Bioactive Small Molecules
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Filtered Search Results
Cayman Chemical Asperphenamate, Purity: ≥95%, CAS: 63631-36-7, 5 mg
A fungal secondary metabolite; inhibits proliferation of T47D and MDA-MB-231 breast and HL-60 leukemia cancer cell lines (IC50s = 92.3, 96.5, and 97.9 μM, respectively); inhibits yeast α-glucosidase activity (IC50 = 8.3 μM)
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TARGETMOL CHEMICALS INC FUCOSTEROL 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. Fucosterol is isolated from E. stolonifera with anti-diabetic anti-adipogenic and anti-cancer activities. It regulates adipogenesis via modulation of PPAR(alpha) and C/EBP(alpha) expression. purity: 99%
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Medchemexpress LLC (3S,9BR)-3-((1H-indol-3-yl)methyl)-9b-methyl-2,3-dihydrooxazolo[2,3-a]isoindol-5(9bH)-one | 1643469-17-3 | 99.3% | 10MM 1ML
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(3S,9BR)-3-((1H-indol-3-yl)methyl)-9b-methyl-2,3-dihydrooxazolo[2,3-a]isoindol-5(9bH)-one | 1643469-17-3 | 99.3% | 10MM 1ML
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Medchemexpress LLC HY-103586 100mg Medchemexpress, GS-441524 CAS:1191237-69-0 Purity:>98%
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Medchemexpress, HY-103586 100mg GS-441524 CAS:1191237-69-0 GS-441524, predominant metabolite of Remdesivir and superior to Remdesivir against Covid-19 , shows comparable efficacy in cell-based models of primary human lung and cat cells infected with coronavirus. GS-441524 could strongly inhibits feline infectious peritonitis virus (FIPV), with an EC50 of 0.78 μM[2][3]. 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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Cayman Chemical CPI-360, Purity: ≥98%, CAS: 1802175-06-9, 10 mg
A selective EZH2 inhibitor (IC50s = 0.5 and 2.5 nM for wild-type EZH2 and Y641N mutant EZH2, respectively); decreases cellular levels of H3K27me3 and H3K27me2 (EC50s = 56 and 65 nM, respectively), triggering cell cycle arrest and ultimately resulting in apoptosis in a large panel of NHL cell lines
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Cayman Chemical Amylose, CAS: 9005-82-7, 250 mg
A polysaccharide made of α-D-glucose units that constitutes about 20% of starch; acts as an indicator, turning blue in the presence of iodine, and has also been coupled to magnetic beads for the isolation and purification of maltose-binding protein fusion proteins
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Medchemexpress LLC Disopyramide | 3737-09-5 | MFCD00057366 | 99.7% | 339.47 g/mol | C21H29N3O | 10MM 1ML
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Disopyramide is a class IA antiarrhythmic agent used in research to investigate ventricular and atrial arrhythmias. It blocks fast inward sodium currents, prolongs cardiac action potential duration, and inhibits hERG-encoded potassium channels, making it useful for electrophysiology and pharmacology studies. Supplied for in vitro use with guidance for solvent preparation and storage.
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Enzo Life Sciences Microcystin-LW (25µg). CAS: 157622-02-1
Analog of microcystin-LR (ALX-350-012) with Trp substituted in place of Arg. Hydrophobic and believed to be more cell permeable than other microcystins. May prove useful in biochemical studies in intact cells. Microcystin-LW has a characteristically different absorption spectrum compared to other microcystins, making it a useful reference compound for HPLC analysis. The Trp confers an absorption maximum at 222nm, whereas most microcystins have a characteristic maximum at 239nm. Purity: ≥95% (HPLC). Solubility: Soluble in 100% methanol. Long Term Storage: -20°C.
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Cayman Chemical ANTIBODY SCH 900776 500ug
A functionally selective inhibitor of Chk1 (Kd = 2 nM; IC50 = 3 nM); interacts synergistically with DNA antimetabolite agents in vitro and in vivo to selectively induce double-strand DNA breaks and cell death in tumor cells
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Cayman Chemical Liproxstatin-1, Purity: ≥95%, CAS: 950455-15-9, 5 mg
A ferroptosis inhibitor; inhibits ferroptotic cell death (IC50 = 22 nM) and lipid peroxidation in inducible Gpx4-/- MEFs at 50 nM; inhibits ferroptosis induced by the ferroptosis-inducing agents BSO, erastin, and (1S,3R)-RSL3 in a concentration-dependent manner in MEFs; inhibits cell death and lipid peroxidation induced by (1S,3R)-RSL3 in human renal proximal tubule epithelial cells; increases survival and decreases TUNEL+ kidney cells in inducible Gpx4-/- mice at 10 mg/kg; reduces tissue injury in a mouse model of hepatic ischemia/reperfusion injury; an antioxidant that inhibits autooxidation of lipids by trapping peroxyl radicals
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Medchemexpress LLC TC-G 1005 | 1415407-60-1 | 99.3% | 399.48 | 100 MG
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TC-G 1005 is a potent, selective, and orally active agonist of the BA receptor Takeda G protein-coupled receptor 5 (TGR5), with EC50s of 0.72 nM for hTGR5 and 6.2 nM for mTGR5. It can reduce glucose levels in vivo.
- Potent and selective TGR5 agonist.
- Orally active.
- Activates human and mouse TGR5.
- Stimulates GLP-1 secretion.
- Reduces blood glucose levels.
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Cayman Chemical MSC2530818, Purity: ≥98%, CAS: 1883423-59-3, 10 mg
A Cdk8 inhibitor (IC50 = 2.6 nM); selective for Cdk8 over a panel of 264 kinases at 1 µM but does inhibit GSK3α (IC50 = 691 nM); inhibits STAT1 phosphorylation in SW620 colorectal cancer cells (IC50 = 8 nM); inhibits Wnt-dependent transcription in LS 174T, COLO 205, and PA-1 cancer cells (IC50s = 32, 9, and 52 nM, respectively, in luciferase reporter assays); reduces tumor growth in a SW620 mouse xenograft model at 50 and 100 mg/kg
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Medchemexpress LLC S2101 | 1239262-36-2 | 99.7% | 311.76 | 1 ML
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S2101 is a lysine-specific demethylase 1 (LSD1) inhibitor with an IC50 of 0.99 μM, Ki of 0.61 μM, and Kinact/Ki of 4560 M/s. It exhibits lower inhibition activity toward MAO-B (Ki=17 μM, Kinact/Ki=18 M/s) and MAO-A (Ki=110 μM, Kinact/Ki=60 M/s). Treatment of HEK293T cells with S2101 leads to a dose-dependent increase in H3K4me2 levels, indicating LSD1 inactivation. It is approximately 50-fold stronger in LSD1 inhibition activity than 2-PCPA in human cells.
- Potent and selective inhibition of LSD1
- Lower inhibition activity toward MAO-B and MAO-A
- Induces dose-dependent increase in H3K4me2 levels
- Approximately 50-fold stronger LSD1 inhibition than 2-PCPA in human cells
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Medchemexpress LLC D-(-)-Lactic acid-13C | 2102426-04-8 | 99.9% | 91.07 | 50 MG
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D-(-)-Lactic acid-13C ((R)-2-Hydroxypropionic acid-13C) is a 13C-labeled D-Lactic acid. It can be utilized as an internal standard and for studies involving metabolic tracing.
- This compound can be used as a tracer.
- It can serve as an internal standard for quantitative analysis using techniques such as NMR, GC-MS, or LC-MS.
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Medchemexpress LLC KP-457 | 1365803-52-6 | 99.18% | 480.55 | 10 MG
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KP-457 is a selective a disintegrin and metalloproteinase 17 (ADAM17) inhibitor, demonstrating higher selectivity for ADAM17 than for other MMPs and ADAM10. It functions by blocking Zn2+ chelation of the catalytic domain of ADAM17.
- Selective ADAM17 inhibitor
- Blocks Zn2+ chelation of ADAM17 catalytic domain
- Retains GPIbα expression on iPSC-derived platelets
- Supports good hemostatic function in iPSC platelets
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