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Manoalide - ≥98%, high purity , CAS No.75088-80-1

  • ≥98%
Item Number
M275478
Grouped product items
SKUSizeAvailabilityPrice Qty
M275478-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$888.90

Irreversible phospholipase C (PLC) inhibitor

View related series
Phospholipase Inhibitors

Basic Description

Synonymsmanoalide|75088-80-1|CHEMBL463914|CHEBI:66666|E1DK0157K9|(2R)-2-hydroxy-3-[(2R,6R)-6-hydroxy-5-[(E)-4-methyl-6-(2,6,6-trimethylcyclohexen-1-yl)hex-3-enyl]-3,6-dihydro-2H-pyran-2-yl]-2H-furan-5-one|UNII-E1DK0157K9|SCHEMBL20551728|DTXSID401028174|HY-N7487|B
Specifications & Purity≥98%
Biochemical and Physiological MechanismsIrreversible phospholipase C (PLC) and phospholipase A2 (PLA2) inhibitor (IC 50 values are 1.5 and 4.7 µM respectively) . Also shown to inhibit calcium channels . Anti-inflammatory and analgesic effects in vivo .
Storage TempStore at -20°C,Argon charged,Desiccated
Shipped InIce chest + Ice pads
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Manoalide irreversibly inhibits the enzyme phospholipase A2. This inhibition is a key point of study in the enzymatic pathways involved in lipid metabolism and cellular signaling. It is used to probe the role of phospholipase A2 in various cellular processes and to understand the structure-activity relationships governing enzyme-ligand interactions. The compound serves as a biochemical tool in experimental applications, helping to dissect complex biological pathways.

Associated Targets

DHX36 Tbio ATP-dependent DNA/RNA helicase DHX36 0 Activities

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

PLA2G4A Tchem Cytosolic phospholipase A2 0 Activities

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

PLA2G2D Tchem Group IID secretory phospholipase A2 0 Activities

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

POLK Tbio DNA polymerase kappa 0 Activities

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

PLA2G1B Tchem Phospholipase A2 0 Activities

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

PLA2G2A Tchem Phospholipase A2, membrane associated 0 Activities

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

Names and Identifiers

IUPAC Name (2R)-2-hydroxy-3-[(2R,6R)-6-hydroxy-5-[(E)-4-methyl-6-(2,6,6-trimethylcyclohexen-1-yl)hex-3-enyl]-3,6-dihydro-2H-pyran-2-yl]-2H-furan-5-one
INCHI InChI=1S/C25H36O5/c1-16(10-12-20-17(2)8-6-14-25(20,3)4)7-5-9-18-11-13-21(29-23(18)27)19-15-22(26)30-24(19)28/h7,11,15,21,23-24,27-28H,5-6,8-10,12-14H2,1-4H3/b16-7+/t21-,23-,24-/m1/s1
InChi Key FGJIDQWRRLDGDB-CPIXEKRISA-N
Canonical SMILES CC1=C(C(CCC1)(C)C)CCC(=CCCC2=CCC(OC2O)C3=CC(=O)OC3O)C
Isomeric SMILES CC1=C(C(CCC1)(C)C)CC/C(=C/CCC2=CC[C@@H](O[C@H]2O)C3=CC(=O)O[C@H]3O)/C
PubChem CID 6437368
Molecular Weight 416.55

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySoluble in DMSO (25mg/ml), 100% ethanol (25mg/ml) or methanol.

Related Documents

Solution Calculators