Free shipping on all orders over $ 500

Tunicamycin

Cat. No. M4798

All AbMole products are for research use only, cannot be used for human consumption.

Tunicamycin Structure
Synonym:

NSC 177382, TN

Size Price Availability Quantity
1mg USD 90 In stock
5mg USD 270 In stock
10mg USD 420 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

Tunicamycin inhibits GlcNAc phosphotransferase (GPT).Tunicamycin blocks the formation of N-glycosidic linkages by inhibiting the first step in glycoprotein synthesis.Tunicamycin can be used to induce autophagy.Tunicamycin induces apoptosis in association with caspase-3 activation, generation of reactive oxygen species (ROS), and downregulation of survivin expression.P38 MAPK (mitogen-activated protein kinase) and the generation of ROS signaling pathway play crucial roles in TN-induced apoptosis in U937 cells.TN modulates multiple components of the apoptotic response of human leukemia cells and raise the possibility of a novel therapeutic strategy for hematological malignancies.

Product Citations
Protocol (for reference only)
Cell Experiment
Cell lines EA.hy926-L2-OE and EA.hy926-NC cells
Preparation method EA.hy926-L2-OE and EA.hy926-NC cells were cultured in six-well plates until they reached 70 % confluence. To induce ERS, the cells were treated with 1 μg/mL of tunicamycin (M4798, AbMole) for 24 h, with DMSO serving as the control.
Concentrations 1 μg/mL
Incubation time 24 h
Animal Experiment
Animal models C57BL/6 and Lect2-KO mice
Formulation DMSO
Dosages 1 mg/kg
Administration Intraperitoneal injection
Chemical Information
Molecular Weight 816.89
Formula C37H60N4O16
CAS Number 11089-65-9
Solubility (25°C) DMSO 30 mg/mL
Storage -20°C, protect from light, dry, sealed
References

[1] Lim EJ, et al. Apoptosis. Tunicamycin promotes apoptosis in leukemia cells through ROS generation and downregulation of survivin expression.

[2] Lauer ME, et al. J Biol Chem. Primary murine airway smooth muscle cells exposed to poly(I,C) or tunicamycin synthesize a leukocyte-adhesive hyaluronan matrix.

[3] Duriez M, et al. J Biol Chem. The hepatitis B virus precore protein is retrotransported from endoplasmic reticulum (ER) to cytosol through the ER-associated degradation pathway.

Related Transferase Products
APO866

APO866 is an effective inhibitor of nicotinamide phosphoribosyltransferase (NMPRTase; NAMPT) with an IC50 of 0.09 nM.

Lonafarnib

Lonafarnib (SCH 66336) is a selectively FPTase inhibitor for H-ras, K-ras-4B and N-ras with IC50 of 1.9 nM, 5.2 nM and 2.8 nM, respectively.

Tolcapone

Tolcapone is a selective, potent and reversible of catechol-O-methyl transferase (COMT) inhibitor with Ki of 30 nM.

Sandoz 58-035

Sandoz 58-035 is a cholesterol acyltransferase (ACAT) inhibitor. Sandoz 58-035 inhibits the accumulation of cholesteryl esters and inhibits the esterification of cholesterol by 95% in arterial smooth muscle cells in culture. Sandoz 58-035 was used to induce simultaneous activation of unfolded protein response (UPR) and pattern recognition receptors (PRRs) in mouse peritoneal macrophages.

OSMI-1

OSMI-1 is a cell permeable inhibitor of OGT (O-GlcNAc transferase) with an IC50 value of 2.7 μM.

  Catalog
Abmole Inhibitor Catalog




Keywords: Tunicamycin, NSC 177382, TN supplier, Transferase, inhibitors, activators

All AbMole products are for research use only, cannot be used for human consumption or veterinary use. We do not provide products or services to individuals. Please comply with the intended use and do not use AbMole products for any other purpose.



Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2026 AbMole BioScience. All Rights Reserved.