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Filtered Search Results
Medchemexpress LLC HY-109059 10mg Medchemexpress, Fulacimstat CAS:1488354-15-9 Purity:>98%
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Medchemexpress, HY-109059 10mg Fulacimstat CAS:1488354-15-9 Fulacimstat is an orally available chymase inhibitor, with IC50s of 4, 3 nM for human and hamster chymase enzyme, 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-111486 10mg Medchemexpress, LSZ-102 CAS:2135600-76-7 Purity:>98%
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Medchemexpress, HY-111486 10mg LSZ-102 CAS:2135600-76-7 LSZ-102 is a potent, orally bioavailable selective estrogen receptor degrader with an IC50 of 0.2 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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Pfaltz & Bauer N-LAURYL ACRYLATE 95% 25G
n-Lauryl acrylate 95%; 25G CAS# 2156-97-0
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Sigma Aldrich Fine Chemicals Biosciences Nisoldipine >=98% (HPLC) | 63675-72-9 | MFCD00478055 | 50MG
Nisoldipine >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 388.41 | 63675-72-9 | MFCD00478055 | 50MG
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Selleck Chemical LLC 3-Aminopropionitrile fumarate S5340-100mg
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3-Aminopropionitrile fumarate (Beta-Aminopropionitrile fumarate) is an organic compound and antirheumatic agent used in veterinary medicine
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Selleck Chemical LLC SC79
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SC79 is a brain-penetrable Akt phosphorylation activator and an inhibitor of Akt-PH domain translocation
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Medchemexpress LLC 3-ethyl 5-methyl 2,6-dimethyl-4-(3-nitrophenyl)-1-(prop-2-yn-1-yl)-1,4-dihydropyridine-3,5-dicarboxylat | 544478-19-5 | MFCD06798381 | 99.5% | 398.41 g/mol | C21H22N2O6 | 25 MG
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MRS1845 is a small-molecule inhibitor of store-operated calcium entry (SOCE) that targets ORAI1 channels. It is used in cellular research to probe SOCE/ORAI1-mediated calcium signaling and calcium entry mechanisms. Reported activity includes an IC50 of 1.7 μM in cellular assays.
- Inhibits store-operated calcium entry (SOCE) and targets ORAI1.
- Reported IC50 of 1.7 μM in HL-60 cellular assays.
- Molecular formula C21H22N2O6; molecular weight 398.41 g/mol.
- Reported purity approximately 99.46% (manufacturer listing).
- Available as solid packs (including 25 mg) and as a 10 mM solution in DMSO for ready reconstitution.
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eMolecules Medchem Express / HTS01037 / 5mg / 446256952 / HY-101503 / / 682741-29-3 / MFCD02681826 / 337.360 / C14H11NO5S2
Medchem Express / HTS01037 / 5mg / 446256952 / HY-101503 / / 682741-29-3 / MFCD02681826 / 337.360 / C14H11NO5S2
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eMolecules Medchem Express / Ciproxifan (maleate) / 5mg / 446265355 / HY-15289 / / 184025-19-2 / MFCD06411563 / 386.404 / C20H22N2O6
Medchem Express / Ciproxifan (maleate) / 5mg / 446265355 / HY-15289 / / 184025-19-2 / MFCD06411563 / 386.404 / C20H22N2O6
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Apexbio Technology LLC KW-2478 819812-04-9 50mg
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KW-2478 (CAS 819812-04-9) is a potent non-ansamycin inhibitor of heat shock protein 90 (Hsp90) Unlike traditional Hsp90 inhibitors such as 17-AAG KW-2478 exhibits improved aqueous solubility and reduced hepatotoxicity In multiple myeloma cell models KW-2478 induces degradation of Hsp90 client proteins and leads to downregulation of IgH translocation products including FGFR3 c-Maf and cyclin D1 thereby inhibiting cell proliferation and promoting apoptosis Additionally KW-2478 reduces levels of Cdk9 and phosphorylated 4E-BP1 further suppressing oncogenic transcriptional regulators This compound is a valuable tool for studying Hsp90-mediated pathways and evaluating therapeutic strategies in hematological malignancies
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Apexbio Technology LLC KW-2478 819812-04-9 10mg
KW-2478 (CAS 819812-04-9) is a potent non-ansamycin inhibitor of heat shock protein 90 (Hsp90) Unlike traditional Hsp90 inhibitors such as 17-AAG KW-2478 exhibits improved aqueous solubility and reduced hepatotoxicity In multiple myeloma cell models KW-2478 induces degradation of Hsp90 client proteins and leads to downregulation of IgH translocation products including FGFR3 c-Maf and cyclin D1 thereby inhibiting cell proliferation and promoting apoptosis Additionally KW-2478 reduces levels of Cdk9 and phosphorylated 4E-BP1 further suppressing oncogenic transcriptional regulators This compound is a valuable tool for studying Hsp90-mediated pathways and evaluating therapeutic strategies in hematological malignancies
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Medchemexpress LLC HY-100242 10mg Medchemexpress, Mivotilate CAS:130112-42-4 Purity:>98%
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Medchemexpress, HY-100242 10mg Mivotilate CAS:130112-42-4 Mivotilate is a nontoxic, potent activator of the aryl hydrocarbon receptor (AhR), and acts as a hepatoprotective agent. 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 3-BROMO-4-CHLOROPYRIDIN-2-A 1G
5000165435 3-BROMO-4-CHLOROPYRIDIN-2-A 1G
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eMolecules Medchem Express / AZD9496 (maleate) / 2mg / 446262010 / HY-12870A / / 1639042-28-6 / MFCD28902196 / 558.554 / C29H29F3N2O6
Medchem Express / AZD9496 (maleate) / 2mg / 446262010 / HY-12870A / / 1639042-28-6 / MFCD28902196 / 558.554 / C29H29F3N2O6
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Apexbio Technology LLC Hydroxypropyl Cellulose 9004-64-2 50mg
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Hydroxypropyl Cellulose (9004-64-2) is a cellulose derivative with modified hydrophilic and organophilic properties due to hydroxypropyl substitution Hydroxypropyl Cellulose is not a small-molecule inhibitor or modulator of a biological target rather it serves as a pharmaceutical excipient and matrix material in biomedical research It is used as a coating agent emulsifier suspending agent tablet binder thickener and viscosity enhancer improving formulation stability solubility and processability In molecular biology Hydroxypropyl Cellulose is applied as a sieving platform for DNA separation enabling size-based molecular discrimination and supporting stable matrix formation during electrophoresis Based on these application properties Hydroxypropyl Cellulose holds research potential in pharmaceutical formulation and nucleic acid electrophoresis
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