Natural Products
Catalog No. | Information |
CFN95543 | Oblongaroside B |
CFN95542 | Tembetarine Tembetarine has anti-inflammatory and anti-injury properties.Tembetarine was antifeedant against S. frugiperda. |
CFN95541 | Methyl lucidenate C |
CFN95540 | Apigenin-6-C-beta-D-glucopyranosyl-8-C-[alpha-L-rhamnopyranosyl-(1->2)]-beta-glucopyranoside |
CFN95539 | Bayin |
CFN95538 | New compound 19 |
CFN95537 | Ganoderic acid beta Ganoderic acid beta(GAB) simultaneously increased IL-10, IFN-γ associated with induction of T-bet and Foxp3, while suppressing IL-5, which was associated with suppression of GATA3, demonstrating unique beneficial cytokine modulatory effect.Ganoderic acid beta, showed significant anti-human immunodeficiency virus (anti-HIV)-1 protease activity. |
CFN95536 | Ganolucidic acid E Ganolucidic acid E inhibits the growth of three types of human cancer cells: Caco-2, HepG2 and HeLa cells. |
CFN95535 | 12-Acetoxy ganoderic acid D |
CFN95534 | Methyl ganoderenate B |
CFN95533 | Mahuannin J |
CFN95532 | Caffeoylcalleryanin Caffeoylcalleryanin exerted strong 15-LOX inhibitory activity; IC50 values was 1.59 μM.A. pulchra leaves ethanol extract (EEAPL) affords compounds with antiviral activity, mainly against DENV-2. respectively, while Caffeoylcalleryanin was the most effective anti-DENV-2 constituent, with a SI of 20.0. |
CFN95531 | (3,4-Dihydroxyphenyl)methyl 3-(beta-D-glucopyranosyloxy)-4-hydroxybenzoate |
CFN95530 | Odontoside |
CFN95529 | Herbacetin 3-sophoroside-8-glucoside |
CFN95528 | Gossypetin 3-sophoroside-8-glucoside |
CFN95527 | New compound 18 |
CFN95526 | Hainanic acid B |
CFN95525 | Regaloside I Regaloside I, which has the structure of phenylpropanolglycerol glycoside, acts as an active compound that inhibits the upregulation of CAPZA1 and inhibits UVA-induced changes in HDF shape, which in turn inhibits collagen reduction. |
CFN95524 | Catechin 7-O-beta-D-glucopyranoside Catechin 7-O-beta-D-glucopyranoside has intestinal anti-inflammatory activity. Catechin 7-O-beta-D-glucopyranoside has a protective effect against STZ-induced cell damage by its antioxidant effects and the attenuation of mitochondrial dysfunction. Catechin 7-O-β-D-glucopyranoside has strong inhibitory activity against α-amylase and α-glucosidase. Catechin 7-O-β-D-glucopyranoside has the activity of inhibiting protein glycation. |
CFN95523 | Dihydroconfertin |
CFN95522 | 5-Hydroxy-4a,8-dimethyl-3-methylen-decahydroazuleno[6,5-b]furan-2(3H)-on |
CFN95521 | Hosenkoside D |
CFN95520 | Hosenkoside L |
CFN95519 | 10-Deacetylcephalomannine 10-Deacetylcephalomannin is also active against PS leukemia in vivo, but it is particularly unstable and forms an equilibrium mixture with its cytotoxic C-7 epimer. 10-Deacetylcephalomannine has growth inhibitory activity against human cancer cell lines such as cervical HeLa adenocarcinoma. |
CFN95518 | Ganoderic acid GS-3 |
CFN95517 | Ganoderenic acid G |
CFN95516 | Ganoderic acid J Ganoderic acid J is a natural terpenoid isolated from the Fungus Ganoderma lucidum. Ganoderic acid J possesses anti-inflammatory anti-inflammatory activity. |
CFN95515 | 12beta-Acetoxy-7beta-hydroxy-3,11,15,23-tetraoxo-5alpha-lanosta-8,20-dien-26-oic acid |
CFN95514 | Ganoderic acid Df Ganoderic acid Df exhibited potent human aldose reductase inhibitory activity, with an IC(50) of 22.8 μM in vitro. Ganoderic acid Df as a potential anticancer agent. |
CFN95513 | Ganolucidic acid B Ganolucidic acids B showd induction ability of hPXR-mediated CYP3A4 expression. |
CFN95512 | Alopecurone A Alopecurone A exhibits potent inhibitory activity on MRP1.Alopecurone A exhibits cytotoxic activity in DU145 (prostate cancer cell line) and MCF-7 (breast cancer cell line) cell lines with IC50 values of 2.44 and 5.44 μg/mL. respectively.Alopecurone A has antibacterial activity against methicillin-resistant Staphylococcus aureus. |
CFN95511 | 2-(2,4-Dihydroxyphenyl)-5,6-methylenedioxybenzofuran (ABF) |
CFN95510 | Sophoraflavone A |
CFN95509 | 8-epi-Confertin |
CFN95508 | 4-O-Coumaroylquinic acid 4-O-Coumaroylquinic acid has potential inhibitory capacity on the spike glycoprotein trimer of SARS-CoV-2.4-O-Coumaroylquinic acid has inhibitory activity against LdNH.4-O-Coumaroylquinic acid has certain antioxidant capacity. |
CFN95507 | 5-O-Coumaroylquinic acid 5-O-Coumaroylquinic acid (3-O-Coumaroylquinic acid), exhibits significant inhibition of PTP1B and a concentration-dependent inhibitory effect on α-glucosidase, thereby demonstrating anti-hyperglycemic properties. Additionally, this compound enhances glucose uptake and inhibits PTP1B in vitro, emphasizing its potential therapeutic applications in glucose regulation. 5-O-Coumaroylquinic acid is a potent, reversible, non-competitive α-amylase inhibitor with an IC50 value of 69.39 μM. |
CFN95506 | Quercetin-3-O-[alpha-L-rhamnose-(1->2)-beta-D-glucopyranosyl]-5-O-beta-D-glucopyranoside |
CFN95505 | 12beta-Acetoxy-3,7,11,15,23-pentaoxo-lanost-8,20-dien-26-oic acid |
CFN95504 | Ganoweberianic acid E |
CFN95503 | Kidjolanin |
CFN95502 | Butesuperin B-7''-O-beta-glucopyranoside |
CFN95501 | erythro-Austrobailignan-6 Erythro-austrobailignan-6 has anticancer activity. EA6-induced apoptosis is mediated by p38 MAPK and caspase-3 activation in both cells. EA6 significantly reduced HER2/EGFR/integrin β3 expression and Src phosphorylation, which was dependent on p38 MAPK activation in 4T-1 and MCF-7 cells.erythro-Austrobailignan-6 induces apoptosis in AGS and NCI-N87 gastric cancer cell lines.Erythro-austrobailignan-6 has antioxidant activity against 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals. Erythro-Austrobailignan-6 has antifungal activity. |
CFN95500 | Massonianoside D |
CFN95499 | beta-Hydroxyacteoside |
CFN95498 | Campneoside II Campneoside II exhibits excellent anti-complement activity. |
CFN95496 | 3-Oxo-alpha-ilexanolic acid |
CFN95495 | Benzylpropyl acetate |
CFN95494 | Isorhamnetin-3-O-rutinoside-7-O-glucoside |
CFN95493 | 2',4'-Dihydroxychalcone 2',4'-Dihydroxychalcone, in combination with nalidixic acid (HY-B0398), exhibits synergistic effects against E. coli by reducing membrane permeability. 2',4'-Dihydroxychalcone (2',4'-DHC) as a compound with Hsp90 inhibitory and antifungal effects. |