Go 6976

CAS No. 136194-77-9

Go 6976( Go-6976 | Go6976 )

Catalog No. M11490 CAS No. 136194-77-9

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

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 173 Get Quote
10MG 257 Get Quote
25MG 434 Get Quote
50MG 618 Get Quote
100MG 860 Get Quote
200MG Get Quote Get Quote
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Biological Information

  • Product Name
    Go 6976
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective protein kinase C (PKC) inhibitor that selectively inhibits PKCα and PKCβ1 with IC50 of 2.3 and 6.2 nM, respectively.
  • Description
    A potent, selective protein kinase C (PKC) inhibitor that selectively inhibits PKCα and PKCβ1 with IC50 of 2.3 and 6.2 nM, respectively; shows no effect on the kinase activity of PKCδ, -ε and -ζ (IC50>3 uM); also inhibits JAK2, FLT3 and mutant FLT3 with significant activity in primary acute myeloid leukaemia cells; 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.HIV Infection Discontinued.
  • In Vitro
    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. UCN-01 is originally identified as a PKC inhibitor. Surprisingly, Go6976 is found to abrogate S and G2 arrest. Dose-response studies reveal that 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. Incubation of cells with UCN-01 or Go6976 alone do not decrease viability compared with control at the concentrations used. Incubation of cells with 5 ng/mL SN38 result in cytostasis, and addition of 50 nM UCN-01 or 100 nM Go6976 to arrested MDA-MB-231 cells cause a dramatic decrease in viable cell number by 96 h.
  • In Vivo
    ——
  • Synonyms
    Go-6976 | Go6976
  • Pathway
    Angiogenesis
  • Target
    PKC
  • Recptor
    PKC
  • Research Area
    Infection
  • Indication
    HIV Infection

Chemical Information

  • CAS Number
    136194-77-9
  • Formula Weight
    378.43
  • Molecular Formula
    C24H18N4O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (132.12 mM)
  • SMILES
    N#CCCN(C1=C2C(CNC3=O)=C3C4=C1N(C)C5=C4C=CC=C5)C6=C2C=CC=C6
  • Chemical Name
    5,6,7,13-Tetrahydro-13-methyl-5-oxo-12H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-12-propanenitrile

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

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. P?tzold 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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