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Filtered Search Results
Medchemexpress LLC HY-B0516 100mg Medchemexpress, Articaine (hydrochloride) CAS:23964-57-0 Purity:>98%
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Medchemexpress, HY-B0516 100mg Articaine (hydrochloride) CAS:23964-57-0 Articaine hydrochloride (Hoe-045) is used in dental. 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 Synthonix / methyl 1-amino-6-bromoisoquinoline-4-carboxylate / 250mg / 779537019 / AC78107 / / 2090332-56-0 / [null] / 281.109 / C11H9BrN2O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502478617.JPG-250.jpg)
eMolecules Synthonix / methyl 1-amino-6-bromoisoquinoline-4-carboxylate / 250mg / 779537019 / AC78107 / / 2090332-56-0 / [null] / 281.109 / C11H9BrN2O2
Synthonix / methyl 1-amino-6-bromoisoquinoline-4-carboxylate / 250mg / 779537019 / AC78107 / / 2090332-56-0 / [null] / 281.109 / C11H9BrN2O2
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Apexbio Technology LLC CA-074 Me 147859-80-1 10mM (in 1mL DMSO)
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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 TRPM8 antagonist 3 | 2102179-29-1 | 99.5% | C13H12N2O4S | 10MG
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TRPM8 antagonist 3 is a potent, selective small-molecule blocker of the TRPM8 ion channel used as a research tool to study cold-sensing and nociception pathways. It shows nanomolar potency (IC50 = 11 nM), a molecular formula of C13H12N2O4S, and is supplied as a high-purity material for in vitro and preclinical research.
- Potent TRPM8 channel blocker with IC50 = 11 nM.
- High purity suitable for research (99.5%).
- Supplied as a solid with option for DMSO solution for easy assay preparation.
- Intended for in vitro and preclinical studies of cold sensation and pain pathways.
- Available in multiple pack sizes to support different experimental scales.
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Medchemexpress LLC BET bromodomain inhibitor 1 | 2411226-02-1 | 99.7% | 100 MG
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BET bromodomain inhibitor 1 is an orally active, selective bromodomain and extra-terminal (BET) bromodomain inhibitor with an IC50 of 2.6 nM for BRD4. It binds to BRD2(2), BRD3(2), BRD4(1), BRD4(2), and BRDT(2) with high affinities (Kd values of 1.3 nM, 1.0 nM, 3.0 nM, 1.6 nM, 2.1 nM, respectively). This inhibitor demonstrates anti-cancer activity.
- Orally active, selective BET bromodomain inhibitor
- High affinity binding to BRD proteins (BRD2(2), BRD3(2), BRD4(1), BRD4(2), BRDT(2))
- Demonstrates anti-cancer activity
- Excellent selectivity for BET bromodomain family
- Does not inhibit five cytochrome P450 enzymes
- Inhibits growth of acute myeloid leukemia and multiple myeloma cell lines
- Exhibits strong antitumor activities in vivo
- Induces G1-phase cell cycle arrest
- Dose-dependent inhibition of c-Myc and upregulation of p21
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eMolecules Ambeed / (E)-(3-Chloroprop-1-en-1-yl)benzene / 5g / 532081312 / A1149049 / / 21087-29-6 / MFCD00000986 / 152.620 / C9H9Cl
Ambeed / (E)-(3-Chloroprop-1-en-1-yl)benzene / 5g / 532081312 / A1149049 / / 21087-29-6 / MFCD00000986 / 152.620 / C9H9Cl
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Medchemexpress LLC ZXH-1-161 | 2407654-51-5 | 98.4% | 468.51 | 5 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
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eMolecules Medchem Express / GGTI298 (Trifluoroacetate) / 1mg / 446266818 / HY-15871 / / 1217457-86-7 / MFCD06409252 / 593.660 / C29H34F3N3O5S
Medchem Express / GGTI298 (Trifluoroacetate) / 1mg / 446266818 / HY-15871 / / 1217457-86-7 / MFCD06409252 / 593.660 / C29H34F3N3O5S
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Enzo Life Sciences Z-D(OMe)E(OMe)VD(OMe)-FMK (5mg)
Inhibitor of caspase-3 and -7. Irreversible, cell permeable inhibitor of caspase-3 and -7. Alternative name: Caspase 3 inhibitor (fluoromethylketone), Caspase 7 inhibitor (fluoromethylketone). Formula: C30H41FN4O12. MW: 668.7. Purity: ≥95% (TLC). Formulation: Lyophilized. Solubility: Soluble in DMSO (20mM) or dimethyl formamide. Long Term Storage: -20°C. Use/Stability: Stable for 1 year after receipt when stored at -20°C. Handling: Packaged under inert gas. After reconstitution, prepare aliquots and store at -20°C.
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eMolecules (R)-TERT-BUTYL 3-(BROMOMETHYL)PIPERIDINE-1-CARBOXYLATE | 1002359-91-2 | MFCD11111932 | 1g
AstaTech | (R)-TERT-BUTYL 3-(BROMOMETHYL)PIPERIDINE-1-CARBOXYLATE | 1g | 449743672 | 78828 | 95.000 | 1002359-91-2 | MFCD11111932 | 278.190 | C11H20BrNO2
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Medchemexpress LLC Z-WEHD-FMK | 210345-00-9 | 98.0% | 763.77 | 5 MG
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Z-WEHD-FMK is a potent, cell-permeable, and irreversible caspase-1/5 inhibitor. It also shows a robust inhibitory effect on cathepsin B activity (IC50=6 μM).
- Blocks C. trachomatis-induced cleavage of golgin-84 and increases GM130 expression in cells.
- Inhibits E. piscicida-induced ZF4 cell cytotoxicity and pyroptotic morphology.
- Inhibits cytotoxicity induced by cytosolic LPS delivery.
- Reduces IL-1β release in bone marrow-derived macrophages (BMDM) depending on metal ion concentration.
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Sigma Aldrich Fine Chemicals Biosciences Citronellyl isobutyrate >=92%, FCC | Purity: >=92% | Mol Wt: 226.36 | 97-89-2 | MFCD00026443 |
Citronellyl isobutyrate >=92%, FCC | 97-89-2 | MFCD00026443 |
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Medchemexpress LLC HY-12466 10mg , Z-DEVD-FMK Caspase-3 Inhibitor CAS:210344-95-9 Purity:98%
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Medchemexpress, HY-12466 10mg Z-DEVD-FMK Caspase-3 Inhibitor CAS:210344-95-9 Formula:C30H41FN4O12 IC50: 18 μM (caspase-3) Purity:98% Z-DEVD-FMK is a specific and irreversible caspase-3 inhibitor with IC 50 of 18 μM. 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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Apexbio Technology LLC CA 074 10MM IN 1ML DMSO
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CA 074 10MM IN 1ML DMSO APEXBIO TECHNOLOGIES
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eMolecules Medchem Express / CA-074 / 1mg / 446258086 / HY-103350 / / 134448-10-5 / MFCD00797531 / 383.445 / C18H29N3O6
Medchem Express / CA-074 / 1mg / 446258086 / HY-103350 / / 134448-10-5 / MFCD00797531 / 383.445 / C18H29N3O6
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