Unsubstituted Phenols
Medchemexpress LLC Protac Bcl-xL ligand-1 | 3029365-95-2 | 99.1% | C32H29IN4O4S2 | 10MG
PROTAC Bcl-xL ligand-1 is a small-molecule ligand for the anti-apoptotic protein Bcl-xL, intended as a building block for proteolysis-targeting chimera (PROTAC) synthesis and related biochemical research. The compound is characterized by CAS 3029365-95-2, molecular formula C32H29IN4O4S2, molecular weight 724.63, and a manufacturer-reported purity of 99.06%. Safety data and handling information are provided in the product SDS.
- High reported purity (99.06%).
- Characterized by CAS number and molecular identifiers.
- Suitable for use in PROTAC synthesis and ligand development.
- Available in multiple small-molecule quantities for research use.
- Safety data sheet and handling guidance available.
eMolecules Medchem Express / Amentoflavone 7474-tetramethyl ether / 1mg / 719836376 / HY-N2756 / / 3778-25-4 / MFCD26406136 / 594.572 / C34H26O10
Medchem Express / Amentoflavone 7474-tetramethyl ether / 1mg / 719836376 / HY-N2756 / / 3778-25-4 / MFCD26406136 / 594.572 / C34H26O10
eMolecules Medchem Express / Isoquercitrin / 10mg / 446275352 / HY-N0768 / / 21637-25-2 / MFCD29050128 / 464.379 / C21H20O12
Medchem Express / Isoquercitrin / 10mg / 446275352 / HY-N0768 / / 21637-25-2 / MFCD29050128 / 464.379 / C21H20O12
Medchemexpress LLC HY-111484 5mg Medchemexpress, GDC-0927 CAS:1642297-01-5 Purity:>98%
Medchemexpress, HY-111484 5mg GDC-0927 CAS:1642297-01-5 GDC-0927 (SRN-927) is a novel, potent, non-steroidal, orally bioavailable, selective estrogen receptor antagonist. 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 Navarixin | 473727-83-2 | 99.3% | 397.42 g/mol | C21H23N3O5 | 10 MG
Navarixin is an orally active, allosteric antagonist of CXCR1 and CXCR2 used as a research compound to study chemokine receptor signaling, neutrophil recruitment, and inflammatory responses in vitro and in vivo.
- Potent, allosteric antagonist of CXCR1 and CXCR2.
- Suitable for in vitro and in vivo pharmacology studies.
- High purity (99.3%) for consistent experimental results.
- Soluble in DMSO at ≥50 mg/mL; several in vivo vehicle formulations reported.
- Recommended storage supports long-term stability of powder and solutions.
- Available in small research quantities for dosing flexibility.
Medchemexpress LLC HY-50662 10mg Medchemexpress, A-769662 CAS:844499-71-4 Purity:>98%
Medchemexpress, HY-50662 10mg A-769662 CAS:844499-71-4 A-769662 is a potent, reversible AMPK activator with EC50 of 0.8 μM. 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 / Hydroxysafflor yellow A / 10mg / 446275172 / HY-N0567 / / 78281-02-4 / MFCD08435942 / 612.537 / C27H32O16
Medchem Express / Hydroxysafflor yellow A / 10mg / 446275172 / HY-N0567 / / 78281-02-4 / MFCD08435942 / 612.537 / C27H32O16
Apexbio Technology LLC MIM1 509102-00-5 10mg
MIM1 (CAS 509102-00-5) is a selective small molecule inhibitor targeting the BH3-binding groove of MCL-1 an anti-apoptotic BCL-2 family protein By binding competitively to MCL-1 MIM1 disrupts its interaction with pro-apoptotic BH3-only proteins thereby neutralizing MCL-1-mediated inhibition of apoptosis In biochemical assays MIM1 displayed IC50 values of 4 7 4 8 M for competing with FITC-MCL-1 SAHBA and FITC-BID BH3 peptides In cellular models of B-ALL MIM1 induced caspase activation and cell death specifically in MCL-1-dependent cells with minimal effects on BCL-XL-dependent counterparts MIM1 is valuable for investigating the role of MCL-1 in apoptosis and for evaluating therapeutic strategies in MCL-1-driven malignancies
eMolecules Medchem Express / AG126 / 5mg / 446259300 / HY-108330 / / 118409-62-4 / MFCD00236448 / 215.168 / C10H5N3O3
Medchem Express / AG126 / 5mg / 446259300 / HY-108330 / / 118409-62-4 / MFCD00236448 / 215.168 / C10H5N3O3
Selleck Chemical LLC Troxerutin 50mg 7085-55-4
Troxerutin, a natural bioflavonoid isolated from Sophora japonica, has been reported to have many benefits and medicinal properties. Troxerutin, also known as vitamin P4, is a tri-hydroxyethylated derivative of natural bioflavonoid rutins which can inhibit the production of reactive oxygen species (ROS) and depress ER stress-mediated NOD activation. *For Research & Development use only. Product is not intended for drug, household, or human consumption.