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1,3-DIHYDRO-1-(1-((4-(6-PHENYL-1H-IMIDAZO[4,5-G]QUINOXALIN-7-YL)PHENYL)METHYL)-4-PIPERIDINYL)-2H-BENZIMIDAZOL-2-ONE TRIFLUOROACETATE SALT HYDRATE

1,3-DIHYDRO-1-(1-((4-(6-PHENYL-1H-IMIDAZO[4,5-G]QUINOXALIN-7-YL)PHENYL)METHYL)-4-PIPERIDINYL)-2H-BENZIMIDAZOL-2-ONE TRIFLUOROACETATE SALT HYDRATE Struktur
616871-83-1
CAS-Nr.
616871-83-1
Englisch 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 TRIFLUOROACETATE SALT HYDRATE
Synonyma:
AKT1/2 KINASE INHIBITOR;AKT-I-1/2;AKT INHIBITOR VIII;AKTI-1/2 TRIFLUOROACETATE SALT HYDRATE;AKT INHIBITOR VIII TRIFLUOROACETATE SALT HYDRATE;1,3-DIHYDRO-1-(1-((4-(6-PHENYL-1H-IMIDAZO[4,5-G]QUINOXALIN-7-YL)PHENYL)METHYL)-4-PIPERIDINYL)-2H-BENZIMIDAZOL-2-ONE TRIFLUOROACETATE SALT HYDRATE;Akt Inhibitor, Isozyme-selective (1,3-Dihydro-1-(1-((4-(6-phenyl-1H-imidazo[4,5-g]quinoxalin-7-yl)phenyl)methyl)-4-piperidinyl)-2H-benzimidazol-2-one;2H-Imidazo[4,5-g]quinoxalin-2-one, 6-[4-[[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]methyl]phenyl]-1,3-dihydro-7-phenyl-, 2,2,2-trifluoroacetate (1:)
CBNumber:
CB5806630
Summenformel:
C36H32F3N7O4
Molgewicht:
683.6789896
MOL-Datei:
Mol file

1,3-DIHYDRO-1-(1-((4-(6-PHENYL-1H-IMIDAZO[4,5-G]QUINOXALIN-7-YL)PHENYL)METHYL)-4-PIPERIDINYL)-2H-BENZIMIDAZOL-2-ONE TRIFLUOROACETATE SALT HYDRATE Eigenschaften

Schmelzpunkt:
>255oC (dec.)
storage temp. 
2-8°C
L?slichkeit
DMSO (Slightly)
Aggregatzustand
powder
Farbe
yellow
InChIKey
CRRPFKCJZALCLQ-UHFFFAOYSA-N
SMILES
[H]O[H].OC(=O)C(F)(F)F.O=C1Nc2ccccc2N1C3CCN(CC3)Cc4ccc(cc4)-c5nc6cc7nc[nH]c7cc6nc5-c8ccccc8

Sicherheit

WGK Germany  3
Speicherklasse 11 - Combustible Solids

1,3-DIHYDRO-1-(1-((4-(6-PHENYL-1H-IMIDAZO[4,5-G]QUINOXALIN-7-YL)PHENYL)METHYL)-4-PIPERIDINYL)-2H-BENZIMIDAZOL-2-ONE TRIFLUOROACETATE SALT HYDRATE Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Akt plays a role in signal transduction pathways of cell proliferation, apoptosis, angiogenesis, and diabetes. Akt1 and Akt2 dual kinase inhibitors are capable of sensitizing tumor cells to certain apoptotic stimuli, and inhibit Akt phosphorylation in vivo. Akt1 kinase activity and its regulation by extracellular signaling factors in vivo in hematopoietic cells suggests the activation of AKT1 involves intracellular translocation of the kinase from cytosol to membrane.

Biochem/physiol Actions

Isozyme selective Akt1/2 kinase inhibitor. In in vitro kinase assays, Akt1/2 kinase inhibitor shows IC50 = 58 nM, 210 nM, and 2.12 mM for Akt1, Akt2, and Akt3, respectively, The inhibition appears to be pleckstrin homology (PH) domain-dependent and the Akt1/2 kinase inhibitor has no 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.

1,3-DIHYDRO-1-(1-((4-(6-PHENYL-1H-IMIDAZO[4,5-G]QUINOXALIN-7-YL)PHENYL)METHYL)-4-PIPERIDINYL)-2H-BENZIMIDAZOL-2-ONE TRIFLUOROACETATE SALT HYDRATE Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


1,3-DIHYDRO-1-(1-((4-(6-PHENYL-1H-IMIDAZO[4,5-G]QUINOXALIN-7-YL)PHENYL)METHYL)-4-PIPERIDINYL)-2H-BENZIMIDAZOL-2-ONE TRIFLUOROACETATE SALT HYDRATE Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 39)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Sigma-Aldrich 021-61415566 800-8193336
orderCN@merckgroup.com China 51395 80
Shanghai Zeye Biotechnology Co., Ltd. 021-57896695 13122364865
sale1@shzysw.net China 9779 58
Kaifeng Mingren Pharmaceutical Co.,LTD 0371-65741762
sales@hasunny.com China 2380 58
Beijing Boorsen Biotechnology Co., Ltd 400-901-9800 18611424007
cis@bioss.com.cn China 9185 58
Huai Hua Binfengchem Co., Ltd 0745-2866851 17711757908
406037272@qq.com China 4383 58
bioleaper 4000880777 17585207275
guojing@bioleaper.com China 5616 58
Cayman Chemical Company --
sales@caymanchem.com China 6838 58
Enzo Biochem Inc --
Enzoname@qq.com China 6174 58
Merck KGaA --
ordercn@merckgroup.com China 6394 58
Santa Cruz Biotechnology Inc --
scbt@scbt.com China 6594 58

  • 1,3-DIHYDRO-1-(1-((4-(6-PHENYL-1H-IMIDAZO[4,5-G]QUINOXALIN-7-YL)PHENYL)METHYL)-4-PIPERIDINYL)-2H-BENZIMIDAZOL-2-ONE TRIFLUOROACETATE SALT HYDRATE
  • AKT-I-1/2
  • AKTI-1/2 TRIFLUOROACETATE SALT HYDRATE
  • AKT INHIBITOR VIII TRIFLUOROACETATE SALT HYDRATE
  • AKT INHIBITOR VIII
  • Akt Inhibitor, Isozyme-selective (1,3-Dihydro-1-(1-((4-(6-phenyl-1H-imidazo[4,5-g]quinoxalin-7-yl)phenyl)methyl)-4-piperidinyl)-2H-benzimidazol-2-one
  • 2H-Imidazo[4,5-g]quinoxalin-2-one, 6-[4-[[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]methyl]phenyl]-1,3-dihydro-7-phenyl-, 2,2,2-trifluoroacetate (1:)
  • AKT1/2 KINASE INHIBITOR
  • 616871-83-1
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