Natural Products
| Catalog No. | Information |
| CFN95336 | Peiioside B |
| CFN95337 | Fuzitine |
| CFN91711 | 6-O-Methylcatalpol 6-O-Methylcatalpol has antiprotozoal activity. |
| CFN95338 | Euphorbia factor L22 Reference standards. Euphorbia factor L1 analogue. |
| CFN95339 | Euphorbia factor L25 Reference standards. Euphorbia factor L1 analogue. |
| 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. |
| 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 |
| 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 |
| 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. |
