Natural Products
| Catalog No. | Information |
| CFN95340 | Deoxy euphorbia factor L1 Deoxy euphorbia factor L1 inhibits the growth of lung cancer A549 cells through the mitochondrial pathway (IC50 value of 17.51 ± 0.85 μM) and induces apoptosis. |
| CFN80137 | Violanthin Violanthin may inhibit COVID-19 by acting on the main protease (3CLpro). Violanthin has potent antioxidant and antibacterial activities. Violanthin inhibits acetylcholinesterase (AChE) with an IC50 value of 79.80 μM. |
| CFN95341 | New compound 8 |
| CFN95342 | New compound 9 |
| CFN95343 | New compound 10 |
| CFN95344 | 4'-O-Methyllucenin II (Diosmetin 6,8-di-C-glucoside) Diosmetin 6,8-di-C-glucoside has antioxidant and anti-aging activities. |
| CFN80138 | Lucenin II Lucenin II has anticonvulsant, antibacterial, anti-inflammatory and antihepatotoxic activity. Lucenin II caused a decrease in the percentage of spore germination, protonemal development and root growth. |
| CFN91710 | Corysamine chloride Corysamine chloride was identified to be active as the inhibitors of ACHE. |
| CFN91709 | Galanthamine 10-Oxide(Galanthamine N-Oxide) Galanthamine N-Oxide inhibits electric eel acetylcholinesterase (AChE) with an EC50 of 26.2 μM. Galanthamine N-Oxide is a prominent inhibitor of substrate accommodation in the active site of the Torpedo californica AChE (TcAChE), hAChE and hBChE enzymes. |
| CFN91708 | O-Desmethyl galanthamine O-Desmethyl Galanthamine (Sanguinine) is galanthamine-type alkaloid. O-Desmethyl Galanthamine is an acetylcholinesterase (AChE) inhibitor, with an IC50 1.83 μM. Sanguinine only shows activity against the fibroblast lineage. |
| CFN91707 | O-Acetylgalanthamine Reference standards. Galanthamine analogue. |
| CFN91706 | Demethylisoencecalin Demethylisoencecalin has antihyperglycemic activity. |
| CFN91705 | Anhydrobyankangelicin Isobyakangelicol is a coumarin that can be found in the roots of Angelica dahurica. Isobyakangelicol inhibits the growth of HeLa and HepG2 cells, with IC50s of 70.04 μM and 17.97 μM. |
| CFN91704 | 3'-Hydroxyxanthyletin 3'-Hydroxyxanthyletin showed antimycobacterial activities against Mycobacterium tuberculosis H(37)R(V) in vitro with MIC values of 16 microg/ml. |
| CFN95345 | Dioscoreside C Dioscoreside C showed mild cytotoxicity against the cancer cell lines, A375, L929, and HeLa, in a dose-dependent manner. |
| CFN95346 | Dioscoreside E Dioscoreside E showed cytotoxic activity and Anti-fungal activity against a panel of tumor cell lines. |
| CFN95347 | Secotubeimoside I Reference standards; tubeimoside I analogue. |
| CFN95348 | Planispine A Planispine A has Anti-inflammatory activity. |
| CFN95349 | trans-Psoralenoside Trans-Psoralenoside has hepatoprotective, kidney protection, antiulcer and anticoagulant activities. |
| CFN91703 | Polyporusterone B Polyporusterone B is a triterpene carboxylic acid isolated from Polyporus umbellatus Fries. Polyporusterone B has inhibitory effect on free radical-induced lysis of red blood cells (hemolysis). Polyporusterone B promotes hair regrowth. and shows potent anticancer activity in HepG2 cells. |
| CFN91702 | (25R)-Spirost-4-ene-3,12-dione (25R)-Spirost-4-ene-3,12-dione has anti-inflammatory and anti-allergic properties. (25R)-Spirost-4-ene-3,12-dione ((-)-(25R)-Spirost-4-ene-3,12-dione) is a natural product that has an inhibitory effect on neutrophil superoxide anion production and histamine release from mast cells |
| CFN91701 | Acetylcytisine N-Acetylcytidine is the Anti-Herbal Chemical Defense Compound in Genista. |
| CFN91700 | 4,4'-Dihydroxy-2,6-dimethoxydihydrochalcone 4,4'-Dihydroxy-2,6-dimethoxydihydrochalcone exhibits COX-1 and COX-2 inhibitory activity. |
| CFN95350 | Isospinosin |
| CFN95351 | New compound 11 |
| CFN95352 | Apigenin 7-[rhamnosyl-(1->2)-galacturonide] |
| CFN95353 | Dipsacussaponin C Dipsacussaponin C potently induces procoagulant activity in platelets and leads to increased thrombus formation. DSC has an antinociceptive effect when it is administered supraspinally and GABAA, NMDA and non-NMDA receptors, but not opioid and GABAB receptors located at the supraspinal level, may be involved in DSC-induced antinociception. Dipsacus saponin C evoked hemolysis directly on the erythrocytes. |
| CFN95354 | Japondipsaponin E1 |
| CFN95355 | Hederagenin 3-O-(2-O-acetyl-alpha-L-arabinopyranoside) Hederagenin 3-O-(2-O-acetyl-α-L-arabinopyranoside) significantly increased alkaline phosphatase (ALP) activity and the level of protein expression of bone sialoprotein (BSP) and osteocalcin (OC) . |
| CFN95356 | 8-Hydroxypinoresinol-4'-O-beta-D-glucopyranoside |
| CFN95357 | Kaempferol 3,4'-di-O-glucoside Kaempferol 3,4'-diglucoside causing the blueing effects on anthocyanin |
| CFN95358 | Acacetin 7-[rhamnosyl-(1->2)-galacturonide] |
| CFN95359 | Dipsacus saponin X |
| CFN91699 | Gosferol |
| CFN91698 | Ilexoside XLVIII Ilexoside XLVIII is an acyl CoA cholesteryl acyl transferase (ACAT) inhibitor. Ilexoside XLVIII is a triterpene saponin isolated from an aqueous extract of the leaves of Ilex kudincha. |
| CFN91697 | Limocitrin 3-O-beta-D-glucopyranoside Limocitrin 3-O-beta-D-glucopyranoside( Limocitrin 3-β-D-glucose) is a flavonoid glycoside. |
| CFN91696 | Cyaonoside A 3-O-β-D-Glucopyranosyl(1→2)-[a-Lrhamnopyranosyl(1→3)]-β-D-glucopyranosyl 28-O-β-D-glucuronopyranoside, a saponin, is isolated from Polaskia chichipe Backbg. 3-O-β-D-Glucopyranosyl(1→2)-[a-Lrhamnopyranosyl(1→3)]-β-D-glucopyranosyl 28-O-β-D-glucuronopyranoside shows ability to inhibit melanin biosynthesis by B16 melanoma cell with inhibitory activity 84.2% at 100μM |
| CFN91695 | Cyaonoside B |
| CFN91694 | Hispidol Hispidol ((Z)-Hispidol) is a potential therapeutic for inflammatory bowel disease; inhibits TNF-α induced adhesion of monocytes to colon epithelial cells with an IC50 of 0.50 μM. Hispidol was found to potently and selectively inhibit an isoform of recombinant human monoamine oxidase-A (MAO-A), with an IC50 value of 0.26 μM, and to inhibit MAO-B, but with lower potency (IC50 = 2.45 μM). Hispidol has antifungal, anti-inflammatory and antidepressant effects. |
| CFN91693 | Limocitrin-3-O-rutinoside |
| CFN95360 | Apigenin 6,8-di-C-alpha-L-arabinopyranoside Apigenin 6,8-di-C-α-L-arabinopyranoside (Apigenin 6,8-di-C-arabinoside) is a natural C-glycosylflavone compound |
| CFN95361 | Foliachinenoside C |
| CFN95362 | ZP-amide C |
| CFN95363 | Eschweilenol C Eschweilenol C has antifungal, anti-inflammatory, antioxidant, antidiabetic activity. 4-(alpha-rhamnopyranosyl)ellagic acid is an inhibitor of human recombinant aldose reductase HRAR (IC50 = 4.1 x 10(-8) M). |
| CFN91692 | Benvitimod (Tapinarof) Benvitimod is targeted as a topical cream treatment for psoriasis, a chronic autoimmune skin disease. Tapinarof (WBI-1001) is a natural aryl hydrocarbon receptor (AhR) agonist with an EC50 of 13 nM. Tapinarof resolves skin inflammation in mice. 3,5-Dihydroxy-4-isopropylstilbene exhibits antioxidant and anticancer activities. |
| CFN91691 | Rehmapicrogenin Rehmapicrogenin, isolated from the root of Rehmannia glutinosa, exhibits potent anti-inflammatory effect by inhibiting iNOS, COX-2 and IL-6. Rehmapicrogenin attenuates kidney damage by reducing inflammatory factor release through the oestrogen signalling pathway. |
| CFN91690 | Dihydrocatalpol Dihydrocatalpol has antidiabetic activity. |
| CFN91689 | Theasaponin E1 Theasaponin E1 has antitumor, anti-inflammatory, QR-inducing activity and obesity prevention effects. Theasaponin E1 inhibits gastric emptying in mice and accelerates gastrointestinal transit. Theasaponin E1 destroys the salt tolerance of yeasts. Theasaponin E1 show antisweet activity. Theasaponin E1 has neuroprotective effects. |
| CFN91688 | Theasaponin E2 Theasaponin E2 has antitumor activity. |
| CFN91687 | 1-Methyl-2-[(6Z,9Z)-6,9-pentadecadiene]-4(1H)-quinolone Methyl-2-[(6Z,9Z)-6,9-pentadecadienyl]-4(1H)-quinolone9 is an antagonist of angiotensin II receptor (IC50=48.2 μM). Methyl-2-[(6Z,9Z)-6,9-pentadecadienyl]-4(1H)-quinolone9 is a quinolone alkaloid from Evodia rutaecarpa.1-methyl-2-[(6Z,9Z)-6,9-pentadecadienyl]-4(1H)-quinolone is an MAO-B inhibitor.1-Methyl-2-[(6Z,9Z)-6,9-pentadecadiene]-4(1H)-quinolone exhibits potent anti-Helicobacter pylori activity with a minimum inhibitory concentration (MIC) value of 10-20 μg/ml. 1-Methyl-2-[(6Z,9Z)-6,9-pentadecadiene]-4(1H)-quinolone exhibits dose-dependent DGAT inhibition with IC 50 of 13.5 μ. |
