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PA 452 - ≥98%(HPLC), high purity , CAS No.457657-34-0, Antagonist of Retinoid X receptor-α

  • Moligand™
  • ≥98%(HPLC)
Item Number
P288123
Grouped product items
SKUSizeAvailabilityPrice Qty
P288123-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$79.90
P288123-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$249.90
P288123-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$399.90
P288123-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$657.90
P288123-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$936.90

RXR antagonist

Basic Description

Synonyms2-[[3-(Hexyloxy)-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl]methylamino]-5-pyrimidinecarboxylic acid
Specifications & PurityMoligand™, ≥98%(HPLC)
Biochemical and Physiological MechanismsRXR antagonist (pA2= 7.11). Triggers dissociation of RXR tetramers. Attenuates cell proliferation and induces apoptosis in MCF-7 breast cancer cells.
Storage TempStore at -20°C,Argon charged
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeANTAGONIST
Mechanism of actionAntagonist of Retinoid X receptor-α

Associated Targets

RXRG Tclin Retinoic acid receptor RXR-gamma 0 Activities

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

RXRB Tclin Retinoic acid receptor RXR-beta 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)

RXRA Tclin Retinoic acid receptor RXR-alpha 3 Activities

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

Names and Identifiers

IUPAC Name 2-[(3-hexoxy-5,5,8,8-tetramethyl-6,7-dihydronaphthalen-2-yl)-methylamino]pyrimidine-5-carboxylic acid
INCHI InChI=1S/C26H37N3O3/c1-7-8-9-10-13-32-22-15-20-19(25(2,3)11-12-26(20,4)5)14-21(22)29(6)24-27-16-18(17-28-24)23(30)31/h14-17H,7-13H2,1-6H3,(H,30,31)
InChi Key JJUUTJCZMGZJDZ-UHFFFAOYSA-N
Canonical SMILES CCCCCCOC1=C(C=C2C(=C1)C(CCC2(C)C)(C)C)N(C)C3=NC=C(C=N3)C(=O)O
Isomeric SMILES CCCCCCOC1=C(C=C2C(=C1)C(CCC2(C)C)(C)C)N(C)C3=NC=C(C=N3)C(=O)O
PubChem CID 9803242
Molecular Weight 439.59

Certificates

Certificate of Analysis(COA)

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10 results found

Lot NumberCertificate TypeDateItem
G2422195Certificate of AnalysisApr 15, 2024 P288123
G2422196Certificate of AnalysisApr 15, 2024 P288123
G2422197Certificate of AnalysisApr 15, 2024 P288123
G2422198Certificate of AnalysisApr 15, 2024 P288123
G2422199Certificate of AnalysisApr 15, 2024 P288123
G2422200Certificate of AnalysisApr 15, 2024 P288123
G2422201Certificate of AnalysisApr 15, 2024 P288123
G2422202Certificate of AnalysisApr 15, 2024 P288123
G2422203Certificate of AnalysisApr 15, 2024 P288123
G2422204Certificate of AnalysisApr 15, 2024 P288123

Chemical and Physical Properties

SolubilitySolvent:DMSO, Max Conc. mg/mL: 43.96, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 4.4, Max Conc. mM: 10

Related Documents

References

1. Takahashi B, Ohta K, Kawachi E, Fukasawa H, Hashimoto Y, Kagechika H.  (2002)  Novel retinoid X receptor antagonists: specific inhibition of retinoid synergism in RXR-RAR heterodimer actions..  J Med Chem,  45  (16): (3327-30).  [PMID:12139443]
2. Nakayama M, Yamada S, Ohsawa F, Ohta Y, Kawata K, Makishima M, Kakuta H.  (2011)  Discovery of a Potent Retinoid X Receptor Antagonist Structurally Closely Related to RXR Agonist NEt-3IB..  ACS Med Chem Lett,  (12): (896-900).  [PMID:24900278]

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