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Go6976

SKU: orb1741480

Description

Go6976

Research Area

Epigenetics & Chromatin, Infectious Disease & Virology, Signal Transduction

Images & Validation

Key Properties

CAS Number136194-77-9
MW378.43
Purity95.89%
FormulaC24H18N4O
SMILESCn1c2ccccc2c2c3C(=O)NCc3c3c4ccccc4n(CCC#N)c3c12
TargetInfluenza Virus,PKC
Solubility10% DMSO+90% Corn Oil:3.3 mg/mL (8.72 mM);DMSO:30 mg/mL (79.27 mM)

Bioactivity

Target IC50
PKCβ1:6.2 nM|PKC:7.9 nM|PKC:20 nM|PKCα:2.3 nM
In Vitro
30 nM Go6976 is sufficient to cause abrogation of S-phase arrest in 6 h and abrogation of G2 arrest followed by lethal mitosis in 24 h. Incubation of cells with 100 nM Go6976 is sufficient to cause complete abrogation of S and G2 arrest at 6 and 24 h, respectively, which is only slightly less potent than in bovine serum. Go6976 is a potent inhibitor of PKC in vitro (IC50 is 20 nM. This compound is structurally related to staurosporine, which is the most potent PKC inhibitor

Storage & Handling

Storagestore at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

Gö 6976, Go6976, PKC
Quality Guarantee

Quality Guarantee

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Key Properties

No computed properties available.

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Protocol Information

Go6976 (orb1741480)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

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1 mg
$ 110.00
5 mg
$ 220.00
1 ml x 10 mM (in DMSO)
$ 230.00
10 mg
$ 320.00
25 mg
$ 440.00
50 mg
$ 720.00
100 mg
$ 980.00
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