Natural Products
Catalog No. | Information |
CFN90109 | Diethyl 2-acetamido-2-(4-octylphenethyl)malonate Reference standards. |
CFN90110 | 3'-Nitroacetophenone Reference standards. |
CFN90111 | 3,5-Dihydroxybenzaldehyde Reference standards. |
CFN90112 | Methyl 3-methoxyacrylate Reference standards. |
CFN90113 | 9-Phenylcarbazole 9-Phenylcarbazole-based dendrons results in the HOMO energy level of -5.36 eV for the 3rd-generation dendrimer, very close to the work function of the ITO/PEDOT electrode (-5.2 eV), which characteristic is very advantageous for the hole injection and transport materials. |
CFN90114 | 3-Bromo-N-phenylcarbazole Reference standards. |
CFN90115 | 3-Methyl-4-nitrobenzoic acid Reference standards. |
CFN90116 | Quinine HCl Quinine HCl produces alpha-adrenergic blockade. Quinine modifies catecholamine- and calcium-induced myocardial contractile force responses. |
CFN97041 | Ferulamide Ferulamide derivatives show potent inhibitory activity against arachidonic acid-induced platelet aggregation. |
CFN97042 | Isobonducellin Isobonducellin exhibits potent cytotoxic activity in Jurkat and HepG2 cells, while moderate growth inhibition against Colon205 cells. |
CFN97043 | 3,9-Dihydroxypterocarpan 3,9-Dihydroxypterocarpan and phaseollidin are all good precursors of the pterocarpan phytoalexin phaseollin. |
CFN97044 | 4-(3,4-Dihydroxyphenyl)-2-butanone 4-(3,4-Dihydroxyphenyl)-2-butanone is a natural product from Taxus yunnanensis. |
CFN90117 | Indoxacarb Given Indoxacarb's effect on adult fleas, egg production and egg viability, this formulation can interrupt flea reproduction on treated cats for at least 6 weeks after treatment. |
CFN90118 | Desoxyanisoin Desoxyanisoin could as efficiently transformed in seven steps into the platinum(II) complexes 1a–c. |
CFN90119 | 1-2-Cyclohexanedione 1,2-Cyclohexanedione, an arginine specific reagent , causes inhibition of transport and a reduction of the capacity of the band 3 protein to bind the specific transport inhibitor H 2DIDS. |
CFN90120 | Propargyl p-toluenesulfonate Propargyl p-toluenesulfonate is a functional initiator. |
CFN90121 | Heptanal oxime Reference standards. |
CFN97045 | Grandifloroside Grandifloroside shows good antioxidative and potent anti-inflammatory activities, it also exhibits potent inhibitory activity against TNF-α and 5α-reductase, suggests that it might be developed as a source of potent anti-oxidative and anti-inflammatory agents and therapeutic agent for benign prostatic hypertrophy (BPH). |
CFN97046 | Cannabispiran Cannabispiran is a natural product from Cannabis sativa L. |
CFN97047 | Vitexilactone Vitexilactone is a HIV-1 reverse transcriptase inhibitor in virtual screening against Indonesian Herbal Database using AutoDock4 performed on HIV-1 reverse transcriptase. It has trypanocidal activity, the minimum lethal concentration against epimastigotes of Trypanosoma cruzi is 66 microM.Vitexilactone is one anticancer component of Vitex trifolia L., which exerts its anti-proliferative effect on cancer cells through inducing apoptosis and inhibiting the cell cycle. |
CFN97048 | Acteoside Acteoside is a lipase inhibitor, has neuroprotective, anti-obesity,anti-inflammatory, antioxidant, anticancer, cytotoxic,antihypertensive, analgesic, and antimetastatic activities. Acteoside can promote nerve growth factor and tropomycin receptor kinase A expression, inhibit arachidonic acid release and prostaglandin E2 production induced by 0.5 microM melittin. Acteoside can protect the cells from X‑ray induced damage through enhancing the scavenging activity of ROS, decreasing the Bax/Bcl-2 ratio and downregulating the activity of procaspase-3, as well as modulating the mitogen‑activated protein kinase signaling pathways. |
CFN97049 | Isoacteoside Isoacteoside exhibits significant inhibition of advanced glycation end product formation with IC50 values of 4.6-25.7 μM; it has neuroprotective, antioxidant, and anti-inflammatory effects. Isoacteoside can stimulate the increase of α7 and α3 proteins in the cultured cells, attenuate the decreased expression of α3 and α7 nAChR subunit proteins and cell viability on SH-SY5Y cells induced by Aβ; it can regulate caspase-1, mitogen-activated protein kinases (c-Jun N-terminal kinase, p38, extracellular signal-regulated protein kinase) and nuclear factor-kappa B pathways. |
CFN97050 | alpha-Mangostin Alpha-Mangostin has neuroprotective, anti-cancer, antifungal, neuroprotective, renoprotective, antioxidant and anti-inflammatory activities. Alpha-Mangostin exhibits peripheral and central antinociception through modulation of opioid and vanilloid receptors, the glutamatergic system, and the larginine/NO/cGMP/PKC/K(+)-ATP pathways; it suppresses phorbol 12-myristate 13-acetate-induced MMP-2/MMP-9 expressions via alphavbeta3 integrin/FAK/ERK and NF-kappaB signaling pathway in human lung adenocarcinoma A549 cells. Alpha-Mangostin is also a novel competitive histamine H1 receptor antagonist in smooth muscle cells. |
CFN97051 | 2,4-Dihydroxyphenylacetic acid 2,4-Dihydroxyphenylacetic acid is a functional moiety in the toxin molecule and the biological action of spider toxin is explained by direct interaction with an Fe-S center which is known to play an important role for the glutamate binding. |
CFN97052 | Vasicine Vasicine, a potential natural cholinesterase inhibitor, has been in development for treatment of Alzheimer's disease. Vasicine can regulate the inflammatory reaction, have great potentials to develop safe medications for respiratory and reproductive medicine.Vasicine is also oxytocic and abortifacient agents. |
CFN90122 | Gomisin D Gomisin D is a natural product from Schizandra chinensis. |
CFN90123 | Gomisin G Gomisin G is a drug candidate for treatment of cardiovascular disease, and it is a good substrate of CYP2C9, and can be easily affected by the inhibitors of CYP2C9. Gomisin G exhibits anti-tumor activities, it exhibits potent anti-HIV activity with EC50 and therapeutic index (TI) values of 0.006 microgram/mL and 300, respectively. |
CFN90124 | Gomisin J Gomisin J is a good substrate of cytochrome P450 3A4(CYP3A4), it has vasodilatory, anti-inflammatory, anti-diabetes, anti-oxidant, and anti-cancer effects, it also has preventive effects on angiotensin II-induced hypertension via an increased nitric oxide bioavailability. Gomisin J has potential benefits in treating nonalcoholic fatty liver disease, it can suppress lipid accumulation by regulating the expression of lipogenic and lipolytic enzymes and inflammatory molecule. Halogenated gomisin J is a potent inhibitor of the cytopathic effects of human immunodeficiency virus type 1 (HIV-1) on MT-4 human T cells (50% effective dose, 0.1 to 0.5 microM). |
CFN90125 | Gomisin N Gomisin N has anti-oxdiant, anti-inflammatory, anti-cancer and anti-hepatitis activities; it produces beneficial sedative and hypnotic bioactivity, which may be mediated by the modification of the serotonergic and GABAergic system. Gomisin N can enhance TNF-α-induced apoptosis by suppressing of NF-κB and EGFR signaling pathways, and potentiate TRAIL-induced apoptosis through ROS-mediated up-regulation of death receptors 4 and 5. |
CFN90126 | Hosenkoside G Hosenkoside G is a natural product from Impatiens balsamina L. |
CFN97053 | 15,16-Epoxy-12R-hydroxylabda-8(17),13(16),14-triene Reference standards. |
CFN97054 | 13-Hydroxy-8,11,13-podocarpatrien-18-oic acid Reference standards. |
CFN97055 | Furomollugin Furomollugin has antiviral activity, it can strongly suppress the secretion of hepatitis B surface antigen (HBsAg), with IC50 = 2.0 micrograms/mL, in human hepatoma Hep3B cells. |
CFN97056 | 11-Methoxyuncarine C Reference standards. |
CFN97057 | Neridienone B Neridienone B has significant effects on calcein accumulation. Neridienone exhibits significant leishmanicidal activity against amastigotes of L. mexicana. |
CFN97058 | Methyl 2-(5-acetyl-2,3-dihydrobenzofuran-2-yl)propenoate Methyl 2-(5-acetyl-2,3-dihydrobenzofuran-2-yl)propenoate is a natural product from Vernonia cinerea. |
CFN97059 | Methyl 2-(6-acetyl-5-hydroxy-2,3-dihydrobenzofuran-2-yl)propenoate Methyl 2-(6-acetyl-5-hydroxy-2,3-dihydrobenzofuran-2-yl)propenoate is a natural product from Vernonia cinerea. |
CFN97060 | 5-O-Methylnaringenin 5-O-Methylnaringenin is a marker, reduced MS detection of 5-O-methylnaringenin indicated that nifedipine may preferably remove a proton from the 5-position OH group in the A ring of the flavonoid skeleton. |
CFN90127 | Dihydrochelerythrine Dihydrochelerythrine has antifungal activity against pathogenic plant fungi; it shows antiparasitic efficacy against Ichthyophthirius multifiliis in richadsin, it has potential application in the therapy of serious infection caused by I. multifiliis. Dihydrochelerythrine affects cell cycle distribution, activates mitochondrial apoptotic pathway, and induces apoptosis and necrosis in HL-60 cells. |
CFN90128 | 2-Carboxybenzaldehyde The major peak of 2-Carboxybenzaldehyde reductase activity in human liver co-purifies with hAFAR protein. Sulphydryl substances and some proteins play important roles in preserving the molecular and catalytic properties of 2-Carboxybenzaldehyde reductase. |
CFN90129 | Octahydroisoindole Reference standards. |
CFN97061 | Deoxycalyciphylline B Deoxycalyciphylline B exhibits hepatic toxicity. Deoxycalyciphylline B and Methyl homosecodaphniphyllate show different inhibitory effects on thephenoloxidase (PO) of Spodoptera exigua (Hbner) and the inhibitor concentrations leading to 50% (IC50) activity lost are estimated to be 2.439 mmol.L-1 for deoxycalyciphyllineB and 0.879mmol.L-1 for methyl homosecodaphniphyllate,respectively. |
CFN97062 | Deoxyisocalyciphylline B Standard reference |
CFN97063 | 4-Hydroxybenzamide 4-Hydroxybenzamide is a natural product from Berberis pruinosa. |
CFN97064 | p-Menthane-1,2,8-triol Standard reference |
CFN97065 | Helichrysetin Helichrysetin has mild anti-HIV-1 PR activity. Helichrysetin has great potentials for development as an anticancer agent, it has cytotoxic effect on four selected cancer cell lines, A549, MCF-7, Ca Ski, and HT-29. |
CFN97066 | Onitisin 2'-O-glucoside Reference standards. |
CFN97067 | epsilon-Viniferin Epsilon-Viniferin is a bacteriostatic stilbenoid as it antagonized the bactericidal activity of vancomycin. Epsilon-viniferin shows a human cytochrome P450 enzymes inhition activity, it exhibits good antioxidant capacity in the DMSO/O(-)(2) polar system (IC50= 0.14 mM). Epsilon-viniferin and epsilon-viniferin pentaacetate slightly reduce cell proliferation but might protect from cell degenerescence.(-)-Trans-epsilon-viniferin is an inhibitor of noradrenaline and 5-hydroxytryptamine uptake and of monoamine oxidase activity, it may be of value as a structural template for the design and development of new antidepressant drugs. |
CFN97068 | alpha-Viniferin Alpha-viniferin is a prostaglandin H2 synthase inhibitor, which has anti-inflammatory, anti-oxidant, anti-arthritis, and anti-tumor activities. Alpha-Viniferin inhibits AChE activity is specific, reversible and noncompetitive, in a dose-dependent manner, and the IC50 values of alpha-Viniferin were 2.0 microM. Alpha-Viniferin exhibits a dose-dependent inhibition on cyclooxygenase activity, where 50% of inhibition (IC50) was shown at a final concentration of about 7 microM, it down-regulates STAT-1-inducible inflammatory genes via inhibiting ERK-mediated STAT-1 activation in IFN-gamma-stimulated macrophages. |
CFN00203 | Valeroidine Reference standards. |