Natural Products
| Catalog No. | Information |
| CFN96450 | Viroallosecurinine Virosecurinine and viroallosecurinine were isolated as two cytotoxic alkaloids from the leaves of Securinega virosa. Viroallosecurinine exhibits a MIC of 0.48 micrograms/ml for Pseudomonas aeruginosa and Staphylococcus aureus. |
| CFN96451 | Virgatic acid Virgatic acid is a natural product from Salvia virgafa. |
| CFN96452 | Victoxinine Victoxinine, the toxic metabolite, considered previously to be a unique product of Helminthosporium victoriae. |
| CFN96453 | Vibralactone K Vibralactone K is a natural product from Basidiomycete Boreostereum vibrans. |
| CFN96454 | Vibralactone D Vibralactones D shows weak inhibitory activities against isozymes of 11beta-hydroxysteroid dehydrogenases (HSD) with IC(50) values of 85.7 microM (human HSD1), 295.2 microM (mouse HSD1), and 87.1 microM (human HSD2). |
| CFN96455 | Vibralactone B Vibralactone B shows antibacterial activity, it can inhibit significantly the growth of E. coli and Pseudomonas aeruginosa, with MBC values of 50 and 100 ug/mL, respectively. |
| CFN96456 | Vernolide B Vernolide B has marginal cytoxicity (ED(50)=3.78, 5.88, 6.42 microg/ml for KB, NCI-661, and Hela, respectively). |
| CFN96457 | Valerosidate Valerosidate is a natural product from Valeriana jatamansi. |
| CFN96458 | Valeriotriate B Reference standards. |
| CFN95010 | Suchilactone Suchilactone may have the potential to be developed as a treatment of Alzheimer's Disease. |
| CFN96459 | Valeriotetrate C Valeriotetrate C is a natural product from Valeriana jatamansi. |
| CFN96460 | Valeriandoid B Reference standards. |
| CFN96461 | Ustusolate C Ustusolate C and ustusolate E exhibit moderate cytotoxicity against A549 and HL-60 cells with IC50 values of 10.5 and 9.0 microM, respectively. |
| CFN96462 | Ustusolate A 1. Ustusolate A shows weak cytotoxicity against HL-60 and A549 cells with IC50 values of 20.6 and 30.0 microM, respectively. |
| CFN96463 | Ustusol C Reference standards. |
| CFN96464 | Ursodeoxycholic acid Ursodeoxycholic acid is a potent inhibitor of apoptosis, it prevents cytochrome c release in apoptosis by inhibiting mitochondrial membrane depolarization and channel formation. Ursodeoxycholic acid can ameliorate experimental ileitis counteracting intestinal barrier dysfunction and oxidative stress, it as a chemopreventive agent in patients with ulcerative colitis and primary sclerosing cholangitis. |
| CFN96465 | Urolignoside Urolignoside shows antioxidant and radical scavenging activity. |
| CFN96466 | Unedone Unedone is a natural product from Lysimachia clethroides. |
| CFN95011 | Glucoliquiritin Reference standards. |
| CFN90873 | Daidzein dimethyl ether Reference standards. |
| CFN90874 | Trimethoxystilbene Trimethoxystilbene has anti-cancer activity, it inhibits cancer cell growth by inducing multipolar cell mitosis. |
| CFN90875 | Agarotetrol Agarotetrol is a chromone derivative isolated from Agarwood. |
| CFN90876 | Hesperetin-7-methyl ether Hesperetin-7-methyl ether is a natural prooduct from Citrus maxima. |
| CFN90877 | 3-O-beta-Allopyranosyl-(1->4)-beta-oleandropyranosyl-11-O-isobutyryl-12-O-acetyltenacigenin B Reference standards. |
| CFN90878 | Schisantherin E Schisantherin E is a natural compound isolated from the active fraction of the fruits of Schisandra sphenanthera Rehd. et Wils. |
| CFN90879 | Pinoresinol dimethyl ether Pinoresinol dimethyl ether, which could be isolated from the wood of the basal tree Humbertieae, show a variety of activities as the inhibitor of cyclic AMP phosphodiesterase. |
| CFN90880 | 1,2-O-Dilinoleoyl-3-O-beta-D-galactopyranosylracglycerol Reference standards. |
| CFN90881 | Pinocembrin 7-O-(3''-galloyl-4'',6''-(S)-hexahydroxydiphenoyl)-beta-D-glucose Pinocembrin 7-O-(3''-galloyl-4'',6''-(S)-hexahydroxydiphenoyl)-beta-D-glucose can moderately inhibit α-amylase activity, with the IC50 value of 0.03 umol/ml. |
| CFN90882 | Brandioside Brandioside shows strong antioxidant, and neuroprotective effects, it significantly attenuates glutamate-induced neurotoxicity at concentrations ranging from 0.1 to 10 microM; it exhibits significant inhibition of advanced glycation end product formation with the IC50 value of 4.6-25.7 uM. Brandioside shows inhibition of smooth muscle cell proliferation, indicates that it may have preventative effects on arteriosclerosis. |
| CFN90883 | Edpetiline Edpetiline is a natural product from Petilium eduardi. |
| CFN90884 | Oleaside A Oleaside A is a natural product from Nerium oleander. |
| CFN96467 | Undulatoside A Undulatoside A has anti-inflammatory activity, it exhibits inhibition on nitric oxide production in lipopolysaccharide induced RAW 264.7 macrophages with the IC50 value of 49.8 uM. |
| CFN96468 | Uncarinic acid E Uncarinic acid E has anti-cancer activity, it induces apoptosis in HepG2 cells via accumulation of p53, alters the Bax/Bcl-2 ratio, and activates caspases, resulting in cytochrome c release from the mitochondria. A mixture of uncarinic acid E and 27-O-p-(E)-coumaroyloxyursolic acid exhibits antiplasmodial activity, with the IC50 value of 2.9 microg/ml. |
| CFN96469 | Ugaxanthone Ugaxanthone is a natural product from Symphonia globulifera L. |
| CFN96470 | Tyramine Tyramine is a major mutagen precursor in soy sauce, being convertible to a mutagen by nitrite; it is the biological precursor of octopamine, both compounds are independent neurotransmitters, acting through various G-protein coupled receptors, they are antagonistic modulators of behavior and metabolism. |
| CFN96471 | Turmeronol A Turmeronol A and turmeronol B are inhibitors of soybean lipoxygenase, they inhibited soybean lipoxygenase at the IC50 values of 16 uM and 9 uM, respectively. |
| CFN96472 | Tryprostatin A Tryprostatin A is an inhibitor of breast cancer resistance protein. Tryprostatin A and tryprostatin B are indole alkaloid-based fungal products that inhibit mammalian cell cycle at the G2/M phase. |
| CFN96473 | Triumbelletin Triumbelletin is a natural product from Wikstroemia indica. |
| CFN96474 | Triptotriterpenic acid A Triptotriterpenic acid A is a natural product from Tripterygium wilfordii Hook.f. |
| CFN96475 | Triptoquinone A Triptoquinone A may be a useful candidate for the development of a drug as a potent inhibitor of iNOS gene over-expression. Triptoquinone A has anti-inflammatory activity, it prevents ndotoxin-or interleukin-1 beta-promoted induction of nitric oxide synthase in vascular smooth muscle, thus inhibiting development of L-arginine-induced vasorelaxation. |
| CFN96476 | Triptonodiol Triptonodiol is a natural product from Tripterygium wilfordii Hook.f. |
| CFN96477 | Triptocalline A Triptocalline A shows an inhibitory effect on rat lens aldose reductase. |
| CFN96478 | Triptobenzene H Triptobenzene H shows the significant immunosuppressive activity. |
| CFN96479 | Triptinin B Triptinin A and triptinin B are leukotriene D4 antagonist constituents. |
| CFN96480 | Trilepisflavan Trilepisflavan shows significant antimicrobial activity. |
| CFN96481 | 3Alaph-Tigloyloxypterokaurene L3 3Alaph-Tigloyloxypterokaurene L3 is a natural product from Wedelia trilobata. |
| CFN96482 | ent-17-Hydroxykaura-9(11),15-dien-19-oic acid ent-17-Hydroxykaura-9(11),15-dien-19-oic acid is a natural product from Wedelia trilobata. |
| CFN95012 | Alloisoimperatorin Alloisoimperatorin is a candidate of AChE inhibitors, it displays potent antioxidant effects against the DPPH radical and against renal epithelial cell injury by using AAPH to generate peroxyl radicals in vitro. Alloisoimperatorin has estrogenic activity on the Ishikawa cell line, it shows strong ability to induce alkaline phosphatase (AP) with the EC50 values of 0.8 microg/mL. |
| CFN96483 | Dehydroglyasperin C Dehydroglyasperin C is a potent NAD(P)H:oxidoquinone reductase (NQO1) and phase 2 enzyme inducer. Dehydroglyasperin C possesses potent antioxidant, cancer chemopreventive, and neuroprotective activities, it has protective effects against chronic diseases caused by reactive oxygen species as well as potential as an antioxidant food additive. Dehydroglyasperin C protects neuronal cells against glutamate-induced oxidative injury through the induction of HO-1 expression, which is, in turn, activated maybe through Nrf2-Keap1 and PI3K/AKT signaling pathways. |
| CFN90885 | Cytosporone B Cytosporone B is a naturally occurring agonist for Nur77, it also is a Salmonella pathogenicity island 1 (SPI-1)-inhibitor, it may have potential in drug development against antibiotic-resistant Salmonella. Cytosporone B can elevate blood glucose levels in fasting C57 mice, an effect that is accompanied by induction of multiple genes involved in gluconeogenesis. Cytosporone B can inhibit transforming growth factor-b (TGF-β)-induced contraction of human corneal fibroblasts (HCFs), likely as a result of its attenuation of the up-regulation of α-SMA expression. |
