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Filtered Search Results
Medchemexpress LLC Methyl α-D-mannopyranoside | 617-04-9 | MFCD00063262 | 98.0% | 194.18 g/mol | C7H14O6 | 1 ML
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Methyl α-D-mannopyranoside is a methylated mannose derivative used as a research reagent in glycobiology and microbiology for lectin-binding studies and as a competitive inhibitor of mannose-binding proteins. It is supplied as a white to off-white solid with high purity and defined storage recommendations.
- Cas number 617-04-9.
- Molecular formula C7H14O6.
- Molecular weight 194.18 g/mol.
- Purity 98.0% (NMR).
- Appearance white to off-white solid.
- Storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
- Typical applications include glycobiology, lectin inhibition, and microbiology research.
- For research use only; not for human therapeutic use.
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Medchemexpress LLC Parecoxib sodium impurity 10 | 198471-06-6 | 97.0% | 356.40 | C18H16N2O4S | 250 MG
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Parecoxib sodium impurity 10 is a characterized impurity of parecoxib sodium supplied as a research reference standard for analytical, synthetic, and impurity-identification work. It is provided for research use only and not for human or clinical applications.
- Used as an analytical reference for impurity profiling and method development.
- Intended for use as a drug intermediate or impurity characterization standard.
- Purity: 97.0% (as listed by supplier).
- Molecular formula C18H16N2O4S; molecular weight 356.40.
- Available in multiple sizes, including 250 mg, to support R&D and analytical needs.
- Store under conditions specified in the certificate of analysis to ensure stability.
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Apexbio Technology LLC cis-Epoxysuccinic acid 16533-72-5 500mg
cis-Epoxysuccinic acid (CAS 16533-72-5) is an epoxysuccinic acid derivative that functions as an agonist of the succinate receptor SUCNR1 (GPR91) Activation of SUCNR1 by cis-Epoxysuccinic acid leads to a marked decrease in intracellular cyclic AMP (cAMP) concentrations with an EC50 of approximately 2 7 M This modulation of cAMP signaling may impact various cellular processes including metabolic regulation and inflammatory responses cis-Epoxysuccinic acid serves as a useful tool compound for investigating SUCNR1-mediated pathways and cAMP-associated signaling in cellular and molecular research
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Medchemexpress LLC 10-camphorsulfonic acid ethyl ester | 108481-13-6 | >95.0% | 260.35 g/mol | C12H20O4S | 250 MG
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10-Camphorsulfonic acid ethyl ester is the ethyl ester derivative of camphorsulfonic acid and is reported as an impurity of the antifungal voriconazole. It is provided for research and analytical use; molecular formula C12H20O4S and molecular weight 260.35 g/mol. Users should consult the certificate of analysis for detailed purity, storage, and handling information.
- Ethyl ester derivative of camphorsulfonic acid.
- Used as an impurity or analytical reference standard in pharmaceutical analysis.
- Identified by CAS number 108481-13-6.
- Molecular formula C12H20O4S and molecular weight 260.35 g/mol.
- Storage and purity information provided in the certificate of analysis.
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![eMolecules 842133-18-0 | Canagliflozin | Ambeed | MFCD18251436 | 444.520 | C24H25FO5S | 95.000 | Cc1ccc(cc1Cc1ccc(s1)-c1ccc(F)cc1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O | 250mg | 525189895](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000128653.jpg-250.jpg)
eMolecules 842133-18-0 | Canagliflozin | Ambeed | MFCD18251436 | 444.520 | C24H25FO5S | 95.000 | Cc1ccc(cc1Cc1ccc(s1)-c1ccc(F)cc1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O | 250mg | 525189895
Canagliflozin | Ambeed | 842133-18-0 | MFCD18251436 | 444.520 | C24H25FO5S | 95.000 | Cc1ccc(cc1Cc1ccc(s1)-c1ccc(F)cc1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O | 250mg | 525189895
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Medchemexpress LLC Glycinexylidide | 18865-38-8 | MFCD05267700 | 95.1% | 178.23 g/mol | C10H14N2O | 250 MG
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Glycinexylidide is the active metabolite of lidocaine supplied as a research reagent for biochemical, pharmacokinetic, and in vitro pharmacology studies. It is used as a reference standard and for investigations into lidocaine metabolism and sodium channel-related activity.
- Active metabolite of lidocaine used in metabolism and pharmacokinetic studies.
- Supplied as a research-grade chemical reagent for laboratory use.
- Available in small analytical quantities suitable for assay and reference standard use.
- Purity around 95.1%, supporting reproducible experimental results.
- Molecular formula C10H14N2O and molecular weight 178.23 g/mol.
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Medchemexpress LLC Anti-B7-H4 VTCN1 Ant 1mg | 1mg
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Anti-B7-H4/VTCN1 Antibody is a CHO-expressed human antibody that targets B7-H4/VTCN1 The Anti-B7-H4/VTCN1 Antibody contains a huIgG1 heavy chain and a hu light chain with a predicted molecular weight (MW) of 145 kDa The isotype control for Anti-B7-H4/VTCN1 Antibody can be referenced as Human IgG1 kappa Isotype Control (HY-P99001)
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Medchemexpress LLC Chloroacetamido-C4-N 250mg
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Chloroacetamido-C4-NHBoc is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs[1]
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Medchemexpress LLC Copanlisib dihydrochloride | 1402152-13-9 | C23H30Cl2N8O4 | 50 MG
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Copanlisib dihydrochloride is a potent, selective, and ATP-competitive pan-class I PI3K inhibitor. It exhibits IC50 values of 0.5 nM for PI3Kα, 0.7 nM for PI3Kδ, 3.7 nM for PI3Kβ, and 6.4 nM for PI3Kγ. This compound demonstrates superior antitumor activity and shows over 2,000-fold selectivity against other lipid and protein kinases, with the exception of mTOR.
- Induces apoptosis in a subset of tumor cell lines resistant to certain treatments.
- Shows complete inhibition of PI3K-mediated AKT phosphorylation in ELT3 cells at 5 nM.
- Potently inhibits cell proliferation in various human tumor cell lines, particularly those with PIK3CA-activating mutations or HER2-positive.
- Significantly increases caspase-9 activities and levels of phosphorylated p53 at Ser15 and cleaved PARP in BT20 breast cancer cells.
- Demonstrates robust antitumor activity in rat KPL4 tumor xenograft models, with high tumor growth inhibition rates.
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Medchemexpress LLC HY-101267 100mg Medchemexpress, CHMFL-BMX-078 CAS:1808288-51-8 Purity:>98%
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Medchemexpress, HY-101267 100mg CHMFL-BMX-078 CAS:1808288-51-8 CHMFL-BMX-078 is a highly potent and selective type II irreversible BMX kinase inhibitor with an IC 50 of 11 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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Medchemexpress LLC HY-18252 100mg Medchemexpress, Avanafil TA1790 CAS:330784-47-9 Purity:98%
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Medchemexpress,HY-18252 100mg Avanafil TA1790 CAS:330784-47-9 Formula:C23H26ClN7O3 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 CERDULATINIB HYDROC 100 mg
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CERDULATINIB HYDROC 100MG
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Medchemexpress LLC CERDULATINIB HYDROC 50 mg
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CERDULATINIB HYDROC 50MG
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Medchemexpress LLC Gusacitinib | 1425381-60-7 | MFCD31692335 | 99.4% | 460.5 g/mol | C24H28N8O2 | 100 MG
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Gusacitinib is an orally active dual spleen tyrosine kinase (SYK) and Janus kinase (JAK) inhibitor supplied for research use in biochemical, cellular, and preclinical studies. The material is characterized by analytical data and supplied with documentation to support research applications.
- Dual SYK/JAK inhibitory activity for immune signaling research.
- High purity suitable for biochemical and cellular assays.
- Supplied as a solid for formulation and dosing flexibility.
- Documented characterization with COA and analytical data.
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Medchemexpress LLC Protac BET degrader-10 | 1957234-97-7 | 99.4% | 783.29 g/mol | C39H39ClN8O6S | 5 MG
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PROTAC BET Degrader-10 is a small-molecule proteolysis-targeting chimera designed to induce degradation of BET family proteins, primarily BRD4. Reported in patent WO2017007612A1 (example 37), the compound links cereblon and BRD4 ligands and has a reported DC50 of 49 nM. Typical analytical data include CAS 1957234-97-7, molecular formula C39H39ClN8O6S, molecular weight 783.29 g/mol, and purity ~99.39%.
- Induces selective BRD4 degradation in cellular assays.
- Reported DC50 of approximately 49 nM for BRD4 degradation.
- Available as solid and as a 10 mM solution in DMSO for assay flexibility.
- High chemical purity suitable for biochemical and cellular studies.
- Applicable to PROTAC mechanism-of-action and epigenetic research.
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