Chemodex

9-Amino-6-chloro-2-methoxyacridine

As low as CHF 258.00
In stock
Only %1 left
CDX-A0099-M02525 mgCHF 258.00
CDX-A0099-M05050 mgCHF 451.00
NEW
 
More Information
Product Details
Synonyms ACMA; 2-Methoxy-6-chloro-9-aminoacridine; 9-Amino-3-chloro-7-methoxyacridine; G 185; NSC 15300
Product Type Chemical
Properties
Formula C14H11ClN2O
MW 258.7
CAS 02.09.3548
RTECS AR7330000
Source/Host Chemicals Synthetic
Purity Chemicals ≥95% (HPLC)
Appearance Yellow to orange powder.
Solubility Soluble in DMSO, DMF or methanol (1mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key IHHSSHCBRVYGJX-UHFFFAOYSA-N
Smiles ClC1=CC=C(C(N)=C(C=C(OC)C=C2)C2=N3)C3=C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
Product Specification Sheet
Datasheet Download PDF
Description
9-Amino-6-chloro-2-methoxyacridine (ACMA) is a cell-permeable ph-sensitive fluorescent probe that intercalates into DNA. It selectively binds to poly(dA-dT) sequences with the fluorescence lifetime decreasing with incorporation of guanosine. It is used for nucleic acid staining/labeling. ACMA fluorescence is pH-dependent and is quenched when a pH gradient is established. Spectral Data: λex 411nm; λem 475nm (in methanol). Excitation of the ACMA-DNA complex (excitation/emission maxima λ419/483 nm) is possible with most UV-light sources, making it compatible for use with both shorter- and longer-wavelength dyes. ACMA also apparently binds to membranes in the energized state and becomes quenched if a pH gradient forms. It has been extensively employed to follow cation and anion movement across membranes and to study the proton-pumping activity of various membrane-bound ATPases. ACMA also inhibits acetylcholinesterase.
Product References
(1) C. Helene, et al.; Biochem. Soc. Trans. 14, 201 (1986) | (2) T. Hard, et al.; J. Phys. Chem. 93, 4338 (1989) | (3) H. Rottenberg & R. Moreno-Sanchez; Biochim. Biophys. Acta 1183, 161 (1993) | (4) S.D. Watts & R.A. Capaldi; J. Biol. Chem. 272, 15065 (1997) | (5) K. Fukui, et al.; J. Photochem. Photobiol. B Biol. 50, 18 (1999) | (6) S. Bencharit, et al.; Chem. Biol. 10, 341 (2003) | (7) I. Carqueijeiro, et al.; Methods Mol. Biol. 1405, 121 (2016) | (8) P. Uzdavinys, et al.; PNAS 114, E1101 (2017)
© 2017 Adipogen Life Sciences. Pictures: © 2012 Martin Oeggerli. All Rights Reserved.