Tunicamycin

Tunicamycin__Autophagy inducer PT-2387

Product Name Tunicamycin
Description

Autophagy inducer

Purity >98% (HPLC) as a mixture of tunicamycin A, B, C and D
CAS No. 11089-65-9
Molecular Formula C39H64N4O16
Molecular Weight 844.95
Storage Temperature -20ºC
Shipping Temperature Shipped Ambient
Product Type Inducer
Solubility Soluble in DMSO (>10 mg/ml) or ethanol (5 mg/ml; warm).
Source Isolated from Streptomyces lysosuperficus
Appearance White solid.
SMILES C@@H2(Oemail protected(Oemail protected1OC@@H(C@@H(O)email protected(O)email protected1NC(=O)C)CO)email protected(NC(=O)C=CCC(C)C)C@@H(O)email protected2O)CC(O)email protected4OC@@H
Safety Phrases Classification: D1A- Very Toxic Material Causing Immediate and Serious Toxic Effects, Highly toxic by ingestion, D2A- Very Toxic Material Causing Other Toxic Effects, Teratogen- Reproductive hazard
Safety Phrases:
S22 – Do not breathe dust.
S24/25 – Avoid contact with skin and eyes.
S36/37/39 – Wear suitable protective clothing, gloves and eye/face protection.
Hazard statements:
H300- Fatal if swallowed.
Precautionary statements:
P264- Wash hands thoroughly after handling.
P301 + P310- IF SWALLOWED: Immediately call a POISON CENTER or doctor/ physician.
Cite This Product Tunicamycin (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-397)
Alternative Names Tunicamycin from Streptomyces sp.
Research Areas Cancer, Autophagy
Scientific Background As a nucleoside antibiotic, Tunicamycin blocks the formation of protein N-glycosidic linkages by inhibiting the transfer of N-acetylglucosamine 1-phosphate to dolichol monophosphate. This causes an induction of glucose-regulated protein 78 (GRP78) mRNA expression, which in turn increases ER stress and subsequently induces autophagy.
References 1. Unal E.S., et al. (2008) Biochim Biophys Acta. 1778(6): 1407-14.
2. Ding W.X., et al. (2007) J Biol Chem. 282(7): 4702-10.
3. Ishii S., et al. (1987) J Neurochem. 49(5): 1606-12.
4. Zhang J., et al. (2013) J Surg Res. 183(2): 929-35.