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Others Other Natural Products

Cat.No.  Name Information
M4748 Pectolinarigenin Pectolinarigenin is a dual inhibitor of COX-2/5-LOX with anti-inflammatory activity.
M19355 Mannitol DL-Mannitol is obtained by combining D-mannitol with a sample of Lmannitol obtained by reduction of L-mannono-1, Clactone.
M27790 Kifunensine Kifunensine, a potent and selective inhibitor of class I α-mannosidases isolated from Actinomycete, prevents α-mannosidases I from trimming mannose residues on glycoproteins. Kifunensine inhibits ERAD.
M4619 Eupalinolide B Eupalinolide B is a germacrane sesquiterpene isolated from Eupatorium lindleyanum. Eupalinolide B demonstrates potent cytotoxicity against A-549, BGC-823 and HL-60 tumour cell lines.
M40431 Isorutarin Isorutarin is a natural product that can be isolated from the seeds of Apium graueolens.
M40430 Specioside Specioside is a novel iridoid glycoside extracted from Catalpa speciosa Warder (Bignoniaceae).
M40429 Tirotundin Tirotundin (Tagitinin D) is a potent anti-inflammatory agent. Tirotundin inhibits the activation of NF-Kβ.
M40428 Angelicide Angelicide is an active compound. Angelicide can be isolated from the medicinal plant dang-gui (A. sinensis).
M40427 Bracteatin Bracteatin is a natural product that can be isolated from Actinidia arguta. Bracteatin has antioxidant effect..
M40426 Henryoside Henryoside, an acylated salicin bis-glucoside from Viburnum veitchii, exhibits spasmolytic and uterotonic properties.
M40425 Maritimein Maritimein is a golden pigment, which is a natural phenol. Maritimein can be isolated from the Chrysanthemum Cinchilla.
M40424 Hannokinol Hannokinol is a potent anti-tumor agent. Hannokinol shows antiproliferative activity. Hannokinol shows antioxidant activities.
M40423 Viteralone Viteralone (compound 5) is a natural product that can be isolated from Vitex negundo. Viteralone is cytotoxic to HL-60 cancer cells.
M40422 Hymexelsin Hymexelsin (Xeroboside) is an apiose-containing scopoletin glycoside, that can be isolated from the stem bark of Hymenodictyon excelsum.
M40421 Isoboldine Isoboldine is a pyridine alkaloid. Isoboldine effectively alleviates inflammation and joint destruction in collagen-induced arthritis in mice.
M40420 Shyobunone Shyobunone (Shyobunon) is a nature product that could be isolated from Acorus calamus rhizomes. Shyobunone has insecticidal and repellant activity.
M40419 Wilforol A Wilforol A ((-)-Wilforol A), plant metabolite, is a pentacyclic triterpenoid. Wilforol A can be used for the research of various biochemical studies.
M40418 Vogeloside Vogeloside is an iridoid that can be isolated from the roots of Triosteum pinnatifidum. Vogeloside inhibits nitric oxide production in LPS-activated macrophages.
M40417 Epinodosin Epinodosin is a diterpenoid. Epinodosin has moderate cytotoxicity against HL-60 cells with IC50 value of 10.4 μM. Epinodosin can be used for the research of inflammatory diseases.
M40416 Jolkinol A Jolkinol A is a natural product that can be found in Euphorbia pubescens. Jolkinol A inhibits cell growth with GI50s of 95.3, 57.3, >100 µM for MCF-7, NCI-460, SF-268 cells, respectively.
M40415 Sericoside Sericoside is a triterpenoid with anti-inflammatory activity, can be isolated form Terminalia. Sericoside has a strong lipolytic activity. Sericoside can also reduce skin wrinkles and ameliorating skin texture.
M40414 Neolitsine Neolitsine ((+)-Neolitsine) is a vasodilator. Neolitsine can be isolated from the herb Cassytha filiformis. Neolitsine exhibits significant vasodilatory effects on precontracted rat aortic preparations with an IC50 of 0.29 μM.
M40413 Paeonoside Paeonoside is a bioactive compound identified in P. suffruticosa that promotes wound healing and migration in osteoblast differentiation. Paeonoside has also been reported to have some antidiabetic activity and may prevent sepsis-induced lethality.
M40412 Caulophine Caulophine is a fluoroketone alkaloid isolated from Caulophyllum robustum MAXIM. Caulophine has antioxidant activity and the ability to protect cardiomyocytes from oxidative and ischemic damage, providing potential value for coronary heart disease research.




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