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Filtered Search Results
Medchemexpress LLC Dxd 5Mg | HY-13631D-5MG
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Dxd 5Mg
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eMolecules 60811-18-9 | 4-Bromo-1-chloro-2-fluorobenzene | Ambeed | MFCD00042519 | 209.44 | C6H3BrClF | 98 | Fc1cc(Br)ccc1Cl | 10g | 525019385
4-Bromo-1-chloro-2-fluorobenzene | Ambeed | 60811-18-9 | MFCD00042519 | 209.440 | C6H3BrClF | 98.000 | Fc1cc(Br)ccc1Cl | 10g | 525019385
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eMolecules 460-00-4 | 1-Bromo-4-fluorobenzene | Ambeed | MFCD00000342 | 175 | C6H4BrF | 95 | Fc1ccc(Br)cc1 | 10g | 518523234
Ambeed | 3-Bromo-5-chloropyrazolo[15-a]pyrimidine | 1g | 525199200 | A373429 | 960613-96-1 | MFCD11520857 | 232.470 | C6H3BrClN3
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Medchemexpress LLC Tolinapant | 1799328-86-1 | 99.81% | 539.68 | 1 ML
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Tolinapant (ASTX660) is an orally bioavailable dual antagonist of cellular inhibitor of apoptosis protein (cIAP) and X-linked inhibitor of apoptosis protein (XIAP).
- Orally bioavailable dual antagonist of cellular inhibitor of apoptosis protein (cIAP) and X-linked inhibitor of apoptosis protein (XIAP)
- Being investigated in a single-agent Phase 1/2 clinical trial in patients with advanced solid tumors and lymphomas
- Demonstrates antiproliferative activity against human MDA-MB-231 cells with an IC50 of 1.8 nM
- Shows efficacy in HCC1806 xenografts in mice by causing moderate tumor growth inhibition
- Available with a purity of 99.81%
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Medchemexpress LLC NVS-SM2 | 1562333-92-9 | 99.15% | 406.52 | 10 MG
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NVS-SM2 is a potent, orally active, and brain-penetrant SMN2 splicing enhancer. It enhances U1-pre-mRNA association, promotes exon 7 inclusion, and restores normal survival motor neuron (SMN) protein expression. This compound is suitable for spinal muscular atrophy (SMA) research.
- Potent, orally active, and brain-penetrant SMN2 splicing enhancer
- Enhances U1-pre-mRNA association
- Promotes exon 7 inclusion
- Restores normal survival motor neuron (SMN) protein expression
- Suitable for spinal muscular atrophy (SMA) research
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Medchemexpress LLC NVS-SM2 | 1562333-92-9 | 99.15% | 406.52 | 5 MG
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NVS-SM2 | 1562333-92-9 | 99.15% | 406.52 | 5 MG
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Medchemexpress LLC Tas-119 | 1453099-83-6 | 98.0% | 506.36 | 50 MG
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TAS-119 is a potent, selective, and orally active Aurora A inhibitor with an IC50 of 1.0 nM. It demonstrates high selectivity for Aurora A over other protein kinases, including Aurora B (IC50 of 95 nM). This compound exhibits potent antitumor activities.
- Enhances the antiproliferative effect of Paclitaxel in various human cancer cell lines, including Paclitaxel-resistant cells.
- Increases cell growth inhibition by taxanes (Paclitaxel, Docetaxel, and Cabazitaxel) in HeLa cells.
- Induces mitotic accumulation predominantly in tumor cells compared to normal diploid fibroblasts.
- Induces phosphorylated histone H3 (pHH3) in nude rats with HeLa-luc xenografts.
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Medchemexpress LLC (R)-GSK-3685032 | 2170140-50-6 | 99.0% | 420.53 | 50 MG
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(R)-GSK-3685032 is the R-enantiomer of GSK-3685032, a first-in-class, non-time-dependent, noncovalently, reversible DNMT1-selective inhibitor with an IC50 of 0.036 μM. It is designed to induce robust loss of DNA methylation, transcriptional activation, and inhibition of cancer cell growth.
- Selective DNMT1 inhibitor
- Target: DNMT1
- Induces loss of DNA methylation and transcriptional activation
- Inhibits cancer cell growth
- Solid storage: 4°C, sealed, away from moisture and light
- Solvent storage: -80°C for 6 months; -20°C for 1 month (sealed, away from moisture and light)
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Medchemexpress LLC WEE1-IN-3 | 2272976-28-8 | 98.6% | 497.59 | 100 MG
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WEE1-IN-3 is a potent inhibitor of Wee1 kinase with an IC50 of less than 10 nM. It demonstrates anticancer activities. WEE1 kinase is crucial for the G2-M cell-cycle checkpoint, which is involved in DNA repair before mitotic entry. While normal cells repair damaged DNA during G1 arrest, cancer cells often have a deficient G1-S checkpoint and rely on a functional G2-M checkpoint for DNA repair. WEE1 is found to be overexpressed in various cancer types. WEE1-IN-3 inhibits cancer cell growth with IC50 values of 100-1000 nM for SW480 cells and less than 100 nM for H23 cells.
- Potent Wee1 kinase inhibitor with an IC50 of <10 nM.
- Exhibits anticancer activities.
- Inhibits cancer cell growth in SW480 and H23 cells.
- Available as solid or solution in DMSO.
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Medchemexpress LLC (R)-GSK-3685032 | 2170140-50-6 | >99.0% | 420.53 | 100 MG
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(R)-GSK-3685032 is the R-enantiomer of GSK-3685032. It is a first-in-class, non-time-dependent, noncovalently, and reversible DNMT1-selective inhibitor, with an IC50 of 0.036 μM. It induces robust loss of DNA methylation, transcriptional activation, and inhibition of cancer cell growth.
- Reversible DNMT1-selective inhibitor
- Induces loss of DNA methylation
- Promotes transcriptional activation
- Inhibits cancer cell growth
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Medchemexpress LLC AHR antagonist 5 | 2247953-39-3 | 98.1% | 550.89 | 50 MG
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AHR antagonist 5 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist, extracted from patent WO2018195397, example 39, with an IC50 of < 0.5 μΜ. It significantly inhibits tumor growth when combined with the checkpoint inhibitor anti-PD-1.
- Potent and orally active aryl hydrocarbon receptor (AHR) antagonist
- Inhibits tumor growth when combined with checkpoint inhibitor anti-PD-1
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Medchemexpress LLC HPK1-IN-3 | 2739844-34-7 | 98.61% | 490.45 | 100 MG
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HPK1-IN-3 is a potent and selective ATP-competitive hematopoietic progenitor kinase 1 (HPK1; MAP4K1) inhibitor with an IC50 of 0.25 nM. It has IL-2 cellular potency with an EC50 of 108 nM in human peripheral blood mononuclear cells (PBMCs).
- Potent and selective ATP-competitive HPK1 (MAP4K1) inhibitor with an IC50 of 0.25 nM.
- Exhibits IL-2 cellular potency with an EC50 of 108 nM in human peripheral blood mononuclear cells (PBMCs).
- Can elevate proinflammatory cytokines IL-6 and TNF-α in human monocyte-derived dendritic cells.
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Medchemexpress LLC HPK1-IN-4 | 2739844-28-9 | 434.49 | 100 MG
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HPK1-IN-4 is an inhibitor of HPK1 (MAPK41), designed as a preclinical immunoresearch tool compound. It exhibits potent activity against HPK1 with a low IC50 value, making it suitable for various research applications targeting the MAPK/ERK pathway. It can be formulated for both in vitro and in vivo studies.
- Inhibits HPK1 (MAPK41) with high potency
- Preclinical immunoresearch tool compound
- Targeted to the MAPK/ERK pathway
- Suitable for in vitro and in vivo applications
- Solubility data available for various solvents and formulations
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Medchemexpress LLC Fosaprepitant dimeglumine | 265121-04-8 | 98.2% | C₃₇H₅₆F₇N₆O₁₆P | 100 MG
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Fosaprepitant dimeglumine (MK-0517) is a proagent of Aprepitant and functions as a neurokinin-1 receptor antagonist. It is developed for the prevention of chemotherapy-induced nausea and vomiting (CINV). For research use only, this product is not sold to patients.
- Proagent of Aprepitant.
- Neurokinin-1 receptor antagonist.
- Developed for preventing chemotherapy-induced nausea and vomiting (CINV).
- Increases the antinociceptive effect in rats when administered intraperitoneally.
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Medchemexpress LLC (Rac)-lunresertib | 2719749-28-5 | 99.7% | C18H20N4O2 | 50 MG
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(Rac)-lunresertib (compound 181) is a potent membrane-associated tyrosine and threonine-specific cdc2-inhibitory kinase (Myt1) (Gene name PKMYT1) inhibitor with an IC50 of <10 nM. It demonstrates anticancer effects.
- Potent Myt1 inhibitor
- Exhibits anticancer effects
- Soluble in DMSO (100 mg/mL)
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