ChemicalBook--->CAS DataBase List--->702681-67-2

702681-67-2

702681-67-2 Structure

702681-67-2 Structure
IdentificationBack Directory
[Name]

CP-868388
[CAS]

702681-67-2
[Synonyms]

CP-868388
(-)-CP-868388
UNII-999KY5ZIGB
CP-868388 free base
(S)-2-(3-(1-((4-Isopropylbenzyloxy)carbonyl)piperidin-3-yl)phenoxy)-2-methylpropanoic acid
2-methyl-2-{3-[(3S)-1-({[4-(propan-2-yl)phenyl]methoxy}carbonyl)piperidin-3-yl]phenoxy}propanoic acid
1-Piperidinecarboxylic acid, 3-[3-(1-carboxy-1-methylethoxy)phenyl]-, 1-[[4-(1-methylethyl)phenyl]methyl] ester, (3S)-
[Molecular Formula]

C26H33NO5
[MDL Number]

MFCD18452851
[MOL File]

702681-67-2.mol
[Molecular Weight]

439.54
Chemical PropertiesBack Directory
[Boiling point ]

584.6±50.0 °C(Predicted)
[density ]

1.161±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: ≥30mg/mL
[form ]

powder
[pka]

3.28±0.10(Predicted)
[color ]

white to off-white
[Optical Rotation]

[α]/D -50 to -65°, c = 0.2 in methanol
[InChIKey]

CSLFIHDRJSTULR-JOCHJYFZSA-N
[SMILES]

CC(C)c1ccc(COC(=O)N2CCC[C@H](C2)c3cccc(OC(C)(C)C(O)=O)c3)cc1
Safety DataBack Directory
[Hazard Codes ]

T,N
[Risk Statements ]

25-50/53
[Safety Statements ]

45-60-61
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

3
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Aquatic Acute 1
Aquatic Chronic 1
Hazard InformationBack Directory
[Uses]

CP-868388 is a potent PPARα agonist with a Ki of 10.8 nM for therapeutic use as hypolipemics, antidiabetics.
[Biological Activity]

CP-868388 is a potent PPARα agonist with a Ki of 10.8 nM.
[in vivo]

CP-868388 (0-3 mg/kg; oral gavage; once daily; for 2 days; male B6/CBF1J mice) treatment shows a robust and highly significant decrease in circulating plasma triglycerides. Triglyceride lowering is dose-dependent with the greatest efficacy achieved at the 3.0 mg/kg dose, with triglyceride decreases of ~50%[1].

Animal Model:Male B6/CBF1J mice[1]
Dosage:0 mg/kg, 0.3 mg/kg, 1 mg/kg, 3 mg/kg
Administration:Oral gavage; once daily; for 2 days
Result:Demonstrated a robust and highly significant decrease in circulating plasma triglycerides.
[IC 50]

hPPARα: 10.8 nM (Ki); hPPARγ: 3.47 μM (Ki)
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