- Natural Products
- Plants
- Berberidaceae
Berberidaceae
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- Epimedium brevicornu Maxim. (36)
- Dysosma versipellis (Hance) M. Cheng ex Ying (12)
- Epimedium koreanum Nakai (12)
- Sinopodophyllum hexandrum (Royle) Ying (10)
- Epimedium wushanense Ying (6)
- Caulophyllum robustum Maxim. (5)
- Epimedium brevicornum Maxim. (4)
- Epimedium sagittatum (Siebold & Zucc.) Maxim. (3)
- Nandina domestica Thunb. (3)
- Epimedium grandiflorum C. Morren (2)
- Podophyllum peltatum L. (2)
- Berberis aristata DC. (1)
- Berberis thunbergii DC. (1)
- Bongardia chrysogonum (L.) Spach (1)
- Caulophyllum thalictroides (L.) Michx. (1)
- Dysosma aurantiocaulis (1)
- Epimedium pubescens Maxim. (1)
- Epimedium sutchuenense Franch. (1)
- Mahonia bealei (Fort.) Carr. (1)
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Berberidaceae (103)
- Formula: C29H32O13
- Molecular Weight: 588.56
Etoposide (VP-16; VP-16-213) is an anti-cancer chemotherapy agent. Etoposide inhibits topoisomerase II, thus stopping DNA replication. Etoposide induces cell cycle arrest, apoptosis and autophagy.
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- Formula: C21H20O6
- Molecular Weight: 368.38
Icaritin (Anhydroicaritin) is a prenylflavonoid derivative from Epimedium brevicornuMaxim. and potently inhibits proliferation of K562 cells (IC50 of 8 µM) and primary CML cells (IC50 of 13.4 µM for CML-CP and 18 µM for CML-BC). Icaritin can regulate MAPK/ERK/JNK and JAK2/STAT3 /AKT signalings, also enhances osteogenesis[3.
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- Formula: C27H30O10
- Molecular Weight: 514.52
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- Formula: C22H22O7
- Molecular Weight: 398.41
Baohuosu is an extract found in abalone cooking broth. Baohuosu contains soluble polysaccharides, polypeptides, free amino acids, various vitamins and minerals.
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- Formula: C24H30O10
- Molecular Weight: 478.49
Epimedoicarisoside A is a 9,10-dihydrophenanthrene derivative found in the aerial parts of Epimedium koreanum.
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- Formula: C22H22O8
- Molecular Weight: 414.41
Podofilox (Podophyllotoxin) is a potent inhibitor of microtubule assembly and DNA topoisomerase II.
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- Formula: C39H50O20
- Molecular Weight: 838.80
Epimedin A, one of the main flavonoid active components in Herba Epimedii, is orally active. Epimedin A can inhibit osteoclastogenesis, differentiation, and bone resorption. Epimedin A also possesses anti-inflammatory activity. Epimedin A can be used in the research of osteoporosis and inflammatory diseases.
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- Formula: C21H16O7
- Molecular Weight: 380.35
Diphyllin is an orally active V-ATPase inhibitor (IC50=17 nM) and HIV-1 inhibitor (IC50=0.38 μM). Diphyllin blocks the acidification of osteoclast lysosomes and bone resorption lacunas (IC50=0.6 nM for acid influx inhibition), thereby inhibiting bone resorption. Diphyllin can effectively inhibit osteoclast-mediated bone resorption and has no effect on osteoblastic bone formation. Diphyllin can be used in the research of bone metabolism-related diseases and has the potential to inhibit diseases related to excessive bone resorption.
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- Formula: C39H50O19
- Molecular Weight: 822.80
Epmedin C (Epimedin-C; Baohuoside-VI) is an orally active anti-inflammatory agent and immunomodulator that binds to multiple key proteins including UCP1, Caspase-1, CDK2 and Keap1. Epmedin C inhibits epithelial cell proliferation by disrupting the complex function of CDK2/Cyclin E. Epmedin C also upregulates Nrf2 expression, reduces ROS levels and inhibits pro-inflammatory cytokine secretion, thereby effectively restoring antibody production and alleviating tissue damage. Epmedin C has good safety with no hepatotoxicity or skin sensitization, and it has been used in studies on diseases such as obesity, Deoxynivalenol (HY-N6684)-induced immunotoxicity and mammary hyperplasia.
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- Formula: C29H32O13
- Molecular Weight: 588.56
Etoposide (Standard) is the analytical standard of Etoposide. This product is intended for research and analytical applications. Etoposide (VP-16; VP-16-213) is an anti-cancer chemotherapy agent. Etoposide inhibits topoisomerase II, thus stopping DNA replication. Etoposide induces cell cycle arrest, apoptosis and autophagy.
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- Formula: C38H48O19
- Molecular Weight: 808.78
Epimedin B, a component extracted from Epimedii Folium, is reported to have antiosteoporotic activity.
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- Formula: C27H30O11
- Molecular Weight: 530.52
Icariside I (GH01) is an orally active metabolite of icalin. Icariside I improves estrogen deficiency-induced osteoporosis by simultaneously regulating osteoblast and osteoclast differentiation. Icariside I promotes ATP (HY-B2176) or Nigericin (HY-127019)-induced mtROS production and NLRP3 inflammasome activation and causes idiosyncratic hepatotoxicity. Icariside I does not alter the activation of NLRC4 and AIM2 inflammasomes. Icariside I inhibits breast cancer proliferation, apoptosis, invasion, and metastasis by targeting the IL-6/STAT3 pathway. Icariside I is a kynurenine-AhR pathway inhibitor that alleviates cancer by blocking tumor immune escape.
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- Formula: C20H20ClNO4
- Molecular Weight: 373.83
Columbamine (Columbamin; Dehydroisocorypalmine) chloride is an organic heterotetracyclic alkaloid extracted from plants. Columbamine chloride is a metabolite of Berberine (HY-N0716). Columbamine chloride inhibits the cytochrome P450 (CYP) isoform CYP3A4 (IC50 = 30.6 µM). Columbamine chloride induces apoptosis in cancer cells. Columbamine chloride can be used for antioxidant, anti-inflammatory, antitumor, antifungal, antiparasite, hepatoprotective, neuroprotective, hypolipidemic and hypoglycemic study.
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- Formula: C39H50O20
- Molecular Weight: 838.80
Epimedin A1 is a flavonoid extracted from Herba Epimedii which is one of commonly used Chinese medicines.
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- Formula: C21H20O8
- Molecular Weight: 400.38
4'-Demethylpodophyllotoxin is an aryltetralin lignin contained in the root of Podophyllum hexandrum and P. peltatum. 4'-Demethylpodophyllotoxin exhibits cytotoxic potential in diverse cancer cell lines.
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- Formula: C₃₃H₄₀O₁₅
- Molecular Weight: 676.66
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- Formula: C20H18O6
- Molecular Weight: 354.35
Desmethylicaritin is a phytoestrogenic molecule, has inducible effect on directional differentiation of embryonic stem cells into cardiomyocytes. Desmethylicaritin also suppresses adipogenesis via Wnt/β-catenin signaling pathway.
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