Pyrroles
=O)C(O)=O.CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C | 500mg | 376013295](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000130328.jpg-250.jpg)
eMolecules 341031-54-7 | Sunitinib Malate | Target Molecule | MFCD08282795 | 532.569 | C26H33FN4O7 | 0.000 | O[C@@H](CC(O)=O)C(O)=O.CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C | 500mg | 376013295
Sunitinib Malate | Target Molecule | 341031-54-7 | MFCD08282795 | 532.569 | C26H33FN4O7 | 0.000 | O[C@@H](CC(O)=O)C(O)=O.CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C | 500mg | 376013295
Medchemexpress LLC (3S,5S)-atorvastatin | 501121-34-2 | MFCD09839951 | 95.0% | 558.64 g/mol | C33H35FN2O5 | 10 MG
(3S,5S)-atorvastatin is the inactive stereoisomer of atorvastatin provided for research use. It is reported to act as a pregnane X receptor (PXR) agonist and is used in pharmacology and metabolic-disease studies. Supplied as a high-purity solid for in vitro and analytical applications.
- Inactive enantiomer of atorvastatin
- Acts as pregnane X receptor (PXR) agonist
- Supplied with reported purity of 95.0%
- Available in a 10 mg quantity for laboratory use
- Suitable for in vitro and analytical research; not for human use
Medchemexpress LLC (S)-bromoenol lactone | 478288-94-7 | 99.1% | 1 MG
(S)-Bromoenol lactone is a chiral, mechanism-based irreversible inhibitor of calcium-independent phospholipase A2β (iPLA2β) used in biochemical and cellular research to investigate arachidonate release pathways. The compound is supplied at high purity as a solution and is typically stored at -20°C for long-term stability.
- Irreversible inhibitor of calcium-independent phospholipase A2β (iPLA2β)
- Reported activity: IC50 ≈ 2 μM for vasopressin-induced arachidonate release in A10 cells
- Molecular weight 317.18 g/mol; formula C16H13BrO2
- Purity 99.1%
- Storage: solution at -20°C; stable for about 2 years
Medchemexpress LLC Antalarmin hydrochloride | 220953-69-5 | MFCD05664721 | 99.9% | 415.01 g·mol⁻¹ | C24H35ClN4 | 5 MG
Antalarmin hydrochloride is the hydrochloride salt of antalarmin, a non-peptide corticotropin-releasing hormone receptor 1 (CRHR1) antagonist used in research to block CRH-induced ACTH secretion and study stress- and anxiety-related pathways. It is supplied as a solid powder with high purity and provided for in vitro and in vivo experimental applications.
- Non-peptide CRHR1 antagonist for research use.
- Purity: 99.87%.
- Molecular weight: 415.01 g·mol⁻¹.
- Physical form: white to light yellow solid powder.
- Storage: store solid at -20°C; in solution, -80°C for up to 6 months.
- Solubility: soluble in DMSO (≈125 mg/mL), DMF, and ethanol; follow vehicle recommendations for in vivo use.
- Supplied in a 5 mg pack for small-scale research studies.
Medchemexpress LLC Pha-665752 | 477575-56-7 | MFCD18632554; MFCD07772270 | 99.9% | 641.61 g/mol | C32H34Cl2N4O4S | 5 MG
PHA-665752 is a selective, ATP-competitive inhibitor of the c-Met (HGFR) receptor tyrosine kinase used in preclinical research to induce apoptosis, cause cell-cycle arrest, and reduce tumor growth in vitro and in vivo. It demonstrates high potency and selectivity versus other kinases and is supplied for research use only.
- Selective ATP-competitive c-Met inhibitor with Ki ≈ 4 nM and IC50 ≈ 9 nM.
- High purity solid (approximately 99.9%) suitable for biochemical assays.
- Molecular formula C32H34Cl2N4O4S; molecular weight 641.61 g/mol.
- Storage: powder at -20°C for long term; in solution store at -80°C when possible.
- Supplied in small preweighed milligram quantities for laboratory research.