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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000351755 ARN-21934 100MG
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![Medchemexpress LLC β-[4-([4-methyl-2-(4-(trifluoromethyl)phenyl)-5-thiazolyl]methoxy)phenyl]-3-isoxazolepropanoic acid | 1011531-27-3 | 99.0% | 488.48 | C24H19F3N2O4S | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000238246.png-250.jpg)
Medchemexpress LLC β-[4-([4-methyl-2-(4-(trifluoromethyl)phenyl)-5-thiazolyl]methoxy)phenyl]-3-isoxazolepropanoic acid | 1011531-27-3 | 99.0% | 488.48 | C24H19F3N2O4S | 10MG
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AM-4668 is a research-grade small-molecule agonist of GPR40 (FFAR1) used in preclinical studies relevant to type 2 diabetes. It activates human GPR40 with low-nanomolar potency in cell-based functional assays and is supplied as a solid for in vitro pharmacology and biochemical studies.
- Low-nanomolar potency at GPR40 (EC50 3.6 nM in A9 cells, 36 nM in CHO cells).
- Suitable for in vitro receptor activation and pharmacology studies.
- High purity solid (99.0%).
- Molecular weight 488.48 and formula C24H19F3N2O4S.
- Available in milligram quantities for laboratory use.
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eMolecules Medchem Express / AZM475271 / 5mg / 446263117 / HY-13561 / / 476159-98-5 / MFCD19690925 / 442.940 / C23H27ClN4O3
Medchem Express / AZM475271 / 5mg / 446263117 / HY-13561 / / 476159-98-5 / MFCD19690925 / 442.940 / C23H27ClN4O3
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Enzo Life Sciences TMTH . hydrochloride (50mg)
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Cyclic hydroxylamine spin probe for in vivo, intraperitoneal and intravenous injections. Lifetime of more than 4 hours in blood plasma, in cells and tissue. Allows quantitative measurements of extracellular O2•– and quantification of intracellular O2•– in cells and tissue samples and in vivo O2•– detection. Alternative name: N-(1-Hydroxy-2,2,6,6-tetramethylpiperidin-4-yl)-2-methylpropanamide . HCl. Purity: ≥99% (EPR). Solubility: Soluble in water, methanol or 100% ethanol. Long Term Storage: -20°C.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
5000411889 CHLORZOXAZONE-D3 5MG
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Medchemexpress LLC SJG-136 | 232931-57-6 | 99.5% | 556.61 | C31H32N4O6 | 50 MG
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SJG-136 is a pyrrolobenzodiazepine-class DNA cross-linking agent supplied as a research reagent. It exhibits potent antitumor activity and an XL50 of 45 nM against pBR322 DNA. The compound is a solid (white to yellow), with formula C31H32N4O6, molecular weight 556.61, and reported purity of 99.47%.
- Pyrrolobenzodiazepine DNA cross-linker with potent antitumor activity.
- XL50 for pBR322 DNA: 45 nM.
- CAS number 232931-57-6.
- Chemical formula C31H32N4O6; molecular weight 556.61.
- Purity reported as 99.47% (certificate of analysis available).
- Appearance: solid, white to yellow.
- Available in multiple package sizes including 50 mg and solution formats.
- Associated documentation available: datasheet, SDS, COA, HNMR, LCMS.
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![eMolecules Medchem Express / BRD4 Inhibitor-20 / 5mg / 788478310 / HY-146208 / / 2490311-14-1 / [null] / 358.410 / C18H18N2O4S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502470648.JPG-250.jpg)
eMolecules Medchem Express / BRD4 Inhibitor-20 / 5mg / 788478310 / HY-146208 / / 2490311-14-1 / [null] / 358.410 / C18H18N2O4S
Medchem Express / BRD4 Inhibitor-20 / 5mg / 788478310 / HY-146208 / / 2490311-14-1 / [null] / 358.410 / C18H18N2O4S
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eMolecules GW2580 | 870483-87-7 | MFCD12024701 | 1g
AstaTech | GW2580 | 1g | 601098372 | 40096 | 95.000 | 870483-87-7 | MFCD12024701 | 366.421 | C20H22N4O3
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![eMolecules Medchem Express / Rogaratinib / 1mg / 446254781 / HY-100019 / / 1443530-05-9 / [null] / 466.560 / C23H26N6O3S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502449217.PNG-250.jpg)
eMolecules Medchem Express / Rogaratinib / 1mg / 446254781 / HY-100019 / / 1443530-05-9 / [null] / 466.560 / C23H26N6O3S
Medchem Express / Rogaratinib / 1mg / 446254781 / HY-100019 / / 1443530-05-9 / [null] / 466.560 / C23H26N6O3S
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eMolecules Medchem Express / AMTB (hydrochloride) / 5mg / 686921644 / HY-100345 / / 926023-82-7 / MFCD18086917 / 430.990 / C23H27ClN2O2S
Medchem Express / AMTB (hydrochloride) / 5mg / 686921644 / HY-100345 / / 926023-82-7 / MFCD18086917 / 430.990 / C23H27ClN2O2S
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Medchemexpress LLC SPP-DM1 | 452072-20-7 | 96.3% | 967.54 | C44H59ClN4O14S2 | 10 MG
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SPP-DM1 is an antibody-drug conjugate (ADC) agent-linker conjugate that links the cytotoxic payload DM1 via an SPP linker to enable targeted delivery of a microtubule-disrupting agent. It is intended for research use in ADC development and preclinical antitumor studies, and is provided with analytical documentation to support characterization and handling.
- Enables targeted delivery of a microtubule-disrupting payload.
- Suitable for ADC development and preclinical antitumor research.
- Provided with analytical documentation such as COA, HNMR, MS, and RP-HPLC.
- Offered at defined purity suitable for research applications.
- Available in small pack sizes for laboratory use.
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![Medchemexpress LLC 8-[5-(difluoromethyl)pyridin-3-yl]-1-(2,3,6,7-tetrahydrooxepin-4-yl)triazolo[4,3-a]quinoxaline | 2763602-59-9 | 99.4% | C21H17F2N5O | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000260771.png-250.jpg)
Medchemexpress LLC 8-[5-(difluoromethyl)pyridin-3-yl]-1-(2,3,6,7-tetrahydrooxepin-4-yl)triazolo[4,3-a]quinoxaline | 2763602-59-9 | 99.4% | C21H17F2N5O | 10MG
BAY-8400 is an orally active, potent, and selective DNA-dependent protein kinase (DNA-PK) inhibitor (IC50 = 81 nM) used in oncology research. It has shown antiproliferative effects in multiple cancer cell lines and oral bioavailability in vivo; supplier data report high purity, defined storage conditions, and good solubility in DMSO, making it suitable for in vitro and in vivo research applications.
- Potent DNA-PK inhibition (IC50 81 nM).
- Orally active with reported in vivo bioavailability.
- Antiproliferative activity in multiple cancer cell lines.
- High reported purity for research use.
- Good DMSO solubility for in vitro assays.
- Stable when stored under recommended conditions.
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![eMolecules Medchem Express / BRD4 Inhibitor-24 / 5mg / 721309706 / HY-147202 / / 309951-18-6 / [null] / 262.265 / C13H14N2O4](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502449213.PNG-250.jpg)
eMolecules Medchem Express / BRD4 Inhibitor-24 / 5mg / 721309706 / HY-147202 / / 309951-18-6 / [null] / 262.265 / C13H14N2O4
Medchem Express / BRD4 Inhibitor-24 / 5mg / 721309706 / HY-147202 / / 309951-18-6 / [null] / 262.265 / C13H14N2O4
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Sigma Aldrich Fine Chemicals Biosciences Phenoxyethanol United States Pharmacopeia (USP) Reference Standard | 122-99-6 | MFCD00002857 | 500MG
Phenoxyethanol United States Pharmacopeia (USP) Reference Standard | Mol Wt: 138.16 | 122-99-6 | MFCD00002857 | 500MG
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Sigma Aldrich Fine Chemicals Biosciences Phenoxyethanol European Pharmacopoeia (EP) Reference Standard | 122-99-6 | MFCD00002857 |
Phenoxyethanol European Pharmacopoeia (EP) Reference Standard | Mol Wt: 138.16 | 122-99-6 | MFCD00002857 |
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