Natural Products
Catalog No. | Information |
CFN95032 | Dactylorhin A Dactylorhin A exhibits moderate inhibitory effect on NO production effects in RAW 264.7 macrophage cells. |
CFN95033 | Gymnoside III Gymnoside III is a natural product from Gymnadenia conopsea. |
CFN95034 | Ginsenoside F5 Ginsenoside F5 is a natural product from Panax ginseng C. A. Mey. |
CFN95035 | 2'-Rhamnoechinacoside 2'-Rhamnoechinacoside is a natural product from Cistanche tubulosa. |
CFN95036 | 20-O-Glucoginsenoside Rf 20-O-Glucoginsenoside Rf is a natural product from Panax ginseng C. A. Mey. |
CFN95037 | Iristectorin A Iristectorin A is a natural product from Iris tectorum. |
CFN95038 | Columbianetin beta-D-glucopyranoside Columbianetin-beta-D-glucopyranoside exhibits anti-inflammatory and analgesic properties, it also shows strong inhibiting activity against platelet aggregation. |
CFN95039 | Arjungenin Arjungenin shows β-glucuronidase inhibitory activity, it shows antiviral, and anti-inflammatory activities. Arjungenin exhibits moderate antibacterial activity against Staphylococcus aureus, Escherichia coli and Enterococcus faecalis (MICs within a range of 64 and 256 ug/mL). Arjungenin shows significant protection against domoic acid induced toxicity in Caco-2 cell line. |
CFN95040 | Cordifolioside A Cordifolioside A possesses immunomodulatory activity, it has a potential in vivo radioprotective effect as well as in vitro cytoprotective activity. |
CFN95041 | 2''-O-Galloylquercitrin 2''-O-Galloylquercitrin is a natural product from Acer ginnala. |
CFN95042 | Carasinol B Carasinol B is a natural product from Carex humilis Leyss. |
CFN95043 | 1,3,6-Tri-O-galloylglucose 1,3,6-Tri-O-galloylglucose shows anti-inflammatory activity. |
CFN95044 | Carasinol D Carasinol D is a natural product from Carex humilis Leyss. |
CFN91012 | 19-Oxocinobufagin 19-Oxocinobufagin is a natural product from Bufo bufo gargarizans Cantor. |
CFN91013 | Resibufagin Resibufagin shows strong cytotoxic activity against HeLa cell line. |
CFN91014 | 20-Hydroxyganoderic acid G Reference standards. |
CFN91015 | bis[6-(5,6-dihydrochelerythrinyl)]amine BIS-[6-(5,6-dihydro-chelerythrinyl)] ether shows strong activity against Aspergillus fumigatus and methicillin-resistant Staphylococcus aureus (MRSA). |
CFN91016 | 19-Oxocinobufotalin 19-Oxocinobufotalin 3-adipoylarginine ester shows significant inhibition effect against human hepatocellular carcinoma cell line SMMC-7721 in vitro. |
CFN91017 | Pseudobufarenogin Pseudobufarenogin(ψ-bufarenogin), a novel anti-tumor compound, suppresses liver cancer growth by inhibiting receptor tyrosine kinase-mediated signaling. ψ-Bufarenogin shows inhibition of human kidney Na(+)/K(+)-ATPase activity. |
CFN91018 | (-)-Anonaine (-)-Anonaine has some anticancer activity, it induces apoptosis through Bax- and caspase-dependent pathways in human cervical cancer (HeLa) cells, it induces DNA damage and inhibits growth and migration of human lung carcinoma h1299 cells. (-)-Anonaine may be considered a potent compound for chemotherapy against cervical cancer or a health food supplement for cancer chemoprevention. (-)-Anonaine has vasorelaxant effect. |
CFN91019 | Roemerine Roemerine is a potential active xanthine oxidase(XOD) inhibitor, XOD is a key enzyme in the pathogenesis of hyperuricemia and also a well-known target for the drug development to treat gout. Roemerine has some anti-prostate cancer effect and alleviates adverse reactions in paclitaxel combination administration. Roemerine shows significant anti-plasmodial activities with IC(50) ranged from 1.2 μM to 52.3 uM. Roemerine also possesses antibacterial activity, it improves the survival rate of septicemic BALB/c mice by increasing the cell membrane permeability of Staphylococcus aureus. |
CFN91020 | 19-Hydroxybufalin Reference standards. |
CFN91021 | Hellebrigenol Hellebrigenol shows cytotoxicity against HepG2 cells. |
CFN91022 | Colutehydroquinone Colutehydroquinone and colutequinone are antifungal isoflavonoids from Colutea arborescens. |
CFN91023 | Odoriflavene Odoriflavene has antioxidant activity, and it also shows inhibition effects on the decrease of glutathione level of rat lens induced by UV irradiation. Odoriflavene shows cytotoxic activity against a SH-SY5Y cell line in vitro. |
CFN91024 | Ganoderenic acid E Reference standards. |
CFN91025 | Lucidone B Reference standards. |
CFN91026 | Methyl Kakuol Reference standards. |
CFN91027 | Eclalbasaponin I Eclalbasaponin I has anti-oxidative, and antitumor activities, it reduces oxidative stress-induced neural cell death by autophagy activation, it can dose-dependently inhibit the proliferation of hepatoma cell smmc-7721 with the IC(50) value of 111.1703 ug/ml. |
CFN91028 | Daidzin 6''-O-malonate Daidzin 6''-O-malonate may have anticancer activity. |
CFN91029 | Angenomalin Reference standards. |
CFN91030 | Dihydromollugin Reference standards. |
CFN91031 | Pendulone Pendulone could be a valuable chemopreventive agent, it shows strong inhibition on the effect of the cell cycle induced by TPA and shows potent anti-tumor-promoting activity for an in vivo two-stage carcinogenesis test. Pendulone displays antibacterial activity against Staphylococcus aureus and methicillin-resistant S. aureus (each IC50 1.44 microg/mL). Pendulone shows potent leishmanicidal, it also shows anti-plasmodial activity with the IC50 value of 7.0 ± 0.8 uM. |
CFN91032 | Lucidin 3-O-glucoside Reference standards. |
CFN94877 | Terpinine-4-ol Terpinine-4-ol is a natural product from Pimpinella yunnanensis. |
CFN95045 | Carasiphenol C Carasiphenol C is a natural product from Carex humilis Leyss. |
CFN95046 | 2''-O-Galloylmyricitrin Reference standards. |
CFN95047 | Betmidin Reference standards. |
CFN95048 | 3''-Galloylquercitrin 1. 3''-Galloylquercitrin possesses the activity for PTK inhibition. |
CFN91033 | Tetrahydromagnolol Tetrahydromagnolol can activate cannabinoid (CB) receptors. |
CFN91034 | 4',5,6,7-Tetramethoxyflavone 4',5,6,7-Tetramethoxyflavone has a hemostatic effect. |
CFN91035 | Micheliolide Micheliolide has antineoplastic, anti-inflammatory and immunomodulatory effects, it inhibits various inflammatory response and may serve as a neuroprotective agent in neuroinflammation-related neurodegenerative disorders. Micheliolide has potential as a candidate drug for the treatment of diabetic nephropathy, it can effectively attenuate the high glucose-stimulated activation of NF-κB, the degradation of IκBα, and the expression of MCP-1, TGF-β1 and FN in rat mesangial cells (MCs). Micheliolide also ameliorates liver steatosis by upregulating PPAR-γ expression, thereby inhibiting NF-κB-mediated inflammation and activating AMPK/mTOR-dependent autophagy. |
CFN91036 | Dihydroseselin Dihydroseselin type of pyranocoumarin possessing a 4'-isovaleryl group is important to suksdorfin's enhanced anti-HIV activity. |
CFN95049 | Arjunglucoside I Arjunglucoside I has anti-inflammatory activity, it exhibits significant activity against carrageenan-induced paw edema in rat. It also shows antiproliferative activity against the A2780 human ovarian cancer cell line with an IC(50) value of 1.2 microM. |
CFN95050 | Poricoic acid B Poricoic acid B shows inhibitory activity against TPA-induced ear inflammatory oedema, it also shows potent inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) activation induced by the tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA). |
CFN93412 | Peujaponiside Reference standards. |
CFN95051 | Tectoruside Tectoruside is a natural product from Iris tectorum. |
CFN95052 | Kakkalide Kakkalide is a potent lactate dehydrogenase (LDH) inhibitor, it has anti-inflammatory effects. Kakkalide can inhibit ROS-associated inflammation and ameliorated insulin-resistant endothelial dysfunction by beneficial effects on IRS-1 function.Kakkalide attenuates ethanol-induced gastric injury in mice by inhibiting the infiltration of neutrophils, it also shows protective effects on ethanol-induced lethality and hepatic injury are dependent on its biotransformation by human intestinal microflora. |
CFN95053 | 1-O-galloyl-6-O-cinnamoylglucose Reference standards. |
CFN95054 | Obovatol Obovatol has antioxidant, neuroprotective, antiinflammatory, antithrombotic and antitumour effects, it is a potent NF-κB inhibitors for Alzheimer's disease treatment. Obovatol shows inhibitory effect on the Salmonella type III secretion system, it could be useful for the prevention and supplementary treatment of bacterial infections. Obovatol inhibits receptor activator of nuclear factor kappa B (NF-κB) ligand (RANKL)-induced osteoclast differentiation in vitro and inflammatory bone loss in vivo, it may be a useful therapeutic agent for the treatment of pathological bone disorders characterized by excessive osteoclastic bone resorption. |