Natural Products
Catalog No. | Information |
CFN90539 | Homoarbutin Reference standards. |
CFN90540 | Homobaldrinal Homobaldrinal has low toxic activity. It has genotoxic activity in the Salmonella/microsome test and the SOS-chromotest. |
CFN90541 | Humulone Humulone, a bone resorption inhibitor, induces apoptosis may via its antioxidative activity in the premyocytic leukemia cell line HL-60 between 1 and 100 micrograms/ml. Humulone is also a potent angiogenic inhibitor, can inhibit cyclooxygenase-2 and may be a novel powerful tool for the therapy of various angiogenic diseases involving solid tumor growth and metastasis. Humulone also has antioxidant, antispasmodic, antiviral and antibacterial activities. |
CFN90542 | Chikusetsusaponin IV Chikusetsusaponin IV may relieve cutaneous symptoms caused by excessive apoptotic cell death in the skin through the Fas/FasL pathway. |
CFN00446 | Glycoside L-F2 Reference standards. |
CFN90543 | Tarasaponin VII Reference standards. |
CFN00447 | 1,2,3,6-Tetragalloylglucose 1,2,3,6-Tetragalloylglucose has antioxidative activity, it also shows the most potent anticomplement activity (IC(50), 34 microM). |
CFN90544 | Isosteviol Isosteviol possesses various biological activities including anti-hyperglycemic, anti-hypertensive, anti-tumor, anti-inflammatory, neuroprotective, antibacterial, antifungal,and antioxidant effects.Isosteviol plays a protective role in a variety of stress-induced cardiac diseases, it can prevent the prolongation of action potential in hypertrophied cardiomyoctyes by regulating transient outward potassium and L-type calcium channels. |
CFN92574 | 3-Oxopomolic acid Reference standards. |
CFN92575 | 6-Hydroxykaempferol 3-Rutinoside -6-glucoside Standard reference |
CFN92576 | Ethyl ganoderate J Standard reference |
CFN92577 | Allo-Yohimbine Alloyohimbine and isoyohimbine have local anesthetic effect. |
CFN92578 | (-)-Lyoniresinol (-)-Lyoniresinol has antioxidant activity. |
CFN92579 | Methyl reserpate 1. Methyl reserpate and reserpinediol, derivatives that incorporate the alkaloid ring system, also competitively inhibit norepinephrine transport into chromaffin vesicles with Ki values of 38 +/- 10 nM and 440 +/- 240 nM, respectively. |
CFN92580 | Reserpinine Reserpinine is a natural product from Rauwolfia vomitoria. |
CFN92581 | Ajmalidine Standard reference |
CFN92582 | 16R-sitsirikine Reference standards. |
CFN92583 | Reserpin N-oxide Reserpin N-oxide shows half the activity of Reserpine. |
CFN92584 | Tetrachlorohydroquinone dimethyl ether |
CFN92585 | Trichloro-1,4-dimethoxybenzene Reference standards. |
CFN92586 | Trans-Pinosylvin dimethyl ether Standard reference |
CFN92587 | 5-Methoxy-3-stilbenol Reference standards. |
CFN92588 | 4'-Hydroxy-7-methoxyflavan 4'-Hydroxy-7-methoxyflavan shows an important cytotoxic effect against human leukemic Molt 4 cells. |
CFN92589 | 6-Methyl-5,6-dihydropyran-2-one 6-Methyl-5,6-dihydropyran-2-on is bactericidal,and antiprotozoal agents. |
CFN92590 | Ethyl 4-methoxysalicylate Reference standards. |
CFN92591 | Dihydrooroxylin A Dihydrooroxylin A has significant antifeeding activity. |
CFN92592 | Bisisorhapontigenin A Standard reference |
CFN92593 | Ginsenoside Rk3 Ginsenoside Rk3 is often used as a major ingredient of the compound preparation for ischemic heart diseases, it could have a role in treating inflammatory diseases. Ginsenoside Rk3 significantly inhibits TNF-α-induced NF-κB transcriptional activity, with an IC50 of 14.24±1.30 μM in HepG2 cells. |
CFN92594 | Ginsenoside Rh4 Ginsenoside Rh4 is a rare saponin obtained from Panax notoginseng. Ginsenoside Rh4 activates Bax, caspase 3, caspase 8, and caspase 9. Ginsenoside Rh4 also induces autophagy. Ginsenoside Rh4 could be safely used as adjuvant with low or non-haemolytic effect; it has cytotoxic activity and its aglycone against cancer cell lines. |
CFN92595 | Ganomycin I Ganomycin I inhibits the activity of HIV-1 protease. |
CFN92596 | Ciwujianoside E Reference standards. |
CFN92597 | Qianhucoumarin E Standard reference |
CFN92598 | 1-O-Acetyl-6beta-O-Isobutyrylbritannilactone Reference standards. |
CFN92599 | Ivangustin Ivangustin exhibits remarkable cytotoxicity against HEp2, SGC-7901 and HCT116 human cancer cell lines. |
CFN92600 | 1beta-Hydroxyalantolactone 1beta-Hydroxyalantolactone has protective effect against AD-like skin inflammation, can as a potential therapeutic agent for AD. |
CFN92601 | Britannilactone Britannilactone significantly reduces melanin production in a dose-dependent manner with the IC50 value of 15.5 uM. |
CFN92602 | Neobritannilactone B Neobritannilactone B has cytotoxic activity. |
CFN90545 | Cineole Cineole has antihypertensive,and anti-inflammatory effects, it regulates nitric oxide and oxidative stress in rats chronically exposed to nicotine. Cineole can attenuate cerulein-induced AP via an anti-inflammatory mechanism and by combating oxidative stress, may can treat neurodegenerative disease. |
CFN90550 | L-Arginine L-Arginine is the nitrogen donor for synthesis of nitric oxide, a potent vasodilator that is deficient during times of sickle cell crisis. L-Arginine exhibits anti-atherosclerotic effect, L-arginine and soy enriched diet are effective in prevention of osteoporosis associated with diabetes mellitus. Exogenous L-Arginine could enhance neonate lymphocyte proliferation through an interleukin-2-independent pathway. |
CFN90551 | L-Citruline L-citrulline is a substance called a non-essential amino acid that is used as a sports performance and cardiovascular health supplement. |
CFN00448 | Sodium barbital Sodium barbital is a depressant of the central nervous system, has sedative/hypnotic effects, it as an inhibitor of rabbit-muscle creatine kinase (CK), it might compete with both creatine and ATP, but mainly with creatine, to inhibit the activity of CK. Sodium barbital is a tumour promoter, it can shorten the otherwise long latency between exposure to toxin and tumourigenesis. Sodium barbital causes progression to the stage of spontaneous renal lesions in Tsc2 mutant rats but do not increase their overall number. |
CFN90546 | Clopidogrel Related Compound A Clopidogrel Related Compound A is a impurity from Clopidogrel. |
CFN90547 | Clopidogrel Related Compound B Reference standards. |
CFN90548 | Clopidogrel Related Compound C Reference standards. |
CFN92603 | Rubinaphthin A Rubinaphthin A is a natural product from Rubia cordifolia. |
CFN92604 | RA VII RA VII is an antitumour agent, shows cytotoxic activity against P-388 cells. RA VII causes the conformational change of F-actin and the stabilization of actin filaments to induce G2 arrest. |
CFN92605 | RA-V RA-V is an potential anti-angiogenic agent, exhibits anti-angiogenic activities in HUVEC and HMEC-1 cell lines with changes in function of these endothelial cells. RA-V also has anti-cancer activity, is a potential anti-metastatic agent in breast cancer, and likely acts via PI3K/AKT and NF-κB signaling pathways in both ER-positive and ER-negative breast cancer cells. |
CFN92606 | RA-XI RA-XI shows potent antitumor activity against P-388. |
CFN92607 | Rhapontigenin Rhapontigenin has antioxidative, antihyperlipidemic, antifungal and anticancer activities. Rhapontigenin inhibits HIF-1α accumulation and angiogenesis in PC-3 prostate cancer cells, suppresses breast cancer cell migration and invasion, which is involved in inhibiting the PI3K-dependent Rac1 signaling pathway. Rhapontigenin exhibits dose-dependent inhibition of tyrosinase activity and melanin synthesis in B16F10 melanoma cells. |
CFN94001 | Cannabisin H Reference standards. |