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Filtered Search Results
Medchemexpress LLC HY-12023 5mg Medchemexpress, Andarine CAS:401900-40-1 Purity:>98%
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Medchemexpress, HY-12023 5mg Andarine CAS:401900-40-1 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-101474A 5mg Medchemexpress, Zanubrutinib CAS:1691249-45-2 Purity:>98%
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Medchemexpress, HY-101474A 5mg Zanubrutinib CAS:1691249-45-2 Zanubrutinib (BGB-3111) is a selective Bruton tyrosine kinase (BTK) inhibitor. 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-111492 5mg Medchemexpress, DIM-C-pPhOCH3 CAS:33985-68-1 Purity:>98%
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Medchemexpress, HY-111492 5mg DIM-C-pPhOCH3 CAS:33985-68-1 DIM-C-pPhOCH3 is a Nur77 agonist. Nerve growth factor-induced Bα (NGFI-Bα, Nur77) is an orphan nuclear receptor. 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 Zingiberen newsaponin | 91653-50-8 | 99.7% | 1047.18 g/mol | C51H82O22 | 10 MG
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Zingiberen newsaponin is an orally active steroid saponin used in preclinical research with reported anticancer and neuroprotective activities. It is provided as a solid for laboratory studies and is intended for research use only.
- Orally active steroid saponin with reported in vitro and in vivo activity.
- Exerts anti-hepatocellular carcinoma effects by inhibiting autophagy and the AKR1C1/JAK2/STAT3 pathway.
- Activates oxidative stress and mitochondrial pathways, promoting cancer cell apoptosis.
- Alleviates cerebral ischemia-reperfusion injury and reduces pro-inflammatory cytokines.
- Enhances antioxidant enzyme activity and protects nerve cells.
- Solid form; white to off-white appearance; store sealed away from moisture and light.
- Analytical purity reported at 99.68%.
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Medchemexpress LLC HY-13311A 5mg Medchemexpress, Infigratinib phosphate CAS:1310746-10-1 Purity:>98%
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Medchemexpress, HY-13311A 5mg Infigratinib phosphate CAS:1310746-10-1 Infigratinib phosphate (BGJ-398 phosphate) is a potent inhibitor of the FGFR family with IC 50 of 0.9 nM, 1.4 nM, 1 nM, and 60 nM for FGFR1 , FGFR2 , FGFR3 , and FGFR4 , 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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FASTER CHEMISTRY LLC Faster Chemistry FastWoRX-M 100 g
FastWoRX Absorbent Powder - 100 g per bottle. FastWoRX products are hydrophobic powders that absorb most organic compounds. With them, liquid-liquid extraction (LLE) for reaction work-ups can be replaced by a simple filtration or magnetic separation. Work-ups can be done in half the time or less. Solvent use can be reduced by 90% or more. Emulsions cannot form. Automation of FastWoRX-based work-ups is much easier than automating LLE.
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Medchemexpress LLC MCOPPB trihydrochloride | 1108147-88-1 | MFCD11840549 | 100.0% | 518.01 g·mol⁻1 | C26H43Cl3N4 | 5 MG
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MCOPPB trihydrochloride is a research-grade nociceptin/orphanin FQ (NOP) receptor agonist supplied as a trihydrochloride salt. It exhibits high affinity for the human NOP receptor (pKi ≈ 10.07) and is intended for use in pharmacological studies, available in both solid and ready-to-use solution formats.
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Medchemexpress LLC HY-12248 10mg Medchemexpress, Telaglenastat CAS:1439399-58-2 Purity:>98%
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Medchemexpress, HY-12248 10mg Telaglenastat CAS:1439399-58-2 Telaglenastat (CB-839) is a first-in-class, selective, reversible and orally active glutaminase 1 (GLS1) inhibitor. Telaglenastat selectively inhibits GLS1 splice variants KGA (kidney-type glutaminase) and GAC (glutaminase C) compared to GLS2. The IC50s are 23 nM and 28 nM for endogenous glutaminase in mouse kidney and brain, respectively. Telaglenastat inudces autophagy and has antitumor activity. 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-14268 10mg Medchemexpress, Febuxostat CAS:144060-53-7 Purity:>98%
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Medchemexpress, HY-14268 10mg Febuxostat CAS:144060-53-7 Febuxostat (TEI 6720) is selective xanthine oxidase inhibitor with a Ki of 0.6 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 98959-89-8 | [4-(Ethanesulfonyl)phenyl]methanamine hydrochloride | MFCD28118402 | 1g
Ambeed | [4-(Ethanesulfonyl)phenyl]methanamine hydrochloride | 1g | 491675091 | A603648 | 98959-89-8 | MFCD28118402 | 235.730 | C9H14ClNO2S
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Medchemexpress LLC HY-111940 5mg Medchemexpress, LUT014 CAS:2274819-46-2 Purity:>98%
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Medchemexpress, HY-111940 5mg LUT014 CAS:2274819-46-2 LUT014 is a B-Raf inhibitor with an IC 50 of 11.7 nM, and developed to reduce dose-limiting acneiform lesions associated EGFR Inhibitors treatment. Extracted from patent WO 2019026065A2 [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 O-desmethyl galanthamine (sanguinine) | 60755-80-8 | MFCD07369289 | 99.7% | 273.33 g/mol | C16H19NO3 | 5 MG
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O-Desmethyl Galanthamine (Sanguinine) is a galanthamine-type alkaloid and an acetylcholinesterase (AChE) inhibitor used in neuropharmacology and biochemical research. It is provided as a high-purity powder and in DMSO solution formats for in vitro assays and mechanistic studies.
- High purity suitable for research-grade assays.
- Validated acetylcholinesterase inhibition; reported IC50 1.83 μM.
- Available as powder and DMSO solutions for flexible preparation.
- Stable when stored under recommended conditions for extended shelf life.
- Supplied in small quantities appropriate for screening and mechanistic work.
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eMolecules 122-99-6 | 2-Phenoxyethanol | Chem-Impex | MFCD00002857 | 138.166 | C8H10O2 | 99.000 | OCCOc1ccccc1 | 1kg | 603112346
2-Phenoxyethanol | Chem-Impex | 122-99-6 | MFCD00002857 | 138.166 | C8H10O2 | 99.000 | OCCOc1ccccc1 | 1kg | 603112346
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eMolecules 16139-79-0 | Diphenylphosphonoacetic acid ethyl ester | Combi-Blocks | MFCD01321165 | 320.281 | C16H17O5P | 95.000 | CCOC(=O)CP(=O)(Oc1ccccc1)Oc1ccccc1 | 5g | 374521585
Diphenylphosphonoacetic acid ethyl ester | Combi-Blocks | 16139-79-0 | MFCD01321165 | 320.281 | C16H17O5P | 95.000 | CCOC(=O)CP(=O)(Oc1ccccc1)Oc1ccccc1 | 5g | 374521585
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Medchemexpress LLC N-[3-[5-chloro-2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]pyrimidin-4-yl]oxyphenyl]propanamide | 1214265-58-3 | MFCD28015100 | 98.0% | 496.99 g·mol⁻1 | C25H29ClN6O3 | 10 MG
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WZ4003 is a potent, selective small-molecule inhibitor of the NUAK family kinases used as a research tool for biochemical and cellular studies. Reported activity includes an IC50 of 20 nM for NUAK1 (ARK5) and 100 nM for NUAK2, with minimal inhibition against a broad kinase panel. Supplied as solid material or as a DMSO solution for laboratory use; manufacturer-reported purity is ~98%.
- Potent inhibition of NUAK1 (IC50 20 nM) and NUAK2 (IC50 100 nM).
- High selectivity with negligible inhibition of approximately 139 other kinases.
- Suitable for biochemical kinase assays and cellular target validation.
- Available as solid (5-200 mg) and as a 10 mM solution in DMSO.
- Manufacturer-reported purity approximately 98% and CAS 1214265-58-3.
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