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Filtered Search Results
Medchemexpress LLC BRD4 inhibitor-24 | 309951-18-6 | 99.3% | C13H14N2O4 | 10MG
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BRD4 Inhibitor-24 is a high-purity small-molecule inhibitor of the BRD4 bromodomain with reported antitumor activity in MCF7 and K562 cells. Supplied for research use, it is characterized for molecular properties, solubility, and storage to support in vitro and in vivo studies.
- High purity (99.3%).
- Molecular formula C13H14N2O4; molecular weight 262.26.
- Reported antitumor activity in MCF7 and K562 cell lines.
- High solubility in DMSO (≥100 mg/mL) and suitable in vivo formulation (≥2.5 mg/mL in 10% DMSO, 90% corn oil).
- Defined storage stability in solution: -80°C for up to 6 months, -20°C for up to 1 month.
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Medchemexpress LLC R-Zanubrutinib 100Mg | HY-101474B-100MG
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R-Zanubrutinib 100Mg
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Medchemexpress LLC HY-13422A 5mg Medchemexpress, Zatebradine CAS:85175-67-3 Purity:>98%
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Medchemexpress, HY-13422A 5mg Zatebradine CAS:85175-67-3 Zatebradine (UL-FS-49 (free base)) is a potent inhibitor of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels with an IC 50 value of 1.96 µM. Zatebradine blocks the slow inward current through human HCN1 , HCN2 , HCN3 and HCN4 channels , with IC 50 values of 1.83 µM, 2.21 µM, 1.90 µM and 1.88 µM, respectively [1] . 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.
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Medchemexpress LLC HY-112606 10mg Medchemexpress, ML-290 CAS:1482500-76-4 Purity:>98%
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Medchemexpress, HY-112606 10mg ML-290 CAS:1482500-76-4 ML-290 is a first-in-class and potent relaxin/insulin-like family peptide receptor (RXFP1) agonist and activator of anti-fibrotic genes, with an EC50 of 94 nM. 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.
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Medchemexpress LLC HY-101279 5mg Medchemexpress, ST034307 CAS:133406-29-8 Purity:>98%
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Medchemexpress, HY-101279 5mg ST034307 CAS:133406-29-8 ST034307 is a potent and selective adenylyl cyclase 1 (AC1) inhibitor, with IC 50 of 2.3 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.
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![Medchemexpress LLC Benzo[b]thiophene-2-carboxylic acid, 5,6-diethoxy-, sodium salt (1:1) | 105102-18-9 | MFCD00864802 | 99.7% | 288.3 g/mol | C13H13O4S.Na | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000245574.png-250.jpg)
Medchemexpress LLC Benzo[b]thiophene-2-carboxylic acid, 5,6-diethoxy-, sodium salt (1:1) | 105102-18-9 | MFCD00864802 | 99.7% | 288.3 g/mol | C13H13O4S.Na | 50 MG
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Tibenelast sodium is the sodium salt form of a benzo[b]thiophene carboxylic acid derivative that functions as a phosphodiesterase (PDE) inhibitor. It is provided as a research-grade small molecule for use in pharmacology and inflammation/respiratory studies, supplied as a solid powder for laboratory experiments.
- High purity (≈99.7%) suitable for research use.
- Phosphodiesterase inhibitor activity for inflammation and respiratory research.
- Sodium salt form for enhanced solubility in polar solvents like DMSO.
- Solid powder presentation convenient for storage and formulation.
- Identified by CAS 105102-18-9 for unambiguous referencing.
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Medchemexpress LLC Mps1-IN-3 hydrochloride | 2989453-29-2 | 98.0% | 574.09 | C26H32ClN7O4S | 25MG
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Mps1-IN-3 hydrochloride is the hydrochloride salt of a potent and selective MPS1 (TTK) kinase inhibitor (reported IC50 ≈ 50 nM) provided for research use. The compound is supplied as a solid with high purity, chemical formula C26H32ClN7O4S, and molecular weight 574.09 g/mol; it is commonly packaged in small quantities for in vitro biochemical and cell-based studies.
- Potent MPS1 kinase inhibitor with reported IC50 ≈ 50 nM.
- High purity solid suitable for research applications.
- Chemical formula C26H32ClN7O4S and molecular weight 574.09 g/mol.
- Hydrochloride salt form to aid solubility for assays.
- Packaged in small quantities for laboratory testing and method development.
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Selleck Chemical LLC Tasquinimod-5mg
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Tasquinimod (ABR-215050) is an orally active antiangiogenic agent by allosterically inhibiting HDAC4 signalling. Phase 3.
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Selleck Chemical LLC ZK756326 2HCl
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ZK756326 is a full agonist of CCR8 Chemokine receptor 8 with an IC50 of 1 8 M dose-responsively eliciting an increase in intracellular calcium and cross-desensitizing the response of the receptor to CCL1
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Medchemexpress LLC HY-111493 10mg Medchemexpress, LRRK2 inhibitor 1 CAS:1802525-61-6 Purity:>98%
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Medchemexpress, HY-111493 10mg LRRK2 inhibitor 1 CAS:1802525-61-6 LRRK2 inhibitor 1 is a potent, selective and oral LRRK2 inhibitor with an pIC50 of 6.8 nM. 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.
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eMolecules 1862238-00-3 | Medchem Express | Sirt2-IN-1 | 5mg | 451965719 | HY-112427 | 557.69 | C28H27N7O2S2
Ambeed | 3-Chloro-4-fluoroacetophenone | 10g | 525146510 | A239344 | 2923-66-2 | MFCD00042203 | 172.580 | C8H6ClFO
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eMolecules 23694-17-9 | Medchem Express | Sultopride hydrochloride | 5mg | 437899520 | HY-42849A | MFCD01319147 | 390.92 | C17H27ClN2O4S
ChemScene | 1-Hydroxycyclobutanecarbonitrile | 100mg | 686911293 | CS-0039879 | 55767-58-3 | MFCD12169298 | 97.117 | C5H7NO
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Selleck Chemical LLC BTK inhibitor 1
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BTK inhibitor 1 (compound 27) is an inhibitor of BTK with an IC50 of 0 11 nM for Btk and inhibits B cell activation in hWB with an IC50 of 2 nM
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Selleck Chemical LLC Erdafitinib
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Erdafitinib is a potent and selective orally bioavailable pan fibroblast growth factor receptor (FGFR) inhibitor with potential antineoplastic activity Erdafitinib also binds to RET (c-RET) CSF-1R PDGFR- /PDGFR- FLT4 Kit (c-Kit) and VEGFR-2 and induces cellular apoptosis
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Selleck Chemical LLC O4I1
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O4I1 is a potent Oct3/4 inducer
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