Prenol lipids
Medchemexpress LLC (5E,9E,13E)-teprenone | 3796-63-2 | 99.9% | 330.56 g/mol | C23H38O | 10 MG
(5E,9E,13E)-teprenone is a geranylgeranyl-derived small molecule used in research to induce heat shock proteins (HSPs) and to study gastric mucosal protection. Supplied as a high-purity reagent suitable for biochemical and cellular assays.
- High purity (99.9%) suitable for research applications.
- CAS number 3796-63-2 for unambiguous identification.
- Chemical formula C23H38O; molecular weight 330.56 g/mol.
- Supplied as a 10 mg pack for small-scale experiments.
- Recommended storage: 4°C; in solvent: -80°C (6 months) or -20°C (1 month) under nitrogen.
Selleck Chemical LLC Phytol S5121-25mg
Phytol (Trans-Phytol) a diterpene alcohol from chlorophyll widely used as a food additive and in medicinal fields shows antinociceptive and antioxidant activities as well as anti-inflammatory and antiallergic effects It is a specific activator of PPAR
Medchemexpress LLC Teprenone | 3796-63-2 | >99.8% | 50 MG
Teprenone, also known as (5E,9E,13E)-Geranylgeranylacetone, is an isomer with antiulcer activity. It induces transcriptional activation of HSP genes, which may enhance gastric mucosal defense under stress conditions. This product is for research use only.
- Isomer with antiulcer activity
- Induces transcriptional activation of HSP genes
- May increase gastric mucosal defense at conditions of stress
- For research use only
Medchemexpress LLC Isophytol (isovegetable alcohol) | 505-32-8 | MFCD00048380 | 99.7% | 296.53 | C20H40O | 100 G
Isophytol (isovegetable alcohol) is a branched-chain diterpenoid alcohol provided for research use as a biochemical assay reagent. It is a clear, oily organic compound (C20H40O, MW 296.53) commonly used in biochemical and analytical applications; manufacturer-stated purity is approximately 99.7%.
- Biochemical assay reagent for life-science research.
- High nominal purity suitable for analytical applications.
- Clear, oily liquid form for easy formulation and handling.
- Supplied in multiple pack sizes for laboratory convenience.
Medchemexpress LLC HY-N0134 5mg Medchemexpress, Tanshinone I CAS:568-73-0 Purity:>98%
Medchemexpress, HY-N0134 5mg Tanshinone I CAS:568-73-0 Tanshinone I is an inhibitor of type IIA human recombinant sPLA 2 ( IC 50 =11 μM) and rabbit recombinant cPLA 2 ( IC 50 =82 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.
Medchemexpress LLC 4,4'-sulfonylbis(2-methylphenol) | 16346-97-7 | MFCD00130281 | 97.0% | 278.32 g·mol-1 | C14H14O4S | 25 MG
Topoisomerase IIα-IN-9 is a bisphenol-derived small-molecule inhibitor of human DNA topoisomerase IIα intended for research use. Reported biochemical activity includes Topo II inhibition (IC50 ≈ 571 μM) and cell growth inhibitory activity in K562 and CHO cells (IC50 ≈ 117 μM and 218 μM, respectively). Molecular formula C14H14O4S and molecular weight 278.32 g·mol-1 are provided; consult the Certificate of Analysis for purity and storage conditions.
- Moderate inhibitor of DNA topoisomerase IIα.
- Exhibits cell growth inhibition in selected cell lines.
- Provided as a characterized small molecule with formula and molecular weight.
- Suitable for biochemical assays and cell-based research applications.
- Certificate of Analysis available for purity and handling details.
Medchemexpress LLC 4,4'-sulfonylbis(2-methylphenol) | 16346-97-7 | MFCD00130281 | 278.32 g/mol | C14H14O4S | 10 MG
Topoisomerase IIα-IN-9 (4,4'-sulfonylbis(2-methylphenol)) is a bisphenol compound that moderately inhibits human DNA topoisomerase II and reduces cell proliferation in selected cell lines. It is supplied for laboratory research; lot-specific purity, solubility, and storage conditions are provided in the product data sheet and Certificate of Analysis.
- Moderate topoisomerase II inhibition (IC50: 571 μM).
- Inhibits K562 cell growth (IC50: 117 μM) and CHO cell growth (IC50: 218 μM).
- Molecular weight 278.32 g/mol and formula C14H14O4S.
- CAS number 16346-97-7 for unambiguous identification.
- Intended for research use; consult Certificate of Analysis for purity and storage.
Apexbio Technology LLC Cryptotanshinone 35825-57-1 20mg
Cryptotanshinone (CAS 35825-57-1) is a bioactive diterpene quinone derived from Salvia miltiorrhiza It modulates cellular signaling pathways by interacting with various molecular targets including components of the STAT3 signaling cascade thereby influencing transcriptional activity Studies indicate that cryptotanshinone alters gene expression profiles associated with cellular stress responses and apoptosis Due to its ability to regulate molecular pathways relevant to cancer biology and oxidative stress cryptotanshinone is widely utilized in biomedical research investigating mechanisms of tumor progression chemoprevention and cytoprotection
eMolecules Tanshinone i | 568-73-0 | MFCD00210563 | 1g
Combi-Blocks, Inc. | Tanshinone i | 1g | 603145422 | QC-9410 | 95.000 | 568-73-0 | MFCD00210563 | 276.291 | C18H12O3
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Medchemexpress LLC Topoisomerase IIα-in-8 | 1251578-67-2 | 314.32 | C15H15FN6O | 1 MG
Topoisomerase IIα-IN-8 is a research-grade small-molecule inhibitor of human DNA topoisomerase IIα reported as a weak inhibitor (IC50 = 462 ± 38.0 μM). It is supplied as a powder for laboratory use, has molecular formula C15H15FN6O and molecular weight 314.32 g·mol-1, and is provided with downloadable product and safety documentation. For research use only.
- Weak inhibitor of human DNA topoisomerase IIα (IC50 = 462 ± 38.0 μM).
- Shows limited antiproliferative activity (GI50 > 100 μM in HEK293 and HT-29 cells).
- Supplied as a powder with specified storage recommendations for powder and solutions.
- Molecular formula C15H15FN6O; molecular weight 314.32 g·mol-1.
- Datasheet and safety data sheet available for handling and purity details.
Medchemexpress LLC Cucurbitacin IIa | 58546-34-2 | 562.73 | 1 ML
Cucurbitacin IIa, also known as Hemslecin A, is an orally active and blood-brain barrier-permeable EGFR inhibitor, demonstrating an IC50 of 1.455 nM against human EGFR. It plays a role in inducing caspase-3-dependent apoptosis, downregulating survivin expression, and enhancing autophagy levels. This compound disrupts the actin cytoskeleton through actin aggregation, arrests the cell cycle at the G2/M phase, and provides anti-inflammatory effects by inhibiting the EGFR-MAPK signaling pathway.
- Orally active, blood-brain barrier-permeable EGFR inhibitor
- Induces caspase-3-dependent apoptosis
- Downregulates survivin expression
- Enhances autophagy levels
- Disrupts actin cytoskeleton via actin aggregation
- Arrests cell cycle at G2/M phase
- Exerts anti-inflammatory activity by inhibiting EGFR-MAPK signaling pathway
- Suitable for research in inflammation-related diseases, depression, and cancers