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T3830

Sigma-Aldrich

Triciribine hydrate

≥97% (HPLC)

Synonym(e):

API-2, Akt/PKB Signaling Inhibitor-2, Inhibitor V, NSC 154020, TCN, VD-0002

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About This Item

Empirische Formel (Hill-System):
C13H16N6O4 · xH2O
CAS-Nummer:
35943-35-2
Molekulargewicht:
320.30 (anhydrous basis)
MDL-Nummer:
MFCD16879015
UNSPSC-Code:
12352200
PubChem Substanz-ID:
329826778
NACRES:
NA.77

Qualitätsniveau

100

Assay

≥97% (HPLC)

Form

powder

Farbe

tan

Löslichkeit

DMSO: >10 mg/mL

Lagertemp.

2-8°C

SMILES String

O.Cn1nc(N)c2cn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c4ncnc1c24

InChI

1S/C13H16N6O4.H2O/c1-18-11-7-5(10(14)17-18)2-19(12(7)16-4-15-11)13-9(22)8(21)6(3-20)23-13;/h2,4,6,8-9,13,20-22H,3H2,1H3,(H2,14,17);1H2/t6-,8-,9-,13-;/m1./s1

InChIKey

SPGRLWCWHWRPHX-DOKXERMVSA-N

Angaben zum Gen

human ... AKT1(207)
mouse ... AKT1(11651)
rat ... AKT1(24185)

Anwendung

Triciribine hydrate has been used to study the effect of diethyldithiocarbamate (DDC) on matrix metalloproteinase-1 (MMP-1) in hepatic stellate cells1. It has also been used to analyze ADAM 10 activation by (-)-epigallocatechin-3-gallate (EGCG) in N2a cells overexpressing Swedish mutant APP (SweAPP N2a cells)2.

Biochem./physiol. Wirkung

Triciribine is a highly selective Akt/PKB inhibitor, that selectively inhibits the cellular phosphorylation/activation of Akt1/2/3.

Leistungsmerkmale und Vorteile

This compound is featured on the PKB/Akt page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Angaben zur Herstellung

Triciribine hydrate is soluble in DMSO at a concentration that is greater than 10 mg/ml.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

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Journal of cellular physiology, 226(3), 822-831 (2010-09-22)
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