Phenols
Medchemexpress LLC RS 67333 hydrochloride | 168986-60-5 | 99.7% | 389.36 g/mol | C19H30Cl2N2O2 | 50 MG
RS 67333 hydrochloride is the hydrochloride salt of a selective partial agonist of the 5-HT4 (serotonin) receptor. Supplied as a solid research reagent, it is used in neuroscience studies of 5-HT4 receptor pharmacology, neuroprotection, and related pathways. For research use only.
- Selective partial agonist of 5-HT4 receptor.
- High purity (99.7%).
- Supplied as a solid suitable for in vitro and in vivo studies.
- Stable when stored sealed at 4°C, away from moisture.
- Available in small laboratory quantities for research applications.
Medchemexpress LLC 4-(3-chloro-4-cyanophenyl)-2-(2-((1R,2R)-2-hydroxy-2-methylcyclopropyl)amino)pyrimidi. | 1610677-37-6 | 99.6% | 535.04 g·mol⁻1 | C28H31ClN6O3 | 1 ML
Luvixasertib hydrochloride is a potent, selective inhibitor of the TTK/Mps1 kinase with low-nanomolar biochemical potency and demonstrated in vitro anticancer activity. Supplied as the hydrochloride salt in a ready-to-use 10 mM DMSO solution, it is intended for preclinical kinase assays and cellular studies probing mitotic checkpoint biology.
- High potency: IC50 1.7 nM for TTK in vitro.
- Hydrochloride salt suitable for formulation and storage.
- Provided as a 10 mM solution in DMSO, 1 mL ready to use.
- High purity (99.63% by supplier analysis).
- Well characterized: CAS 1610677-37-6; molecular weight 535.04 g·mol⁻1.
- Applications: preclinical kinase inhibition and cellular mitotic checkpoint studies.
eMolecules Fenretinide | 65646-68-6 | MFCD00792674 | 100mg
Apollo Scientific | Fenretinide | 100mg | 562460510 | BIFK0053 | 99.000 | 65646-68-6 | MFCD00792674 | 391.555 | C26H33NO2
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Medchemexpress LLC Luvixasertib hydrochloride | 1610677-37-6 | 99.6% | 535.04 g/mol | C28H31ClN6O3 | 50 MG
Luvixasertib hydrochloride is a selective, orally bioavailable small-molecule inhibitor of TTK/Mps1 used for preclinical research. It inhibits TTK/Mps1 with an in vitro IC50 of 1.7 nM and has demonstrated anticancer activity in cell-based studies.
- Selective TTK/Mps1 inhibition with IC50 of 1.7 nM.
- Orally bioavailable scaffold suitable for in vivo studies.
- Hydrochloride salt form improves solubility and handling.
- High reported purity (≈99.6%) for research reproducibility.
- Supplied in small research quantities for assay development and compound characterization.
Cambridge Isotope Laboratories 4-Isopropyl-3-methylphenol (isopropyl-13C3 99%) 100 ug/mL in methanol 1 2 mL
4-Isopropyl-3-methylphenol (isopropyl-13C3 99%) 100 ug/mL in methanol 1 2 mL
Cambridge Isotope Laboratories Acetaminophen (ring-13C6 98%) 1 mg
Acetaminophen (ring-13C6 98%) 1 mg
Medchemexpress LLC AFM-30a hydrochloride | 99.8% | 502.97 | 100 MG
AFM-30a hydrochloride is a potent and selective protein arginine deiminase 2 (PAD2) inhibitor. It binds to PAD2 with an EC50 value of 9.5 μM and inhibits H3 citrullination with an EC50 value of 0.4 μM. This compound is suitable for research into certain cancers and various autoimmune diseases, including rheumatoid arthritis (RA), multiple sclerosis, lupus, and ulcerative colitis.
- Exhibits high potency and selectivity for PAD2.
- Effectively inhibits H3 citrullination.
- Has shown low cytotoxicity in HEK293T/PAD2 cells.
- Can suppress NLRP3 signaling, decreasing airway remodeling in PAD2-/- transgenic mice.
Medchemexpress LLC HIF-1α-IN-2 hydrochloride | 98.1% | 397.92 | 10 MG
HIF-1α-IN-2 hydrochloride is an effective HIF-1α inhibitor with anticancer potencies (IC50s of 28 nM and 15 nM in MDA-MB-231 and MiaPaCa-2 cells, respectively). It suppresses HIF-1α expression by blocking transcription and protein translation.
- Effective HIF-1α inhibitor
- Suppresses HIF-1α expression by blocking transcription and protein translation
- Anticancer potencies (IC50s of 28 nM and 15 nM in MDA-MB-231 and MiaPaCa-2 cells)
Cambridge Isotope Laboratories 440mL Lecture bottle CGA 580 packless brass angle ea
440mL Lecture bottle CGA 580 packless brass angle ea
Cayman Chemical JWH 073 N 3hydroxybutyl meta
Expected product of the metabolism of JWH 073 by human liver microsomes in vitro, generated by the oxidation of the aminoalkyl chain; biological actions are unknown; intended for research and forensic applications