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Adrenochrome - 98%, high purity , CAS No.54-06-8

  • ≥98%
Item Number
D133484
Grouped product items
SKUSizeAvailabilityPrice Qty
D133484-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$185.90
D133484-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$583.90
D133484-250mg
250mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,156.90

Basic Description

SynonymsAdrenochrome|54-06-8|Adraxone|3-Hydroxy-1-methyl-5,6-indolinedione|3-Hydroxy-1-methylindoline-5,6-dione|1-Adrenochrome|D,L-Adrenochrome|2,3-Dihydro-3-hydroxy-1-methyl-1H-indole-5,6-dione|1H-Indole-5,6-dione, 2,3-dihydro-3-hydroxy-1-methyl-|70G54NQL71|3-hy
Specifications & Purity≥98%
Biochemical and Physiological MechanismsAdrenochrome is an oxidation product of adrenaline (ephinephrine, norepinephrine). It inhibits COMT (Catechol-O-methyltransferase), promotes the synthesis of prostaglandins in brain tissue in vitro, promotes the secretion of nerve growth factor by L-M ce.
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Product Description

An inhibitor of catechol-o-methyltransferase

Associated Targets

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 0 Activities

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

VDR Tclin Vitamin D3 receptor 0 Activities

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

KAT2A Tchem Histone acetyltransferase KAT2A 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)

RECQL Tbio ATP-dependent DNA helicase Q1 0 Activities

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

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 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)

THRB Tclin Thyroid hormone receptor beta 0 Activities

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

MAPT Tclin Microtubule-associated protein tau 0 Activities

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

Names and Identifiers

IUPAC Name 3-hydroxy-1-methyl-2,3-dihydroindole-5,6-dione
INCHI InChI=1S/C9H9NO3/c1-10-4-9(13)5-2-7(11)8(12)3-6(5)10/h2-3,9,13H,4H2,1H3
InChi Key RPHLQSHHTJORHI-UHFFFAOYSA-N
Canonical SMILES CN1CC(C2=CC(=O)C(=O)C=C21)O
Isomeric SMILES CN1CC(C2=CC(=O)C(=O)C=C21)O
PubChem CID 5898
Molecular Weight 179.17

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySoluble in water (0.3 mg/ml), ethanol, and 1 M sodium hydroxide (50 mg/ml, gives a dark brown solution).

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H302:Harmful if swallowed

Precautionary Statements

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P270:Do not eat, drink or smoke when using this product.

P330:Rinse mouth.

P301+P317:IF SWALLOWED: Get medical help.

Related Documents

Solution Calculators