2. Natural Products
  3. Plants
  4. Magnoliaceae

Magnoliaceae

 

Magnoliaceae (80):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-N0003
    Honokiol 35354-74-6 99.90%
    Honokiol is a bioactive, biphenolic phytochemical that possesses potent antioxidative, anti-inflammatory, antiangiogenic, and anticancer activities by targeting a variety of signaling molecules. It inhibits the activation of Akt. Honokiol can readily cross the blood brain barrier.
    Honokiol
  • HY-N0163
    Magnolol 528-43-8 99.84%
    Magnolol, a natural lignan isolated from the stem bark of Magnolia officinalis, is a dual agonist of both RXRα and PPARγ, with EC50 values of 10.4 µM and 17.7 µM, respectively.
    Magnolol
  • HY-N0334A
    (+)-Magnoflorine iodide 4277-43-4 99.74%
    (+)-Magnoflorine (α-Magnoflorine) iodide is an orally active aporphine alkaloid with multiple biological activities. (+)-Magnoflorine iodide promotes Parkin/PINK1 -mediated mitochondrial autophagy, inhibits the activation of NLRP3/Caspase-1 pathway, regulates the intestinal microbiota, and exhibits significant anti-inflammatory and immunomodulatory activities. (+)-Magnoflorine iodide inhibits JNK and TLR4/NF-κB signaling pathways, activates Sirt1/AMPK pathway, alleviates neuronal oxidative stress and apoptosis. Magnoflorine upregulates miR-410-3p, inhibits HMGB1/NF-κB pathway, and has anti-tumor activity. (+)-Magnoflorine iodide also has significant antifungal activity.
    (+)-Magnoflorine iodide
  • HY-116637
    Tetrahydromagnolol 20601-85-8 99.89%
    Tetrahydromagnolol (Magnolignan), the main metabolite of Magnolol, is a potent and selective cannabinoidCB2 receptor agonist (EC50 =170 nM) and GPR55 antagonist. The Ki of Tetrahydromagnolol for CB2 is 416 nM, 20-fold higher than for the CB1 receptor. Magnolol shows antifungal, anti-inflammatory and analgesic effects.
    Tetrahydromagnolol
  • HY-N2180
    (+)-Eudesmin 29106-36-3 99.91%
    Pinoresinol dimethyl ether ((+)-Eudesmin) is a non-phenolic furanoid lignin. Pinoresinol dimethyl ether can be isolated from Magnolia biondii. Pinoresinol dimethyl ether activates MAPK, PKC, and PKA upstream pathways and inhibits NO levels. Pinoresinol dimethyl ether has neuroprotective activity.
    (+)-Eudesmin
  • HY-135015
    Tetradecanenitrile 629-63-0
    Tetradecanenitrile is a nitrogen-containing saturated long-chain aliphatic nitrile that can be found in Pseudomonas veronii R02. Tetradecanenitrile can be used for the research of multiresistant Staphylococcus aureus infection.
    Tetradecanenitrile
  • HY-N17491
    Sesaminone 157207-93-7
    Sesaminone is a lignan found in the leaves of Magnolia coco.
    Sesaminone
  • HY-N17496
    Cyathisterol 159736-32-0
    Cyathisterol is a steroidal compound that inhibits LPS (HY-D1056)-induced nitric oxide production. Cyathisterol can be used for the research of inflammatory diseases.
    Cyathisterol
  • HY-N8259
    Obovatol 83864-78-2 99.60%
    Obovatol is a biphenyl ether lignan isolated from the leaves of Magnolia obovata Thunb.
    Obovatol
  • HY-126535
    Magnoloside B 116872-05-0 99.69%
    Magnoloside B is an α-glucosidase inhibitor (IC50=0.69 mM), which can be obtained from Magnolia officinalis stem bark. Magnoloside B shows moderate inhibitory activity against MGC-803 and HepG2 cells. Magnoloside B has the potential to study cancer and diabetes.
    Magnoloside B
  • HY-N1374
    Magnolin 31008-18-1 99.98%
    Magnolin, a major component of Magnolia liliiflora, inhibits the Ras/ERKs/RSK2 signaling axis by targeting the active pocket of ERK1 and ERK2 with IC50s of 87 nM and 16.5 nM, respectively.
    Magnolin
  • HY-N0719
    Fargesin 31008-19-2 99.52%
    Fargesin is a bioactive neolignan isolated from magnolia plants, with antihypertensive and anti-inflammatory effects.
    Fargesin
  • HY-U00450
    4-O-Methyl honokiol 68592-15-4 98.76%
    4-O-Methyl honokiol is a natural neolignan isolated from Magnolia officinalis, acts as a PPARγ agonist, and inhibtis NF-κB activity, used for cancer and inflammation research.
    4-O-Methyl honokiol
  • HY-N3376
    Liriodenine 475-75-2
    Liriodenine (Spermatheridine; VLT045) is an aporphine alkaloid isolated from the plant?Mitrephora sirikitiae?and has anti-cancer activities. Liriodenine induces cell apoptosis, activates the intrinsic pathway by induction of caspase-3 and caspase-9.
    Liriodenine
  • HY-32135
    N-Phenethylbenzamide 3278-14-6 99.56%
    N-Phenethylbenzamide is an active compound. N-Phenethylbenzamide can be extracted from Liriodendron tulipifera. N-Phenethylbenzamide can be used for the research of inflammatory diseases.
    N-Phenethylbenzamide
  • HY-N2357
    Eudesmin 526-06-7 99.96%
    Eudesmin ((-)-Eudesmin) impairs adipogenic differentiation via inhibition of S6K1 signaling pathway. Eudesmin possesses diverse therapeutic effects, including anti-tumor, anti-inflammatory, and anti-bacterial activities.
    Eudesmin
  • HY-N13742
    Dihydrohonokiol B 219565-74-9 99.29%
    Dihydrohonokiol B (Dihydrohonokiol) is an anxiolytic agent. Dihydrohonokiol B can reduce the neurotoxicity induced by amyloid β protein by stimulating the GABAC receptor. Dihydrohonokiol B can be used in the research of neurodegenerative diseases such as Alzheimer's disease.
    Dihydrohonokiol B
  • HY-N12545
    Magnoloside F 1945997-27-2 98.73%
    Magnoloside F is a natural compound that can be isolated from the Magnolia officinalis, and has antioxidant activity.
    Magnoloside F
  • HY-N2544
    Dehydroglaucine 22212-26-6 98.49%
    Dehydroglaucine is a potent antimicrobial alkaloid.
    Dehydroglaucine
  • HY-N12496
    Di-O-methylhonokiol 68592-18-7 99.59%
    Di-O-methylhonokiol is a natural phenolic compound that can be isolated from magnolia flowers. Di-O-methylhonokiol has significant antibacterial activity against Gram-positive bacteria, acid-fast bacilli, and yeast-like and filamentous fungi. Di-O-methylhonokiol can be used in the study of fungal infections.
    Di-O-methylhonokiol