Acrylic acids and derivatives
Sigma Aldrich Fine Chemicals Biosciences Cefepime hydrochloride | 123171-59-5 | 100MG
Cefepime hydrochloride | Mol Wt: 571.5 | 123171-59-5 | 100MG
Medchemexpress LLC N-(3-chloro-4-methylphenyl)-3-(3-((1-(2,6-dioxopiperidin-3-yl)-2,5-dioxo-2,5-dihydro-1H- | 2438124-79-7 | 98.6% | 494.93 g/mol | C25H23ClN4O5 | 5 MG
ALV1 is a small-molecule molecular glue degrader that induces proteasomal degradation of Ikaros (IKZF1) and Helios (IKZF2) via binding to cereblon (CRBN). It is supplied as a high-purity solid for research use.
- Potent degrader of Ikaros and Helios (DC50 2.5 nM and 10.3 nM, respectively).
- Binds cereblon with IC50 of 0.55 μM.
- High purity solid, light yellow to green-yellow appearance.
- Soluble in DMSO (50 mg/mL); in vivo formulation examples available.
- Stable when stored as powder at -20°C (3 years) or 4°C (2 years).
Medchemexpress LLC HY-15232B 100mg Medchemexpress, GS-7340 (hemifumarate) Tenofovir alafenamide hemifumarate CAS:1392275-56-7 Purity:98%
Medchemexpress,HY-15232B 100mg GS-7340 (hemifumarate) Tenofovir alafenamide hemifumarate CAS:1392275-56-7 Formula:C21H29N6O5P.1/2 C4H4O4 GS-7340 (Tenofovir alafenamide) hemifumarate is an investigational oral prodrug of the HIV-1 nucleotide reverse transcriptase inhibitor Tenofovir (TFV). 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.
eMolecules Medchem Express / Salvianolic acid C / 5mg / 434310703 / HY-N0319 / / 115841-09-3 / MFCD16660675 / 492.436 / C26H20O10
Medchem Express / Salvianolic acid C / 5mg / 434310703 / HY-N0319 / / 115841-09-3 / MFCD16660675 / 492.436 / C26H20O10
Medchemexpress LLC Rilmenidine (hemifumarate) | 207572-68-7 | 99.8% | 238.28 g/mol | C10H16N2O · 1/2 C4H4O4 | 10 MG
Rilmenidine hemifumarate is an orally active research compound that selectively agonizes I1 imidazoline receptors and α2-adrenoceptors. It is used in cellular studies to induce autophagy and modulate apoptotic pathways, and is supplied as a high-purity solid for laboratory research.
- Selective I1 imidazoline receptor and α2-adrenoceptor agonist.
- Reported to induce autophagy and affect mitochondrial apoptosis pathways in cell models.
- High-purity solid suitable for research applications.
- Stable when stored under recommended conditions (solid: -20°C; in solution: -80°C or -20°C as specified).
- Supplied in small research pack sizes for experimental use.
Enzo Life Sciences Parthenolide (50 mg). CAS: 20554-84-1
Sesquiterpene lactone. Widely used as an herbal remedy for arthritis and migraine. Has anti-inflammatory, antisecretory and spasmolytic activity. Specifically inhibits activation of NF-κB by preventing the degradation of IκBα and IκBβ. Inhibits activation of MAP kinase (MAPK/ERK) and generation of leukotriene B4 and thromboxane B2. Potent anticancer agent. Induces apoptosis in various cancer cell lines. Specifically inhibits histone deacetylase 1 (HDAC1) without affecting other class I/II HDACs. Inhibits tubulin carboxypeptidase (TCP) activity. Alternative name: (1aR-[1aR*,4E,7aS*,-10aS*,-10bR*])-2,3-6,7,7a,8,10a,10b-Octahydro-1a,5-dimethyl-8-methyleneoxireno[9,10]cyclo deca[1,2-b]furan-9(1aH)-one. Purity: ≥97% (HPLC, TLC). Solubility: Soluble in DMSO (100mg/ml), dichloromethane (50mg/ml) or 100% ethanol (20mg/ml). Long Term Storage: -20°C.
Enzo Life Sciences Ro 48-8071 (50mg). CAS: 189197-69-1
Inhibits cholesterol biosynthesis at the level of 2,3-oxidosqualene cyclase (OSC). Blocks OSC and cholesterol synthesis in HepG2 cells in the nanomolar range. A novel lipid lowering agent. Purity: ≥95% (HPLC). Solubility: Soluble in water (25 mg/ml). Long Term Storage: Ambient.
eMolecules Medchem Express / PD150606 / 5mg / 446255688 / HY-100529 / / 179528-45-1 / MFCD00949076 / 306.120 / C9H7IO2S
Medchem Express / PD150606 / 5mg / 446255688 / HY-100529 / / 179528-45-1 / MFCD00949076 / 306.120 / C9H7IO2S
Medchemexpress LLC (+)-Kavain | 500-64-1 | 99.1% | 5 MG
(+)-Kavain is a primary kavalactone derived from Piper methysticum, known for its anticonvulsive properties. It functions by interacting with voltage-dependent Na+ and Ca2+ channels, thereby attenuating vascular smooth muscle contraction. Additionally, it has been shown to bind to the α4β2δ GABAA receptor, enhancing GABA efficacy. Its anti-inflammatory actions have been extensively researched, making it a subject of study for inflammatory disease treatments.
- Attenuates vascular smooth muscle contraction by interacting with voltage-dependent Na+ and Ca2+ channels.
- Potentiates GABAA receptors by binding to the α4β2δ subtype.
- Exhibits anti-inflammatory effects.