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Filtered Search Results
eMolecules 292058-49-2 | 5-(5-Chlorobenzooxazol-2-yl)-2-methylphenylamine | Oakwood Chemical | MFCD00656147 | 258.710 | C14H11ClN2O | 0.000 | Cc1ccc(cc1N)-c1nc2cc(Cl)ccc2o1 | 100mg | 537675270
5-(5-Chlorobenzooxazol-2-yl)-2-methylphenylamine | Oakwood Chemical | 292058-49-2 | MFCD00656147 | 258.710 | C14H11ClN2O | 0.000 | Cc1ccc(cc1N)-c1nc2cc(Cl)ccc2o1 | 100mg | 537675270
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Medchemexpress LLC Berotralstat (BCX7353) | 1809010-50-1 | MFCD33023491 | 99.7% | 562.6 g/mol | C30H26F4N6O | 5 MG
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Berotralstat is a selective, orally active plasma kallikrein inhibitor used in research and clinical development, including prophylaxis studies for hereditary angioedema and investigational work on edema and glioblastoma models. This item is provided as a research-grade solid standard (5 mg) intended for analytical, preclinical, and formulation studies, with documented batch-level characterization and supporting analytical data.
- Selective plasma kallikrein inhibitor for HAE and related research
- Supplied as a 5 mg research-grade solid suitable for analytical use
- High HPLC purity (reported ~99.7%) for reliable results
- Documented certificate of analysis and batch data available
- Suitable for biochemical assays, formulation studies, and reference standards
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Medchemexpress LLC HY-103483 5mg Medchemexpress, MD2-IN-1 CAS:111797-22-9 Purity:>98%
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Medchemexpress, HY-103483 5mg MD2-IN-1 CAS:111797-22-9 MD2-IN-1 is an inhibitor of Myeloid differentiation protein 2 (MD2) with a KD of 189 μM for the recombinant human MD2 (rhMD2). 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 89464-87-9 | 3-Methoxy-5-methylpyrazin-2-amine | Combi-Blocks, Inc. | MFCD09750038 | 139.158 | C6H9N3O | 98.000 | COc1nc(C)cnc1N | 1g | 569293461
3-Methoxy-5-methylpyrazin-2-amine | Combi-Blocks, Inc. | 89464-87-9 | MFCD09750038 | 139.158 | C6H9N3O | 98.000 | COc1nc(C)cnc1N | 1g | 569293461
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Enzo Life Sciences SB-3CT (5mg). CAS: 292605-14-2
Competitive, mechanism-based inhibitor of matrix metalloproteinases 2 and 9 (MMP-2 and MMP-9). It possesses Ki values in the nanomolar range against the gelatinases (14nM for MMP-2; 600nM for MMP-9), but in the micromolar range against other metalloproteinases (206µM for MMP-1, 15µM for MMP-3, 96µM for MMP-7, and 4µM for ADAM17/TACE). This inhibitor has also been used in vitro, in vivo, and in tissue culture. In vivo, it is metabolized to an even more potent gelatinase inhibitor. Purity: ≥98% (TLC). Solubility: Soluble in DMSO (at least 30mM) or 100% ethanol. Long Term Storage: -20°C.
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Medchemexpress LLC Mirificin | 103654-50-8 | 5 MG
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Mirificin is an isoflavone found in Puerariae Lobatae Radix. It acts as a tyrosinase (TYR) inhibitor with an IC50 of 12.66 μM.
- Purity of 99.66%
- Also known as Puerarin apioside
- Inhibits tyrosinase with an IC50 of 12.66 μM
- Molecular weight of 548.49
- Chemical formula C26H28O13
- Solid appearance
- Color ranges from white to light yellow
- Classified as flavonoid, isoflavone, phenol, and polyphenol
- Initially sourced from plants
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eMolecules 201943-63-7 | Medchem Express | LY341495 | 5mg | 446271395 | HY-70059 | MFCD00949707 | 353.374 | C20H19NO5
Medchem Express | MAGL-IN-5 | 5mg | 716993582 | HY-119283 | 359714-55-9 | MFCD12912259 | 355.350 | C18H17N3O5
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Medchemexpress LLC R-Zanubrutinib 100Mg | HY-101474B-100MG
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R-Zanubrutinib 100Mg
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Medchemexpress LLC RVX-297 100mg | 1044871-04-6 | 100 MG
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RVX-297 is a BD2-selective BET bromodomain inhibitor provided as a research compound for studying bromodomain-mediated regulation of gene expression and inflammation. It is supplied as a powder with defined purity and storage recommendations for laboratory use.
- BD2-selective BET bromodomain inhibitor for in vitro and in vivo research.
- Shown to suppress inflammatory gene expression in multiple immune cell models.
- Supplied as a powder with specified storage conditions to maintain stability.
- Common applications include studies of inflammation, autoimmunity, and epigenetic regulation.
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eMolecules 1780259-94-0 | Medchem Express | ZK756326 (dihydrochloride) | 5mg | 446256361 | HY-101038A | MFCD09038571 | 429.38 | C21H30Cl2N2O3
Medchem Express | AICAR | 50mg | 446262850 | HY-13417 | 2627-69-2 | 258.234 | C9H14N4O5
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Medchemexpress LLC Dihydrodiol-ibrutinib | 1654820-87-7 | 99.9% | 474.51 g/mol | C25H26N6O4 | 5 MG
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Dihydrodiol-ibrutinib is a dihydrodiol active metabolite of ibrutinib that retains BTK inhibitory activity at a lower potency than the parent compound. Supplied as a white to off-white solid for laboratory research use, it is suitable for in vitro assays and formulation studies and can be prepared in common solvents for dosing formulations.
- Active metabolite with measurable BTK inhibition (~15x lower than parent)
- High reported purity, suitable for research applications
- White to off-white solid for convenient handling
- Soluble in DMSO and compatible with multiple in vivo formulation vehicles
- Stable under recommended cold storage conditions for extended periods
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Medchemexpress LLC Mps1-IN-3 hydrochloride | 2989453-29-2 | 98.0% | 574.09 | C26H32ClN7O4S | 25MG
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Mps1-IN-3 hydrochloride is the hydrochloride salt of a potent and selective MPS1 (TTK) kinase inhibitor (reported IC50 ≈ 50 nM) provided for research use. The compound is supplied as a solid with high purity, chemical formula C26H32ClN7O4S, and molecular weight 574.09 g/mol; it is commonly packaged in small quantities for in vitro biochemical and cell-based studies.
- Potent MPS1 kinase inhibitor with reported IC50 ≈ 50 nM.
- High purity solid suitable for research applications.
- Chemical formula C26H32ClN7O4S and molecular weight 574.09 g/mol.
- Hydrochloride salt form to aid solubility for assays.
- Packaged in small quantities for laboratory testing and method development.
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Medchemexpress LLC GSK2945 hydrochloride | 98.5% | 457.80 | 100 MG
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GSK2945 hydrochloride is a class of tertiary amine, and is a highly specific Rev-erbα/REV-ERBα (mouse/human reverse erythroblastosis virus α) antagonist with EC50s of 21.5 μM and 20.8 μM, respectively. It enhances cholesterol 7α-hydroxylase (CYP7A1) level and cholesterol metabolism.
- Dose-dependently enhances the transcriptional activity of Rev-erbα and a Bmal1 (a target gene of REV-ERBs) luciferase reporter (EC50 of 2.05 μM).
- Treatment (20 μM; 12 hours and 24 hours; mouse and human primary hepatocytes) increases levels of Cyp7a1/CYP7A1 in mouse and human primary hepatocytes.
- Treatment (20 μM) also increases Lrh-1/LRH-1 (a known hepatic activator of Cyp7a1/CYP7A1) mRNA and protein.
- Treatment (0-10 mg/kg; intraperitoneal injection; twice every day; for 7 days; male C57BL/6 mice) increases hepatic mouse cholesterol 7α-hydroxylase (Cyp7a1) level and lowers plasma cholesterol in wild-type mice.
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Selleck Chemical LLC BAW2881
BAW2881 (NVP-BAW2881) is a novel vascular endothelial growth factor (VEGF) receptor tyrosine-kinase inhibitor that potently inhibits VEGFR1-3 at 1 0-4 3 nanomolar (nM) concentrations and inhibits PDGFR c-Kit and RET (c-RET) at 45-72 nM concentrations
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Medchemexpress LLC Benzo[b]thiophene-2-carboxylic acid, 5,6-diethoxy-, sodium salt | 105102-18-9 | MFCD00864802 | >98.0% | 288.30 g/mol | C13H13NaO4S | 100 MG
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Tibenelast sodium is the sodium salt of benzo[b]thiophene-2-carboxylic acid, 5,6-diethoxy- (synonym LY-186655), a small-molecule phosphodiesterase inhibitor supplied for laboratory research use. It is identified by CAS 105102-18-9 and has a molecular weight of 288.30 g/mol.
- Phosphodiesterase inhibitor activity useful for biochemical and pharmacology studies.
- Provided as a research reagent for laboratory use only, not for human or veterinary applications.
- Reported purity greater than 98.0%.
- Small-package quantities suitable for early-stage research, such as 25-100 mg.
- Chemical formula C13H13NaO4S and molecular weight 288.30 g/mol.
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