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Natural Products

Cat.No.  Name Information
M10867 Obovatol Obovatol, a biphenyl ether lignan isolated from the leaves of Magnolia obovata Thunb, possesses antioxidant, neuroprotective, anti-inflammatory, anti-thrombotic, and antitumor activities. In addition, Obovatol targets the pan-apoptosis (PANoptosis)-related molecule NLRP3/AIM2.
M10830 Corynantheine Corynantheine (Hirsuteine) is an indole alkaloid extracted from Uncaria rhynchophylla. Corynantheine (Hirsuteine) antagonizes nicotine-mediated dopamine release non-competitively by blocking ion permeation through nicotinic receptor channel complexes.
M10801 Calcitonin (salmon) Calcitonin salmon is a calcium-regulating hormone that is a dual agonist of amylin and calcitonin receptors that stimulate bone production and inhibit bone resorption.
M10674 Prosapogenin A Prosapogenin A is a natural product from Veratrum, induces apoptosis in human cancer cells in vitro via inhibition of the STAT3 signaling pathway and glycolysis.
M10673 Procyanidin C1 Procyanidin C1 (PCC1) is a natural polyphenol, which causes DNA damage, cell cycle arrest and induces apoptosis. Procyanidin C1 decreases the level of Bcl-2, but enhances BAX, caspase 3 and 9 expression in cancer cells.
M10672 Thonningianin A Thonningianin A is an ellagitannin with anti-cancer activities. Thonningianin A also has antioxidant properties of radical scavenging, anti-superoxide formation and metal chelation.
M10671 Garcinone E Garcinone E is the most active xanthone from mangosteen, which has potent cytotoxic effect against hepatocellular carcinoma cell lines. Garcinone E might inhibit metastasis of an oral cancer cell line by blocking invasion, migration and MMP production.
M10663 Alcesefoliside Alcesefoliside is a flavonoid isolated from Nitraria sibirica Pall, with antioxidant activity
M10662 Camelliaside A Camelliaside A is a flavonoid from the methanol extract of tea (Camellia oleifera) seed pomace.
M10661 Tabersonine Tabersonine is an indole alkaloid mainly isolated from Catharanthus roseus. Tabersonine has anti-inflammatory activities and acts as a potential therapeutic candidate for the treatment of ALI/ARDS.
M10660 (-)-Syringaresinol (-)-Syringaresinol has anti-cancer activity. (-)-Syringaresinol inhibits the proliferation of human promyelocytic HL-60 cells through G1 arrest and induction of apoptosis.
M10659 Picfeltarraenin IV Picfeltarraenin IV is an acetylcholinesterase (AChE) inhibitor, which is obtained from Picriafel-terrae Lour (P.fel-terrae).
M10658 Calenduloside E Calenduloside E (CE) is a natural pentacyclic triterpenoid saponin extracted from Aralia elata. Calenduloside E (CE) has anti-apoptotic potent by targeting heat shock protein 90 (Hsp90).
M10657 Purpureaside C Purpureaside C is a phenolic glycoside which has significant proinflammatory activity.
M10656 Bergaptol Bergaptol is a hydroxylated psoralen that acts as a potent inhibitors of debenzylation activity of CYP3A4 enzyme with an IC50 value of 24.92 uM.
M10655 Picfeltarraegenin X Picfeltarraenin X is an AChE inhibitor, which is a triterpenoid isolated from Picria fel-terrae Lour.
M10654 Ajmalicine (Raubasine) Ajmalicine (Raubasine) is an adrenolytic agent which preferentially blocks alpha 1-adrenoceptor than alpha 2-adrenoceptor. Ajmalicine (Raubasine) is an reversible non-competitive nicotine receptor antagonist with an IC50 of 72.3 μM.
M10653 Dehydroevodiamine Dehydroevodiamine has an antiarrhythmic effect in guinea-pig ventricular myocytes. Dehydroevodiamine inhibits LPS-induced iNOS, COX-2, prostaglandin E2 (PGE2) and nuclear factor-kappa B (NF-κB) expression in murine macrophage cells.
M10652 Voacamine Voacamine is an indole alkaloid, exhibits potent cannabinoid CB1 receptor antagonistic activity. Voacamine also inhibits P-glycoprotein (P-gp) action in multidrug-resistant tumor cells.
M10651 Shikimic acid Shikimic acid is an important metabolic intermediate with various applications. Shikimic acid is an industrially important compound that acts as a precursor in the synthesis of many chemical substances like oseltamivir phosphate.

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