Hot Products

2,4,6-Trihydroxybenzoic acid
Catalog No: CFN70208

2,4,6-Trihydroxybenzoic acid may mediate its effects through a CDK- and SLC5A8-dependent pathway contributing to the prevention of colorectal cancer.

2',4'-Dihydroxy-3',6'-dimethoxychalcone
Catalog No: CFN99391

2',4'-Dihydroxy-3',6'-dimethoxychalcone has cytotoxic, anti-inflammatory activity and anti-cholinesterase activities, it has significant NO inhibitory activity.

2,4-Dihydroxyacetophenone
Catalog No: CFN97463

2,4-Dihydroxyacetophenone is a plant metabolite that can act as a qualitative reagent for ferric iron.

2,4-Dihydroxybenzoic acid
Catalog No: CFN70215

2,4-Dihydroxybenzoic acid is found frequently as a pollutant in natural waters and represents a threat to water quality because it is a precursor to the formation of quinones which are highly toxic. It could as a novel eluent in single column anion chromatography. 2,4-Dihydroxybenzoic acid shows strong inhibitory effects against α-glucosidase enzyme with IC50 values of 549 μg/mL .

2,4'-Dihydroxybenzophenone
Catalog No: CFN92400

Reference standards.

2',4'-Dihydroxychalcone
Catalog No: CFN95493

2',4'-Dihydroxychalcone, in combination with nalidixic acid (HY-B0398), exhibits synergistic effects against E. coli by reducing membrane permeability. 2',4'-Dihydroxychalcone (2',4'-DHC) as a compound with Hsp90 inhibitory and antifungal effects.

2',4'-Dihydroxydihydrochalcone
Catalog No: CFN70401

2',4'-Dihydroxydihydrochalcone has cytotoxic, and anti-inflammatory activities.

2,4-Dihydroxyphenylacetic acid
Catalog No: CFN97051

2,4-Dihydroxyphenylacetic acid is a functional moiety in the toxin molecule and the biological action of spider toxin is explained by direct interaction with an Fe-S center which is known to play an important role for the glutamate binding.

2',5,6',7-Tetrahydroxyflavone
Catalog No: CFN80131

2',5,6',7-Tetrahydroxyflavone inhibited hepatic testosterone 6beta-hydroxylation (CYP3A4) activity with a IC50 of 7.8 microM.

2,5-Dihydroxyacetophenone
Catalog No: CFN93182

2,5-Dihydroxyacetophenone is an uncompetitive inhibitor of murine tyrosinase (K(I) 0.28mm), it strongly inhibits both melanogenesis and cellular tyrosinase activity, it possesses anti-inflammatoryanti-anxiety, and neuroprotective qualities. 2,5-Dihydroxyacetophenone treatment can induce a sustained activation of JNK, ERK1/2, and p38 MAPKs, it also can potentiate the pro-apoptotic and anti-proliferative effects of bortezomib in U266 cells.