trans-AUCB

trans-AUCB

T648371-5mg

5mg

≥98%

-20°C储存

超低温冰袋运输

trans-AUCB (t-AUCB) is a potent, orally active and selective soluble epoxide hydrolase (sEH) inhibitor with IC 50 s of 1.3 nM, 8 nM, 8 nM for hsEH, mouse sEH and rat sEH, respectively. trans-AUCB has anti-glioma activity In Vitro trans-AUCB (t-AUCB; 25-300 μM; 48 hours) suppresses U251 and U87 cell growth in a dose-dependent manner. ?\ntrans-AUCB (200 μM; 48 or 96 hours) induces cell-cycle G0/G1 phase arrest in U251 and U87 cells. ?\ntrans-AUCB (200 μM; 10 min-4 hours) can increase the phosphorylation levels of p65 after 10 min, reaching to peak after 30 min and lasting for at least 2 hours. ?\ntrans-AUCB (200 μM; 48 hours) suppresses U251 and U87 cell growth by activating NF-jB-p65. ?\ntrans-AUCB (10 μM; 30 min) efficiently inhibits sEH activities in human glioblastoma cell lines (U251, U87) and human hepatocellular carcinoma cell line (HepG2 cells). MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: U251, U87 cells Concentration: 25, 50, 100, 200, or 300 μM Incubation Time: 48 hours Result: Suppressed U251 and U87 cell growth in a dose-dependent manner. Cell Cycle AnalysisCell Line: U251, U87 cells Concentration: 200 μM Incubation Time: 48 or 96 hours Result: Induced cell-cycle G0/G1 phase arrest in U251 and U87 cells. Western Blot AnalysisCell Line: U251, U87 cells Concentration: 200 μM Incubation Time: 10 min, 30 min, 1 hour, 2 hours, or 4 hours Result: Increased the phosphorylation levels of p65 after 10 min, reached to peak after 30 min and lasted for at least 2 hours. In Vivo trans-AUCB (t-AUCB; p.o.; 0.1, 0.5, 1 mg/kg) ameliorates the LPS-induced hypotension in a dose-dependent manner. ?\ntrans-AUCB (p.o.; 0.1, 0.5, 1 mg/kg) has t 1/2 values of 20, 30, 15 min and C max values of 30, 100, 150 nmol/L for p.o. of 0.1, 0.5, 1 mg/kg. ?\ntrans-AUCB (s.c.; 1, 3, 10 mg/kg) has t 1/2 values of 60, 85, 75 min and C max values of 245, 2700, 3600 nmol/L for s.c. of 1, 3, 10 mg/kg. ?\ntrans-AUCB (i.v.; 0.1 mg/kg) has t 1/2 values of 70 min and 10 hours for distribution (α) and elimination (β) phases. trans-AUCB has a CL of 0.7 L/h?kg and a V dss was 17 L/kg. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Mice (male CFW strain, 7 weeks old, 24-30 g; and male C57BL/6 strain, 8 weeks old, 22-25 g)Dosage: 0.1, 0.5, 1 mg/kg Administration: PO Result: Ameliorated the LPS-induced hypotension in a dose-dependent manner. Animal Model: Mice (male CFW strain, 7 weeks old, 24-30 g; and male C57BL/6 strain, 8 weeks old, 22-25 g)Dosage: 0.1, 0.5, 1 mg/kg (Pharmacokinetic Analysis) Administration: PO Result: Had t 1/2 values of 20, 30, 15 min and C max values of 30, 100, 150 nmol/L for p.o. of 0.1, 0.5, 1 mg/kg, respectively. Form:Solid IC50& Target:IC50: 1.3 nM (hsEH), 8 nM (mouse sEH) and 8 nM (rat sEH)

反式-AUCB（t-AUCB）是一种强效、口服活性和选择性可溶性环氧化物水解酶（sEH）抑制剂，对 hsEH、小鼠 sEH 和大鼠 sEH 的 IC 50 s 分别为 1.3 nM、8 nM 和 8 nM。

885012-33-9

C24H32N2O4

412.52 g/mol

16038368

C1CC(CCC1NC(=O)NC23CC4CC(C2)CC(C4)C3)OC5=CC=C(C=C5)C(=O)O

4-[4-(1-adamantylcarbamoylamino)cyclohexyl]oxybenzoic acid

1S/C24H32N2O4/c27-22(28)18-1-5-20(6-2-18)30-21-7-3-19(4-8-21)25-23(29)26-24-12-15-9-16(13-24)11-17(10-15)14-24/h1-2,5-6,15-17,19,21H,3-4,7-14H2,(H,27,28)(H2,25,26,29)

KNBWKJBQDAQARU-UHFFFAOYSA-N

C1CC(CCC1NC(=O)NC23CC4CC(C2)CC(C4)C3)OC5=CC=C(C=C5)C(=O)O

16038368

DMSO : 100 mg/mL (242.41 mM; Need ultrasonic)

3

4

5

412.236 Da

412.236 Da

87.700 Ų

30

0

608.000

0

1

4.600