Hot Products

3,8'-Biapigenin
Catalog No: CFN99025

3, 8''-Biapigenin can modulate intracellular ROS production.

3,8-Di-O-methylellagic acid
Catalog No: CFN98217

3,3'-Di-O-methylellagic acid reveals moderate antibacterial activity, it also shows strong DPPH radical scavenging activities with SC50 of 123.3 ug/mL. It has a lower capacity of stimulating murine peritoneal macrophages to release nitric oxide and tumoural-alpha necrose factor. 3,3'-Di-O-methylellagic acid may be a useful as pharmacological agent for the treatment of neurodegenerative diseases.

3,9-Dihydroxypterocarpan
Catalog No: CFN97043

3,9-Dihydroxypterocarpan and phaseollidin are all good precursors of the pterocarpan phytoalexin phaseollin.

3-Acetyl-ginsenoside F1
Catalog No: CFN95238

Reference standards.

3alpha-Akebonoic acid
Catalog No: CFN99067

3α-Akebonoic acid shows interesting in vitro growth inhibitory activity against human tumor A549 and HeLa cell lines, it also shows significant in vitro α-glucosidase inhibitory activity. 3α-Akebonoic acid can interfer with presenilin-1 (PS1)/ β-site APP-cleaving enzyme 1 (BACE1) interaction and reduces Aβ production, the chemical interference of PS1/BACE1 interaction is a promising strategy for Alzheimer’s disease therapeutics.

3alpha-Hydroxytanshinone IIA
Catalog No: CFN90352

Reference standards.

3beta-Hydroxylanosta-8,24-diene-21-al
Catalog No: CFN92365

3beta-Hydroxylanosta-8,24-diene-21-al may have cancer cell growth inhibitory activity against P388, HL-60, L1210 and KB cell lines.

3beta-Methoxy-2,3-dihydrowithaferin A
Catalog No: CFN91105

3beta-Methoxy-2,3-dihydrowithaferin A has cytoprotective activity, it protects normal cells against stress.

3-beta-O-(trans-p-Coumaroyl)maslinic acid
Catalog No: CFN92210

3-beta-O-(trans-p-Coumaroyl)maslinic acid is a DNA polymerase B" inhibitor. It shows antimicrobial activity on Gram-positive bacteria and yeasts.

3-Butylidenephthalide
Catalog No: CFN99588

(Z)-3-butylidenephthalide has antihyperglycemic effect is due to inhibition of α-glucosidase at the intestinal level, inhibited the activity of yeast-α-glucosidase (IC(50) 2.35 mM) in a noncompetitive fashion with a K(i) of 4.86 mM. It can induce a dose-dependent antinociceptive action in the hot-plate assay, it is also effective for controlling the pain provoked by chemical irritation at the doses of 10 and 31.6 mg/kg.