Natural Products
| Catalog No. | Information |
| CFN00165 | Calystegine B5 Reference standards. |
| CFN00166 | Calystegine A3 Calystegines A3, B2, and C1 are glycosidase inhibitors. Calystegines A3 and B2 can effectively stabilize β-glucocerebrosidase, and consequently increase intracellular β-glucocerebrosidase activities in N370S fibroblasts. |
| CFN00167 | Calystegine A7 Calystegine A7 is a glycosidase inhibitor. |
| CFN00168 | Calystegine A6 Reference standards. |
| CFN00169 | Calystegine A5 Reference standards. |
| CFN00170 | 8-Azabicyclo-3.2.1-octan-3-ol Reference standards. |
| CFN98937 | Asperglaucide Asperglaucide shows some nematocidal property against M. incognita. |
| CFN98938 | Methyl lycernuate A Reference standards. |
| CFN98939 | Porson Porson exhibited anti-tubercular activity against Mycobacterium tuberculosis H37Rv in vitro and MICs values of 40.0 μg/mL. |
| CFN98940 | 3-(2,4-Dihydroxyphenyl)propionic acid 3-(2,4-Dihydroxyphenyl)propionic acid and l-ascorbic acid show tyrosinase inhibition activity, a synergistic effect on tyrosinase inhibition was observed when the two compounds were mixed. |
| CFN98941 | 5,6,7,8-Tetramethoxycoumarin Standard reference |
| CFN98942 | Hedychenone Hedychenone has anti-inflammatory activity, it also shows potent in vitro cytotoxic activity against cancerous cells. |
| CFN98943 | Tirotundin Tirotundin is a PPARα/γ dual agonist, it exerts anti-diabetic effect through PPARγ pathway. It shows anti-inflammatory activity, it inhibits inhibit the activation of NF-kappa B, thereby, the synthesis of inflammatory mediators such as cytokines and chemokines is reduced. |
| CFN98944 | Hop-17(21)-en-3-ol Standard reference |
| CFN98945 | Methyl eichlerianate Standard reference |
| CFN98946 | Eichlerianic acid Eichlerianic acid is a trypanocidal compound with an IC50 value of 10 mg/mL. Eichlerianic acid may have antiviral activity against Herpes simplex virus types I and II in vitro. Eichlerianic acid shows weak cytotoxicity (IC50 6.87 to >40 μM) against human cancer cell (HL-60, SMMC-7721, A-549, MCF-7 and SW480). |
| CFN98947 | 4,9-Dihydroxy-alpha-lapachone 4,9-Dihydroxy-alpha-lapachone has antitumor-promoting effects, it exhibits significant inhibitory activity against 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced Epstein-Barr virus early antigen (EBV-EA) activation in Raji cells. 4,9-Dihydroxy-alpha-lapachone exhibits potent inhibitory effects on lipopolysaccharide-induced NO synthesis in RAW 264.7 cells , with IC(50) value of 2.73 microM. |
| CFN98948 | Hinokiol Hinokiol has anti-inflammatory activity, it has significant inhibitory effects on 5-hydroxy-eicosa-tetra-enoic acid (5-HETE) and leukotriene B(4) (LTB4) formations. Hinokiol demonstrates potent activity against clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA). |
| CFN98949 | Steppogenin Steppogenin exhibits significant tyrosinase inhibition activity, it also shows strong mushroom tyrosinase inhibitory activity with IC(50) values lower than 50 microM, more potent than kojic acid (IC(50) = 71.6 microM), a well-known tyrosinase inhibitor. |
| CFN98950 | Phenylalanine betaine Standard reference |
| CFN98951 | Scopoletin acetate Reference standards. |
| CFN98952 | Tanshinone IIA Tanshinone IIA is an estrogen receptor partial agonist with antiandrogenic properties, it has neuroprotective effects against cerebral ischemia/reperfusion injury and traumatic injury of the spinal cord in rats. Tanshinone IIA has anti-leukemia, anti-inflammatory and anti-oxidative properties, inhibits the release of inflammatory cytokines, such as, IL-1 β, IL-6 α, TNF-α. |
| CFN98953 | Tanshinone I Tanshinone I is an inhibitor of type IIA human recombinant sPLA2 (IC50=11 μM) and rabbit recombinant cPLA2 (IC50=82 μM). Tanshinone I possesses hepatocyte protective, anticancer, neuroprotection, and nephroprotective properties. Tanshinone I pretreatment causes significant suppression of skin cell death induces by solar simulated UV and riboflavin-sensitized UVA. |
| CFN98954 | 8-Demethyleucalyptin Reference standards. |
| CFN98955 | Platyphyllenone Platyphyllenone has shown promising anti-filarial activity both in vitro and in vivo studies. It can inhibit the biosynthesis of violacein in C. violaceum CV026. |
| CFN98956 | 9,9'-Di-O-(E)-feruloylsecoisolariciresinol 1,4-O-Diferuloylsecoisolariciresinol(9,9'-Di-O-(E)-feruloylsecoisolariciresinol),and pierreione B, two novel inhibitors of mTOR signaling, have strong anticancer activity. (+)-9,9′-O-Diferuloylsecoisolariciresinol has significant cytotoxic activity against the DU145, LNCaP, and A549 cell lines. |
| CFN98957 | Penduletin Penduletin has anti-inflammatory,anti-tumor cells, and anti-bacterical activities,it inhibits growth of the Gram-negative pathogen neisseria gonorrhoeae. Penduletin has strong activity in vitro against EV71 with low cytotoxicity. |
| CFN98958 | Xanthohumol Xanthohumol has anti-hepatitis C virus, anti-carcinogenic, free radical-scavenging, and anti-inflammatory activities, it can inhibit HIV-1 induced cytopathic effects, the production of viral p24 antigen and reverse transcriptase in C8166 lymphocytes at non-cytotoxic concentration. Xanthohumol may play a role in improving cognitive flexability in young animals. Xanthohumol has beneficial effects on markers of metabolic syndrome, it lowers body weight and fasting plasma glucose in obese male Zucker fa/fa rats. |
| CFN98959 | Stigmasta-5,8-dien-3-ol |
| CFN98960 | 4'-Hydroxywogonin 4'-Hydroxywogonin has positive effect on inhabiting those human tumor lines in vitro, with IC50 value is 8.3-38.4ug/mL . |
| CFN98961 | Avicularin Avicularin exhibits anti-inflammatory activity through the suppression of ERK signaling pathway in LPS-stimulated RAW 264.7 macrophage cells; it inhibits the accumulation of the intracellular lipids by decreasing C/EBPα-activated GLUT4-mediated glucose uptake in adipocytes and potently inhibiting fatty acid synthase. |
| CFN98962 | Engeletin Engeletin, a bioactive flavonoid, has multiple biological activities such as anti-diabetic and anti-inflammatory effects. Engeletin possesses potent inhibition of PGE2 release with IC50 values of 19.6 μg/ml; it inhibits a recombinant human aldose reductase (IC50 value=1.16 microM). |
| CFN98963 | Boehmenan (±)-Boehmenan shows potent protein-tyrosine phosphatase 1B (PTP1B) inhibitory activity in vitro with the IC(50) values of 43.5 uM, it inhibits PTP1B activity in a competitive manner. Boehmenan exhibits the potent cytotoxic effects against many cancer cell lines, boehmenan-mediated anti-tumor property is mediated by modulation of mitochondria and EGFR signaling pathway in A549 NSCLC cells. |
| CFN98964 | Liriodendrin Liriodendrin has anti-inflammatory, antinociceptive, hypoglycemic activities, it plays protective role in sepsis-induced acute lung injury, it regulates lung inflammation, the phosphorylation of the NF-kB (p65) and expression of vascular endothelial growth factor (VEGF). Liriodendrin has protective effects on dopamine-induced cytotoxicity via its anti-oxidative properties by reducing ROS level and anti-apoptotic effect via protection of mitochondrion membrane potential (ΔΨm). It may be a potent suppressor of CaCl(2)-induced arrhythmias, the prophylactic administration of liriodendrin is effective in prolonging latency of arrhythmia and reducing the occurrence of ventricular fibrillation from 75% to 25%. Liriodendrin has inhibitory activities on gastritis and gastric ulcer, it can inhibit colonization of Helicobacter pylori effectively, it could be utilized for the treatment and/or protection of gastritis and gastric ulcer. |
| CFN98965 | Dihydroepistephamiersine 6-acetate Reference standards. |
| CFN98966 | 8-O-Acetylshanzhiside methyl ester 8-O-Acetylshanzhiside methyl ester(ND01) has potential against cerebral ischemic injury and experimental myocardial ischemia injury, it can increase angiogenesis and improve functional recovery after stroke. ND01 protects diabetic brain against I/R injury by alleviating diabetic cerebral I/R injury and attenuating blood–brain barrier (BBB) breakdown, and its protective effects may involve HMGB-1 and NF-κB signalling pathway. |
| CFN00171 | Nortropacocaine Reference standards. |
| CFN00172 | Isoporoidine Isoporoidine is a natural product from Duboisia myoporoides. |
| CFN00173 | Nortropinyl cinnamate Reference standards. |
| CFN00174 | Belladonnine Reference standards. |
| CFN00175 | Beta-Belladonnine Reference standards. |
| CFN00176 | Alpha-Belladonnine Reference standards. |
| CFN00177 | Bellendine Reference standards. |
| CFN00178 | 2,3-Dihydrobellendine Reference standards. |
| CFN00179 | Alkaloid C Reference standards. |
| CFN00180 | Alkaloid KD1 Reference standards. |
| CFN98967 | p-Menth-8-ene-1,2-diol Reference standards. |
| CFN98968 | Stigmast-4-ene-3,6-dione Stigmast-4-ene-3,6-dione has anti-inflammatory and anti-allergic properties. |
| CFN98969 | Carpachromene Carpachromene could be a potential anti-inflammatory agent, it blocks protein expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) in LPS-stimulated macrophages.Carpachromene shows significant α-glucosidase inhibitory activity. It also exhibits significant cytotoxicity against HepG2, PLC/PRF/5 and Raji cancer cell lines in vitro. |
| CFN98970 | Sucrose Sucrose is used extensively as a food and a sweetener, it is the most efficient large-scale crop capable of supplying sufficient carbon substrate, in the form of Sucrose, needed during fermentative feedstock production. |
