Click Here for 5% Off Your First Aladdin Purchase!

JP 1302 dihydrochloride - ≥99%, high purity , CAS No.80259-18-3, Antagonist of α 2C-adrenoceptor

  • Moligand™
  • ≥99%
Item Number
J335104
Grouped product items
SKUSizeAvailabilityPrice Qty
J335104-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$175.90
J335104-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$733.90

a selective α2C-AR

View related series
α2C-adrenoceptor Antagonist

Basic Description

Synonyms80259-18-3|N-(4-(4-Methyl-1-piperazinyl)phenyl)-9-acridinamine|JP1302|N-[4-(4-methylpiperazin-1-yl)phenyl]acridin-9-amine|GNF-PF-3427|TCMDC-123912|JP 1302|JP-1302|MMV006172|N-(4-(4-methylpiperazin-1-yl)phenyl)acridin-9-amine|CHEMBL106525|9-Acridinamine, N
Specifications & PurityMoligand™, ≥99%
Storage TempStore at -20°C,Desiccated
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeANTAGONIST
Mechanism of actionAntagonist of α 2C-adrenoceptor
Product Description

JP 1302 dihydrochloride is a potent and selective α2C-AR adrenoreceptor antagonist. JP 1302 dihydrochloride strongly antagonizes adrenaline-stimulated 35GTPγS binding|in vitro|.

Product Properties

Ki Dataα2C-AR: Ki= 28 nM (human); α2B-AR: Ki= 1.47 μM (human); α2D-adrenoceptor : Ki= 1.70 μM (human); α2A-AR: Ki= 3.15 μM (human)

Associated Targets

RORC Tchem Nuclear receptor ROR-gamma 0 Activities

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

FEN1 Tchem Flap endonuclease 1 0 Activities

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

WRN Tbio Werner syndrome ATP-dependent helicase 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)

POLI Tchem DNA polymerase iota 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)

BLM Tchem Bloom syndrome protein 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)

ADRA2B Tclin Alpha-2B adrenergic receptor 0 Activities

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

ADRA2C Tclin Alpha-2C adrenergic receptor 3 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)

GLA Tclin Alpha-galactosidase A 0 Activities

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

ADRA2A Tclin Alpha-2A adrenergic receptor 0 Activities

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

SLC2A1 Tchem Solute carrier family 2, facilitated glucose transporter member 1 0 Activities

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

KCNH2 Tclin Potassium voltage-gated channel subfamily H member 2 0 Activities

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

Names and Identifiers

IUPAC Name N-[4-(4-methylpiperazin-1-yl)phenyl]acridin-9-amine
INCHI InChI=1S/C24H24N4/c1-27-14-16-28(17-15-27)19-12-10-18(11-13-19)25-24-20-6-2-4-8-22(20)26-23-9-5-3-7-21(23)24/h2-13H,14-17H2,1H3,(H,25,26)
InChi Key QZKGUNQLVFEEBA-UHFFFAOYSA-N
Canonical SMILES CN1CCN(CC1)C2=CC=C(C=C2)NC3=C4C=CC=CC4=NC5=CC=CC=C53
Isomeric SMILES CN1CCN(CC1)C2=CC=C(C=C2)NC3=C4C=CC=CC4=NC5=CC=CC=C53
RTECS AR7147000
PubChem CID 540335
Molecular Weight 441.4

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Chemical and Physical Properties

SolubilitySoluble in DMSO (5 mM), and water (100 mM).
Refractive Indexn20D1.71

Safety and Hazards(GHS)

RTECS AR7147000

Related Documents

Solution Calculators