Unsubstituted Phenols
eMolecules Medchem Express / 2OH-BNPP1 / 2mg / 446257661 / HY-102081 / / 833481-73-5 / MFCD28120704 / 297.362 / C16H19N5O
Medchem Express / 2OH-BNPP1 / 2mg / 446257661 / HY-102081 / / 833481-73-5 / MFCD28120704 / 297.362 / C16H19N5O
eMolecules Medchem Express / FX-11 / 5mg / 482204411 / HY-16214 / / 213971-34-7 / MFCD22572764 / 350.414 / C22H22O4
Medchem Express / FX-11 / 5mg / 482204411 / HY-16214 / / 213971-34-7 / MFCD22572764 / 350.414 / C22H22O4
Medchemexpress LLC 2-Amino-2',5-dichlorobenzophenone | 2958-36-3 | MFCD00007840 | 100.0% | 266.12 | 10 G
(2-Amino-5-chlorophenyl)(2-chlorophenyl)methanone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. It is for research use only and not sold to patients.
- Used as a biological material or organic compound
- Suitable for life science related research
- For research use only
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.
Selleck Chemical LLC Ginkgolic Acid-1mg
Ginkgolic acid, toxic phenolic compounds present in the fruits and leaves of Ginkgo biloba L., is a potent sumoylation inhibitor also reported to inhibit histone acetylation transferase (HAT).
Medchemexpress LLC Procyanidin C1 (PCC1) | 37064-30-5 | 5 MG
Procyanidin C1 (PCC1) is a natural polyphenol with oral activity. It causes DNA damage, cell cycle arrest, and induces apoptosis. It decreases Bcl-2 levels while enhancing BAX, caspase 3, and caspase 9 expression in cancer cells. Procyanidin C1 also exhibits senotherapeutic activity and extends the lifespan in mice.
- Natural polyphenol
- Oral activity
- Causes DNA damage
- Induces cell cycle arrest
- Induces apoptosis by decreasing Bcl-2 and enhancing BAX, caspase 3, and 9 expression in cancer cells
- Shows senotherapeutic activity
- Increases lifespan in mice
eMolecules Medchem Express / Epimedin A / 5mg / 446274882 / HY-N0257 / / 110623-72-8 / MFCD30496681 / 838.809 / C39H50O20
Medchem Express / Epimedin A / 5mg / 446274882 / HY-N0257 / / 110623-72-8 / MFCD30496681 / 838.809 / C39H50O20
Medchemexpress LLC Ko 143 | 461054-93-3 | MFCD19053160 | 99.9% | 469.57 g·mol⁻¹ | C26H35N3O5 | 50 MG
Ko 143 is a potent, selective inhibitor of the ATP-binding cassette subfamily G member 2 (ABCG2/BCRP) used as a research reagent to investigate transporter-mediated drug efflux and multidrug resistance. It exhibits nanomolar activity in biochemical and cell-based assays and shows substantial selectivity versus other transporters. Supplied as a research-grade small molecule for laboratory use only.
- Potent ABCG2 inhibition at nanomolar concentrations.
- High selectivity over P-gp and MRP-1.
- Suitable for studies of transporter activity and drug resistance.
- Supplied in milligram quantities for laboratory experiments.
- Stable as powder when stored appropriately at low temperature.
Sigma Aldrich Fine Chemicals Biosciences Diethylstilbestrol >=99% (HPLC) | 56-53-1 | MFCD00002373 | 1G
Diethylstilbestrol >=99% (HPLC) | Purity: >=99% (HPLC) | Mol Wt: 268.35 | 56-53-1 | MFCD00002373 | 1G
eMolecules Medchem Express / SYP-5 / 5mg / 446255902 / HY-100693 / / 1384268-04-5 / MFCD30534394 / 312.380 / C18H16O3S
Medchem Express / SYP-5 / 5mg / 446255902 / HY-100693 / / 1384268-04-5 / MFCD30534394 / 312.380 / C18H16O3S
eMolecules Medchem Express / Col003 / 5mg / 455326227 / HY-124817 / / 328565-16-8 / MFCD00852947 / 257.245 / C14H11NO4
Medchem Express / Col003 / 5mg / 455326227 / HY-124817 / / 328565-16-8 / MFCD00852947 / 257.245 / C14H11NO4
Medchemexpress LLC Taxifolin 7-O-α-L-rhamnoside | 137592-12-2 | 20 MG
Taxifolin 7-O-rhamnoside (Taxifolin 7-O-α-L-rhamnoside) is a flavonoid isolated from *Hypericum japonicum*. It is intended for research use only.
- Purity: 98.13%
- Appearance: Solid, off-white to light yellow
- Molecular weight: 450.39
- Formula: C21H22O11
- Soluble in DMSO at 125 mg/mL
- Storage: 4°C, protected from light
- In solvent, -80°C for 6 months or -20°C for 1 month (protect from light)
Enzo Life Sciences Tyrphostin AG 527 (25mg). CAS: 133550-32-0
Alternative name: Tyrphostin B44, (-)-(R)-N-(alpha-Methylbenzyl)-3,4-dihydroxybenzylidenecyanoacetamide. Formula: C18H16N2O3. MW: 308.3. Purity: ≥98% (HPLC). Solubility: Soluble in DMSO or 100% ethanol. Long Term Storage: -20°C. Handling: Store tightly sealed in the dark. Protect from light.
Medchemexpress LLC Dehydroxymethylepoxyquinomicin | 287194-40-5 | 99.8% | 261.23 | 2 MG
Dehydroxymethylepoxyquinomicin, also known as (-)-DHMEQ, is a potent, selective, and irreversible NF-κB inhibitor that covalently binds to a cysteine residue. This chemical compound is known to inhibit the nuclear translocation of NF-κB, which plays a crucial role in various cellular processes. It exhibits significant anti-inflammatory and anticancer activities.
- Potent and selective NF-κB inhibitor
- Irreversibly binds to a cysteine residue
- Inhibits nuclear translocation of NF-κB
- Exhibits anti-inflammatory activity
- Demonstrates anticancer activity
Medchemexpress LLC Ko 143 | 461054-93-3 | MFCD19053160 | 100.0% | 469.6 g/mol | C26H35N3O5 | 1 ML
Potent, selective ABCG2 (BCRP) inhibitor used to probe transporter function and multidrug resistance. Shows over 200-fold selectivity versus P-gp and MRP-1; supplied as a 10 mM solution in 1 mL for laboratory use.
- Potent and selective ABCG2 (BCRP) inhibitor for transporter studies.
- Displays greater than 200-fold selectivity over P-gp and MRP-1.
- Supplied as a 10 mM solution in 1 mL for convenient dosing.
- Molecular weight 469.6 g/mol and formula C26H35N3O5.
- CAS number 461054-93-3 for unambiguous identification.