Free shipping on all orders over $ 500

A-366

Cat. No. M8529

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

A-366 Structure
Synonym:

A366

Size Price Availability Quantity
1mg USD 40 In stock
5mg USD 90 In stock
10mg USD 125 In stock
25mg USD 250 In stock
50mg USD 490 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

A-366 is a potent and highly selective peptide-competitive inhibitor of histone methyltransferase G9a, with IC50s of 3.3 nM and 38 nM for G9a and GLP, respectively, and is more than 1,000-fold selective for G9a and GLP over 21 other methyltransferases. A-366 is also a potent inhibitor of Spindlin1-H3K4me3 interaction (IC50=182.6 nM).A-366 shows high affinity for human H3R (Ki=17 nM) and exhibits subtype selectivity between subpopulations of the histaminergic and dopaminergic receptor families. It can be used for induction and maintenance of pluripotent stem cells in mice.

Chemical Information
Molecular Weight 329.44
Formula C19H27N3O2
CAS Number 1527503-11-2
Form Solid
Solubility (25°C) DMSO: 10 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Mohammad Rafiqul Islam, et al. A unified genotypic classification of infectious bursal disease virus based on both genome segments

[2] Christos I Papagiannopoulos, et al. The histone methyltransferase inhibitor A-366 enhances hemoglobin expression in erythroleukemia cells upon co-exposure with chemical inducers in culture

[3] Xianglan Wang, et al. Genetic variation in ZmVPP1 contributes to drought tolerance in maize seedlings

[4] William N Pappano, et al. The Histone Methyltransferase Inhibitor A-366 Uncovers a Role for G9a/GLP in the Epigenetics of Leukemia

[5] Xuhong Ye, et al. A gyrB-targeted PCR for rapid identification of Salmonella

Related Histone Methyltransferase Products
BIX 01294 Trihydrochloride

BIX 01294 Trihydrochloride is a potent inhitor of G9a histone methyltransferase with IC50 of 2.7 μM.

EPZ-5676

EPZ-5676 is a potent and selective aminonucleoside inhibitor of DOT1L histone methyltransferase.

EPZ004777

EPZ004777 is a potent, selective, small-molecule inhibitor of DOT1L with IC50 of 0.4 nM.

3-Deazaneplanocin A

3-deazaneplanocin A (DZNeP), an analog of adenosine, is a competitive inhibitor of S-adenosylhomocysteine hydrolase with Ki of 50 pM.

EPZ004777 hydrochloride

EPZ004777 hydrochloride is the hydrochloride salt of EPZ004777, which is a potent, selective DOT1L inhibitor with IC50 of 0.4 nM.

  Catalog
Abmole Inhibitor Catalog




Keywords: A-366, A366 supplier, Histone Methyltransferase, 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.