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Filtered Search Results
Medchemexpress LLC HY-16901 10mg Medchemexpress, Firsocostat CAS:1434635-54-7 Purity:>98%
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Medchemexpress, HY-16901 10mg Firsocostat CAS:1434635-54-7 Firsocostat (ND-630; GS-0976; NDI-010976) is an acetyl-CoA carboxylase (ACC) inhibitor; inhibits human ACC1 and ACC2 with IC50 values of 2.1 and 6.1 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 HY-16568 50mg Medchemexpress, Irinotecan (hydrochloride trihydrate) CAS:136572-09-3 Purity:>98%
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Medchemexpress, HY-16568 50mg Irinotecan (hydrochloride trihydrate) CAS:136572-09-3 Irinotecan hydrochloride trihydrate ((+)-Irinotecan hydrochloride trihydrate) is a topoisomerase I inhibitor with antitumor activity. 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 AR-C102222 hydrochloride | 1781934-50-6 | 99.8% | 10 MG
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AR-C102222 hydrochloride is the hydrochloride salt of AR-C102222, a potent, competitive, orally active, and highly selective inducible nitric oxide synthase (iNOS) inhibitor (IC50 = 37 nM). It is supplied as a white to off-white solid for research use.
- Potent, selective iNOS inhibitor (IC50 = 37 nM).
- White to off-white solid with high purity.
- Soluble in DMSO; may require sonication and warming.
- Store sealed at 4°C; solutions stable at -20°C to -80°C for extended storage.
- Available in small research pack sizes suitable for laboratory use.
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Medchemexpress LLC HY-N0133 10mg Medchemexpress, Tangeretin CAS:481-53-8 Purity:>98%
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Medchemexpress, HY-N0133 10mg Tangeretin CAS:481-53-8 Tangeretin (Tangeritin), a flavonoid from citrus fruit peels, has been proven to play an important role in anti-inflammatory responses and neuroprotective effects in several disease models, and was also selected as a Notch-1 inhibitor. 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-122816 5mg Medchemexpress, HLY78 CAS:854847-61-3 Purity:>98%
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Medchemexpress, HY-122816 5mg HLY78 CAS:854847-61-3 HLY78 is an activator of the Wnt/β-catenin signaling pathway, which targets the DIX domain of Axin and potentiates the Axin-LRP6 association to promote Wnt signaling transduction [1] . 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 Phenoxyacetone 1g | 621-87-4 | 150.18 g/mol | C9H10O2 | 1 G
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Phenoxyacetone (1-phenoxy-2-propanone) is a small-molecule research chemical reported as a competitive acetylcholinesterase (AChE) inhibitor. It is supplied as a light yellow to yellow liquid and is accompanied by analytical documentation to support experimental use and safe handling.
- Competitive acetylcholinesterase (AChE) inhibitor for biochemical research.
- Molecular formula C9H10O2 and molecular weight 150.18 g/mol.
- High purity (99.38%) confirmed by certificate of analysis.
- Available in laboratory-scale sizes, including 1 g vials for small-scale experiments.
- Provided with a safety data sheet for handling, storage, and hazard information.
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Medchemexpress LLC 1-cyclobutyl-3-(2,6-dimethylphenyl)-3,4-dihydro-pyrimido[4,5-d]pyrimidin-2(1H)-one (methoxy-piperazinyl substituted) | 2172617-15-9 | 99.8% | 5 MG
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YKL-06-061 is a potent, selective, second-generation salt-inducible kinase (SIK) inhibitor for research use. It inhibits SIK1, SIK2, and SIK3 with IC50 values of 6.56 nM, 1.77 nM, and 20.5 nM, respectively. The compound is supplied as a high-purity solid with good DMSO solubility for biochemical and cellular studies.
- Potent inhibition of SIK1, SIK2, and SIK3 at low-nanomolar concentrations.
- High purity suitable for research applications.
- Soluble in DMSO at 16.67 mg/mL (31.59 mM).
- Solid storage recommended at -20°C; in solution store at -80°C for long-term stability.
- Available in small research sizes for assay development.
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Medchemexpress LLC 4-Phenoxybenzylamine | 107622-80-0 | 98.45% | 199.25 | 500 MG
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4-Phenoxybenzylamine inhibits the function of the NS3 protein by stabilizing an inactive conformation with an IC50 of about 500 μM against FL NS3/4a. It is for research use only and not sold to patients.
- Appearance: Liquid
- Color: Colorless to light yellow
- Shipping: Room temperature in continental US; may vary elsewhere
- Storage: 4°C, protect from light
- Inhibits the function of the NS3 protein by stabilizing an inactive conformation
- Represents a new class of direct acting antiviral agents
- Identified to bind at an allosteric site located at the interface between the protease and helicase domains of the Hepatitis C Virus (HCV) NS3 protein
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Medchemexpress LLC HY-12001 5mg Medchemexpress, WZ-3146 CAS:1214265-56-1 Purity:>98%
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Medchemexpress, HY-12001 5mg WZ-3146 CAS:1214265-56-1 WZ3146 is a mutant selective EGFR inhibitor with IC 50 s of 2, 2, 5, 14 and 66 nM for EGFR L858R , EGFR L858R/T790M , EGFR E746_A750 , EGFR E746_A750/T790M and EGFR, 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-112316B 5mg Medchemexpress, (rac)-BAY1238097 CAS:1564268-19-4 Purity:>98%
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Medchemexpress, HY-112316B 5mg (rac)-BAY1238097 CAS:1564268-19-4 (rac)-BAY1238097 is a BET inhibitor, with an IC 50 of 1.02 μM for BRD4. Used in cancer research [1] . 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 ARN-21934 | 2230854-93-8 | 98.1% | 360.46 g·mol⁻1 | C21H24N6 | 5 MG
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ARN-21934 is a selective small-molecule inhibitor of human topoisomerase IIα with demonstrated blood-brain barrier penetration. It inhibits DNA relaxation activity and is supplied for research use in solid form and as DMSO solutions; molecular data and CAS are provided for compound characterization.
- Selective inhibition of human topoisomerase IIα
- Demonstrated blood-brain barrier penetration
- Supplied as solid and as 10 mM DMSO solutions
- High purity suitable for biochemical and cellular studies
- Molecular formula and weight documented for compound characterization
- Available in multiple pack sizes to support varied study scales
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MEDCHEMEXPRESS LLC ETOSALAMIDE 10MG
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501874295 ETOSALAMIDE 10MG
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Medchemexpress LLC HY-108597 5mg Medchemexpress, TC-S 7005 CAS:1082739-92-1 Purity:>98%
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Medchemexpress, HY-108597 5mg TC-S 7005 CAS:1082739-92-1 TC-S 7005 is a Polo-like kinases (Plks) inhibitor with IC 50 s of 4 nM, 24 nM and 214 nM for Plk2, Plk3, and Plk1, respectively [1] . 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-119243 5mg Medchemexpress, LY2794193 CAS:2173037-97-1 Purity:>98%
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Medchemexpress, HY-119243 5mg LY2794193 CAS:2173037-97-1 LY2794193 is a highly potent and selective mGlu3 receptor agonist ( hmGlu3 K i =0.927 nM, EC 50 =0.47 nM; hmGlu2 K i =412 nM, EC 50 =47.5 nM) [1] . 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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Apexbio Technology LLC Bufexamac 2438-72-4 50mg
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Bufexamac (CAS 2438-72-4) is a small molecule that functions as an inhibitor of cyclooxygenase (COX) modulating enzymatic pathways involved in inflammatory responses It has been shown to promote the release of interferon-alpha (IFN- ) with an EC50 of 8 9 M indicating its potency in modulating cytokine production Bufexamac is utilized in biomedical research to investigate COX-mediated signaling pathways and the regulation of interferon-related immune responses
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