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ChemicalBook--->CAS DataBase List--->1256341-22-6

1256341-22-6

1256341-22-6 Structure

1256341-22-6 Structure
IdentificationBack Directory
[Name]

2-[[[2-(Tetradecyl)phenyl]amino]carbonyl]benzoic acid
[CAS]

1256341-22-6
[Synonyms]

CX08005
CX08005,CX-08005
CX08005 >=98% (HPLC)
2-[[[2-(Tetradecyl)phenyl]amino]carbonyl]benzoic acid
Benzoic acid, 2-[[[2-(tetradecyloxy)phenyl]amino]carbonyl]-
[Molecular Formula]

C28H39NO4
[MDL Number]

MFCD30480928
[MOL File]

1256341-22-6.mol
[Molecular Weight]

453.61
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

powder
[color ]

white to beige
Hazard InformationBack Directory
[Uses]

CX08005 is a competitive PTP1B inhibitor (IC50 = 0.781 μM). Binds catalytic P-loop of enzyme. Improves insulin sensitivity in obese mice in the glucose tolerance test and the homeostasis model assessment of insulin resistance index (HOMA-IR). Enhances insulin-induced glucose uptake in adipocytes and myotubes in vitro. Exhibits some selectivity for PTP1B over other protein tyrosine phosphatases, except TCPTP.
[Biological Activity]

CX08005 is a cell-permeable benzoic acid based compoundpotent and substrate-competitive PTP1B/TCPTP dual inhibitor with anti-diabetic efficacy both in vitro and in vivo. CX08005 targets protein tyrosine phosphatase 1B (PTP1B) catalytic P-loop and acts as a substrate-competitive inhibitor against PTP1B and TCPTP (IC50 = 781 and 475 nMrespectively) with much reduced potency toward LARSHP1and VHR (by 52%89%and 60%respectively at 10 μM). CX08005 enhances insulin-dependent cellular signaling (Eff. conc. 10 nM; HepG2 cells) and glucose uptake (Eff. conc. 100-500 nM; 3T3-L1 adipocityes and C2C12 myoblasts) in vitroas well as improves glucose tolerance and insulin sensitivity in diet-induced obesity (DIO) mice and KKAy type 2 diabetes mice (50-200 mg/kg/day i.p.) in vivo with good pharmacokinetics in SD rats (Cmax = 7425.9 ng/mLTmax = 6.67 h,  t1/2
[storage]

Store at -20°C
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