology research.
- High purity: 99.9% by assay.
- Molecular weight: 467.34 g/mol.
- Chemical formula: C25H20Cl2N2O3.
- Physical appearance: white to light yellow solid.
- Available as solid and as 10 mM solution in DMSO.
- Suitable for studies of VEGF regulation and DHODH-related pathways.
- Offered in multiple package sizes including 50 mg.
Medchemexpress LLC Emvododstat | 1256565-36-2 | 99.9% | 467.34 g·mol-1 | C25H20Cl2N2O3 | 10MG
PTC299 (Emvododstat) is a small-molecule research inhibitor that suppresses vascular endothelial growth factor (VEGF) protein translation and inhibits dihydroorotate dehydrogenase (DHODH). Supplied as a 10 mg powder with high reported purity, it is intended for laboratory research use and includes specified storage recommendations. CAS 1256565-36-2; molecular formula C25H20Cl2N2O3; molecular weight 467.34 g·mol-1.
- Inhibits VEGF protein translation and DHODH activity.
- High reported purity suitable for research use.
- Provided as a 10 mg powder for laboratory applications.
- Recommended storage: powder -20°C (up to 3 years) or 4°C (up to 2 years).
- Includes CAS identifier for unambiguous compound tracking.
eMolecules AstaTech / 4-TERT-BUTOXYANILINE / 0.25g / 721956548 / AB10504 / 95.000 / 57120-36-2 / MFCD11196184 / 165.236 / C10H15NO
AstaTech / 4-TERT-BUTOXYANILINE / 0.25g / 721956548 / AB10504 / 95.000 / 57120-36-2 / MFCD11196184 / 165.236 / C10H15NO
Selleck Chemical LLC Agerafenib
Agerafenib (CEP-32496) is a highly potent inhibitor of BRAF(V600E/WT) and c-Raf with Kd of 14 nM/36 nM and 39 nM also potent to Abl-1 c-Kit Ret (c-Ret) PDGFR and VEGFR2 respectively insignificant affinity for MEK-1 MEK-2 ERK-1 and ERK-2 Phase 1/2
Medchemexpress LLC HY-103318 2mg Medchemexpress, PD173212 CAS:217171-01-2 Purity:>98%
Medchemexpress, HY-103318 2mg PD173212 CAS:217171-01-2 PD173212 is a selective N-type voltage sensitive calcium channel (VSCC) blocker, with an IC50 of 36 nM in IMR-32 assays. 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.
Medchemexpress LLC HY-U00422 5mg Medchemexpress, K-756 CAS:130017-40-2 Purity:>98%
Medchemexpress, HY-U00422 5mg K-756 CAS:130017-40-2 K-756 is a direct and selective tankyrase ( TNKS ) inhibitor, which inhibits the ADP-ribosylation activity of TNKS1 and TNKS2 with IC 50 s of 31 and 36 nM, respectively. 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.
Medchemexpress LLC Gne-371 | 1926986-36-8 | 98.2% | 431.5 g/mol | C24H25N5O3 | 5 MG
GNE-371 is a potent, selective chemical probe that targets the second bromodomain of human transcription-initiation factor TFIID subunit 1 (TAF1). It is provided as a research-grade small molecule for biochemical and cellular assays with reported low-nanomolar activity against TAF1(2).
- Potent, selective TAF1(2) bromodomain inhibitor with IC50 ≈ 10 nM.
- Suitable as a chemical probe for biochemical and cellular studies.
- High purity (98.2%).
- Molecular formula C24H25N5O3.
- Molecular weight 431.5 g/mol.
- CAS number 1926986-36-8.
- Soluble in DMSO for assay preparation.
![Medchemexpress LLC β-[4-([4-methyl-2-(4-(trifluoromethyl)phenyl)-5-thiazolyl]methoxy)phenyl]-3-isoxazolepropanoic acid | 1011531-27-3 | 99.0% | 488.48 | C24H19F3N2O4S | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000238246.png-250.jpg)
Medchemexpress LLC β-[4-([4-methyl-2-(4-(trifluoromethyl)phenyl)-5-thiazolyl]methoxy)phenyl]-3-isoxazolepropanoic acid | 1011531-27-3 | 99.0% | 488.48 | C24H19F3N2O4S | 10MG
AM-4668 is a research-grade small-molecule agonist of GPR40 (FFAR1) used in preclinical studies relevant to type 2 diabetes. It activates human GPR40 with low-nanomolar potency in cell-based functional assays and is supplied as a solid for in vitro pharmacology and biochemical studies.
- Low-nanomolar potency at GPR40 (EC50 3.6 nM in A9 cells, 36 nM in CHO cells).
- Suitable for in vitro receptor activation and pharmacology studies.
- High purity solid (99.0%).
- Molecular weight 488.48 and formula C24H19F3N2O4S.
- Available in milligram quantities for laboratory use.
Medchemexpress LLC HY-W002304 100mg Medchemexpress, (R)-5-Oxopyrrolidine-2-carboxylic acid CAS:4042-36-8 Purity:>98%
Medchemexpress, HY-W001080 100mg 3,4-Dihydroxybenzeneacetic acid CAS:102-32-9 3,4-Dihydroxybenzeneacetic acid is the main neuronal metabolite of dopamine. 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.