Hot Products

Calystegine B2
Catalog No: CFN00161

Calystegine B2 can inhibit the alpha-galactosidase and enzymes beta-glucosidase activities.

Calystegine B3
Catalog No: CFN00162

Calystegine B3 is a highly specific inhibitor for Man2C1 among various α-mannosidases prepared from rat liver, it could thus serve as a potent tool for the development of a highly specific in vivo inhibitor for Man2C1.

Calystegine B4
Catalog No: CFN00163

Calystegine B4 inhibits almond beta-glucosidase and pig kidney trehalase in a competitive manner, with a Ki value of 7.3 microM and 1.2 microM, respectively.

Calyxin B
Catalog No: CFN99693

Calyxin B exhibits potent activity against human HT-1080 fibrosarcoma cells with an ED50 value of 0.69 microM. A methylated product of calyxin A and an epimeric mixture of Calyxin B, showed greatly reduced activity suggesting that phenolic hydroxyl groups are involved in the inhibitory activity.

Camaldulenic acid
Catalog No: CFN96017

Standard reference

Camellianin A
Catalog No: CFN90992

Camellianin A has anticancer activity, it can inhibit the proliferation of the human hepatocellular liver carcinoma Hep G2 and human breast adenocarcinoma MCF-7 cell lines in a dose-dependent manner and induce the significant increase of the G0/G1 cell population. Camellianin A also shows angiotensin converting enzyme (ACE) inhibitory activity.

Camelliaside A
Catalog No: CFN93559

Camelliaside A is a natural product from Camellia oleifera Abel.

Camelliaside B
Catalog No: CFN93560

Camelliaside B is a natural product from Camellia oleifera Abel.

Campestanol
Catalog No: CFN93818

Campestanol, which shares the same basic structure and intestinal absorption pathway with cholesterol, does not accumulate when fed, and may be incorporated into the diet to block cholesterol absorption.

Campesterol
Catalog No: CFN92204

Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects, it and other plant sterols often decrease LDL cholesterol levels overall. Campesterol has anti-inflammatory effect, it inhibits several pro-inflammatory and matrix degradation mediators typically involved in osteoarthritis- induced cartilage degradation, also sometimes used to treat some specific prostate conditions.