Natural Products
| Catalog No. | Information |
| CFN97717 | Lup-20(29)-ene-2alpha,3beta-diol Standard reference |
| CFN97718 | Uzarigenin digitaloside Reference standards. |
| CFN90261 | Acetylaconitine 3-Acetylaconitine, aconitine, and deoxyaconitine are main toxic components of the roots of Aconitum pendulum. |
| CFN90262 | Safflor Yellow A Safflor Yellow A protects cultured rat cardiomyocytes against A/R injury, maybe via inhibiting cellular oxidative stress and apoptosis. |
| CFN90263 | Lycorine Lycorine is a toxic crystalline alkaloid found in various Amaryllidaceae species that weakly inhibits acetylcholinesterase (AChE) and ascorbic acid biosynthesis.Lycorine has antiviral, and anti-cancer effects, the mechanisms of Lycorine on the multiple myeloma cell line ARH-77 are associated with G1 phase cell cycle arrest, mitochondrial dysfunction, reactive oxygen species (ROS) generation, ATP depletion, and DNA damage. |
| CFN97719 | Epipterosin L 2'-O-glucoside Reference standards. |
| CFN97720 | Homopterocarpin Homopterocarpin and Pterocarpus extract offer gastroprotection against indomethacin- induced ulcer by antioxidative mechanism and the modulation of gastric homeostasis, homopterocarpin may be responsible for, or contribute to the antiulcerogenic property of P. erinaceus. Homopterocarpin can contribute to the hepatoprotective and antioxidant potentials of P. erinaceus extract in acetaminophen-provoked hepatotoxicity. It can inhibit (lower concentration) or kill (higher concntration) human^s liver cancer cells under the cultured condition, they have anticancer activity. (-)-Homopterocarpin has active insect antifeedant against both S. litura and R. speratus. (+)-Homopterocarpin also has antimitotic effect. |
| CFN97721 | Serpentinic acid Reference standards. |
| CFN97722 | Nimbin Nimbin is an anti-pyretic, can be used to treat arthritis, hypoglycaemia, peptic ulcers, anti-secretory activity, and it can also be used as an antibiotic. Nimbin requires to elicit a 50% inhibition of this steroid hydroxylase activity in the three insect species examined ranged from approximately 2 x 10(-5) to 1 x 10(-3). Nimbin also shows anti-feedant activity and toxicity against larvae of three species of Lepidoptera, Spodoptera littoralis (Boisd), Spodoptera frugiperda (FE Smith) and Helicoverpa armigera (Hübner) and nymphs of the locusts Schistocerca gregaria (Forskål) and Locusta migratoria (L). |
| CFN90264 | Cyclo(Ile-Val) Cyclo(Ile-Val) shows moderate antifungal and weak antitumor activities in vitro. |
| CFN90265 | Cyclo(Val-Hpro) Cyclo(Val-Hpro) is isolated from Ascotricha genus. |
| CFN90266 | Cyclo(Ala-Phe) Cyclo(Phe-Ala) displays significant anti-diatom activity with the inhibitory rate of 50% at the concentration of 50 microg/mL. |
| CFN90267 | Cyclo(Ala-Tyr) Cyclo(Val-Tyr) is a product from the culture of Pseudomonas putida. |
| CFN90268 | Cyclo(Tyr-Val) Reference standards. |
| CFN90269 | Cyclo(Tyr-Gly) Reference standards. |
| CFN90270 | Cyclo(Pro-Pro) Cyclo(Pro-Pro) tasted bitter.Verpacamides A-D, a sequence of C11N5 diketopiperazines relating cyclo(Pro-Pro) to cyclo(Pro-Arg), from the marine sponge Axinella vaceleti is possible biogenetic precursors of pyrrole-2-aminoimidazole alkaloids. |
| CFN90271 | Cyclo(Phe-Pro) Cyclo(Phe-Pro) inhibition of cholera toxin and toxin-coregulated pilus production correlated with reduced transcription of the virulence regulator tcpPH and was alleviated by overexpression of tcpPH.Cyclo(Phe-Pro) has been shown to inhibit cancer cell growth and induce apoptosis in HT-29 colon cancer cells. |
| CFN90272 | Cyclo(Pro-Gly) Cyclo(Pro-Gly) is an active metabolite of piracetam-N-phenylacetyl-L-prolylglycine (GWS-111), it shows a greater resistance to an enzymatic effect than natural neuropeptides. Cyclo-(Gly-Pro) shows cytotoxicity at the concentration of 10 umol/L, it inhibits the growth of Bacillus subtilis with the minimal inhibitory concentration (MIC) value of 0.8, 0.8 g/L. |
| CFN90273 | Cyclo(Phe-Leu) Cyclo(Phe-Leu) is a new cell cycle inhibitor. |
| CFN97723 | Isopimaric acid Isopimaric acid is active against MDR and MRSA strains of S. aureus which are becoming increasingly resistant to antibiotics, the minimum inhibitory concentrations (MIC) are 32-64 microg/mL . Isopimaric acid is also possible that an antagonistic interaction with reserpine may render the antibiotics inactive. |
| CFN97724 | Rhamnocitrin Rhamnocitrin can enhance the immune function, improve the formation of spleen cells of mice serum hemolysin of chicken red blood cell immune. Rhamnocitrin possesses significant anticataract activity and acts most likely due to its antioxidant property, it shows a significant protection against cloudiness in lenses induced by hydrogen peroxide and hydrocortisone in a dose dependent manner.Rhamnocitrin and kaempferol can augment cellular antioxidant defense capacity, at least in part, through regulation of HO-1 expression and MAPK signal transduction; they not only protect low-density lipoprotein from oxidation but also prevent atherogenesis through suppressing macrophage uptake of oxidized low-density lipoprotein. |
| CFN97725 | Beta-Amyrenonol acetate Reference standards. |
| CFN97726 | Durantoside I Durantoside I has inhibitory activity on the growth of lettuce seedling. It also displays DPPH scavenging activity. |
| CFN90292 | Ganoderic acid D Ganoderic acid D treatment for 48h inhibits the proliferation of HeLa human cervical carcinoma cells with an IC(50) value of 17.3 +/- 0.3 microM. |
| CFN90293 | Ganoderic acid N 23-Dihydroganoderic Acid N has anticancer effects. |
| CFN90294 | Ganoderic acid Y Ganoderic acid Y significantly inhibits the replication of the viral RNA (vRNA) of EV71 replication through blocking EV71 uncoating. |
| CFN90295 | Ganoderic acid Z The binding affinities of ganoderic acid DM and ganoderic acid Z (ΔGbind, −16.83 and−10.99 kcal mol−1) are comparable to that of current commercial drug oseltamivir (−23.62 kcal mol−1);Ganoderic acid DM is a potential source of anti-influenza ingredient, with novel binding pattern and advantage over oseltamivir, it has steric hindrance on the 150 cavity of N1 protein, and exerts activities across the H274Y and N294S mutations, is the attractive candidates of novel neuraminidase (NA) inhibitors.Ganoderic acid zeta has cytotoxicity in vitro against Meth-A and LLC cell lines. |
| CFN90296 | Ganoderic acid AM1 Ganoderic acid AM1 treatment for 48 h inhibited the proliferation of HeLa human cervical carcinoma cells with IC(50) values of 19.8+/-0.7 microM. |
| CFN90297 | Ganoderic acid LM2 Ganoderic acid LM2 exhibits potent enhancement of ConA-induced mice splenocytes proliferation in vitro. |
| CFN90298 | Ganoderic acid TN Reference standards. |
| CFN90299 | Ganolucidic acid A Ganolucidic acid A exhibits cytotoxicity, has inhibitory activities against human HeLa cervical cancer cell lines. It shows significant anti-human immunodeficiency virus (anti-HIV)-1 protease activity with IC50 values of 20-90 microM. |
| CFN90300 | Ganoderenic acid D Ganoderenic acid D is most cytotoxic with IC50 values of 0.14 ± 0.01, 0.18 ± 0.02 and 0.26 ± 0.03 mg/mL in Hep G2, Hela and Caco-2 cells, respectively. |
| CFN90301 | Ganoderenic acid F Reference standards. |
| CFN90302 | Ganoderenic acid H Ganoderenic acid H is one compound of triterpenoids isolated from Ganoderma lucidum, triterpenoids exhibit a broad spectrum of anti-cancer properties, including anti-proliferative, anti-metastatic and anti-angiogenic activities. |
| CFN90303 | Ganoderone A Ganoderone A exhibits potent inhibitory activity against herpes simplex virus. Ganoderone A exhibits strong inhibitory activities against Vero cells (IC50 is 0.3 ug/mL); it also has inhibition against cancer cell lines K562, SW620, and HL60, the 50% inhibiting concentration( IC50) are 9. 61, 22. 38, 7. 14 mg/L, respectively. |
| CFN97727 | Durantoside II Standard reference |
| CFN90304 | Lucialdehyde A Lucialdehydes A-C (1-3) are new lanostante-type triterpene aldehydes, show cytotoxic effects on tumor cells, including Lewis lung carcinoma (LLC), T-47D, Sarcoma 180, and Meth-A tumor cell lines. |
| CFN90305 | Lucialdehyde B Lucialdehyde B exhibits potent inhibitory activity against herpes simplex virus. It shows cytotoxic effects on Lewis lung carcinoma (LLC), T-47D, Sarcoma 180, and Meth-A tumor cell lines. |
| CFN97728 | 4,9,9'-Trihydroxy-3,3'-dimethoxy-8,4'-oxyneolignan Reference standards. |
| CFN97729 | Dehydroadynerigenin digitaloside Reference standards. |
| CFN97730 | 3,5-Diprenyl-4-hydroxybenzaldehyde Reference standards. |
| CFN90306 | Ganoderal A The oxygenated sterols( 26-oxygenosterols ganoderol A, ganoderol B, ganoderal A, and ganoderic acid Y) from G. lucidum can inhibit cholesterol biosynthesis via conversion of acetate or mevalonate as a precursor of cholesterol. |
| CFN90274 | Cyclo(Phe-Val) Cyclo(Phe-Val) is a new cell cycle inhibitor, it shows cyctoxic activity in vitro. |
| CFN90275 | Cyclo(Pro-Val) Cyclo(Pro-Val) shows cyctoxic, moderate antifungal and weak antitumor activities in vitro, it can inhibit the growth of Bacillus subtilis with the minimal inhibitory concentration (MIC) value of 0.8 g/L. Cyclo(Pro-Val) and cyclo(Pro-Tyr) are toxic to both suspension cells and seedlings of Pinus thunbergii, which may offer some clues to research the mechanism of pine wilt disease caused by pine wood nematode. |
| CFN90276 | Cyclo(Tyr-Pro) Cyclo(Tyr-Pro) shows antibacterial activity towards several marine bacterial species, it also shows weak antagonistic activity against VEGFR2 -CD. Cyclo(Tyr-Pro) and cyclo(Pro-Val) are toxic to both suspension cells and seedlings of Pinus thunbergii, which may offer some clues to research the mechanism of pine wilt disease caused by pine wood nematode. |
| CFN90277 | Cyclo(Pro-Trp) Cyclo(Pro-Trp) and cyclo(Phe-Pro) show broad spectrum antibacterial properties. |
| CFN90278 | Cyclo(Tyr-Phe) Cyclo-(Phe-Tyr) shows anticoagulant activities. |
| CFN90279 | Cyclo(Tyr-Hpro) Reference standards. |
| CFN90280 | Cyclo(Phe-Hpro) Reference standards. |
| CFN97731 | Allamandicin Allamandicin shows antifeedant and insecticidal activities against fifth instar larvae of Pieris rapae larvae , the AFC50 value is 0.045 mg/mL after 48 hours. |
