Linear 1 3-diarylpropanoids
Medchemexpress LLC Tetra(p-bromophenyl)porphyrin | 29162-73-0 | 95.0% | 930.32 | C44H26Br4N4 | 5 G
Tetra(p-bromophenyl)porphyrin is a brominated tetrakisphenylporphyrin used as a fluorescent dye and as a synthetic intermediate in porphyrin chemistry. It is employed as a porphyrin scaffold for derivatization and photophysical studies.
- Fluorescent tetrakisphenylporphyrin with four p-bromophenyl groups.
- CAS number 29162-73-0 and formula C44H26Br4N4.
- Molecular weight 930.32 g·mol-1.
- Light blue to blue solid, purity ~95.0%.
- Suitable as a building block for perfluoroalkyl-substituted porphyrins and other derivatives.
- Store protected from light and under inert atmosphere; cold storage recommended for solutions.
Medchemexpress LLC (S)-(+)-1,2-Propanediol | 4254-15-3 | 99.8% | C₃H₈O₂ | 100 G
(S)-(+)-1,2-Propanediol is an endogenous metabolite that can be used as an organic solvent and diluent in drug preparations. It also serves as a chiral synthetic intermediate and a substrate for enzyme research.
- Used as an organic solvent and diluent
- Serves as a chiral synthetic intermediate
- Acts as a substrate for enzyme research
- Endogenous metabolite
Selleck Chemical LLC Avobenzone S1904-200mg
Avobenzone (Butyl methoxydibenzoylmethane BF2AVB) is an oil soluble ingredient used in sunscreen products to absorb the full spectrum of UVA rays and a dibenzoylmethane derivative
Medchemexpress LLC Dibenzoylmethane | 120-46-7 | MFCD00003085 | 98.0% | 224.26 | 25 G
Dibenzoylmethane, a minor ingredient in licorice, activates Nrf2 and prevents various cancers and oxidative damage. It is an analog of curcumin and results in dissociation from Keap1 and nuclear translocation of Nrf2. It is for research use only and not sold to patients.
- Activates Nrf2.
- Helps prevent various cancers and oxidative damage.
- Functions as an analog of curcumin.
- Leads to dissociation of Keap1 and nuclear translocation of Nrf2.
- Available in solid form, off-white to light yellow in color.
- Suitable for in vitro and in vivo studies.
- Stable for 3 years when stored as a solid at room temperature.
eMolecules 32864-38-3 | tert-Butyl ethyl propanedioate | ChemScene | MFCD00009193 | 188.223 | C9H16O4 | 95.000 | CCOC(=O)CC(=O)OC(C)(C)C | 25g | 791179218
tert-Butyl ethyl propanedioate | ChemScene | 32864-38-3 | MFCD00009193 | 188.223 | C9H16O4 | 95.000 | CCOC(=O)CC(=O)OC(C)(C)C | 25g | 791179218
TARGETMOL CHEMICALS INC Naringenin 1G
Also available in 1 mL, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Naringenin (NSC-11855) is a flavanone that is considered to have a bioactive effect on human health as antioxidant, free radical scavenger, antiinflammatory, carbohydrate metabolism promoter, immunity system modulater. This substance has also been shown to repair DNA. Purity 98.81%
Medchemexpress LLC (E)-Naringenin chalcone | 25515-46-2 | 1 MG
(E)-Naringenin chalcone is an orally active anti-allergic agent that also possesses antioxidant and anti-inflammatory activities. It can improve adipocyte functions and inhibits histamine release from rat peritoneal mast cells. This product is for research use only.
- Orally active anti-allergic agent
- Possesses antioxidant activities
- Exhibits anti-inflammatory activities
- Improves adipocyte functions
- Inhibits histamine release from rat peritoneal mast cells
Medchemexpress LLC (±)-Naringenin (Standard) | 67604-48-2 | 98.8% | 272.25 | 100 MG
(±)-Naringenin (Standard) is the analytical standard of (±)-Naringenin, intended for research and analytical applications. It is a naturally-occurring flavonoid that displays a vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes.
- Analytical standard grade
- Naturally-occurring flavonoid
- Used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS
- Appearance: solid, white to light yellow
- Structure classification: flavonoids, phenols
- Initial source: plants other families
- Displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes.