Products

AKT Inhibitors

본문

 
AKT Inhibitors
 
 
Product Name: Akt Inhibitor VIII, Isozyme-Selective, Akti-1/2
 
 
   클릭하시면 닫힙니다.이미지 저장을 원하시면 마우스 오른쪽클릭후 '다른이름으로 저장'을 하세요
 
A cell-permeable quinoxaline compound that potently and selectively inhibits Akt1/Akt2 activity (IC50 = 58 nM, 210 nM, and 2.12 µM for Akt1, Akt2, and Akt3, respectively, in in vitro kinase assays). The inhibition appears to be pleckstrin homology
(PH) domain-dependent. It does not exhibit any inhibitory effect against PH domain-lacking Akts, or other closely related 
AGC family kinases, PKA, PKC, and SGK, even at concentrations as high as 50 µM. Overcomes Akt1/Akt2-mediated resistance to chemotherapeutics in tumor cells and is shown to block basal and stimulated phosphorylation/activation of Akt1/Akt2 both in cultured cells in vitro and in mice in vivo.
 
Details
Chemical Formula:
 
C34H29N7O
CAS No.:
 
612847-09-3
Molecular weight:
 
551.6
Purity:
98% by HPLC
Appearance:
 
Light yellow solid
Chemical name:
 
 1,3-Dihydro-1-(1-((4-(6-phenyl-1H-imidazo[4,5-g]quinoxalin-7-yl)phenyl)methyl)-4-
piperidinyl)-2H-benzimidazol-2-one
Solubility:
 
DMSO (5mg/mL)
Storage:
Protect from light. Packaged under inert gas
 
References
 
 
Product Name: Akt Inhibitor X, PH-domain Independent
 
 
   클릭하시면 닫힙니다.이미지 저장을 원하시면 마우스 오른쪽클릭후 '다른이름으로 저장'을 하세요
 
A cell-permeable, reversible, and selective inhibitor of the phosphorylation of Akt and its in vitro kinase activity (complete
inhibition < 5 µM) with minimal effect on PI 3-K, PDK1, or SGK1. Shown to suppress growth of Rh (rhabdomyosarcoma) cell
lines (IC50 = 2-5 μM), inhibit IGF-I-stimulated nuclear translocation of Akt, and prevent phosphorylation of the downstream
targets, mTOR, p70S6 kinase, and S6 ribosomal protein. Unlike Akti1/2 (Cat # CD0223), the mode of inhibition is not PH
domain-dependent. Also shown to induce neuronal autophagy in an Akt- and mTOR-independent manner and enhances the
clearance of misfolded protein.
 
Details
Chemical Formula:
 
C20H25CIN2O∙HCI
CAS No.:
 
925681-41-0
Molecular weight:
 
381.4
Purity:
98% by HPLC
Appearance:
 
White solid
Chemical name:
 
 10-(4′-(N-diethylamino)butyl)-2-chlorophenoxazine hydrochloride
Solubility:
 
DMSO (60 mg/mL), water (1 mg/mL)
Storage:
Protect from light. Packaged under inert gas
 
References
 
 
Ordering informations
 
Catalog No.
Product Name
Size
CD0223
AKT inhibitor VIII
1mg, 5mg, 10mg & 25mg
CD0225
AKT inhibitor X
1mg, 5mg, 10mg & 25mg
 
 
       
 
▣ 관련 페이지 ; Chemdea
 
 
 
 

댓글목록

등록된 댓글이 없습니다.

Copyright by Sambo Medical Co. All rights reserved.