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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
68 Results for "
antioxidant capacity
" in MedChemExpress (MCE) Product Catalog:
Products (68)
68 Results for "antioxidant capacity" in MCE Product Catalog:
31
31 Publications Verification
Synonyms: (+)-Dihydroquercetin; (+)-Taxifolin
14
4
4 Cited Publications
Cat. No.: HY-N2025
CAS No.: 57396-78-8
Category:
Flavonoids Flavones Metabolic Disease Plants Bignoniaceae Oroxylum indicum (Linn.) Bentham ex Kurz Disease Research Fields
Target:
3
3 Cited Publications
Cat. No.: HY-N0385
CAS No.: 66280-25-9
Category:
Cardiovascular Disease Monophenols Lignans Phenols Phenylpropanoids Plants Schisandraceae Disease Research Fields Schisandra chinensis (Turcz.) Baill.
Target:
2
2 Cited Publications
Cat. No.: HY-W011757
CAS No.: 303136-82-5
Target:
Research Areas:
Neocuproine hydrochloride monohydrate, 99% can be used to prepare complex solutions for studying antioxidant capacity determination in biological samples based on copper reduction complexes.
1
Category:
Stilbenes Vitis vinifera cv. Zalema Phenols Polyphenols Plants Vitaceae Disease Research Fields Inflammation/Immunology
Target:
1
1 Cited Publications
Cat. No.: HY-N0310
CAS No.: 51330-27-9
1
1 Cited Publications
Cat. No.: HY-N3433
CAS No.: 99882-10-7
Category:
Flavonols Flavonoids Sauropus spatulifolius Beille Other Diseases Phenols Polyphenols Euphorbiaceae Plants Disease Research Fields
Target:
1
1 Cited Publications
Synonyms: (+)-Dihydroquercetin (Standard); (+)-Taxifolin (Standard)
Category:
Flavanonols other families Flavonoids Phenols Polyphenols Plants
1
1
1 Cited Publications
Cat. No.: HY-N7832A
CAS No.: 28500-02-9
Category:
Anthocyans Flavonoids Other Diseases Vitis amurensis Rupr. Phenols Polyphenols Plants Vitaceae Disease Research Fields
Target:
Cat. No.: HY-W017982
CAS No.: 55965-84-9
Synonyms: CMI/MI
Research Areas:
CMIT/MIT (14.5% in water) (CMI/MI) is a mixture of CMIT and MIT, and is also a preservative and skin sensitizer. CMIT/MIT (14.5% in water) increases the levels of phosphorylated ERK1/2, p38, JNK1/2, p53, p21 and Bax, decreases the level of Bcl-2, and activates the Nrf-2/HO-1 signaling pathway. CMIT/MIT (14.5% in water) increases LDH release and lipid peroxidation levels, impairs antioxidant defense capacity, promotes pro-inflammatory cytokine release, induces apoptosis, triggers cell cycle arrest, exhibits neurotoxicity in neuroblastoma cells, and causes dysregulation of Th2/Th17 immune responses. CMIT/MIT (14.5% in water) can be used in studies related to allergy, atopic dermatitis and lung injury .
Cat. No.: HY-W012997
CAS No.: 542-28-9
Synonyms: δ-valerolactone
Target:
Target:
Category:
Triterpenes Verbenaceae Terpenoids Plants Disease Research Fields Inflammation/Immunology Lantana camaraLinn.
Target:
Cat. No.: HY-N7541
CAS No.: 656830-24-9
Target:
Synonyms: Cy 3-soph
Category:
Target:
Cat. No.: HY-W540232
CAS No.: 2284-20-0
Synonyms: 4-Methylphenyl ITC
Research Areas:
4-Methoxyphenyl isothiocyanate (4-Methylphenyl ITC) is an antioxidant, with a IC50 value of 1.25 mM for scavenging DPPH radicals. ORAC testing indicates its antioxidant capacity as 11.7 mM TE (indicating that the antioxidant efficacy of this compound is equivalent to 11.7 mmol of Trolox (HY-101445, a standard antioxidant) under the same conditions), and it extends the oxidation process by approximately 9180 seconds in the Briggs–Rauscher reaction. Additionally, 4-Methoxyphenyl isothiocyanate exhibits moderate cholinesterase inhibitory activity, with an inhibition rate of 30.4% against acetylcholinesterase (AChE) and 17.9% against butyrylcholinesterase (BChE). 4-Methoxyphenyl isothiocyanate holds potential for research in the fields of antioxidation and neurological disorders .
Cat. No.: HY-76779
CAS No.: 25392-41-0
Target:
Research Areas:
4-(Chloromethyl)-7-hydroxycoumarin (compound 4) is a hydroxycoumarin derivative with potent antioxidant effect and high hydroxyl radical-scavenging property. 4-(Chloromethyl)-7-hydroxycoumarin contains a methyl group and a chlorine group in the heterocyclic ring. A series of coumarins incorporating hydroxy-, chloro- and/or chloromethyl-moieties has been investigated as potent inhibitors of the zinc enzyme carbonic anhydrase, expecially tumor-associated isoforms CA IX and XII .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
