Product overview

Name Splitomicin
Purity >98%
Description Potent,selective, cell permeable yeast NAD+-dependent HDAC Sir2p inhibitor
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Biological Data

Biological description Potent, selective and cell permeable yeast NAD+-dependent histone deacetylase (HDAC) Sir2p inhibitor. Displays higher activity in vivo than in vitro. Sensitizes mammalian cells to a variety of DNA-damaging agents by abrogating Sir2p activity on p53. Acts by either altering or blocking access to the acetylated histone binding pocket. Shown to have diverse effects also in mammalian cells.

Solubility & Handling

Storage instructions +4°C
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.

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Chemical Data

Purity >98%
Chemical name 1,2-Dihydro-3H-naphtho[2,1-b]pyran-3-one
Molecular Weight 198.2
Chemical structure Splitomicin [5690-03-9] Chemical Structure
Molecular Formula C13H10O2
CAS Number 5690-03-9
PubChem identifier 5269
SMILES O=C1CCC2=C(O1)C=CC1=CC=CC=C21
InChiKey ISFPDBUKMJDAJH-UHFFFAOYSA-N
Appearance White to off-white solid