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PRE-084 hydrochloride - ≥99%(HPLC), high purity , CAS No.138847-85-5, Agonist of sigma non-opioid intracellular receptor 1

  • Moligand™
  • ≥99%(HPLC)
Item Number
P288761
Grouped product items
SKUSizeAvailabilityPrice Qty
P288761-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$153.90
P288761-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$636.90

Highly selective σ1agonist

Basic Description

SynonymsPre-084|138847-85-5|Pre 084|2-(4-Morpholino)ethyl-1-phenylcyclohexane-1-carboxylate|2-morpholin-4-ylethyl 1-phenylcyclohexane-1-carboxylate|2-Morpholinoethyl 1-Phenylcyclohexanecarboxylate|Cyclohexanecarboxylic acid, 1-phenyl-, 2-(4-morpholinyl)ethyl este
Specifications & PurityMoligand™, ≥99%(HPLC)
Biochemical and Physiological MechanismsHigh affinity, selectiveσ1agonist (Kivalues are 2.2 and 13091 nM forσ1andσ2receptors respectively). Selective over PCP receptors (IC50> 100000 nM) and several other receptor systems. Produces antiamnesic and antitussive effectsin vivo. Also exhibits prote
Storage TempRoom temperature
Shipped InNormal
GradeMoligand™
Action TypeAGONIST
Mechanism of actionAgonist of sigma non-opioid intracellular receptor 1

Associated Targets

CYP1A2 Tchem Cytochrome P450 1A2 0 Activities

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

CYP2D6 Tclin Cytochrome P450 2D6 0 Activities

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

CYP2C19 Tchem Cytochrome P450 2C19 0 Activities

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

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

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

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 0 Activities

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

CYP2C9 Tchem Cytochrome P450 2C9 0 Activities

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

KMT2A Tchem Histone-lysine N-methyltransferase 2A 0 Activities

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

HDAC6 Tclin Histone deacetylase 6 0 Activities

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

SLC6A3 Tclin Sodium-dependent dopamine transporter 0 Activities

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

TMEM97 Tchem Sigma intracellular receptor 2 0 Activities

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

SIGMAR1 Tclin Sigma non-opioid intracellular receptor 1 2 Activities

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

PRCP Tchem Lysosomal Pro-X carboxypeptidase 0 Activities

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

RGS4 Tchem Regulator of G-protein signaling 4 0 Activities

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

PKM Tchem Pyruvate kinase PKM 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)

CHRM1 Tclin Muscarinic acetylcholine receptor M1 0 Activities

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

ALDH1A1 Tchem Retinal dehydrogenase 1 0 Activities

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

ARSA Tbio Arylsulfatase A 0 Activities

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

Names and Identifiers

IUPAC Name 2-morpholin-4-ylethyl 1-phenylcyclohexane-1-carboxylate
INCHI InChI=1S/C19H27NO3/c21-18(23-16-13-20-11-14-22-15-12-20)19(9-5-2-6-10-19)17-7-3-1-4-8-17/h1,3-4,7-8H,2,5-6,9-16H2
InChi Key RQHKZUBCUZVZEF-UHFFFAOYSA-N
Canonical SMILES C1CCC(CC1)(C2=CC=CC=C2)C(=O)OCCN3CCOCC3
Isomeric SMILES C1CCC(CC1)(C2=CC=CC=C2)C(=O)OCCN3CCOCC3
PubChem CID 126402
Molecular Weight 353.89

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySolvent:water, Max Conc. mg/mL: None, Max Conc. mM: 25; Solvent:DMSO, Max Conc. mg/mL: 26.54, Max Conc. mM: 75

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