Tubacin

Bezeichnung:Tubacin

CAS-Nr537049-40-4

Englisch Name:Tubacin

CBNumberCB32519138

SummenformelC41H43N3O7S

Molgewicht721.86

MOL-Datei537049-40-4.mol

Tubacin physikalisch-chemischer Eigenschaften

Schmelzpunkt	155 - 157°C
storage temp.	-20°C
Löslichkeit	DMSO: ≥10mg/mL
Aggregatzustand	powder
Farbe	white to tan
InChIKey	BHUZLJOUHMBZQY-UHHSDZQINA-N
SMILES	C(NC1=CC=C([C@H]2O[C@@H](CSC3=NC(C4=CC=CC=C4)=C(C4=CC=CC=C4)O3)C[C@@H](C3=CC=C(CO)C=C3)O2)C=C1)(=O)CCCCCCC(NO)=O \|&1:6,8,29,r\|

Sicherheit

WGK Germany

Gefahreninformationscode (GHS)

Tubacin Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung
Tubacin: an HDAC6 Selective Inhibitor.
Tubacin (tubulin acetylation inducer) is a highly potent and selective, reversible, cell-permeable inhibitor of HDAC6 (IC50=0.004μM). It dose-dependently boosted the release of influenza A virus (IAV) progeny through the increase of acetylated microtubules to effectively move viral components to the plasma membrane. It could reduce the Replication of the Japanese Encephalitis Virus via the Decrease of Viral RNA Synthesis. Tubacin was demonstrated as a host-targeting agent with preventive and therapeutic activities against the Japanese encephalitis virus. Concentration in cell culture experiments typically ranges from 2-50μM[1].
Verwenden
Tubacin is tubulin acetylation inducer that selectively inhibits histone deacetylase (HDAC6).
Definition
ChEBI: N-[4-[(2R,4R,6S)-4-[[(4,5-diphenyl-2-oxazolyl)thio]methyl]-6-[4-(hydroxymethyl)phenyl]-1,3-dioxan-2-yl]phenyl]-N'-hydroxyoctanediamide is a member of 1,3-oxazoles.
Biochem/physiol Actions
Tubacin triggers the release of reactive oxygen species and mediates caspase-3-independent apoptosis of Epstein-Barr virus (EBV)-positive Burkitt lymphoma cells. It suppresses the proliferation of acute lymphoblastic leukemia (ALL) cells and enhances the effect of chemotherapy to treat ALL cells. Tubacin prevents the epileptic activity and neuronal migration defects caused due to lowered expression of Srpx2 in rats.
target
HDAC6
Einzelnachweise
[1] Chien-Yi Lu. “Tubacin, an HDAC6 Selective Inhibitor, Reduces the Replication of the Japanese Encephalitis Virus via the Decrease of Viral RNA Synthesis.” International Journal of Molecular Sciences 18 5 (2017).

Tubacin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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