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Filtered Search Results
Medchemexpress LLC Dicyclomine impurity 1 | 60263-54-9 | MFCD00129987 | 98.0% | 210.31 g/mol | C13H22O2 | 250 MG
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Dicyclomine impurity 1 is an impurity of dicyclomine supplied as a research-grade reference standard for analytical method development, impurity profiling, and quality control.
- High purity for analytical applications (98%).
- Solid with molecular formula C13H22O2 and molecular weight 210.31 g/mol.
- Supplied in small reference sizes suitable for method development and stability studies.
- Includes product datasheet and analytical characterization information.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Sigma Aldrich Fine Chemicals Biosciences Prednisone European Pharmacopoeia (EP) Reference Standard | 53-03-2 | MFCD00003608 |
Prednisone European Pharmacopoeia (EP) Reference Standard | Mol Wt: 358.43 | 53-03-2 | MFCD00003608 |
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Medchemexpress LLC (2S,3R,4S,5R)-2-amino-3,4,5,6-tetrahydroxyhexanal hydrochloride | 5505-63-5 | MFCD00064557 | 98.0% | 215.63 g/mol | C6H14ClNO5 | 25 G
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D-Mannosamine hydrochloride is the hydrochloride salt of D-mannosamine, a six-carbon amino monosaccharide used in glycobiology and metabolic research. It is supplied as a high-purity solid reagent for laboratory use in studies of glycosylation pathways, lipopolysaccharide biosynthesis, and cell-surface carbohydrate interactions.
- High chemical purity suitable for analytical and preparative work.
- Soluble in water for aqueous assays and reactions.
- Serves as a building block in glycoconjugate synthesis and metabolic labeling.
- Stable when stored under recommended conditions.
- Offered in multiple laboratory pack sizes for experimental scalability.
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Medchemexpress LLC 3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(1H-indol-3-yl)pyrrolidine-2,5-dione | 1239986-50-5 | MFCD18917093 | 95.2% | 369.42 | C23H19N3O2 | 10 MG
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(Rac)-Tivantinib is the racemic form of Tivantinib, a selective c-Met tyrosine kinase inhibitor provided for use as an experimental control in biochemical and cellular research. Supplied as a powder with recommended low-temperature storage, it has CAS 1239986-50-5 and a molecular weight of 369.42 g·mol⁻1.
- Racemic isomer suitable as an experimental control in c-Met inhibition studies.
- Powder form allows accurate weighing and formulation of stock solutions.
- Purity typically reported near 95% for research-grade applications.
- Stable under recommended low-temperature storage for extended shelf life.
- Soluble in common organic solvents for preparation of assay concentrations.
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Medchemexpress LLC Plerixafor | 110078-46-1 | MFCD05662218 | 99.9% | 502.78 g/mol | C28H54N8 | 50 MG
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Plerixafor is a small-molecule CXCR4 antagonist used in research to mobilize hematopoietic stem cells and to probe CXCR4-mediated signaling pathways. It is provided as a solid reagent for in vitro and ex vivo studies and has reported antiviral activity in cell-based assays.
- Selective CXCR4 antagonist with reported IC50 ≈ 44 nM
- Mobilizes hematopoietic stem cells for ex vivo applications
- Useful tool for CXCR4 pathway, chemotaxis, and signaling studies
- Documented in vitro antiviral activity against HIV strains
- Supplied as a powder suitable for laboratory reagent use
- High reported purity and well-defined chemical identity
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Sigma Aldrich Fine Chemicals Biosciences Lumefantrine United States Pharmacopeia (USP) Reference Standard | 82186-77-4 | MFCD05662268 | 100MG
Lumefantrine United States Pharmacopeia (USP) Reference Standard | Mol Wt: 528.94 | 82186-77-4 | MFCD05662268 | 100MG
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Medchemexpress LLC HY-P9921 5mg Medchemexpress, Trastuzumab emtansine CAS:1018448-65-1 Purity:>98%
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Medchemexpress, HY-P9921 5mg Trastuzumab emtansine CAS:1018448-65-1 Trastuzumab emtansine (Ado-Trastuzumab emtansine) is an antibody-drug conjugate (ADC) that incorporates the HER2-targeted antitumor properties of trastuzumab with the cytotoxic activity of the microtubule-inhibitory agent DM1 (derivative of maytansine). Trastuzumab emtansine can be used for the research of advanced breast cancer. 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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Cerilliant Corporation S(+)AMPHETAMINE HCL, 1MG/ML
S(+)-Amphetamine, 1.0 mg/mL; 1 mL/ampoule
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Cerilliant Corporation MORPHINE GLUCURONIDE 1MG/ML
Morphine-3-beta-D-glucuronide, 1.0 mg/mL; 1 mL/ampoule
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Selleck Chemical LLC Enalaprilat Dihydrate 50mg 84680-54-6 MK-422 Dihydrate
Enalaprilat (MK-422) is an angiotensin-converting enzyme (ACE) inhibitor with IC50 of 1.94 nM. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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Sigma Aldrich Fine Chemicals Biosciences Lamivudine for system suitability 1 European Pharmacopoeia (EP) Reference Standard | 134678-17-4 | MFCD00869739 |
Lamivudine for system suitability 1 European Pharmacopoeia (EP) Reference Standard | Mol Wt: 229.26 | 134678-17-4 | MFCD00869739 |
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Sigma Aldrich Fine Chemicals Biosciences Galactose European Pharmacopoeia (EP) Reference Standard | 59-23-4 | MFCD00151230 |
Galactose European Pharmacopoeia (EP) Reference Standard | MW: 180.16 | 59-23-4 | MFCD00151230
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AdipoGen Dimethylsulfoniopropionate (DMSP) . Hydrochloride
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Dimethylsulfoniopropionate (DMSP) . hydrochloride, AdipoGen Life Sciences. Chemical. CAS: 4337-33-1. Formula: C5H10O2S . HCl. MW: 134.2 . 36.5. Synthetic. Naturally occurring organosulfur compound. Osmolyte, osmoprotectant. Antioxidant. Cryoprotectant. Neuroprotective agent. Neuritogenic. Acts against immune-deficient diseases (e.g. cancer). Important in geochemistry, ecology and algal/plant physiology. Metabolite produced primarily by marine phytoplankton and is the main precursor to the climatically important gas dimethylsulfide (DMS).
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Cayman Chemical Itraconazole 100mg
An antifungal agent and hedgehog pathway inhibitor; inhibits hedgehog signaling (IC50 = 0.8 μM); binds to 14-α sterol demethylase/CYP51 isoform B (Kd = 31 nM for A. fumigatus enzyme expressed in E. coli); inhibits ergosterol biosynthesis in C. neoformans (IC50 = 6 nM after 16 hours); inhibits C. neoformans growth by 50% at 3.2 nM; suppresses growth of medulloblastomas in a Ptch+/-p53-/- mouse allograft model at 100 mg/kg twice daily; reduces viral titers of several enteroviruses in infected cells from 1.25-100 µM
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TARGETMOL CHEMICALS INC FENTICONAZOLE NITRATE 50MG
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Also available in 10 mg 25 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Fenticonazole Nitrate (Lomexin) is an azole agent with antifungal activity. purity: 97%
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