Natural Products
| Catalog No. | Information |
| CFN95141 | Pueroside B Pueroside B may can treat coronary heart disease, it can interact with two or more targets[peroxisome proliferator activated receptor γ (PPAR-γ), angiotensin-converting enzyme (ACE), hydroxymethylglutaryl coenzyme A receptor (HMGR), cyclooxygenase-2 (COX2), and thrombin]. |
| CFN95140 | 7-(4-Hydroxyphenyl)-1-phenyl-4-hepten-3-one 7-(4-Hydroxyphenyl)-1-phenyl-4-hepten-3-one as a beneficial compound to ameliorate the deleterious effects of Aβ on dendrite integrity and cell survival, and may provide new insights on drug discovery of Alzheimer's disease (AD). |
| CFN95139 | 7-(4-hydroxy-3-methoxyphenyl)-1-phenylhept-4-en-3-one (DPHB) Reference standards. |
| CFN95137 | 5-Hydroxy-1-(4-hydroxyphenyl)-7-phenyl-3-heptanone (AO 2210) (±)-5-hydroxyl-1-(4′-hydroxyphenyl)-7-phenyl-3-heptanone have digestibility inhibition in vitro in cow rumen fluid. |
| CFN95136 | Orientalide Reference standards. |
| CFN95135 | 5-Hydroxy-7-(4'-hydroxy-3'-methoxyphenyl)-1-phenyl-3-heptanone (DHPA) 5-Hydroxy-7-(4'-hydroxy-3'-methoxyphenyl)-1-phenyl-3-heptanone (DHPA) is a pancreatic lipase inhibitor, it shows antihyperlipidemic activity. |
| CFN95134 | Rhamnocitrin 3-glucoside Reference standards. |
| CFN95133 | Gardenin D Gardenin D has antioxidant, and antiproliferative activities. |
| CFN91105 | 3beta-Methoxy-2,3-dihydrowithaferin A 3beta-Methoxy-2,3-dihydrowithaferin A has cytoprotective activity, it protects normal cells against stress. |
| CFN91095 | Gardoside Reference standards. |
| CFN95132 | Emodin-8-O-beta-gentiobioside Reference standards. |
| CFN95131 | Torosachrysone 8-O-beta-gentiobioside Reference standards. |
| CFN95130 | Cassiaglycoside II Reference standards. |
| CFN91094 | 6-Hydroxyluteolin 7-glucoside Reference standards. |
| CFN91093 | Neoastilbin Neoastilbin may have antioxidant and anti-inflammatory activities, it shows potent inhibition of lens aldose reductase. |
| CFN91088 | Bacoside A3 Bacoside A3 has antioxidant potential, it shows comparatively higher neuroprotective response analysed as higher cell viability and decreased intracellular ROS. Bacoside A3 shows a newer potential role in the clinical management of opioid withdrawal induced depression. Bacoside A3 inhibited both basal activity as well as verapamil-stimulated ATPase activity, thus its affinity towards P-gp; the interaction of bacosides (A3/A) with Tryptophan hydroxylase (TPH) might up-regulate its activity to elevate the biosynthesis of 5-HT, thereby enhances learning and memory formation. |
| CFN91082 | Bacopaside X Bacopaside X (9.06 μM) showed binding affinity towards the D1 receptor. |
| CFN91079 | Sterebin E Sterebin E may have anti-inflammatory activity. |
| CFN91078 | Sterebin A Sterebin A may have anti-inflammatory activity. |
| CFN95129 | 1-Phenyl-2-propanol Reference standards. |
| CFN95128 | Yuankanin Reference standards. |
| CFN95127 | Yuanhuanin Reference standards. |
| CFN95126 | Maculosidin Maculosidine affect the PS I electron acceptors on leaf discs, it can inhibit ATP synthesis, basal, phosphorylating and uncoupled electron transport acting as Hill reaction inhibitors on spinach chloroplasts. |
| CFN95125 | Microgrewiapine A Microgrewiapine A is a selective cytotoxic agent for colon cancer cells over normal colon cells and to exhibit nicotinic receptor antagonistic activity for both the hα3β4 and hα4β2 receptor subtypes. |
| CFN95124 | Asiaticoside B Asiaticoside B has notable cytotoxicity against HepG2 and MCF-7 cancer cell lines. |
| CFN95123 | 3'-Angeloyloxy-4'-senecioyloxy-2',3'-dihydrooroselol Reference standards. |
| CFN95121 | Cistantubuloside C1 Reference standards. |
| CFN95120 | Cassiaside C Reference standards. |
| CFN95119 | Isorubrofusarin 10-gentiobioside Isorubrofusarin 10-gentiobioside shows promising inhibitory activity against AChE/BACE1. |
| CFN95118 | Polygalin C Reference standards. |
| CFN91072 | 19 alpha-Hydroxyasiatic acid 19 alpha-Hydroxyasiatic acid shows significant anticoagulant effect on the extrinsic pathway. |
| CFN91070 | Isosilybin A Isosilybin A is a partial PPARγ agonist, it significantly induced ABCA1 protein expression, it inhibited both monophenolase (IC50 = 1.7-7.6 µM) and diphenolase (IC50 = 12.1-44.9 µM) of tyrosinase. Isosilybin A shows anti-angiogenic efficacy, it has anti-prostate cancer (PCA) activity that is mediated via cell cycle arrest and apoptosis induction. |
| CFN91066 | Zerumbone Zerumbone is a potential antimicrobial and antibiofilm agent indicated for the therapeutic management of nosocomial medical device-related infections induced by dual-species biofilms of C. albicans and S. aureus. Zerumbone protects the neuronal injury and ameliorates the cognitive function by stimulating the proliferation of endogenous neural stem cells; it suppresses enterotoxigenic bacteroides fragilis infection-induced colonic inflammation through inhibition of NF-κΒ. Zerumbone exhibits a hepatoprotective effect against ALI through its antioxidant and anti-inflammatory activities and the possible mechanism might be mediated by the TLR4/NF-κB/COX-2 pathway. Zerumbone can be a potential candidate for development of immunosuppressive agent. |
| CFN91065 | Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside can effectively induce apoptosis via p53, MAPKs and the mitochondrial apoptotic pathways. |
| CFN91060 | Niga-ichigoside F1 Niga-ichigoside F1(NI) has anti-inflammatory, gastroprotective ,antinociceptive, and cytotoxic effects. NI showed an inhibition zone on β-glucosidase and anti-acetylcholinesterase assays. The dietary NI could prevent HFD-induced hepatic steatosis, possibly via interacting with HFD to activate Nrf2 nuclear translocation to maintain a redox status, thus regulating lipid metabolism genes expressions. |
| CFN95117 | Polygalasaponin XLIX Reference standards. |
| CFN95116 | Rhamnetin 3-galactoside Reference standards. |
| CFN95115 | Hamaudol Hamaudol has analgesic and anti-inflammary activities, it showed inhibitory activity on COX-1 and COX-2 activities with values of 0.30, 0.57 mM, respectively. |
| CFN95114 | 1-Isomangostin 1-Isomangostin has cytotoxic, and anticomplement activities. |
| CFN95113 | Macrophylloside D Reference standards. |
| CFN95112 | 3'-Methoxymirificin Reference standards. |
| CFN95111 | 2-O-cinnamoyl-beta-D-glucose Reference standards. |
| CFN95110 | Pilosidine Pilosidine has vasoconstrictor activity, it showed facilitating effect on adrenaline evoked contractions in rabbit aorta isolated preparations. |
| CFN95109 | Orcinol 1-O-beta-D-apiofuranosyl-(1->6)-beta-D-glucopyranoside Orcinol 1-O-beta-D-apiofuranosyl-(1->6)-beta-D-glucopyranoside has antioxidative activity. |
| CFN95108 | Tangshenoside I Tangshenoside I might be a potential bioactive marker related to the hematopoietic and immunologic functions of Codonopsis Radix, which could be recommended as the index compound. It has α-glucosidase inhibition activity. |
| CFN95107 | Tuberosin Tuberosin shows anti-inflammatory and antioxidant activities.It demonstrated a significantly potent inhibition on yeast α-glucosidase in a dose dependent manner. |
| CFN95106 | Isololiolide Isololiolide has phytotoxicity, it inhibited seedling growth of cress and barnyard grass. It also showed in vitro activity against both trypomastigote and intracellular amastigotes of Trypanosoma cruzi, with IC50 values of 32 μM and 40 μM, respectively. Isololiolide is an antioxidant response element (ARE) inducer, it has anti-inflammatory activity. It can exert a selective cytotoxic activity on hepatocarcinoma HepG2 cells as well as induce apoptosis through the modulation of apoptosis-related proteins. |
| CFN93556 | Luteolin 7-rutinoside Luteolin 7-rutinoside has antiallergic, antimicrobial, antimutagenic and radical scavenging activities, it showed antimutagenic effects on TA1537 and TA1535 strains. Luteolin 7-rutinoside also displayed potent rat lens aldose reductase inhibitory activities with IC(50) values ranging from 0.19 to 5.37 μM. |
| CFN93694 | Irilone Irilone has immunomodulatory, and α-amylase inhibitory activities, it exhibits the selective inhibition toward CYP3 A4 rather than other major human CYPs. Irilone exhibited prominent antioxidant activities with the IC50 value of 10.46μM. Irilone potentiated the effect of progesterone in both endometrial and ovarian cancer cell lines, it protected dopaminergic neurons against LPS-induced injury through inhibition of microglia activation and proinflammatory factors generation. |
| CFN95105 | 6-O-(E)-Caffeoylglucopyranose Reference standards. |
