Yttrium (Y)
Yttrium was discovered in 1794 and is found in nearly all of the rare-earth minerals.
Relatively stable in air, yttrium has a silver-metallic luster. However, fine pieces of the metal will ignite in air at temperatures greater than 400 °C.
Natural yttrium contains one isotope, but nineteen unstable isotopes have also been characterized. Lunar rock samples show relatively high content levels of yttrium.
It is recovered commercially from monazite sand and from bastnasite. Yttrium oxide is used to make compounds that provide the red color in television tubes and to produce yttrium-iron-garnets used as microwave filters.
Yttrium ingot/button,≈50.8mm (2.0 in.) dia. x 11mm (0.43 in.) thick, 99% (REO)
CAS: 7440-65-5 Molecular Formula: Y Molecular Weight (g/mol): 88.91 MDL Number: MFCD00011468 InChI Key: VWQVUPCCIRVNHF-UHFFFAOYSA-N Synonym: yttrium, elemental,yttrium-89,ion,ytrio,hydride,unii-58784xqc3y,yttrium, metal and compounds,ingot,foil,element PubChem CID: 23993 ChEBI: CHEBI:33331 IUPAC Name: yttrium SMILES: [Y]
Yttrium powder, -40 mesh, 99.6% (REO)
CAS: 7440-65-5 Molecular Formula: Y Molecular Weight (g/mol): 88.91 MDL Number: MFCD00011468 InChI Key: VWQVUPCCIRVNHF-UHFFFAOYSA-N Synonym: yttrium, elemental,yttrium-89,ion,ytrio,hydride,unii-58784xqc3y,yttrium, metal and compounds,ingot,foil,element PubChem CID: 23993 ChEBI: CHEBI:33331 IUPAC Name: yttrium SMILES: [Y]
Yttrium ingot, 99.9% (REO)
CAS: 7440-65-5 Molecular Formula: Y Molecular Weight (g/mol): 88.91 MDL Number: MFCD00011468 InChI Key: VWQVUPCCIRVNHF-UHFFFAOYSA-N Synonym: yttrium, elemental,yttrium-89,ion,ytrio,hydride,unii-58784xqc3y,yttrium, metal and compounds,ingot,foil,element PubChem CID: 23993 ChEBI: CHEBI:33331 IUPAC Name: yttrium SMILES: [Y]
Medchemexpress LLC PROTAC RAR Degrader-1 | 1351169-27-1 | 97.9% | 917.14 | 10 MG
PROTAC RAR Degrader-1 (Compound 9) is a potent and selective RAR PROTAC Degrader that incorporates apoptotic protein inhibitors (IAPs) ligands, also known as SNIPERs. It reduces RARα levels in HT1080 cells in a concentration-dependent manner, a process that is blocked by the proteasome inhibitor MG132. This product is suitable for studying nuclear receptor-related diseases.
- Potent and selective RAR PROTAC Degrader.
- Consists of apoptotic protein inhibitors (IAPs) ligands (SNIPERs).
- Reduces RARα levels in HT1080 cells in a concentration-dependent manner.
- Useful in the study of nuclear receptor-related diseases.
Medchemexpress LLC 1-(3-methyl-3-((3-(trifluoromethyl)phenyl)amino)pyrrolidin-1-yl)prop-2-en-1-one | 2416417-65-5 | 99.4% | C15H17F3N2O | 10MG
MYF-01-37 is a small-molecule covalent inhibitor of TEAD that targets cysteine 380 and produces reversible inhibition of the YAP-TEAD protein-protein interaction. It is characterized for research use with defined molecular properties and high analytical purity.
- Targets cysteine 380 on TEAD, enabling covalent engagement.
- Inhibits YAP-TEAD interaction relevant to Hippo/Wnt signaling pathways.
- High purity for reproducible experimental results.
- Available as solid and as DMSO solution for flexible assay setup.
- Intended for research use only; not for clinical or diagnostic use.
Medchemexpress LLC Crocin | 42553-65-1 | 976.96 | 5 MG
Crocin is an orally active natural product isolated from the stigma of Crocus sativus. It inhibits tumor cell proliferation and promotes apoptosis through the JAK pathway, while also exhibiting anti-inflammatory, antioxidant, and antitumor activities.
- Isolated from the stigma of Crocus sativus
- Inhibits tumor cell proliferation and promotes apoptosis
- Exhibits anti-inflammatory, antioxidant, and antitumor activities
- Weakens colon cancer cell vitality in a concentration-dependent manner
- Facilitates apoptosis of HCT-116 cells
- Decreases levels of key signaling proteins (p-JAK2, p-STAT3, p-ERK)
- Shows antioxidant, anti-inflammatory, and antifibrotic effects in rat models
- Reduces expression of TLR4, IL-10, TNF-α, and TGF-β1
- Purity of 99.30%
- Appears as a solid, brown to reddish brown substance
Medchemexpress LLC BA-53038B 5mg | 2306195-65-1 | 5 MG
BA-53038B (CAS 2306195-65-1) is an HBV core protein allosteric modulator that binds the HAP pocket and modulates capsid assembly. It exhibits antiviral activity against hepatitis B virus (EC50 = 3.32 μM) and is supplied as a solid for research use.
- Chemical name: N-(3-chlorophenyl)bicyclo[4.1.0]heptane-7-carboxamide.
- Cas number: 2306195-65-1.
- Molecular formula: C14H16ClNO.
- Molecular weight: 249.74 g·mol⁻¹.
- Purity: 98.7%.
- Storage: powder at -20°C for long-term stability.
- Available pack sizes: 5 MG and larger quantities.
- Intended for research use only; not for human or clinical use.
Medchemexpress LLC BA-53038B 50mg | 2306195-65-1 | 50 MG
BA-53038B is a hepatitis B virus (HBV) core protein allosteric modulator that binds the HAP pocket and modulates HBV capsid assembly. It exhibits antiviral activity against HBV (reported EC50 3.32 μM) and is intended for preclinical research use.
- High purity (reported 98.73%).
- Molecular formula: C14H16ClNO.
- Molecular weight: 249.74 g·mol^-1.
- Available in multiple pack sizes for research use.
- Storage: powder at -20°C for long-term; in solvent at -80°C for short-term.
Medchemexpress LLC BA-53038B 100mg | 2306195-65-1 | 100 MG
BA-53038B is a hepatitis B virus (HBV) core protein allosteric modulator used in research to modulate capsid assembly and assess antiviral activity (reported EC50 3.32 μM). It is supplied as a high-purity solid and as DMSO stock solutions for in vitro studies.
- Acts as an HBV core protein allosteric modulator targeting the HAP pocket.
- Demonstrated antiviral activity (EC50 3.32 μM) in cell-based assays.
- High purity (98.73%) and white to off-white solid appearance.
- Chemical formula C14H16ClNO; molecular weight 249.74 g·mol⁻¹.
- Available as solid quantities (up to 100 mg) and as a 10 mM DMSO solution.
- Store powder at -20°C for long-term stability; store solutions at -80°C.
Medchemexpress LLC BA-53038B 10mg | 2306195-65-1 | 10 MG
BA-53038B is a hepatitis B virus (HBV) core protein allosteric modulator that binds the HAP pocket and modulates capsid assembly. It shows antiviral activity against HBV (EC50 = 3.32 μM) with low cytotoxicity (CC50 > 100 μM). Supplied as a solid research reagent with high reported purity and good solubility in DMSO.
- Modulates HBV capsid assembly by binding the HAP pocket.
- Antiviral activity: EC50 = 3.32 μM; low cytotoxicity (CC50 > 100 μM).
- Solid form with reported purity of 98.73%.
- Highly soluble in DMSO (250 mg/mL); may require ultrasonication.
- Recommended storage: powder at -20°C (up to 3 years) or 4°C (2 years); in solvent at -80°C (6 months).
Medchemexpress LLC PGAM1-IN-1 | 2438637-65-9 | 99.8% | 50 MG
PGAM1-IN-1 is a phosphoglycerate mutase 1 (PGAM1) inhibitor that inhibits H1299 proliferation with an IC50 of 14.1±1.9 μM. It appears as a solid with a light yellow to yellow color.
- Phosphoglycerate mutase 1 (PGAM1) inhibitor
- Has an IC50 of 6.4 μM for PGAM1
- Inhibits H1299 proliferation with an IC50 of 14.1±1.9 μM
- Solid, light yellow to yellow appearance
Medchemexpress LLC Annonacin | 111035-65-5 | 1 MG
Annonacin is an acetylgenin that inhibits the mitochondrial complex pathway and ATPase pumps. It is known to increase tau phosphorylation and exhibits significant killing effects on various cancer cells, including ovarian, cervical, breast, bladder, and skin cancer lines. Annonacin induces apoptosis through Bax and Caspase-3-related pathways.
- Promotes selective cancer cell death via NKA-dependent and SERCA-dependent pathways.
- Arrests cancer cells at the G1 phase.
- Induces apoptosis through Bax and Caspase-3-related pathways.
- Increases tau phosphorylation.
- Exhibits anti-cancer effects in mouse models of skin tumors.
- Has a purity of 98.09%.
Medchemexpress LLC Hardwickiic acid | 1782-65-6 | 1 MG
Hardwickiic acid is a diterpenoid compound that can block tetrodotoxin-sensitive voltage-dependent sodium channels. It possesses multiple activities including insecticidal, antinociceptive, and neurotransmitter release-regulating effects. It is used in the study of neurological diseases.
- Neuroprotectant
- Blocks tetrodotoxin-sensitive voltage-dependent sodium channels
- Possesses insecticidal activity
- Exhibits antinociceptive activity
- Regulates neurotransmitter release