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Filtered Search Results
Abcam 25-Hydro x yvitamin D3 (Calcifediol), metabolite of vitamin D3, 5MG
MW 400.6 Da, Purity >98%. Principal cholecalciferol (ab143594) metabolite. Downregulates TLR4 and JAK1/STAT3 signaling. Hydroxylates to calcitriol (ab141456) *in vivo*. Anti-inflammatory effects. Orally active.
The product is subject to the following: Abcam Restricted Use Statement
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Medchemexpress LLC Ticagrelor impurity 10 | 98.5% | 562.63 g·mol⁻¹ | C26H32F2N6O4S | 10 MG
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Ticagrelor impurity 10 is a research-grade impurity of the antiplatelet agent ticagrelor, supplied for analytical reference, impurity profiling, and method development. The material is provided at high stated purity (98.51%) and is characterized by a molecular weight of 562.63 g·mol⁻¹. Small-mass packages are offered for laboratory use, and accompanying documentation (SDS, COA) is available.
- Research-grade impurity for analytical and QC applications.
- High stated purity (98.51%) for reliable reference standards.
- Available in small milligram quantities suitable for method development.
- Characterized molecular weight for analytical confirmation.
- SDS and COA available to support safe handling and verification.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000693181 DIAVERIDINE 100G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000695355 RIVAROXABAN IMPURITY 1G
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Sigma Aldrich Fine Chemicals Biosciences Trehalose United States Pharmacopeia (USP) Reference Standard | 6138-23-4 | MFCD00071594 | 400MG
Trehalose United States Pharmacopeia (USP) Reference Standard | Mol Wt: 378.33 | 6138-23-4 | MFCD00071594 | 400MG
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5000784612 FLECAINIDE IMPURITY 50G
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Medchemexpress LLC Lapatinib ditosylate monohydrate | 388082-78-8 | 100.0% | 50 MG
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Lapatinib ditosylate monohydrate is a potent, orally active inhibitor of the ErbB-2 and EGFR tyrosine kinase domains. It has demonstrated IC50 values against purified EGFR and ErbB-2 of 10.2 and 9.8 nM, respectively. This compound is for research use only.
- Potent, orally active inhibitor of ErbB-2 and EGFR tyrosine kinase domains.
- Inhibits receptor autophosphorylation of EGFR and ErbB-2.
- Selectively inhibits proliferation of human tumor cell lines overexpressing EGFR or ErbB-2.
- Induces G1 arrest in HN5 cells.
- Inhibits tumor xenograft growth in vivo.
- Associated with numerous clinical trials for various cancers.
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Sigma Aldrich Fine Chemicals Biosciences Levosimendan | 141505-33-1 | MFCD00867135 | 10mg
Levosimendan | Purity: 98% | Mol Wt: 280.28 | 141505-33-1 | MFCD00867135 | 10mg
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U.S. Pharmacopeia Salicylic Acid, 69-72-7, MFCD00002439, 125mg
Molecular formula C7H6O3, Molecular weight 138.12, Melting point 314.6 - 321.8 °F (157 - 161 °C) ; 76 ° C (sublimes), Boiling point 411.8 °F (211 °C) at 20 mm Hg, Flash point 315.00 °F (157.22 °C) Closed Cup
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![Medchemexpress LLC Phosphonic acid, P-[[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl] hydrate | 206184-49-8 | MFCD11519982 | 99.5% | C10H16N5O4P·H2O | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000260772.png-250.jpg)
Medchemexpress LLC Phosphonic acid, P-[[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl] hydrate | 206184-49-8 | MFCD11519982 | 99.5% | C10H16N5O4P·H2O | 10MG
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Tenofovir hydrate is an antiviral nucleotide reverse transcriptase inhibitor provided for research use. It is used in studies of HIV and chronic hepatitis B and is supplied as a high-purity white to off-white powder suitable for biochemical and cell-based assays. This product is intended for laboratory research and not for clinical use.
- High purity suitable for research applications.
- White to off-white powder, easy to weigh and dissolve.
- Available as solid, solution in DMSO, or pre-dissolved formats.
- Suitable for biochemical and cell-based antiviral assays.
- Batch-specific certificate of analysis available for validation.
- Intended for research use only; not for human or clinical use.
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5000695551 RIBOCICLIB IMPURITY 5G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000695069 GRAZOPREVIR IMPURITY 5MG
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Medchemexpress LLC Doxazosin | 74191-85-8 | 99.9% | C23H25N5O5 | 25 MG
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Doxazosin is a quinazoline-derivative that selectively antagonizes postsynaptic α1-adrenergic receptors. It is a long-lasting inhibitor of α1-adrenoceptors used to treat benign prostatic hyperplasia and lower urinary tract symptoms.
- Selectively antagonizes postsynaptic α1-adrenergic receptors.
- Long-lasting inhibitor of α1-adrenoceptors.
- Used to treat benign prostatic hyperplasia.
- Used to treat lower urinary tract symptoms.
- May inhibit cholesterol synthesis and reduce LDL cholesterol.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000784883 TELMISARTAN IMPURITY 50G
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Apexbio Technology LLC APEXBIO TECHNOLOGY LLC
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5000568287 EDETATE-CALCIUM-DISODIUM-300G
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