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Filtered Search Results
Medchemexpress LLC Bambuterol-d9 hydrochloride | 1794810-59-5 | 99.9% | 412.96 | 5 MG
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Bambuterol-d9 hydrochloride is a deuterium-labeled form of Bambuterol, a long-acting beta-adrenoceptor agonist (LABA) and prodrug of terbutaline, primarily used in the treatment of asthma. This compound is also valuable as a tracer and internal standard for quantitative analysis in various spectroscopic methods.
- Can be used as a tracer.
- Functions as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Deuteration can affect pharmacokinetic and metabolic profiles of drugs.
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eMolecules Medchem Express / Toremifene (citrate) / 100mg / 446271899 / HY-B0005 / / 89778-27-8 / MFCD01729016 / 598.090 / C32H36ClNO8
Medchem Express / Toremifene (citrate) / 100mg / 446271899 / HY-B0005 / / 89778-27-8 / MFCD01729016 / 598.090 / C32H36ClNO8
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![Medchemexpress LLC N-[(3R,4S)-3-hydroxy-2,2-dimethyl-6-(4,4,4-trifluorobutoxy)chroman-4-yl]-N-methylmethanesulfonamide | 223749-46-0 | MFCD12756323 | 100.0% | 411.44 | C17H24F3NO5S | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000244141.png-250.jpg)
Medchemexpress LLC N-[(3R,4S)-3-hydroxy-2,2-dimethyl-6-(4,4,4-trifluorobutoxy)chroman-4-yl]-N-methylmethanesulfonamide | 223749-46-0 | MFCD12756323 | 100.0% | 411.44 | C17H24F3NO5S | 10 MG
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HMR 1556 is a chromanol-derived small molecule that selectively inhibits the I_Ks (slow delayed rectifier potassium) current. It exhibits potent activity in cardiac myocytes with reported IC50 values in the low nanomolar range and is supplied as a high-purity research reagent in solid and solution formats.
- Potent and selective Iks channel blocker.
- Reported IC50s of 10.5 nM (canine) and 34 nM (guinea pig).
- High reported purity (99.95%).
- Available as solid and as DMSO solution formats.
- Multiple package sizes to suit experimental scale.
- For research use only; not for human or clinical use.
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Medchemexpress LLC HY-12382 5mg Medchemexpress, NMS-P715 CAS:1202055-32-0 Purity:>98%
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Medchemexpress, HY-12382 5mg NMS-P715 CAS:1202055-32-0 NMS-P715 is a selective, ATP-competitive inhibitor of MPS1, with an IC50 of 182 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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Accela Chembio Inc 2-(trifluoromethoxy)benzonitrile | 25g | 63968-85-4 | MFCD00042409 | 97+% | D: 1.245 | Shelf Life: 2160 Days | Regular
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2-(trifluoromethoxy)benzonitrile | 25g | 63968-85-4 | MFCD00042409 | 97+% | D: 1.245 | Shelf Life: 2160 Days | Regular
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eMolecules 2-Amino-4-ethoxybenzoic acid | 61484-98-8 | MFCD01464112 | 250mg
Ambeed | 2-Amino-4-ethoxybenzoic acid | 250mg | 600841054 | A466624 | | 61484-98-8 | MFCD01464112 | 181.191 | C9H11NO3
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eMolecules ZM447439 | 331771-20-1 | MFCD08703125 | 10mg
Ambeed | ZM447439 | 10mg | 524996360 | A107524 | | 331771-20-1 | MFCD08703125 | 513.598 | C29H31N5O4
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Medchemexpress LLC HY-101676 5mg Medchemexpress, RG-12525 CAS:120128-20-3 Purity:>98%
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Medchemexpress, HY-101676 5mg RG-12525 CAS:120128-20-3 RG-12525 is a a specific, competitive and orally effective antagonist of the peptidoleukotrienes, LTC4, LTD4 and LTE4, inhibiting LTC4-, LTD4- and LTE4-inducd guinea pig parenchymal strips contractions, with IC50s of 2.6 nM, 2.5 nM and 7 nM, respectively; RG-12525 is also a peroxisome proliferator-activated receptor gamma (PPAR-gamma) agonist with IC50 of appr 60 nM and a potent inhibitor of CYP3A4, with a Ki value of 0.5 µM. 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-100639 5mg Medchemexpress, Roflumilast N-oxide CAS:292135-78-5 Purity:>98%
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Medchemexpress, HY-100639 5mg Roflumilast N-oxide CAS:292135-78-5 Roflumilast N-oxide is a PDE type 4 inhibitor. 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-116790A 10mg Medchemexpress, (+)-Penbutolol CAS:38363-41-6 Purity:>98%
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Medchemexpress, HY-116790A 10mg (+)-Penbutolol CAS:38363-41-6 (+)-Penbutolol is a β-adrenoceptor antagonist, with an IC50 of 0.74 μM. (+)-Penbutolol is an optical isomer of l-penbutolol with Na+ channel-blocking action. 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-124960 5mg Medchemexpress, CTPB CAS:586976-24-1 Purity:>98%
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Medchemexpress, HY-124960 5mg CTPB CAS:586976-24-1 CTPB is a good activator of p300 histone acetyl transferase (HAT) enzyme. 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-103318 2mg Medchemexpress, PD173212 CAS:217171-01-2 Purity:>98%
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Medchemexpress, HY-103318 2mg PD173212 CAS:217171-01-2 PD173212 is a selective N-type voltage sensitive calcium channel (VSCC) blocker, with an IC50 of 36 nM in IMR-32 assays. 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 JJKK 048 | 1515855-97-6 | 99.6% | 434.44 | 10 MG
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JJKK 048 | 1515855-97-6 | 99.6% | 434.44 | 10 MG
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Sigma Aldrich Fine Chemicals Biosciences Pirodavir >=98% (HPLC) | 124436-59-5 | MFCD00866965 | 25MG
Pirodavir >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 369.46 | 124436-59-5 | MFCD00866965 | 25MG
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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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