- Go 6983
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- $36.00 / 1mg
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2024-11-19
- CAS:133053-19-7
- Min. Order:
- Purity: 99.04%
- Supply Ability: 10g
- GO 6983
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- $9.80 / 1.79999995231628KG
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2020-01-13
- CAS:133053-19-7
- Min. Order: 1g
- Purity: ≥99%
- Supply Ability: 100kg
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| | GO 6983 Basic information |
| Product Name: | GO 6983 | | Synonyms: | gǒ 6983;GOE 6983;Gδ 6983;1H-Pyrrole-2,5-dione, 3-[1-[3-(dimethylamino)propyl]-5-methoxy-1H-indol-3-yl]-4-(1H-indol-3-yl)-;Go6983(96 %);G 6983 - GO 6983 | Goe 6983;CS-674;G 6983 - CAS 133053-19-7 - Calbiochem | | CAS: | 133053-19-7 | | MF: | C26H26N4O3 | | MW: | 442.51 | | EINECS: | | | Product Categories: | Smad;TGF-beta;Inhibitors;TGF-beta/Smad | | Mol File: | 133053-19-7.mol |  |
| | GO 6983 Chemical Properties |
| Boiling point | 709.0±60.0 °C(Predicted) | | density | 1.31±0.1 g/cm3(Predicted) | | storage temp. | -20°C | | solubility | DMSO: 20 mg/mL, clear, red | | form | powder | | pka | 8.02±0.60(Predicted) | | color | red | | Stability: | Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month. |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | HS Code | 2933998090 |
| | GO 6983 Usage And Synthesis |
| Description | Go-6983 (133053-19-7) potent and pan-specific, ATP-competitive protein kinase C inhibitor. PKC isotype IC50s= 7, 7, 6, 10 and 60 nM for PKC α, β, γ, δ, ζ respectively.1 Suppresses stress induced HSP27 disassociation.2 Maintains rat embryonic stem cell pluripotency.3 Attenuates myocardial ischemia/reperfusion injury.4 | | Uses | Go 6983, is a protein kinase C (PKC) inhibitor.Potent PKC Inhibitor | | Uses | GO6983 has been used as a protein kinase C (PKC) inhibitor to study its effects on the nuclear import. It has also been used as a supplement in Fc medium to culture mouse embryonic stem (mES) cells on mitomycin C treated mouse embryonic fibroblasts (MEFs). | | Definition | ChEBI: 3-[1-[3-(dimethylamino)propyl]-5-methoxy-3-indolyl]-4-(1H-indol-3-yl)pyrrole-2,5-dione is a member of indoles and a member of maleimides. | | Biological Activity | Broad spectrum protein kinase C (PKC) inhibitor (IC 50 values are 7, 7, 6, 10, 60 and 20000 nM for PKC α , PKC β , PKC γ , PKC δ , PKC ζ and PKC μ respectively). Displays cardioprotective properties; reduces polymorphonuclear leukocyte adherence and infiltration following myocardial ischemia/reperfusion injury. | | Biochem/physiol Actions | Protein kinase C (PKC) inhibitor that selectively inhibits several PKC isozymes (IC50 = 7 nM for PKCα and PKCβ; 6 nM for PKCγ; 10 nM for PKCδ; and 60 nM for PKCζ), but does not inhibit PKCμ (IC50 = 20 mM). | | storage | -20°C | | References | 1) Gschwendt et al. (1996), Inhibition of protein kinase C mu by various inhibitors. Differentiation from protein kinase C isoenzymes; FEBS Lett., 392 77
2) Kato et al. (2001), Protein kinase inhibitors can suppress stress-induced dissociation of Hsp27; Cell Stress Chaperones, 6 16
3) Rajendran et al. (2013), Inhibition of protein kinase C signaling maintains rat embryonic stem cell pluripotency; J. Biol. Chem., 288 24351
4) Young et al. (2005), Go 6983: a fast acting protein kinase C inhibitor that attenuates myocardial ischemia/reperfusion injury; Cardiovasc, Drug Rev., 23 255 |
| | GO 6983 Preparation Products And Raw materials |
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