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Filtered Search Results
Medchemexpress LLC Oleanolic acid hemip | 50MG
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Oleanolic acid hemip | 50MG
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eMolecules 41204-08-4 | A-BRMO-3,4-DICHLOROPHENYLACETIC ACID ETHYL ESTER | AstaTech | MFCD04116366 | 311.980 | C10H9BrCl2O2 | 95.000 | CCOC(=O)C(Br)c1ccc(Cl)c(Cl)c1 | 5g | 397208736
A-BRMO-3,4-DICHLOROPHENYLACETIC ACID ETHYL ESTER | AstaTech | 41204-08-4 | MFCD04116366 | 311.980 | C10H9BrCl2O2 | 95.000 | CCOC(=O)C(Br)c1ccc(Cl)c(Cl)c1 | 5g | 397208736
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Medchemexpress LLC ZXH-1-161 | 2407654-51-5 | 98.4% | 468.51 | 100 MG
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ZXH-1-161 is a potent CRBN modulator that selectively induces the degradation of GSPT1 in a CRBN-dependent manner. It can inhibit the proliferation of multiple myeloma cells and exhibits antitumor activity.
- Potent CRBN modulator.
- Selectively induces degradation of GSPT1.
- Inhibits proliferation of multiple myeloma cells.
- Exhibits antitumor activity.
- IC50 of 0.039 μM in MM1.S wild-type cells for antiproliferative activity.
- Induces GSPT1 degradation in MM1.S cells at 0.01-10 μM (4 h).
- Reduces GSPT1 levels in MM1.S cells in a dose-dependent manner.
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Medchemexpress LLC Silvestrol | 697235-38-4 | >98.0% | 654.66 g/mol | C34H38O13 | 5 MG
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Silvestrol is a natural eukaryotic translation initiation factor 4A (eIF4A) inhibitor isolated from Agave americana, used as a research reagent to study translation initiation, autophagy, and apoptosis pathways. It exhibits cytotoxic activity in cellular models and is applied in mechanistic studies of protein synthesis and anti-cancer research.
- Selective eIF4A inhibitor for translation initiation studies.
- Induces autophagy and caspase-mediated apoptosis in cell models.
- High purity (>98%) suitable for in vitro experiments.
- Molecular formula C34H38O13; molecular weight 654.66 g/mol.
- Supplied in small research quantities for laboratory use.
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eMolecules 1402148-68-8 | tert-butyl 4-amino-4-isopropyl-piperidine-1-carboxylate | MFCD22681610 | 1g
ChemScene | 1-Benzyl 2-ethyl piperazine-12-dicarboxylate | 100mg | 717420971 | CS-0528785 | 1822509-89-6 | MFCD24849997 | 292.335 | C15H20N2O4
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eMolecules 6290-49-9 | METHYL METHOXYACETATE | AstaTech | MFCD00008451 | 104.105 | C4H8O3 | 95.000 | COCC(=O)OC | 25g | 722710498
METHYL METHOXYACETATE | AstaTech | 6290-49-9 | MFCD00008451 | 104.105 | C4H8O3 | 95.000 | COCC(=O)OC | 25g | 722710498
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eMolecules 210344-95-9 | Medchem Express | Z-DEVD-FMK | 1mg | 446261296 | HY-12466 | MFCD23380217 | 668.672 | C30H41FN4O12
Ambeed | 24-Dimethylpyrimidin-5-ol | 100mg | 552592946 | A153597 | 412003-95-3 | MFCD18072447 | 124.143 | C6H8N2O
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Medchemexpress LLC HY-13229 5mg Medchemexpress, BOC-D-FMK CAS:634911-80-1 Purity:>98%
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Medchemexpress, HY-13229 5mg BOC-D-FMK CAS:634911-80-1 Boc-D-FMK is a cell-permeable, irreversible and broad spectrum caspase inhibitor. Boc-D-FMK inhibits apoptosis stimulated by TNF-α with an IC50 of 39 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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eMolecules 147859-80-1 | Medchem Express | CA-074 methyl ester | 1mg | 446255232 | HY-100350 | MFCD00797532 | 397.472 | C19H31N3O6
Pharmablock | 1-benzothiophene-5-carboxylic acid | 25mg | 724442882 | PBSL0127 | 2060-64-2 | MFCD04974042 | 178.210 | C9H6O2S
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Medchemexpress LLC HY-112430 10mg Medchemexpress, TRPM8 antagonist 2 CAS:259674-19-6 Purity:>98%
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Medchemexpress, HY-112430 10mg TRPM8 antagonist 2 CAS:259674-19-6 TRPM8 antagonist 2 is a potent and selective TRPM8 antagonist, with an IC50 of 0.2 nM, used in the research of neuropathic pain syndromes. 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-12466 1mg Medchemexpress, Z-DEVD-FMK CAS:210344-95-9 Purity:>98%
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Medchemexpress, HY-12466 1mg Z-DEVD-FMK CAS:210344-95-9 Z-DEVD-FMK is a specific and irreversible caspase-3 inhibitor with an IC50 of 18 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 PTP1B-IN-4 | 765317-72-4 | 99.6% | 741.45 g/mol | C26H19Br2N3O7S3 | 10 MG
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PTP1B-IN-4 is a small-molecule, non-competitive allosteric inhibitor of protein tyrosine phosphatase 1B (PTP1B) with a reported IC50 of approximately 8 μM. It is intended for biochemical and cellular research into PTP1B-related signaling pathways, including studies of metabolism, obesity, and diabetes. The compound is supplied as a powder or as a DMSO solution for research use.
- Non-competitive allosteric inhibitor of PTP1B (IC50 ≈ 8 μM).
- High purity (99.55%).
- Available as powder and as 10 mM solution in DMSO.
- Pack sizes suitable for small-scale research (1-100 mg).
- Recommended storage: powder at -20°C; in solvent at -80°C (long term).
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Apexbio Technology LLC CA 074 134448-10-5 10mg
CA 074 (CAS 134448-10-5) is a selective inhibitor of cathepsin B a cysteine protease involved in diverse pathological mechanisms By targeting cathepsin B CA 074 alleviates neurotoxicity induced by amyloid-activated microglia and inhibits proteolytic cascades associated with cell growth suppression and plasminogen activation Additionally CA 074 treatment modulates immune responses by shifting CD4 T cells from a Th2 to a Th1 phenotype reducing IgE and IgG1 levels In vivo studies indicate that CA 074 can attenuate TNF- -induced hepatic injury highlighting its relevance as a research tool in inflammation immunology and neurodegenerative disease investigations
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Apexbio Technology LLC CA-074 Me 147859-80-1 5mg
CA-074 Me (CAS 147859-80-1) is a cell-permeable methyl ester derivative of CA-074 functioning primarily as a selective inhibitor of cathepsin B It exhibits potent inhibitory activity against cathepsin B (IC50 36 3 nM) In cultured human gingival fibroblasts CA-074 Me effectively suppresses cathepsin B activity while moderately reducing combined cathepsin B and L activities Under strong reducing conditions (e g presence of DTT or GSH) CA-074 Me inhibits cathepsin L substantially Thus it is widely utilized in biomedical research to study lysosomal enzyme functions and roles of cathepsins in cellular processes
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Medchemexpress LLC HY-16658 1mg Medchemexpress, Z-VAD(OMe)-FMK CAS:187389-52-2 Purity:>98%
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Medchemexpress, HY-16658 1mg Z-VAD(OMe)-FMK CAS:187389-52-2 Z-VAD(OMe)-FMK (Z-Val-Ala-Asp(OMe)-FMK) is a cell-permeable and irreversible pan-caspase inhibitor. Z-VAD(OMe)-FMK is an ubiquitin carboxy-terminal hydrolase L1 (UCHL1) inhibitor. Z-VAD(OMe)-FMK irreversibly modifies UCHL1 by targeting the active site of UCHL1[2]. 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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