Malabaricone B - ≥99.0%, high purity , CAS No.63335-24-0

  • ≥99%
Item Number
M650981
Grouped product items
SKUSizeAvailabilityPrice Qty
M650981-5mg
5mg
Available within 8-12 weeks(?)
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$390.90

Phenols Polyphenols Ketones, Aldehydes, Acids

Basic Description

SynonymsMalabaricone B | 63335-24-0 | 1-(2,6-dihydroxyphenyl)-9-(4-hydroxyphenyl)nonan-1-one | NSC630196 | 1-(2,6-Dihydroxyphenyl)-9-(4-hydroxyphenyl)-1-nonanone | Malabaricon-B | CHEMBL489354 | DTXSID80212720 | 1-Nonanone, 1-(2,6-dihydroxyphenyl)-9-(4-hydroxyphenyl)- | HY-N8517 | B
Specifications & Purity≥99%
Biochemical and Physiological MechanismsMalabaricone B, a naturally occurring plant phenolic, is an orally active α-glucosidase inhibitor with an IC 50 of 63.7 µM. Malabaricone B has anticancer , antimicrobial, anti-oxidation and antidiabetic activities.
Storage TempProtected from light,Store at -80°C
Shipped InIce chest + Ice pads
Product Description

Malabaricone B, a naturally occurring plant phenolic, is an orally active α-glucosidase inhibitor with an IC 50 of 63.7 µM. Malabaricone B has anticancer, antimicrobial, anti-oxidation and antidiabetic activities .

In Vitro

Malabaricone B shows selective toxicity to human lung cancer (A549), malignant melanoma (A375) and T cell leukemia (Jurkat) cell lines, without showing toxicity to human normal intestinal (INT407), human kidney (HEK293) and lung fibroblast (WI-38) cells. Among the chosen cancer cell lines, Malabaricone B shows maximum cytotoxicity to the A549 cells (IC 50 = 8.1 μM), which is significantly better than that of curcumin (IC 50 = 26.7 μM). The Malabaricone B-induced apoptosis is mediated by an increase in the intracellular reactive oxygen species (ROS). Malabaricone B (2.5, 5, 10 and 20 µM) increases the BAX level while simultaneously decreasing the BCL-2 and BCL-XL levels in the A549 cells, triggering the mitochondrial apoptotic pathway as revealed from the release of cytochrome c, and the activation of caspase-9 and caspase-3. Malabaricone B exhibits a good level of antimicrobial activity when tested against avariety of microorganisms, including Staphylococcus aureus and Candida albicans. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Malabaricone B (100 mg/kg; p.o; alternate day, 23 days) inhibits lung tumor (xenograft) growth in SCID mice . MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

Associated Targets(Human)

SGMS2 Tchem Phosphatidylcholine:ceramide cholinephosphotransferase 2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALB Tchem Serum albumin (2651 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AMY2A Tclin Pancreatic alpha-amylase (74 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SGMS2 Tchem Phosphatidylcholine:ceramide cholinephosphotransferase 2 (194 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SGMS1 Tchem Phosphatidylcholine:ceramide cholinephosphotransferase 1 (149 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Enterococcus durans (113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
L6 (7924 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Cholinesterase (8742 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
nanA Sialidase A (49 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

IUPAC Name 1-(2,6-dihydroxyphenyl)-9-(4-hydroxyphenyl)nonan-1-one
INCHI InChI=1S/C21H26O4/c22-17-14-12-16(13-15-17)8-5-3-1-2-4-6-9-18(23)21-19(24)10-7-11-20(21)25/h7,10-15,22,24-25H,1-6,8-9H2
InChi Key KOAPDMKKECXPHX-UHFFFAOYSA-N
Canonical SMILES C1=CC(=C(C(=C1)O)C(=O)CCCCCCCCC2=CC=C(C=C2)O)O
Isomeric SMILES C1=CC(=C(C(=C1)O)C(=O)CCCCCCCCC2=CC=C(C=C2)O)O
Alternate CAS 63335-24-0
PubChem CID 163001
NSC Number 287967
MeSH Entry Terms malabaricone B
Molecular Weight 342.43

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilityDMSO : 100 mg/mL (292.03 mM; Need ultrasonic)

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Solution Calculators