Natural Products
Catalog No. | Information |
CFN96405 | Licoisoflavone B Licoisoflavone B is an inhibitor of germ tube growth in the arbuscular mycorrhizal (AM) fungus Gigaspora margarita, it can strongly inhibit germ tube growth at 0.63 ug/disc, and it can completely inhibit hyphal branching induced by a lupin strigolactone, orobanchyl acetate, in G. margarita at 0.16 ug/disc. Licoisoflavone B exhibits inhibitory activity against the growth of Helicobacter pylori in vitro, it also shows anti-H. pylori activity against a clarithromycin (CLAR) and amoxicillin (AMOX)-resistant strain.Licoisoflavone B exhibits antimutagenic activity against carcinogenic N-methyl-N-nitrosourea (MNU), it is important to prevent DNA damage by N-nitrosamines for cancer chemoprevention. |
CFN96406 | Delta-Tocotrienol Delta-tocotrienol is a potential angiogenic inhibitor, it (2.5-5 microM) can significantly suppress human colorectal adenocarcinoma cells (DLD-1-CM) -induced tube formation, migration, and adhesion on human umbilical vein endothelial cells.It is also a nontoxic activator of mir-34a which can inhibit nonsmall cell lung cancer cells (NSCLC) cell proliferation, induce apoptosis and inhibit invasion, and thus offering a potential starting point for the design of novel anticancer agents. Delta-tocotrienol displays significant radioprotective effects, it protects mouse and human hematopoietic progenitors from gamma-irradiation through extracellular signal-regulated kinase/mammalian target of rapamycin signaling. |
CFN93805 | Vitisin B Vitisin B can stimulate osteoblastogenesis via estrogen receptor-mediated pathway, it can inhibits migration through inhibition of PDGF signaling and enhancement of cell adhesiveness in cultured vascular smooth muscle cells. (-)-Vitisin B can significantly inhibit cell proliferation through inducing cell apoptosis in human HL-60 promyelocytic leukemia cells, it induces apoptosis of leukemia cells might be mediated through activation of JNK and Fas death-signal transduction. |
CFN96407 | Delta-Caesalpin Reference standards. |
CFN96408 | Beta-Furoyleupatolide Reference standards. |
CFN96409 | Beta-Aflatrem Standard reference |
CFN96410 | Alpha-Onocerin diacetate Standard reference |
CFN96411 | Alpha-Obscurine Standard reference |
CFN96412 | Yunnanxane Standard reference |
CFN96413 | Yunaconitoline Reference standards. |
CFN96414 | Ylangenyl acetate Standard reference |
CFN96415 | Ylangenol Standard reference |
CFN96416 | Yangambin Yangambin is a selective antagonist of the cardiovascular effects of platelet activating factor (PAF); it has hypotensive effect, which is probably due to a peripheral vasodilatation that involves, at least, the inhibition the Ca2+ influx through voltage-gated Ca2+ channels. Yangambin has central nervous system activity, it presents a depressant activity in the open field, forced swimming and pentobarbital sleeping time tests. |
CFN90869 | Pennogenin 3-O-beta-chacotrioside |
CFN90870 | Tetrahydropiperin Reference standards. |
CFN90871 | Maltotetraose Maltotetraose and stachyose are potent inhibitors of TNF-α-induced intercellular adhesion molecule-1 (ICAM-1) expression, maltotetraose may be beneficial in the suppression of early atherosclerosis development and could be developed as a dietary supplement for cardiovascular health. |
CFN90872 | Maltohexaose Maltohexaose is a natural saccharide, and can be produced from amylose, amylopectin and whole starch. |
CFN96417 | Yadanzioside P Yadanzioside P has antileukemic and antitumor activities. |
CFN96418 | Yadanzioside M Yadanzioside M has antitumor activity. |
CFN96419 | Yadanzioside L Yadanzioside L shows strong antiviral activity. |
CFN96420 | Yadanzioside K Yadanzioside K is a natural product from Brucea javanica. |
CFN96421 | Yadanzioside I Yadanzioside I shows strong antiviral activity. |
CFN96422 | Yadanzioside G Yadanzioside G has antileukemic activity. |
CFN96423 | Yadanzioside F Yadanzioside F has antileukemic activity. |
CFN96424 | Yadanzioside C Yadanzioside C has antileukemic activity. |
CFN96425 | Yadanzioside A Yadanzioside A has antileukemic activity. |
CFN96426 | Yadanziolide C Yadanziolide C induces differentiation with cultured HL-60 promyelocytic leukemia cells. |
CFN96427 | Yadanziolide B Yadanziolide B exhibits cytotoxic activities with IC50 values of 3.00-5.81 uM. |
CFN96428 | Yadanziolide A Yadanziolide A shows strong antiviral activity. |
CFN96429 | Xanthyletin Xanthyletin has anti-inflammatory, anti-tumor and anti-bacterial activities, it also inhibits symbiotic fungus cultivated by leaf-cutting ants. Xanthyletin exhibits potent inhibition (IC50 values ≤ 4.79 ug/mL) of superoxide anion generation by human nutrophils in response to N-formyl-L-methionyl-L-leucyl-L-phenylalanine/cytochalasin B (fMLP/CB); it inhibits fMLP/CB-induced elastase release with IC50 values ≤ 5.48 ug/mL. |
CFN96430 | Xanthopurpurin Xanthopurpurin shows antiviral activity, it can effectively inhibit rotavirus multiplication by promoting virus-induced apoptosis in MA-104 cells. Xanthopurpurin shows mainly strong inhibition of collagen-induced platelet aggregation. |
CFN96431 | Germacrone 4,5-epoxide (4S,5S)-(+)-Germacrone-4,5-epoxide inhibits certain subtypes of cytochrome P450 (CYP). |
CFN96432 | Bisacurone Bisacurone has anti-oxidant, anti-inflammatory, and anti-metastatic activities, it may have a protective effect against ethanol-induced liver injury by suppressing hepatic oxidation and inflammation. |
CFN96440 | Cauloside A Cauloside A exhibits concentration- and time-dependent mitochondriotoxic activities. |
CFN96433 | Withaperuvin C Withaperuvin C may have anti-inflammatory activity with lipopolysaccharide (LPS)-activated murine macrophage RAW 264.7 cells. |
CFN96434 | Withanolide S Reference standards. |
CFN96435 | Withanolide C Withanolide C is a natural product from Physali alkekengi. |
CFN96436 | Wedelobatin B Wedelobatin B is a natural product from Wedelia trilobata. |
CFN96437 | Wedelobatin A Wedelobatin A is a natural product from Wedelia trilobata. |
CFN96438 | Wedeliatrilolactone A Wedeliatrilolactone A is a natural product from Wedelia trilobata. |
CFN96439 | Wedelialactone A Reference standards. |
CFN96441 | Walsuralactam A Walsuralactam A in the formula I, which is used as an active ingredient, and is used for treating and preventing the tumour. |
CFN96442 | Vomicine Vomicine is a natural product from Strychnos nux-vomica, the S. nux-vomica extracts show antihyperglycemic activity in experimental animals. |
CFN96443 | Volvaltrate B Volvaltrate B shows cytotoxic activity against the lung adenocarcinoma (A549), metastatic prostate cancer (PC-3M), colon cancer (HCT-8), and hepatoma (Bel7402) cell lines, with IC50 values of 8.5, 2.0, 3.2, and 6.1 uM, respectively. |
CFN96444 | Vogeloside Vogeloside shows inhibition of nitric oxide production in lipopolysaccharide-activated macrophages; its activity is comparable to that of aminoguanidine, a classic inhibitor. |
CFN96445 | Voafinidine Voafinidine is a natural product from Tabernaemontana divaricata. |
CFN96446 | Vitexolide D Vitexolide D shows moderate antibacterial activity against a panel of 46 Gram-positive strains. It also shows cytotoxic activities against the HCT-116 cancer cell line and human fetal lung fibroblast MRC5 cell line (1 < IC50s < 10 uM). |
CFN96447 | Vitexin 2''-O-(4'''-O-acetyl)rhamnoside Reference standards. |
CFN96448 | Vitedoin A Vitedoin A shows stronger antioxidative activity than alpha-tocopherol using the ferric thiocyanate method, it also shows higher radical-scavenging effect on the stable free radical, 1,1-diphenyl-2-picrylhydrazyl, than L-cysteine. |
CFN96449 | Virosine B Reference standards. |