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Filtered Search Results
Keyence Corp Of America KEYENCE MK-10 INK CARTRIDGE MK
Keyence MK-10 ink cartridge MK-K01 (1 cartridge)
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Medchemexpress LLC Osilodrostat | 928134-65-0 | 99.9% | 227.24 | 100 MG
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Osilodrostat | 928134-65-0 | 99.9% | 227.24 | 100 MG
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Medchemexpress LLC Flunarizine dihydrochloride | 30484-77-6 | MFCD00058198 | 99.9% | 500 MG
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Flunarizine dihydrochloride is a potent dual Na+/Ca2+ channel (T-type) blocker. It also acts as a D2 dopamine receptor antagonist, exhibiting anticonvulsive and antimigraine activities, along with peripheral vasodilator effects.
- Potent dual Na+/Ca2+ channel (T-type) blocker
- D2 dopamine receptor antagonist
- Demonstrates anticonvulsive activity
- Exhibits antimigraine activity
- Provides peripheral vasodilator effects
- Blocks sodium currents and calcium currents (INa and ICa)
- Protects against LPS-induced acute lung injury
- Suppresses LPS-induced cell influx, protein leakage, and inflammatory cytokines release
- Inhibits pulmonary inflammation
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Medchemexpress LLC Ziconotide acetate (SNX-111 acetate) | 914454-03-8 | 99.2% | 2639.13 (free base) | 10 MG
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Ziconotide acetate is a peptide that acts as a potent and selective antagonist of N-type calcium channels. It reduces synaptic transmission and is suitable for chronic pain research.
- Potent and selective N-type calcium channel antagonist
- Reduces synaptic transmission
- Used for chronic pain research
- Partially reduces high-voltage-activated calcium currents
- Delivers antinociceptive efficacy by reducing pronociceptive neurotransmitters
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Medchemexpress LLC HY-129336 5mg Medchemexpress, CDK4/6-IN-4 CAS:2138499-06-4 Purity:>98%
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Medchemexpress, HY-129336 5mg CDK4/6-IN-4 CAS:2138499-06-4 CDK4/6-IN-4, the active metabolite of Abemaciclib, is a selective CDK4/6 inhibitor for the treatment of cancer. 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-14369 5mg Medchemexpress, Elagolix sodium CAS:832720-36-2 Purity:>98%
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Medchemexpress, HY-14369 5mg Elagolix sodium CAS:832720-36-2 Elagolix sodium is a human GnRH receptor (GnRHR) antagonist with an IC50 and Ki of 0.25 and 3.7 nM, 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 Gsk-2793660 free base | 1613458-70-0 | 357.45 | 10 MG
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GSK-2793660 (free base) is an oral, irreversible inhibitor of Cathepsin C (CTSC) and can be used for the research of bronchiectasis. At equivalent molar concentrations, both the salt and free forms of a compound exhibit comparable biological activity, however, the salt form usually boasts enhanced water solubility and stability. It is intended for research use only.
- Oral, irreversible inhibitor of Cathepsin C (CTSC).
- Useful for research related to bronchiectasis, cystic fibrosis, non-cystic fibrosis bronchiectasis, and anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis.
- Free base form offers comparable biological activity to the salt form.
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Selleck Chemical LLC Nirogacestat
Nirogacestat (PF-03084014 PF-3084014) is a selective gamma-secretase inhibitor with IC50 of 6 2 nM in a cell-free assay Nirogacestat (PF-03084014 PF-3084014) induces apoptosis Phase 2
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Selleck Chemical LLC Darapladib
Darapladib is a reversible lipoprotein-associated phospholipase A2 (Lp-PLA2) inhibitor with IC50 of 0 25 nM Phase 3
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Biotium DIOC14(3)
DiOC14(3) is a DiO derivative, but is more soluble in aqueous media than the latter because it has shorter hydrocarbon chains. Also offered as ready-to-use CellBrite™ Cell Membrane Labeling Solutions. Properties: Ex/ Em(MeOH) = 484/501nm; e (MeOH) = 150,000; Orange solid soluble in methanol, ethanol or DMSO; Store desiccated at 4°C; C47H74N2O6S; MW: 795
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VEOLIA WTS 900 SNGLE-PT VERIFICTN SET 5MG
NC3840797 900 SNGLE-PT VERIFICTN SET 5MG
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Medchemexpress LLC Parsaclisib hydrochloride | 1995889-48-9 | 99.3% | 469.34 | 100 MG
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Parsaclisib hydrochloride is a potent, selective, and orally active inhibitor of PI3Kδ, exhibiting an IC50 of 1 nM at 1 mM ATP. It demonstrates approximately 20000-fold selectivity over other PI3K class I isoforms and is used for research into relapsed or refractory B-cell malignancies.
- Potent and selective PI3Kδ inhibitor.
- Orally active.
- High selectivity (approximately 20000-fold) over other PI3K class I isoforms.
- Useful for research of relapsed or refractory B-cell malignancies.
- Inhibits proliferation of MCL and DLBCL cell lines.
- Inhibits anti-IgM-induced pAKT (Ser473) in Ramos Burkitt's lymphoma cell line.
- Inhibits proliferation of human, dog, rat, and mouse primary B cells after receptor activation.
- Inhibits tumor growth in BALB/c mice bearing A20 murine lymphoma cells.
- Slows Pfeiffer xenograft tumor growth in a dose-dependent manner and is well tolerated.
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Medchemexpress LLC PT-2385 | 1672665-49-4 | MFCD28963916 | 5 mg
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PT-2385 | Purity: 99.48% | Mol Wt: 383.35 | 1672665-49-4 | MFCD28963916 | 5 mg
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eMolecules 1674-38-0 | 1-Phenyldodecan-1-one | Combi-Blocks | MFCD00008967 | 260.421 | C18H28O | 98.000 | CCCCCCCCCCCC(=O)c1ccccc1 | 25g | 267172321
1-Phenyldodecan-1-one | Combi-Blocks | 1674-38-0 | MFCD00008967 | 260.421 | C18H28O | 98.000 | CCCCCCCCCCCC(=O)c1ccccc1 | 25g | 267172321
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Medchemexpress LLC HY-15823 1mg Medchemexpress, CAY10566 CAS:944808-88-2 Purity:>98%
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Medchemexpress, HY-15823 1mg CAY10566 CAS:944808-88-2 CAY10566 is a potent, orally bioavailable and selective stearoyl-CoA desaturase1 ( SCD1 ) inhibitor with IC 50 s of 4.5 and 26 nM in mouse and human enzymatic assays, respectively.CAY10566 also shows excellent cellular activity in blocking the conversion of saturated long-chain fatty acid-CoAs (LCFA-CoAs) to monounsaturated LCFA-CoAs in HepG2 cells (IC 50 =7.9 nM or 6.8 nM) [1] [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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