GO 6976 manufacturers
- Go6976
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- $78.00 / 1mg
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2024-11-06
- CAS:136194-77-9
- Min. Order:
- Purity: 95.89%
- Supply Ability: 10g
- G? 6976
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- $1.00 / 1g
-
2020-01-13
- CAS:136194-77-9
- Min. Order: 1g
- Purity: 95-99%
- Supply Ability: 1ton
- GO 6976
-
- $1.00 / 1g
-
2020-01-13
- CAS:136194-77-9
- Min. Order: 1g
- Purity: 99%
- Supply Ability: 200kg
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| | GO 6976 Basic information |
| Product Name: | GO 6976 | | Synonyms: | InSolution? G? 6976;5,6,7,13-Tetrahydro-13-methyl-5-oxo-12H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-12-propanenitrile;Go6976,5,6,7,13-Tetrahydro-13-Methyl-5-oxo-12H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-12-propanenitrile;PD406976;12-(2-CYANOETHYL)-6,7,12,13-TETRAHYDRO-13-METHYL-5-OXO-5H-INDOLO(2,3-A)PYRROLO(3,4-C)-CARBAZOLE;12-2(2-CYANOETHYL)-6,7,12,13-TETRAHYDRO-13-METHYL-5-OXO-5H-INDOLO[2,3-A]PYRROLO[3,4-C]CARBAZOLE;GO 6976;G6976 | | CAS: | 136194-77-9 | | MF: | C24H18N4O | | MW: | 378.43 | | EINECS: | 200-258-5 | | Product Categories: | Inhibitors;Inhibitor | | Mol File: | 136194-77-9.mol |  |
| | GO 6976 Chemical Properties |
| Melting point | >221°C (dec.) | | Boiling point | 652.3±55.0 °C(Predicted) | | density | 1.41±0.1 g/cm3(Predicted) | | storage temp. | Sealed in dry,2-8°C | | solubility | Acetonitrile (Very Slightly, Heated), DMSO (Slightly), Methanol (Very Slightly) | | form | Off-white solid | | pka | 14.39±0.20(Predicted) | | color | White to Off-White |
| Safety Statements | 22-24/25 | | HS Code | 2933998090 |
| | GO 6976 Usage And Synthesis |
| Uses | Go 6976 is a potent FLT3 inihibtor which is been shown to initiate cytotoxicity involving acute leukemia. Also known as a PKC inhibitor, which results into apoptosis and tumor destruction. Cancer therapeutic agent. | | Definition | ChEBI: Goe 6976 is an organic heterohexacyclic compound and an indolocarbazole. It has a role as an EC 2.7.11.13 (protein kinase C) inhibitor. | | Biological Activity | Potent protein kinase C (PKC) inhibitor (IC 50 = 7.9 nM). In vitro, discriminates between Ca 2+ -dependent and -independent isoforms of PKC; selectively inhibits PKC α and PKC β 1 (IC 50 values are 2.3 and 6.2 nM respectively) but does not inhibit the activity of PKC δ , - ε , or - ζ (IC 50 > 3 μ M). Also inhibits TrkA, TrkB, JAK2 and JAK3 tyrosine kinases (IC 50 values are 5, 30, 130 and 370 nM respectively). | | storage | -20°C (desiccate) | | references | [1]. gschwendt, m., et al., inhibition of protein kinase c mu by various inhibitors. differentiation from protein kinase c isoenzymes. febs lett, 1996. 392(2): p. 77-80.
[2]. qatsha, k.a., et al., go 6976, a selective inhibitor of protein kinase c, is a potent antagonist of human immunodeficiency virus 1 induction from latent/low-level-producing reservoir cells in vitro. proc natl acad sci u s a, 1993. 90(10): p. 4674-8.
[3]. joksovic, p.m., et al., mechanisms of inhibition of t-type calcium current in the reticular thalamic neurons by 1-octanol: implication of the protein kinase c pathway. mol pharmacol, 2010. 77(1): p. 87-94.
[4]. taube, e., et al., a novel treatment strategy for egfr mutant nsclc with t790m-mediated acquired resistance. int j cancer, 2012. 131(4): p. 970-9.
[5]. yoshida, a., et al., go6976, a flt3 kinase inhibitor, exerts potent cytotoxic activity against acute leukemia via inhibition of survivin and mcl-1. biochem pharmacol, 2014. 90(1): p. 16-24. |
| | GO 6976 Preparation Products And Raw materials |
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