ChemicalBook--->CAS DataBase List--->1356497-91-0

1356497-91-0

1356497-91-0 Structure

1356497-91-0 Structure
IdentificationBack Directory
[Name]

3-[[[4-(Hexylamino)-2-methoxyphenyl]amino]sulfonyl]-2-thiophenecarboxylic acid methyl ester
[CAS]

1356497-91-0
[Synonyms]

ST247
ST247 >=98% (HPLC)
3-[[[4-(Hexylamino)-2-methoxyphenyl]amino]sulfonyl]-2-thiophenecarboxylicacidmethyleste
3-[[[4-(Hexylamino)-2-methoxyphenyl]amino]sulfonyl]-2-thiophenecarboxylic acid methyl ester
2-Thiophenecarboxylic acid, 3-[[[4-(hexylamino)-2-methoxyphenyl]amino]sulfonyl]-, methyl ester
[Molecular Formula]

C19H26N2O5S2
[MOL File]

1356497-91-0.mol
[Molecular Weight]

426.55
Chemical PropertiesBack Directory
[Boiling point ]

595.0±60.0 °C(Predicted)
[density ]

1.285±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: soluble10mg/mL (clear solution)
[form ]

powder
[pka]

8.53±0.50(Predicted)
[color ]

white to beige
[InChI]

1S/C19H26N2O5S2/c1-4-5-6-7-11-20-14-8-9-15(16(13-14)25-2)21-28(23,24)17-10-12-27-18(17)19(22)26-3/h8-10,12-13,20-21H,4-7,11H2,1-3H3
[InChIKey]

MRWCGEOYGFZZCJ-UHFFFAOYSA-N
[SMILES]

CCCCCCNc1ccc(NS(=O)(=O)c2ccsc2C(=O)OC)c(OC)c1
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-41
[Safety Statements ]

26-39
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

ST247 a potent PPARβ/δ inverse agonist. ST247 has a higher affinity to PPARβ/δ. ST247 modulates expression of the activation marker CCL2 in the opposite direction. ST247 efficiently induces the interaction with corepressors. ST247 inhibits the agonist-induced transcriptional activity of PPARβ/δ[1].
[Biological Activity]

ST247 is a PPAR β/δ selective inverse agonist. The compound is based on the structure of GSK0660and is 10-fold more potent in blocking the transcription of endogenous target genes: ST247 IC50 = 19 nm vs. GSK0660 IC50 = 210 nM.
[IC 50]

PPARβ/δ
[References]

[1] Naruhn S, et al. High-affinity peroxisome proliferator-activated receptor β/δ-specific ligands with pure antagonistic or inverse agonistic properties. Mol Pharmacol. 2011 Nov;80(5):828-38. DOI:10.1124/mol.111.074039
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