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Filtered Search Results
eMolecules 1141934-97-5 | Medchem Express | Emixustat (hydrochloride) | 2mg | 446270158 | HY-19720A | MFCD28400873 | 299.84 | C16H26ClNO2
Medchem Express | DMH-1 | 10mg | 446260894 | HY-12273 | 1206711-16-1 | MFCD18384963 | 380.451 | C24H20N4O
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Medchemexpress LLC (R)-3-(2-chlorophenyl)-N-(1-(3-methoxyphenyl)ethyl)propan-1-amine hydrochloride | 177172-49-5 | MFCD16038895 | 99.7% | 340.3 g/mol | C18H23Cl2NO | 50 MG
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Tecalcet hydrochloride is the hydrochloride salt of a calcimimetic research compound that allosterically and positively modulates the calcium-sensing receptor (CaSR), increasing receptor sensitivity to extracellular calcium. It is provided for research use in solid form or as DMSO solutions for in vitro studies of CaSR signaling and calcium homeostasis.
- Allosteric positive modulator of the calcium-sensing receptor for CaSR signaling studies.
- Orally active compound used in pharmacology and cellular assays.
- High reported purity suitable for research applications.
- Available as solid and as DMSO solutions for flexible dosing.
- Stable when stored sealed and protected from moisture; solvent storage at low temperatures recommended.
- Well characterized chemically with reported molecular weight and structural identifiers.
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Medchemexpress LLC Bi 639667 (compound 19n) | 1295298-26-8 | 98.9% | 10 MG
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BI 639667 is a small-molecule CCR1 antagonist chemical probe with low-nanomolar potency in biochemical and cellular assays. It is intended for in vitro pharmacology and target-validation studies exploring CCR1-mediated chemotaxis and signaling.
- Chemical probe for CCR1 with potent receptor antagonism.
- Ca2+ flux IC50 ≈ 1.8 nM; SPA binding ~5.4 nM; chemotaxis IC50 ~2.4 nM.
- CAS 1295298-26-8; molecular formula C22H18FN5O3S; molecular weight 451.47 Da.
- High chemical purity (reported 98.87%).
- Supplied as a 10 mg sample suitable for in vitro assays.
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eMolecules 2748943-41-9 | 2-Benzyloxycarbonylamino-3 -(5 -phenyl-pyridin-2-yl)-acrylic acid methyl ester | Oakwood Chemical388.423 | C23H20N2O4 | 97.000 | COC(=O)C(\NC(=O)OCc1ccccc1)=C\c1ccc(cn1)-c1ccccc1 | 100mg | 534152923
2-Benzyloxycarbonylamino-3 -(5 -phenyl-pyridin-2-yl)-acrylic acid methyl ester | Oakwood Chemical | 2748943-41-9388.423 | C23H20N2O4 | 97.000 | COC(=O)C(\NC(=O)OCc1ccccc1)=C\c1ccc(cn1)-c1ccccc1 | 100mg | 534152923
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Medchemexpress LLC Phenoxyacetone 10mM 1mL | 621-87-4 | 150.17 g/mol | C9H10O2 | 1 ML
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Phenoxyacetone is a small-molecule acetylcholinesterase (AChE) inhibitor supplied as a ready-to-use 10 mM solution in DMSO (1 mL) for in vitro research and enzymatic assays.
- Ready-to-use 10 mM solution in DMSO, 1 mL.
- Suitable for in vitro acetylcholinesterase assays and biochemical screening.
- High purity reported on accompanying certificate of analysis (COA).
- Safety data sheet (SDS) and COA are available for documentation and compliance.
- Also offered as solid quantities for preparation of custom stock solutions.
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Medchemexpress LLC 5-O-Methylvisammioside | 84272-85-5 | 452.45 | 100 MG
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5-O-Methylvisammioside is a natural compound isolated from *Saposhnikovia divaricata*.
- 99.90% purity
- White to off-white solid appearance
- Soluble in DMSO and H2O for in vitro use
- Compatible with various in vivo dissolution protocols
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Medchemexpress LLC HY-112642 5mg Medchemexpress, 9-Methoxycanthin-6-one CAS:74991-91-6 Purity:>98%
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Medchemexpress, HY-112642 5mg 9-Methoxycanthin-6-one CAS:74991-91-6 9-Methoxycanthin-6-one, a canthin-6-one alkaloid, is present in intact plant parts and in callus tissues of different explants. 9-Methoxycanthin-6-one shows anti-tumor 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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Sigma Aldrich Fine Chemicals Biosciences Atomoxetine Related Compound A United States Pharmacopeia (USP) Reference Standard | 42142-52-9 | MFCD00674078 | 10MG
Atomoxetine Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 165.23 | 42142-52-9 | MFCD00674078 | 10MG
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eMolecules 2955-56-8 | 3-Eicosanone | Toronto Research Chemicals | MFCD00026673 | 296.539 | C20H40OCCCCCCCCCCCCCCCCCC(=O)CC | 100mg | 601588909
3-Eicosanone | Toronto Research Chemicals | 2955-56-8 | MFCD00026673 | 296.539 | C20H40OCCCCCCCCCCCCCCCCCC(=O)CC | 100mg | 601588909
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Biotang Inc Silodosin (Rapaflo) > 99%, 10MG, CAS#160970-54-7, M.W.495.53, Formula: C25H32F3N3O4, SYON:KAD 3213, KMD 3213. RS041-10MG
Silodosin (Rapaflo) > 99%, 10MG, CAS#160970-54-7, M.W.495.53, Formula: C25H32F3N3O4, SYON:KAD 3213, KMD 3213. RS041-10MG.
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Medchemexpress LLC HY-100419 5mg Medchemexpress, BFH772 CAS:890128-81-1 Purity:>98%
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Medchemexpress, HY-100419 5mg BFH772 CAS:890128-81-1 BFH772 is a potent oral VEGFR2 inhibitor, which is highly effective at targeting VEGFR2 kinase with an IC50 value of 3 nM. 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 380584-15-6 | 5-(4-Chlorophenyl)-4-(4-ethoxybenzoyl)-1,5-dihydro-3-hydroxy-1-(2-thiazolyl)-2H-pyrrol-2-one | Oakwood Chemicals | MFCD02989816 | 440.900 | C22H17ClN2O4S | 95.000 | CCOc1ccc(cc1)C(=O)C1=C(O)C(=O)N(C1c1ccc(Cl)cc1)c1nccs1 | 10mg | 480151905
5-(4-Chlorophenyl)-4-(4-ethoxybenzoyl)-1,5-dihydro-3-hydroxy-1-(2-thiazolyl)-2H-pyrrol-2-one | Oakwood Chemicals | 380584-15-6 | MFCD02989816 | 440.900 | C22H17ClN2O4S | 95.000 | CCOc1ccc(cc1)C(=O)C1=C(O)C(=O)N(C1c1ccc(Cl)cc1)c1nccs1 | 10mg | 480151905
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Active Motif RVX-208
Active Motif's RVX-208 is a potent BET bromodomain antagonist with (IC50 = 0.51 uM for BD2) with approximately 170-fold selectivity over BD1 (ref 1,2). It increases apolipoprotein A-1 and HDL cholesterol in vitro and in vivo, and it reduces atherosclerosis.
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Medchemexpress LLC HY-112610 10mg Medchemexpress, CF53 CAS:1808160-52-2 Purity:>98%
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Medchemexpress, HY-112610 10mg CF53 CAS:1808160-52-2 CF53 is a highly potent, selective and orally active inhibitor of BET protein, with a Ki of <1 nM, Kd of 2.2 nM and an IC50 of 2 nM for BRD4 BD1. CF53 binds to both the BD1 and BD2 domains of BRD2, BRD3, BRD4, and BRDT BET proteins with high affinities, very selective over non-BET bromodomain-containing proteins. CF53 shows potent anti-tumor activity both in vitro and in vivo. 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 Futibatinib (TAS-120) | 1448169-71-8 | 418.45 g/mol | C22H22N6O3 | 100 MG
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Futibatinib (TAS-120) is an orally bioavailable, irreversible fibroblast growth factor receptor (FGFR) inhibitor used in research to study FGFR-driven signaling and oncology models. It inhibits FGFR1-4 and retains activity against several FGFR2 mutants, making it a tool compound for in vitro and in vivo pathway inhibition studies.
- Molecular weight: 418.45 g/mol.
- CAS number: 1448169-71-8.
- Chemical formula: C22H22N6O3.
- Target: FGFR1-4, including mutant FGFR2 variants.
- Potency: low-nanomolar IC50 values against FGFRs.
- Typical applications: biochemical assays and cellular or animal studies of FGFR signaling.
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