Natural Products
Catalog No. | Information |
CFN95609 | (E)-1-methoxy-2-O-(p-coumaroyl)-myo-inositol |
CFN95610 | Protocatechuoylcalleryanin-3-O-beta-glucopyranoside |
CFN95611 | Norbergenin Norbergenin, the O-demethyl derivative of bergenin, shows moderate antioxidant activity (IC50 13 μM in DPPH radical scavenging; 32 μM in superoxide anion scavenging). |
CFN95612 | N-Methylarmepavine |
CFN95613 | Ellagic acid 4-O-alpha-L-arabinofuranoside |
CFN95614 | Schizotenuin A |
CFN95615 | Tlatlancuayin |
CFN95616 | New compound 24 |
CFN95617 | New compound 25 |
CFN95618 | Ellagic acid-4-O-beta-D-xylopyranoside Ellagic acid 4-O-β-D-xylopyranoside, an ellagitannin found naturally, exhibits antimicrobial properties and acts as an inhibitor of xanthine oxidase, displaying an IC50 value of 2.1 μg/mL. |
CFN95619 | Akebia saponin E |
CFN95620 | Rhamnocitrin-3-O-neohesperoside-4'-O-glucoside |
CFN91539 | Magnoloside B Magnoloside B shows moderate inhibitory activity against MGC-803 and HepG2 cells. IC50 & Target;IC50: α-glucosidase (0.69 mM) |
CFN91538 | Poricoic acid AM Poricoic acid AM is a triterpenoid with ant-tumor activities |
CFN91537 | Tetradehydropodophyllotoxin Tetradehydropodophyllotoxin possesses antifungal activity. |
CFN91536 | Epirosmanol Epirosmanol is a nature diterpene lactone from S. officinalis. Epirosmanol shows anti-cancer activity and inhibits melanin biosynthesis against melanoma cells. Epirosmanol also exhibits DPPH radical scavenging activity |
CFN91535 | Calythropsin |
CFN91534 | Cephalandole B cephalandole B, an indole alkaloid isolated from cyanide, significantly inhibited IL-17A gene expression and suppressed IL-17A luciferase reporter in Jukat cells in a dose-dependent manner. |
CFN91533 | Dipetalolactone |
CFN91532 | Dihydroparadol |
CFN91531 | (E)-[6]-Dehydroparadol (E)-[6]-Dehydroparadol, an oxidative metabolite of [6]-Shogaol (HY-14616), is a potent Nrf2 activator. IC50 & Target: Nrf2 |
CFN91530 | 8-Methoxyflindersine |
CFN91529 | Hydroxylinderstrenolide |
CFN91528 | Kaempferol 7-O-rutinoside |
CFN91527 | Tamarixetin 7-O-neohesperidoside Tamarixetin 7-O-neohesperidoside has moderate hepatoprotective activity. |
CFN91526 | 25,28-Di-epi-cyasterone |
CFN91525 | Mangostanaxanthone IV |
CFN91524 | Garcixanthones B |
CFN91523 | 11-hydroxy-1-isomangostin |
CFN91522 | Ectoine Ectoine ( THP(B)) is a natural amino acid derivate with membrane stabilizing and inflammation reducing capacities. IC50 & Target: Bacterial |
CFN91521 | Chloramphenicol Chloramphenicol is an orally active, potent and broad-spectrum antibiotic. Chloramphenicol shows antibacterial activity. Chloramphenicol represses the oxygen-labile transcription factor and hypoxia inducible factor-1 alpha (HIF-1α) in hypoxic A549 and H1299 cells. Chloramphenicol suppresses the mRNA levels of vascular endothelial growth factor (VEGF) and glucose transporter 1, eventually decreasing VEGF release. Chloramphenicol can be used for anaerobic infections and lung cancer research IC50 & Target: JNK MMP13 |
CFN91520 | Triethyl citrate |
CFN91519 | 5-Hydroxymethyl-2-furoic acid |
CFN91518 | Cyclo(L-Leu-L-Pro) Cyclo(L-Leu-L-Pro) inhibits accumulation of NA by A. parasiticus NFRI-95 and inhibits spore formation. Cyclo(L-Leu-L-Pro) inhibits aflatoxin production with an IC50 of 0.2 mg/mL in A. parasiticus SYS-4. |
CFN91517 | Cyclo(L-Pro-L-Ile) |
CFN91516 | Cyclo(L-Pro-L-Val) Cyclo(L-Pro-L-Val) is a 2,5-diketopiperazine, with toxic activity against phytopathogenic microorganisms (such as R. fascians LMG 3605). Cyclo(L-Pro-L-Val) shows toxicity similar to Chloramphenicol (HY-B0239) with comparable concentration. Cyclo(L-Pro-L-Val) can also inhibit gram-positive phytopathogenic bacterium. Cyclo(L-Pro-L-Val) has potential development as biopesticide. |
CFN91515 | Leucocyanidin Leucocyanidin is an active anti-ulcerogenic ingredient was extracted from Litchi Chinensis. Leucocyanidin demonstrates a significant protective effect against Aspirin-induced erosions in rat models. |
CFN91514 | Nepetin 7-O-beta-D-glucopyranoside |
CFN91513 | Bigelovin Bigelovin, a sesquiterpene lactone isolated from Inula hupehensis, is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation. |
CFN91512 | Aromaticin |
CFN91511 | Carpesiolin |
CFN91510 | 8-epi-Helenalin 8-epi-Helenalin is a semitterpene lactone with anti-tumor activity that can be isolated from Inula britannicaL. var. chinensis (Rupr.) Reg. and the ED50 values of 8-epi-Helenalin for HL-60, A549, MCF7, HCT-15, SK-OV-3 and Malme-3M are 12.2 μM, 53.8 μM, 9.1 μM, 8.7 μM, 18.7 μM and 8.3 μM, respectively. 8-epi-Helenalin can be used for anti-tumor studies. |
CFN95621 | 1-Methyl-6,8-dimethoxyquinoline-2 1H-one |
CFN95622 | New compound 26 |
CFN95623 | 4-(2-Hydroxyethyl)benzoic acid |
CFN95624 | Patrinia saponin H3 |
CFN95625 | alpha-[4-[(1E)-2-Carboxyethenyl]-2-hydroxyphenoxy]-beta,3,4-trihydroxybenzenepropanoic acid |
CFN95626 | Cimiricaside E |
CFN95627 | 24-epi-7,8-Didehydrocimigenol 3-xyloside |
CFN95628 | 24-epi-24-O-acetyl-7,8-didehydrohydroshengmanol-3-O-beta-D-xylopyranoside |