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Filtered Search Results
Medchemexpress LLC HY-15186 100mg , GDC-0068 Ipatasertib;RG7440 CAS:1001264-89-6 Purity:98%
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Medchemexpress, HY-15186 100mg GDC-0068 Ipatasertib;RG7440 CAS:1001264-89-6 Formula:C24H32ClN5O2 IC50: 5±7 nM (Akt1), 18±10 nM (Akt2), 8±9 nM (Akt3), 3100±705 nM (PKA) Purity:98% GDC-0068 is a highly selective pan-Akt inhibitor targeting Akt1 / Akt2 / Akt3 with IC 50 of 5/18/8 nM, 620-fold selectivity over PKA. 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-12082A 2mg Medchemexpress, GSK369796 Dihydrochloride CAS:1010411-21-8 Purity:>98%
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Medchemexpress, HY-12082A 2mg GSK369796 Dihydrochloride CAS:1010411-21-8 GSK369796 Dihydrochloride is an affordable and effective antimalarial and inhibits hERG potassium ion channel repolarization with an IC50 of 7.5 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 Erythromycin | 114-07-8 | 98.0% | 1 ML
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Erythromycin is a macrolide antibiotic derived from Streptomyces erythreus, offering a broad spectrum of antimicrobial activity. It functions by binding to bacterial 50S ribosomal subunits, thereby inhibiting RNA-dependent protein synthesis through the blockage of transpeptidation and/or translocation reactions. Beyond its antibiotic properties, Erythromycin has shown promise with antitumor and neuroprotective effects in various research areas.
- Binds to bacterial 50S ribosomal subunits
- Inhibits RNA-dependent protein synthesis
- Blocks transpeptidation and/or translocation reactions
- Demonstrates antitumor effects
- Shows neuroprotective effects
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![Medchemexpress LLC 3-[(2-methylphenyl)methylsulfanyl]-6-pyridin-2-ylpyridazine | 894002-50-7 | ≥98.0% | 293.39 g·mol-1 | C17H15N3S | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000264345.png-250.jpg)
Medchemexpress LLC 3-[(2-methylphenyl)methylsulfanyl]-6-pyridin-2-ylpyridazine | 894002-50-7 | ≥98.0% | 293.39 g·mol-1 | C17H15N3S | 5 MG
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LDN-212320 is a small-molecule activator of the glutamate transporter GLT-1 (EAAT2) used in research to increase EAAT2 expression and probe glutamate transport-related biology, including pain models. It is supplied as a powder and in solution formats suitable for in vitro and in vivo studies.
- Activates GLT-1/EAAT2 at the translational level.
- Small molecule; chemical formula C17H15N3S; molecular weight 293.39 g·mol-1.
- High purity (≥98.0% by HPLC).
- Available in mg-scale vials and as a 10 mM solution in DMSO for stock preparation.
- Soluble in DMSO (50 mg/mL); in vivo formulations achievable at ≥2.5 mg/mL with appropriate co-solvents.
- Storage: powder -20°C (long term) or 4°C (short term); in solvent -80°C recommended.
- Used in preclinical studies to modulate glutamate uptake and attenuate nociceptive and chronic pain phenotypes.
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Medchemexpress LLC Wyc-210 (tazarotene derivative) | 2131803-93-3 | 99.2% | 340.40 | C18H16N2O3S | 5 MG
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WYC-210 is a tazarotene-derivative small-molecule retinoid intended for research use. The compound contains an alkyne functional group and is used as a click-chemistry reagent; it has been reported to exhibit relatively low anticancer activity. The material is supplied with a high purity specification and explicit storage recommendations for solid and solution forms.
- Contains an alkyne group suitable for click chemistry.
- Tazarotene-derived retinoid scaffold.
- High reported purity, suitable for analytical and synthetic applications.
- Available in small-mass packages for laboratory-scale experiments.
- Recommended storage conditions specified for powder and solutions.
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Medchemexpress LLC PF-04957325 | 1305115-80-3 | C14H15F3N8OS | 5 MG
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PF-04957325 is a highly potent and selective PDE8 inhibitor, with IC50s of 0.7 nM for PDE8A and 0.3 nM for PDE8B. It inhibits breast cancer cell migration and greatly potentiates steroidogenesis in WT adrenal cells.
- Highly potent and selective PDE8 inhibitor
- IC50s of 0.7 nM for PDE8A and 0.3 nM for PDE8B
- Inhibits breast cancer cell migration
- Potentiates steroidogenesis in WT adrenal cells
- Increases steroid production in WT Leydig cells or MA10 cells
- Synergistically potentiates steroid production with rolipram
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eMolecules 7177-48-2 | AstaTech | AMPICILLIN TRIHYDRATE | 50g | 392632363 | 42357 | 95 | MFCD00072036 | 403.45 | C16H25N3O7S
AstaTech | AMPICILLIN TRIHYDRATE | 50g | 392632363 | 42357 | 95.000 | 7177-48-2 | MFCD00072036 | 403.450 | C16H25N3O7S
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Medchemexpress LLC HY-11087 10mg Medchemexpress, SD 0006 CAS:271576-80-8 Purity:>98%
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Medchemexpress, HY-11087 10mg SD 0006 CAS:271576-80-8 SD 0006 (SD-06) is an orally active, selective, ATP-competitive and potent diaryl pyrazole inhibitor of p38α MAP kinase, with an IC50 of 110 nM for p38α. 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-114703 5mg Medchemexpress, Eslicarbazepine CAS:104746-04-5 Purity:>98%
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Medchemexpress, HY-114703 5mg Eslicarbazepine CAS:104746-04-5 Eslicarbazepine is an oral anticonvulsant indicated for the adjunctive treatment of partial seizures. 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 1018675-35-8 | Medchem Express | CVT-12012 | 5mg | 437899099 | HY-11034 | MFCD18251587 | 434.419 | C21H21F3N4O3
Ambeed | 1-Chloro-4-iodobutane | 10g | 525135067 | A222627 | 10297-05-9 | MFCD00039415 | 218.460 | C4H8ClI
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Cayman Chemical AzIthromycIn-13C-d3 500ug
An internal standard for the quantification of azithromycin by GC- or LC-MS
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Medchemexpress LLC SRI-011381 | 1629138-41-5 | MFCD01475985 | 99.6% | 329.48 g/mol | C20H31N3O | 25 MG
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SRI-011381 is a small-molecule research compound that acts as an orally active agonist of the TGF-β/Smad signaling pathway and has reported neuroprotective effects. It is supplied for research use only and is characterized by defined analytical identifiers and purity.
- Orally active TGF-β/Smad pathway agonist with reported neuroprotective effects.
- High purity, typically around 99.6%.
- Available in multiple solid pack sizes and as a DMSO solution for assay use.
- Characterized by CAS 1629138-41-5 and molecular formula C20H31N3O.
- Intended for research use only; not for human use.
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Medchemexpress LLC HY-101422 5mg Medchemexpress, GAL-021 CAS:1380341-99-0 Purity:>98%
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Medchemexpress, HY-101422 5mg GAL-021 CAS:1380341-99-0 GAL-021 a new intravenous BKCa-channel blocker. 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-100224 10mg Medchemexpress, SANT-1 CAS:304909-07-7 Purity:>98%
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Medchemexpress, HY-100224 10mg SANT-1 CAS:304909-07-7 SANT-1 is a potent Smo antagonist, inhibits Hedgehog signaling, with IC50s of 20 nM and 30 nM in Shh-LIGHT2 and SmoA1-LIGHT2 assay, respectively. 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-12018 10mg Medchemexpress, Vatalanib (dihydrochloride) CAS:212141-51-0 Purity:>98%
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Medchemexpress, HY-12018 10mg Vatalanib (diHCl) CAS:212141-51-0 Vatalanib dihydrochloride (PTK787 dihydrochloride) is an inhibitor of VEGFR2/KDR with IC50 of 37 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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