Free shipping on all orders over $ 500

Toyocamycin

Cat. No. M7419

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

Toyocamycin Structure
Synonym:

Vengicide

Size Price Availability Quantity
1mg USD 25 In stock
5mg USD 50 In stock
10mg USD 75 In stock
25mg USD 150 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

Toyocamycin is a adenosine analog; antifungal antibiotic. Toyocamycin (Vengicide) inhibits RNA self-cleavage in HEK79 cells and PI 3-kinase activity in A431 epidermoid carcinoma cell membrane fractions. Toyocamycin (Vengicide) also inhibits thapsigargin-induced XBP1-luciferase activation and induces apoptosis in multiple myeloma cell lines. Toyocamycin specifically inhibits CDK9.

Chemical Information
Molecular Weight 291.26
Formula C12H13N5O4
CAS Number 606-58-6
Solubility (25°C) DMSO ≥ 60 mg/mL
Storage -20°C, dry, sealed
References

[1] Ikuko Takahara, et al. PLoS One . Toyocamycin attenuates free fatty acid-induced hepatic steatosis and apoptosis in cultured hepatocytes and ameliorates nonalcoholic fatty liver disease in mice

[2] Ri M, et al. Blood Cancer J. Identification of Toyocamycin, an agent cytotoxic for multiple myeloma cells, as a potent inhibitor of ER stress-induced XBP1 mRNA splicing.

[3] Nishioka H, et al. J Antibiot (Tokyo). Inhibition of phosphatidylinositol kinase by toyocamycin.

Related Apoptosis Products
23-Hydroxybetulinic acid

23-Hydroxybetulinic acid is a novel anticancer substance.

TH-302 (Evofosfamide)

TH-302 is a highly potent and selective hypoxia-activated procompound targeting hypoxic regions of solid tumors with IC50 of 19 nM.

Se-Methylselenocysteine

Se-methylselenocysteine, a precursor of methyl selenium, has strong cancer chemoprophylaxis and antioxidant activity. Se-Methylselenocysteine has oral biological activity, can induce apoptosis.

Aloperine

Aloperine is exhibits anti-inflammatory, antibacterial, antiviral, and anti-tumor properties.

Ezatiostat

Ezatiostat (TER199, TLK199) is a glutathione analog inhibitor of glutathione S-transferase (GST) P1-1. Ezatiostat leads to JNK activation by inhibiting GSTP1. Ezatiostat stimulates both lymphocyte production and bone marrow progenitor proliferation.

  Catalog
Abmole Inhibitor Catalog




Keywords: Toyocamycin, Vengicide supplier, Apoptosis, 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.