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4-O-Methyl honokiol - 99%, high purity , CAS No.68592-15-4

  • ≥99%
Item Number
O648808
Grouped product items
SKUSizeAvailabilityPrice Qty
O648808-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$150.90
O648808-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$240.90
O648808-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$480.90
O648808-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$760.90
O648808-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,200.90

Phenylpropanoids Lignans Phenols Monophenols

Basic Description

Synonyms4-O-Methylhonokiol|68592-15-4|4-O-Methyl honokiol|METHYLHONOKIOL|4-methoxyhonokiol|4'-O-Methylhonokiol|TUH6B83HJW|4'-METHOXY-3',5-DI-2-PROPENYL-(1,1'-BIPHENYL)-2-OL|CHEMBL89700|NSC-293101|[1,1'-Biphenyl]-2-ol, 4'-methoxy-3',5-di-2-propenyl-|(1,1'-Biphenyl
Specifications & Purity≥99%
Biochemical and Physiological Mechanisms4-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.
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Product Description

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.

In Vitro

4-O-Methyl honokiol is a natural neolignan isolated from Magnolia officinalis , acts as a PPARγ agonist, and inhibtis NF-κB activity. 4-O-Methyl honokiol (20 μM) increases the expression, transcription and DNA binding activities, and nuclear translocation of PPARγ in both in prostate PC-3 and LNCap cells. 4-O-Methyl honokiol (0-30 μM) inhibits LNCaP and PC-3 cancer cells growth, causes G0/G1 phase arrest and induces apoptotic cell death, and such effects can be reversed by PPARγ antagonist. 4-O-Methyl honokiol inhibits NF-κB activity and cancer cell growth, but such effects as well as its activation of PPARγ can be abolished by knock-down of p21. 4-O-methylhonokiol (0.5, 1 and 2 μM) reduces LPS-induced release of NO, PGE2, ROS, TNF-α and IL-1β in cultured astrocytes, and amyloidogenesis in cultured astrocytes and microglial BV-2 cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

4-O-Methyl honokiol (40 or 80 mg/kg, i.p. everyday for 4 weeks) inhibits the growth of SW620 and PC3 tumours in SW620 and PC3 xenograft model. 4-O-Methyl honokiol significantly increases the expression of p21 and PPARγ in the tumour tissues . 4-O-Methyl honokiol (0.5 or 1 mg/kg/day daily for 3 weeks) significantly ameliorates LPS-induced memory impairment, and inhibits LPS-induced iNOS and COX-2 expression in mice. 4-O-Methyl honokiol also shows inhibitory activities against the Aβ 1-42 accumulation, and activates astrocytes and microglia in LPS-injected mice brain. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Viscous liquid

IC50& Target:PPARγ NF-κB

Associated Targets

CNR2 Tchem Cannabinoid receptor 2 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GABRA1 Tclin Gamma-aminobutyric acid receptor subunit alpha-1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTGS1 Tclin Prostaglandin G/H synthase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTGS2 Tclin Prostaglandin G/H synthase 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALOX5 Tclin Arachidonate 5-lipoxygenase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 2-(4-methoxy-3-prop-2-enylphenyl)-4-prop-2-enylphenol
INCHI InChI=1S/C19H20O2/c1-4-6-14-8-10-18(20)17(12-14)15-9-11-19(21-3)16(13-15)7-5-2/h4-5,8-13,20H,1-2,6-7H2,3H3
InChi Key OQFHJKZVOALSPV-UHFFFAOYSA-N
Canonical SMILES COC1=C(C=C(C=C1)C2=C(C=CC(=C2)CC=C)O)CC=C
Isomeric SMILES COC1=C(C=C(C=C1)C2=C(C=CC(=C2)CC=C)O)CC=C
Alternate CAS 131845-16-4,68592-15-4
PubChem CID 155160
NSC Number 293101
MeSH Entry Terms 4-O-methylhonokiol
Molecular Weight 280.36

Certificates

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Chemical and Physical Properties

SolubilityDMSO : 100 mg/mL (356.68 mM; Need ultrasonic)

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