Unsubstituted Phenols
Medchemexpress LLC HY-50662 10mg Medchemexpress, A-769662 CAS:844499-71-4 Purity:>98%
Medchemexpress, HY-50662 10mg A-769662 CAS:844499-71-4 A-769662 is a potent, reversible AMPK activator with EC50 of 0.8 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.
eMolecules 833481-73-5 | Medchem Express | 2OH-BNPP1 | 2mg | 446257661 | HY-102081 | MFCD28120704 | 297.362 | C16H19N5O
Medchem Express | 2OH-BNPP1 | 2mg | 446257661 | HY-102081 | 833481-73-5 | MFCD28120704 | 297.362 | C16H19N5O
eMolecules 53527-42-7 | Medchem Express | Luteolin-3-O-beta-D-glucuronide | 5mg | 434310729 | HY-N4099 | 462.363 | C21H18O12
Medchem Express | Luteolin-3-O-beta-D-glucuronide | 5mg | 434310729 | HY-N4099 | 53527-42-7 | 462.363 | C21H18O12
Medchemexpress LLC Icilin | 36945-98-9 | 99.3% | 311.29 | 100 MG
Icilin (AG-3-5) is a super-agonist of the transient receptor potential M8 (TRPM8) ion channel. It activates TRPM8 in EGTA in a dose-dependent manner (EC50=1.4 μM) and is considered a "super-cooling agent". Icilin also helps to reduce autoimmune neuroinflammation by modulating the T-cell response.
- Activates TRPM8 in EGTA in a dose-dependent manner (EC50=1.4 μM).
- Considered a "super-cooling agent".
- Modulates T-cell response to reduce autoimmune neuroinflammation.
Medchemexpress LLC HY-N0208 5mg Medchemexpress, Kaempferol-3-O-glucorhamnoside CAS:40437-72-7 Purity:>98%
Medchemexpress, HY-N0208 5mg Kaempferol-3-O-glucorhamnoside CAS:40437-72-7 Kaempferol-3-O-glucorhamnoside, a flavonoid derived from plant Thesium chinense Turcz, inhibits inflammatory responses via MAPK and NF-κB pathways in vitro and in vivo. 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 HY-N0163 10mg Medchemexpress, Magnolol CAS:528-43-8 Purity:>98%
Medchemexpress, HY-N0163 10mg Magnolol CAS:528-43-8 Magnolol, a natural lignan isolated from the stem bark of Magnolia officinalis, is a dual agonist of both RXRα and PPARγ , with EC 50 values of 10.4 µM and 17.7 µM, respectively. 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.
ILEX LIFE SCIENCES LLC TRYPSIN/EDTA P10-028100 100ML
PAN-Biotech Trypsin 0.25% / 1 mM EDTA 4 Na in DPBS, w/o: Ca and Mg (100 ml). DESCRIPTION: Trypsin 0.25% / 1 mM EDTA 4 Na in PBS, w/o: Ca and Mg is a porcine pancreas-derived enzyme plus EDTA-4Na in a PBS solution. Trypsin-EDTA solution is commonly used for the dissociation of anchorage-dependent (adherent) mammalian cells and tissues from culture surfaces. The concentration of trypsin necessary to dislodge cells from their substrate is dependent on the cell type and the age of the culture. Ethylenediaminetetraacetic acid (EDTA), a chelating agent, is often added to trypsin solutions to enhance enzymatic activity by neutralizing calcium and magnesium ions that enhance cell-to-cell adhesion and obscure the peptide bonds on which trypsin acts. LIQUID/POWDER: Liquid. PHENOL RED: Without Phenol Red. Ca/Mg CONTENT: Without Ca and Mg. TRYPSIN: 0.25% Trypsin. EDTA: 0.042 % (1.00 mM) EDTA-Na4 x 2H2O. STERILE: Yes. STORAGE TEMP: -20°C. MANUFACTURER: PAN-Biotech GmbH (Germany).
Medchemexpress LLC Methyl caprooyl tyrosinate | 1104874-94-3 | 98.6% | 293.36 g/mol | C16H23NO4 | 25 MG
MHP (methyl caprooyl tyrosinate) is a small-molecule activator of sphingosine kinase 1 (SPHK1) used as a research reagent. It is supplied as a solid (white to off-white) with reported purity of 98.6%, molecular formula C16H23NO4, and CAS 1104874-94-3. The compound is highly soluble in DMSO and can be prepared for in vivo dosing with common co-solvent systems.
Medchemexpress LLC Tert-butyl 3-[(3S,6S,12aS)-6-isobutyl-9-methoxy-1,4-dioxopyrazino...propanoate | 461054-93-3 | MFCD19053160 | 100.0% | 469.6 g/mol | C26H35N3O5 | 100 MG
Ko 143 is a potent, selective inhibitor of the ABCG2 (BCRP) efflux transporter used in biochemical and cellular research to study transporter-mediated drug resistance and pharmacokinetics. It exhibits greater than 200-fold selectivity over P-gp and MRP-1, and is supplied as a high-purity research-grade small molecule suitable for in vitro applications.
- Potent and selective ABCG2 (BCRP) inhibition.
- >200-fold selectivity over P-gp and MRP-1.
- High purity suitable for research applications.
- Available as a solid or as a DMSO solution for convenient use.
- Suitable for in vitro transporter assays and drug resistance studies.
- CAS number provided for unambiguous identification.
Medchemexpress LLC HY-N1454 5mg Medchemexpress, Apigenin-7-glucuronide CAS:29741-09-1 Purity:>98%
Medchemexpress, HY-N1454 5mg Apigenin-7-glucuronide CAS:29741-09-1 Apigenin-7-glucuronide could inhibit Matrix Metalloproteinases (MMP) activities, with IC 50 s of 12.87, 22.39, 17.52, 0.27 μM for MMP-3, MMP-8, MMP-9, MMP-13, respectively. 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 Hesperetin 7-O-glucoside | 31712-49-9 | 99.4% | 464.42 g·mol⁻¹ | C22H24O11 | 5MG
Hesperetin 7-O-glucoside is a flavanone monoglucoside provided for laboratory research with reported anti-inflammatory and antihypertensive activity. It is intended for research use only and not for human or clinical applications. The product is supplied with supporting documentation including a datasheet, certificate of analysis, and safety data sheet.
- Flavanone monoglucoside structure with molecular formula C22H24O11.
- Molecular weight 464.42 g·mol⁻¹.
- High purity (~99.4%) as indicated on the COA.
- Supplied in small research pack sizes suitable for assay development.
- Includes datasheet, certificate of analysis, and safety data sheet.
- Commonly used in studies of flavonoid metabolism and enzyme inhibition.
Medchemexpress LLC Procyanidin B3 | 23567-23-9 | 5 MG
Procyanidin B3 is a natural product that exhibits antioxidant activity and oral bioavailability. It has good blood-brain barrier penetration and acts as a selective inhibitor of histone acetyltransferase (HAT). It inhibits p300 HAT-mediated acetylation of the androgen receptor and can alleviate intervertebral disc degeneration (IVDD) by inhibiting the formation of the TLR4/MD-2 complex. Procyanidin B3 is suitable for research related to prostate cancer and arthritis.
- Natural product
- Antioxidant activity
- Oral bioavailability
- Good blood-brain barrier penetration
- Selective inhibitor of histone acetyltransferase (HAT)
- Inhibits p300 HAT-mediated acetylation of the androgen receptor
- Alleviates intervertebral disc degeneration (IVDD) by inhibiting the formation of the TLR4/MD-2 complex
- Can be used in research on prostate cancer and arthritis
Medchemexpress LLC Combretastatin A-1 | 109971-63-3 | 97.0% | 100 MG
Combretastatin A-1 (CAS 109971-63-3) is a microtubule polymerization inhibitor supplied as a research-grade solid. It is used as an analytical standard and reagent for studying tubulin dynamics, cell biology assays, and biochemical experiments. Common handling involves dissolution in DMSO to prepare concentrated stock solutions for in vitro use.
- Microtubule polymerization inhibitor for tubulin-related studies.
- Suitable as an analytical standard and research reagent.
- High purity appropriate for biochemical and cell-based assays.
- Stable as a powder when stored under recommended frozen conditions.
- Soluble in DMSO for preparation of concentrated stock solutions.
eMolecules 118409-62-4 | Medchem Express | AG126 | 5mg | 446259300 | HY-108330 | MFCD00236448 | 215.168 | C10H5N3O3
Ambeed | N1-(3-Aminopropyl)butane-14-diamine | 1g | 627733185 | A128137 | 124-20-9 | MFCD00008229 | 145.250 | C7H19N3
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Medchemexpress LLC 3,6-Dihydroxyflavone | 108238-41-1 | 5 MG
3,6-Dihydroxyflavone is an anti-cancer agent. It dose- and time-dependently decreases cell viability and induces apoptosis by activating caspase cascade and cleaving poly (ADP-ribose) polymerase (PARP). It also increases intracellular oxidative stress and lipid peroxidation.
- Anti-cancer agent
- Induces apoptosis by activating caspase cascade and cleaving PARP
- Increases intracellular oxidative stress and lipid peroxidation
- Purity: 98.06%