Natural Products
| Catalog No. | Information |
| CFN92215 | 5,2',6'-Trihydroxy-6,7,8-trimethoxyflavone 5,2',6'-Trihydroxy-6,7,8-trimethoxyflavone (ED 50 =4.5 ug/ml ) shows cytotoxicity against L1210 cell and has inhibiting effects on ATPase from the cell. |
| CFN92216 | Skullcapflavone II Skullcapflavone II is a flavonoid derived from Scutellaria baicalensis, a widely used herbal medicine in anti-inflammatory and anticancer therapy in Korea. Skullcapflavone II may have therapeutic potential for the treatment of allergic asthma. |
| CFN92217 | Rivularin Reference standards. |
| CFN92218 | Norwogonin Norwogonin(IC 50 = 1.1 microM) shows potent inhibitory activity toward VHR. |
| CFN92219 | Bavachromene 1. Bavachromene exhibits a significant inhibitory effect on baculovirus-expressed BACE-1 in vitro. |
| CFN92220 | Isobavachromene Isobavachromene is an inhibitor of NADH-Ubiquinone oxidoreductase and ornithine decarboxylase. Isobavachromene has antifungal activity. |
| CFN92221 | Bavachalcone Bavachalcone has antibiotic or anticancer activities, it may be useful as a therapeutic drug for bone resorption-associated diseases.Bavachalcone can protect the endothelial function by increasing AMPK activity and MnSOD expression and reducing mitochondrial oxidative stress. |
| CFN92222 | Neobavaisoflavone Neobavaisoflavone, exhibits inhibitory activity against DNA polymerase and platelet aggregation, it also has striking anti-inflammatory and anti-cancer effects, Neobavaisoflavone can significantly inhibit the production of reactive oxygen species (ROS), reactive nitrogen species (RNS) and cytokines: IL-1β, IL-6, IL-12p40, IL-12p70, TNF-α in LPS+IFN-γ- or PMA- stimulated RAW264.7 macrophages. |
| CFN92223 | Isoneobavaisoflavone Reference standards. |
| CFN92224 | Psoralenoside Psoralenoside is a narture product from Psoralea corylifolia. |
| CFN92225 | Isopsoralenoside Isopsoralenoside shows estrogen-like, osteoblastic proliferation accelerating, antitumor, and antibacterial effects. |
| CFN92226 | Corylifol A Corylifol A is a naturally occurring potent inhibitor of hCE2 and UDP-glucuronosyltransferase 1A1 (UGT1A1); it could be the potential uncouplers of neuronal nitric oxide synthase-postsynaptic density protein-95. Corylifol A displays cytotoxic activity against HepG2 and Hep3B hepatocellular carcinoma cell lines, with IC50 values of 4.6 and 13.5 ug/ml, respectively. Corylifol A has antiinflammatory activity, it shows an inhibitory effect on IL-6-induced STAT3 promoter activity in Hep3B cells with IC50 values of 0.81 ± 0.15 uΜ, it also inhibits STAT3 phosphorylation induced by IL-6 in Hep3B cells. |
| CFN92227 | Corylifol B Reference standards. |
| CFN92228 | Corylifol C Corylifol C and, to a lesser extent, xanthoangelol are potent protein kinase inhibitors (inhibitory concentration 50% values for epidermal growth factor receptor (EGFR): 1.1 and 4.4 × 10(-6) μg/ml, respectively). |
| CFN92229 | Bakuchalcone Reference standards. |
| CFN92230 | Brosimacutin G Reference standards. |
| CFN92231 | Erythrinin A |
| CFN92232 | 13-Hydroxylupanine 13-Hydroxylupanine is a natural product from Cytisus scoparius. |
| CFN92233 | Angustifoline Angustifoline has activity against gram-positive bacteria. It inhibits human colon cancer cell growth by inducing autophagy along with mitochondrial-mediated apoptosis, suppression of cell invasion and migration and stimulating G2/M cell cycle arrest. |
| CFN92234 | Lucidal Lucialdehyde C (Lucidal) exhibits potent cytotoxicity against LLC, T-47D, Sarcoma 180, and Meth-A tumor cells with ED(50) values of 10.7, 4.7, 7.1, and 3.8 microg/ml, respectively. |
| CFN92235 | Ganoderic acid TR Ganoderic acid TR, a new lanostanoid with 5α-reductase inhibitory activity from the fruiting body of Ganoderma lucidum. |
| CFN92236 | Ganoderenic acid A Ganoderenic acid A has a potent hepatoprotective, and cytotoxic effects, it shows inhibitory activity on human aldose reductase in vitro. |
| CFN92237 | Ganoderic acid T-Q Ganoderic acid T-Q and TR are two inhibitors of H5N1 and H1N1 NAs. |
| CFN92238 | Ganoderenic acid C Reference standards. |
| CFN92239 | Delta 5-avenasterol Delta 5-avenasterol has antioxidant activity. |
| CFN92240 | Delta 7-avenasterol Delta 7-avenasterol has antioxidant activity. |
| CFN92241 | 15,16-Dihydrotanshindiol B Reference standards. |
| CFN90499 | Strictosidine Strictosidine has DNA damaging activity in yeast RS 188N mutant, assessed as drug level required to produce 12 mm zone of inhibition. |
| CFN92242 | 15,16-Dihydrotanshindiol C Reference standards. |
| CFN92243 | Salvinolone Salvinolone, demethyl cryptojaponol and taxodione show potent activity with 4-10 microg/mL of MIC against MRSA and 4-16 microg/mL of MIC against VRE. |
| CFN92244 | 12-Hydroxysapriparaquinone 12-Hydroxysapriparaquinone is a natural product from Salvia prionitis. |
| CFN92245 | Prionoid B Prionoid B is a natural product from Salvia prionitis. |
| CFN92246 | 6,7-Dehydroferruginol 6,7-Dehydroferruginol has potent activity against F. palustris . 6,7-Dehydroferruginol and sugiol are weakly active against Heterosigma akashiwo. |
| CFN92247 | 1-Ketoaethiopinone Reference standards. |
| CFN92248 | Salpriolactone Reference standards. |
| CFN92249 | Methylenedihydrotanshinquinone Methylenedihydrotanshinquinone has cytotoxic activity. |
| CFN92250 | Miltipolone Miltipolone is a good and broad-spectrum inhibitor against the growth of cancer cells. It also possibly acts as a Fe(2+) chelator to conduct its inhibitory activity. |
| CFN92251 | Tuberostemonin Reference standards. |
| CFN92252 | Voacangine Voacangine is a novel transient receptor potential vanilloid type 1 (TRPV1) antagonist, it shows mod. cytotoxic activity, also some CNS, brachycardial and hypotensive action.Voacangine significantly suppresses in vitro angiogenesis, such as VEGF-induced tube formation and chemoinvasion. |
| CFN92253 | (-)-Haplomyrfolin (-)-Haplomyrfolin is a natural product from Platycladus orientalis. |
| CFN92254 | Kusunokinin Kusunokinin displays significant activity against intracellular amastigotes (IC(50) = 17 µM) and trypomastigotes (IC(50) = 51 µM) without hemolytic activity. |
| CFN92255 | (-)-Hinokinin (-)-Hinokinin has anti-genotoxic and anticarcinogenic potential. (-)-Hinokinin is an anti-chagasic drug, has no mutagenic effects in animal cell and bacterial systems, anxiety that target the DAT, NET, and GAT-1 transporters, it may serve as a tool to develop new therapeutic drugs for attention deficit hyperactivity disorder. |
| CFN92256 | Daphnelantoxin B Daphnelantoxin B shows inhibition on aphid body detoxify enzyme system. |
| CFN92257 | Daphnenone Daphnenone shows cytotoxic activity against the tumor cells of human melanoma A375-S2 , with the IC(50) value of 29.8 uM. |
| CFN92258 | Daphneolone Daphneolone analogues are potentially active against plant pathogenic fungi, Rhizoctonia solani, Gibberella zeae, Bipolaris maydis, Sclerotia sclerotium and Botrytis cirerea. |
| CFN92259 | Ponicidin Ponicidin has anti-leukemia, immunoregulatory and anti-inflammatory functions, it also has anti-viral function especially in the upper respiratory tract infection. Ponicidin has anti-cancer activity against gastric carcinoma and lung cancer; can inhibit growth and induce apoptosis of gastric carcinoma cell line MKN28, via the signaling pathway regulated by Janus kinase 2 (JAK2) and signal transducers and activators of transcription 3 (STAT3). |
| CFN92260 | Augustifolin Reference standards. |
| CFN92261 | 6-epi-Augustifolin Reference standards. |
| CFN92262 | Effusanin E Effusanin E shows antibacterial and anti-cancer activities, it significantly inhibits cell proliferation and induces apoptosis in NPC cells by suppressing p50/p65 proteins to down-regulate COX-2 expression . |
| CFN92263 | Lushanrubescensin H Lushanrubescensin H is a natural product from Isodon rubescens. |
