
SR11237
CAS No. 146670-40-8
SR11237( BMS-649 )
Catalog No. M27716 CAS No. 146670-40-8
SR11237 is a Pan retinoid X receptor (RXR) agonist. SR11237 causes RXR/RXR homodimers to form and transactivate a reporter gene containing a RXR-response element.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 170 | Get Quote |
![]() ![]() |
10MG | 258 | Get Quote |
![]() ![]() |
25MG | 520 | Get Quote |
![]() ![]() |
50MG | 750 | Get Quote |
![]() ![]() |
100MG | 1035 | Get Quote |
![]() ![]() |
500MG | 2061 | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameSR11237
-
NoteResearch use only, not for human use.
-
Brief DescriptionSR11237 is a Pan retinoid X receptor (RXR) agonist. SR11237 causes RXR/RXR homodimers to form and transactivate a reporter gene containing a RXR-response element.
-
DescriptionSR11237 is a Pan retinoid X receptor (RXR) agonist. SR11237 causes RXR/RXR homodimers to form and transactivate a reporter gene containing a RXR-response element.(In Vitro):SR11237 is effective at transactivating a chloramphenicol acetyltransferase reporter gene through RXRs but not retinoic acid receptors in COS-1 cells.(In Vivo):In Sprague-Dawley rats, SR11237 (BMS-649) (25 mg/kg; i.p.) Caused disturbed ossification and bone morphology in rats, including premature growth plate closure and infiltration of ossified tissue through the central epiphysis.
-
In VitroUsing nuclear receptor co-transfection assays in COS-1 cells, that SR11237 is effective at transactivating a chloramphenicol acetyltransferase reporter gene through RXRs but not retinoic acid receptors.
-
In VivoSR11237 (BMS-649) (25 mg/kg; i.p.; daily from post-natal days 5 to 15) causes irregular ossification and premature closure of the growth plate. Animal Model:Sprague-Dawley rats Dosage:25 mg/kg Administration:I.p.; daily from post-natal days 5 to 15 Result:Caused disturbed ossification and bone morphology in rats, including premature growth plate closure and infiltration of ossified tissue through the central epiphysis.
-
SynonymsBMS-649
-
PathwayOthers
-
TargetOther Targets
-
RecptorAurora A
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number146670-40-8
-
Formula Weight380.484
-
Molecular FormulaC24H28O4
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 5 mg/mL (13.14 mM)
-
SMILESCC1(C)CCC(C)(C)c2cc(ccc12)C1(OCCO1)c1ccc(cc1)C(O)=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Ando R, et al. 3-Cyano-6-(5-methyl-3-pyrazoloamino)pyridines: selective Aurora A kinase inhibitors. Bioorg Med Chem Lett. 2010;20(15):4709-4711.
molnova catalog



related products
-
(S)-VU0637120
(S)-VU0637120 is a selective neuropeptide Y(4)R-mutant antagonist used in the study of metabolic disorders.
-
Triphenyl bismuth
Triphenyl bismuth is an additive for making biomedical resins visible on x-ray images and can be used as a radiopaque agent for orthopaedic bone cements.
-
BI-6015
BI 6015 is an antagonist of HNF4α. HNF4α is a nuclear receptor that regulates gene expression in the intestine cells, liver cells, and pancreas-β cells.