2. Natural Products
  3. Plants
  4. Magnoliaceae

Magnoliaceae

 

Magnoliaceae (64):

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 99.92%
    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-U00450
    4-O-Methyl honokiol 68592-15-4 98.18%
    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-N0334A
    (+)-Magnoflorine iodide 4277-43-4 99.69%
    (+)-Magnoflorine iodide (Magnoflorine iodide), an aporphine alkaloid found in Acoruscalamus, reduces the formation of C. albicans biofilm. (+)-Magnoflorine iodide has anti-fungal, anti-antidiabetic and anti-oxidative activity.
    (+)-Magnoflorine iodide
  • HY-N8259
    Obovatol 83864-78-2 99.78%
    Obovatol is a biphenyl ether lignan isolated from the leaves of Magnolia obovata Thunb.
    Obovatol
  • HY-N12496
    Di-O-methylhonokiol 68592-18-7
    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
  • HY-N0003R
    Honokiol (Standard) 35354-74-6
    Honokiol (Standard) is the analytical standard of Honokiol. This product is intended for research and analytical applications. 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 (Standard)
  • HY-N0163R
    Magnolol (Standard) 528-43-8
    Magnolol (Standard) is the analytical standard of Magnolol. This product is intended for research and analytical applications. 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 (Standard)
  • 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 99.91%
    Fargesin is a bioactive neolignan isolated from magnolia plants, with antihypertensive and anti-inflammatory effects.
    Fargesin
  • HY-N2180
    Pinoresinol dimethyl ether 29106-36-3 99.39%
    Pinoresinol dimethyl ether ((+)-Eudesmin) is a non-phenolic furofuran lignan isolated from Magnolia biondii with neuritogenic activity. Pinoresinol dimethyl ether ((+)-Eudesmin) can induce neuritis outgrowth from PC12 cells by stimulating up-stream MAPK, PKC and PKA pathways.
    Pinoresinol dimethyl ether
  • HY-116637
    Tetrahydromagnolol 20601-85-8 99.79%
    Tetrahydromagnolol (Magnolignan), a main metabolite of Magnolol, is a potent and selective cannabinoid CB2 receptor agonist with an EC50 of 170 nM and a Ki of 416 nM. Tetrahydromagnolol possesses 20-fold more selective for CB2 receptor than CB1 receptor. Tetrahydromagnolol is also a weak GPR55 receptor antagonist.
    Tetrahydromagnolol
  • 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-N2544
    Dehydroglaucine 22212-26-6 98.49%
    Dehydroglaucine is a potent antimicrobial alkaloid.
    Dehydroglaucine
  • HY-N5023
    Veraguensin 19950-55-1 99.71%
    Veraguensin is a lignan compound derived from Magnolia sp.. Veraguensin can inhibit bone resorption
    Veraguensin
  • HY-N5101
    Kobusin 36150-23-9 99.93%
    Kobusin is a bisepoxylignan isolated from the Pnonobio biondii Pamp. Kobusin is an activator of CFTR and CaCCgie chloride channels and a inhibitor of ANO1/CaCC (calcium-activated chloride channel) channel.
    Kobusin
  • HY-N9300
    1,6-Dihydro-4,7-epoxy-1-methoxy-3,4-methylenedioxy-6-oxo-3,8-lignan 57430-03-2
    1,6-Dihydro-4,7-epoxy-1-methoxy-3,4-methylenedioxy-6-oxo-3,8-lignan, a lignan derivative from the ethyl acetate soluble fraction of twigs of Magnolia denudate (Magnoliaceae), exhibits anti-platelet-activating factor (PAF) activity. PAF is a potent lipid mediator in inflammation and asthma.
    1,6-Dihydro-4,7-epoxy-1-methoxy-3,4-methylenedioxy-6-oxo-3,8-lignan
  • HY-N10763
    N-Methylcorydaldine 6514-05-2
    N-Methylcorydaldine, an alkaloid, shows promising anti-secretory activity.
    N-Methylcorydaldine
  • HY-N11694
    9-O-Acetyl-fargesol 449172-61-6
    9-O-Acetyl-fargesol is a lignan, which can be isolated from the seeds of Magnolia praecocissima.
    9-O-Acetyl-fargesol