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Go 6976

Chemical Structure : Go 6976

CAS No.: 136194-77-9

Go 6976 (Go-6976;Go6976)

Catalog No.: PC-60684Not For Human Use, Lab Use Only.

Go 6976 is a potent, selective protein kinase C (PKC) inhibitor that selectively inhibits PKCα and PKCβ1 with IC50 of 2.3 and 6.2 nM, respectively.

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2 mg $148 In stock
5 mg $258 In stock
10 mg $398 In stock
25 mg $598 In stock
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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Go 6976 is a potent, selective protein kinase C (PKC) inhibitor that selectively inhibits PKCα and PKCβ1 with IC50 of 2.3 and 6.2 nM, respectively.
Go 6976 shows no effect on the kinase activity of PKCδ, -ε and -ζ (IC50>3 uM).
Go 6976 also inhibits JAK2, FLT3 and mutant FLT3 with significant activity in primary acute myeloid leukaemia cells.
Go 6976 inhibits HIV-1 proviral induction from latent/low-level-producing infectious states, inhibits signalling, survival and proliferation in cells expressing the leukaemia-associated TEL-JAK2 fusion protein and the MPD-associated JAK2 V617F mutant.

Physicochemical Properties

M.Wt 378.43
Formula C24H18N4O
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

5,6,7,13-Tetrahydro-13-methyl-5-oxo-12H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-12-propanenitrile

References

1. Martiny-Baron G, et al. J Biol Chem. 1993 May 5;268(13):9194-7.

2. Qatsha KA, et al. Proc Natl Acad Sci U S A. 1993 May 15;90(10):4674-8.

3. Pätzold S, et al. Antiviral Res. 1993 Dec;22(4):273-83.

4. Grandage VL, et al. Br J Haematol. 2006 Nov;135(3):303-16.

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