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Orsellinic acid , CAS No.480-64-8

  • ≥97%
Item Number
O329655
Grouped product items
SKUSizeAvailabilityPrice Qty
O329655-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$42.90
O329655-250mg
250mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$72.90
O329655-1g
1g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$229.90

a benzoic acid compound shown to block PAF-mediated neuronal apoptosis

View related series
Aromatic Ring Compounds

Basic Description

SynonymsOrsellinic acid|2,4-Dihydroxy-6-methylbenzoic acid|480-64-8|o-Orsellinic acid|Orsellic acid|Orcinolcarboxylic acid|4,6-Dihydroxy-o-toluic acid|2,4-dihydroxy-6-methyl-benzoic acid|Benzoic acid, 2,4-dihydroxy-6-methyl-|CHEBI:32807|MFCD00210536|2,4-Dihydroxy
Specifications & Purity≥97%
Storage TempProtected from light,Store at -20°C
Shipped InIce chest + Ice pads
Product Description

Orsellinic acid is a compound produced by Lecanoric acid treated with alcohols. Lecanoric acid is a lichen depside isolated from a Parmotrema tinctorum specimen.

Associated Targets

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

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

PTPN1 Tchem Tyrosine-protein phosphatase non-receptor type 1 0 Activities

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

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 0 Activities

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

SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 0 Activities

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

GAA Tclin Lysosomal alpha-glucosidase 0 Activities

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

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase 0 Activities

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

Names and Identifiers

IUPAC Name 2,4-dihydroxy-6-methylbenzoic acid
INCHI InChI=1S/C8H8O4/c1-4-2-5(9)3-6(10)7(4)8(11)12/h2-3,9-10H,1H3,(H,11,12)
InChi Key AMKYESDOVDKZKV-UHFFFAOYSA-N
Canonical SMILES CC1=CC(=CC(=C1C(=O)O)O)O
Isomeric SMILES CC1=CC(=CC(=C1C(=O)O)O)O
PubChem CID 68072
Molecular Weight 168.15

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySoluble in water, DMSO or 100% ethanol.
SensitivityLight sensitive
Melt Point(°C)176° C

Safety and Hazards(GHS)

Merck Index 5.36180555555556

Related Documents

Solution Calculators