Hot Products
Catalog No. | Information |
CFN92578 | (-)-Lyoniresinol (-)-Lyoniresinol has antioxidant activity. |
CFN96732 | (-)-Lyoniresinol 9'-O-glucoside (-)-Lyoniresinol 9'-O-glucoside is a natural product from Phyllostachys heterocycla MITF. |
CFN98030 | (-)-Maackiain (-)-Maackiain, a phytoalexin, which is an anti-allergic compound that suppresses the up-regulation of the histamine H1 receptor (H1R) gene. It shows significant growth inhibitory action on the growth of the human lymphoblastoid cell lines Molt and Raji, and shows a strong larvicidal effect against 4th instar larvae of Aedes aegypti(LC50=21.95±1.34ug/mL). |
CFN70079 | (-)-Myrtenol (-)-Myrtenol has gastroprotective, and anxiolytic-like activities, which could be related to GABAA -receptor activation and antioxidant activity. |
CFN91089 | (-)-Perillaldehyde (-)-Perillaldehyde shows antibacterial activity. |
CFN92287 | (-)-Pinoresinol Pinoresinol is the precursor of other dietary lignans that are present in whole-grain cereals, legumes, fruits, and other vegetables, PIN can cause an upregulation of the CDK inhibitor p21(WAF1/Cip1) both at mRNA and protein levels; PIN can ameliorate CCl4-induced acute liver injury, and this protection is likely due to anti-oxidative activity and down-regulation of inflammatory mediators through inhibition of NF-kappaB and AP-1. (+)-Pinoresinol possesses fungicidal activities and therapeutic potential as an antifungal agent for the treatment of fungal infectious diseases in humans. |
CFN96948 | (-)-Pinoresinol 4-O-glucoside (-)-Pinoresinol 4-O-glucoside is a natural product from Lonicera japonica THUNB. |
CFN89475 | (-)-Sativan (-)-Sativan is a phytoalexin. |
CFN90180 | (-)-Sparteine Sparteine is a class 1a antiarrhythmic agent, a sodium channel blocker. The deficient debrisoquine hydroxylation of Sparteine is due to the absence of P-450IID1 protein in the livers of poor metabolizers. |
CFN92500 | (-)-Syringaresinol (-)-Syringaresinol inhibits the proliferation of human promyelocytic HL-60 cells through G(1) arrest and induction of apoptosis, may be a potential chemotherapeutic agent for the treatment of cancer. |