Natural Products
| Catalog No. | Information |
| CFN92509 | (+)-Isoajmaline Reference standards. |
| CFN92510 | Kaempferol 5-methyl ether Standard reference |
| CFN92511 | 6-Formyllimetin Reference standards. |
| CFN92512 | 5-Hydroxyseselin Reference standards. |
| CFN92513 | (-)-Toddanol Reference standards. |
| CFN92514 | Toddanone Standard reference |
| CFN92515 | Inokosterone Inokosterone is an analgesic drug. It also shows high insect moulting hormone activity. |
| CFN92516 | Chikusetsusaponin IVa Chikusetsusaponin IVa is a novel AMPK activator, can induce insulin secretion from βTC3 cells via GPR40 mediated calcium and PKC pathways, may be developed into a new potential for therapeutic agent used in T2DM patients.Chikusetsusaponin IVa exerts antithrombotic effects, including minor hemorrhagic events. |
| CFN92517 | Zingibroside R1 Zingibroside R1 has anti-HIV-1 activity. |
| CFN92518 | Peucedanocoumarin I Standard reference |
| CFN92519 | Peucedanocoumarin II Peucedanocoumarin II shows only partial relaxation. |
| CFN92520 | 5,6,7,4'-Tetrahydroxyflavanone 6,7-diglucoside Reference standards. |
| CFN92521 | 6-Hydroxykaempferol-3,6,7-triglucoside 6-Hydroxykaempferol 3,6,7-tri-O-glucoside and 6-hydroxykaempferol 3,6-di-O-glucoside can inhibit platelet aggregation induced by collagen, they also show weak inhibitory effects on the adenosine 5'-diphosphate (ADP)- induced platelet aggregation. |
| CFN92522 | 25-Anhydrocimigenol 3-O-beta-D-xyloside 25-Anhydrocimigenol 3-O-beta-D-xyloside has notable cytotoxicity against HepG2 and MCF-7 cancer cell lines. |
| CFN92523 | Paederoside Paederoside is a potent deterrent against the beetle was isolated from the aphid.It displays high anti-tumor promoting activity against the Epstein-Barr virus activation. |
| CFN92524 | Paederosidic acid Paederosidic acid has significant anti-tumor, anticonvulsant and sedative effects. Paederosidic acid increases brain gamma-aminobutyric acid and decreases glutamic acid in the brain, and it up-regulates expressions of GAD 65, may be a promising future therapeutic agent for treatment of epilepsy. |
| CFN92525 | Paederosidic acid methyl ester Paederosidic acid methyl ester has antinociception, is possibly related to the pathway of NO-cGMP-ATP sensitive K(+) channels. |
| CFN92526 | Kihadanin A Kihadanin A is a natural product from Phellodendron amurense. |
| CFN92527 | Kihadanin B Kihadanin B can repress the adipogenesis by decreasing lipid accumulation through the suppression of the Akt-FOXO1-PPARγ axis in 3T3-L1 adipocytes. |
| CFN92528 | Methyl 4-caffeoylquinate Reference standards. |
| CFN92529 | Cyclohexanecarboxylic acid Standard reference |
| CFN92530 | Kobophenol A Kobophenol A has antimicrobial, and anti-inflammatory activities, it might be a candidate for treatment of inflammatory bone diseases relevant to osteoblast cell death. Kobophenol A inhibits AChE activity in a dose-dependent manner, and the IC50 value is 115.8mM. Kobophenol A has protective effect against nitrosative/oxidative or mitochondrial damages resulted in the inhibition of the ROS, intracellular calcium ion level, and mitochondrial transmembrane potential changes on SH-SY5Y cells. Kobophenol A, identified through docking studies, is the first compound that inhibits SARS-CoV-2 binding to cells through blocking S1-RBD to the host ACE2 receptor and thus may serve as a good lead compound against COVID-19. |
| CFN92531 | Hopeachinol B Hopeachinol B is a potent immunosuppressive polyphenol. |
| CFN92532 | Cudraflavanone B Standard reference |
| CFN92533 | Kurarinol Kurarinol is a potent inhibitor of sortase A, with an IC50 value of 107.7 ± 6.6 μM. Kurarinol has extremely strong tyrosinase inhibitory activity, exerts varying degrees of inhibition on tyrosinase-dependent melanin biosynthesis, is a candidate as skin-whitening agents. |
| CFN92534 | Kushenol K Kushenol K is a potent and Selective Inhibitor of cGMP Phosphodiesterase 5, it also has inhibitory effects on diacylglycerol acyltransferase (DGAT). Kushenol K shows weak antiviral activity against Herpes simplex virus types I and II. |
| CFN92535 | Scandoside Scandoside exerts anti-inflammatory effect via suppressing NF-κB and MAPK signaling pathways in LPS-induced RAW 264.7 macrophages.It also inhibits LDL-oxidation. |
| CFN92536 | Digiferruginol Digiferruginol has cytotoxic activity. Digiferruginol and hederagenin show weak effect on porcine respiratory and reproductive syndrome virus (PRRSV) with an IC50 value of 80.5 ± 16.9 uM(SI = 19.9) and 43.2 ± 7.4 uM (SI = 13.1), respectively. |
| CFN92537 | 2-Anthraquinonecarboxylic acid Anthraquinone-2-carboxylic acid is a novel electron shuttling mediator, shows potent anti-inflammatory and antinociceptive activities in vivo, thus contributing to the immune regulatory role of fruits and herbs. |
| CFN92538 | 4,6-Dimethoxy-2H-1-benzopyran-2-one Reference standards. |
| CFN92539 | 1,3,5,6-Tetrahydroxyxanthone 1,3,5,6-Tetrahydroxyxanthone shows moderate hepatoprotective activity with EC(50) values of 160.2 +/- 0.6 microM against tacrine-induced cytotoxicity in HepG2 cells. It can inhibit angiotensin-I-converting-enzyme activity in a dose-dependent manner. |
| CFN92540 | 1,3,6-Trihydroxy-5-methoxyxanthone Standard reference |
| CFN90504 | Noroxyhydrastinine Noroxyhydrastinine exhibits potent melanogenesis-inhibitory activities, it inhibits melanogenesis, at least in part, by inhibiting the expression of protein levels of tyrosinase, TRP-1, and TRP-2 in α-MSH-stimulated B16 melanoma cells. |
| CFN90505 | Palmatrubine Palmatrubine binds to double-stranded DNA most probably via an intercalating mode. |
| CFN92541 | 1,3,6,8-tetrahydroxy-4-(3-methyl-2-buten-1-yl)-9H-Xanthen-9-one Reference standards. |
| CFN92542 | Alisol A Alisol A may be an autophagic inducer, it has anti-cancer activity, it presents inhibitory effects on cancer cell lines tested(HepG2, MDA-MB-231, and MCF-7 cells). |
| CFN92543 | 25-O-Methylalisol A Reference standards. |
| CFN92544 | Alisol A 23-acetate Alisol A 23-acetate may possess therapeutic effects through their modulation of AR, PR, and GR pathways. |
| CFN92545 | Alisol C Alisol C can improve glucose uptake in Hep G2 cells, it may be one of the therapeutic material basis in hypoglycemic activities in A. orientalis. Alisol C,16,23-oxido-alisol B and alisol O in Zexie may cause nephrotoxicity. |
| CFN92546 | Alisol E 23-acetate Reference standards. |
| CFN92547 | 16-Oxoalisol A Reference standards. |
| CFN92548 | Alisol G Alisol G has hCE2 inhibitory effects. |
| CFN92549 | Trans-caffeic acid Trans-caffeic acid stearyl ester is posited to inhibit melanogenesis signaling while suppressing cAMP levels and, subsequently, MC1R, MITF, tyrosinase, TRP-2 and TRP-1 down-regulation, resulting in the suppression of tyrosinase activity, DOPA oxidase activity and melanin synthesis. |
| CFN92550 | Icariside I Icariside I is a metabolite product of Icariin. |
| CFN92551 | 2''-O-Rhamnosylicariside II 2″-O-Rhamnosylicariside II shows potent antioxidant activity, with IC50 values of 11.5 ug/mL and 90.5 uM. It shows potent inhibitory activities on osteoclast-like cell formation at a concentration of 2 uM without toxic effects. |
| CFN92552 | Eriosematin A Eriosematin A exhibits antifungal activity against Cladosporium cucumerinum and Candida albicans in TLC bioautographic assays. |
| CFN92553 | Isorhyncophylline Isorhyncophylline and rhyncophylline can directly inhibit the contractile responses induced by several agonists in small blood vessels of rat, they also can inhibit the hypertensive effect of angiotensin Ⅱ. |
| CFN92554 | Phellolactone Phellolactone is a natural product from Phellodendron chinense. |
| CFN92555 | Skimmianin Skimmianine is a new inhibitor against the Leishmania APRT enzyme, it is also a strong acetylcholinesterase (AChE) inhibitor. Skimmianine has anti-inflammatory, immunomodulatory, and leishmanicidal properties, it has a selective inhibitory effect on the 5-hydroxytryptamine-induced vasopressor responses of rats. |
| CFN92556 | 3,8-Dihydroxy-2,4,6-trimethoxyxanthone Standard reference |
