210584-54-6

Amustaline dihydrochloride Chemical Structure
210584-54-6

Chemical Structure

Amustaline dihydrochloride

Synonym(s): S-303 dihydrochloride

  • CAS No.: 210584-54-6
  • Formula:C22H27Cl4N3O2
  • Molecular Weight:507.28

IUPAC Name: 2-(bis(2-chloroethyl)amino)ethyl 3-(acridin-9-ylamino)propanoate dihydrochloride

InChIKey: WEOLKSYHLNAIRH-UHFFFAOYSA-N

SMILES: O=C(CCNC1=C2C=CC=CC2=NC3=CC=CC=C31)OCCN(CCCl)CCCl.[H]Cl.[H]Cl

Biological Activity: Amustaline (S-303) dihydrochloride, a nucleic acid-targeted alkylator, is an efficient pathogen inactivation agent for blood components containing red blood cells. Amustaline dihydrochloride has three components: an acridine anchor (an intercalator that targets nucleic acids non-covalently), an effector (a bis-alkylator group that reacts with nucleophiles), and a linker (a small flexible carbon chain containing a labile ester bond that hydrolyzes at neutral pH to yield non-reactive breakdown products)[1][2].

Cat. No. Product Name Purity Description Pricing
HY-106991A
Amustaline dihydrochloride 95.0% Amustaline (S-303) dihydrochloride, a nucleic acid-targeted alkylator, is an efficient pathogen inactivation agent for blood components containing red blood cells. Amustaline dihydrochloride has three components: an acridine anchor (an intercalator that targets nucleic acids non-covalently), an effector (a bis-alkylator group that reacts with nucleophiles), and a linker (a small flexible carbon chain containing a labile ester bond that hydrolyzes at neutral pH to yield non-reactive breakdown products).
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HY-106991AR
Amustaline dihydrochloride (Standard) ≥98% Amustaline (dihydrochloride) (Standard) is the analytical standard of Amustaline (dihydrochloride). This product is intended for research and analytical applications. Amustaline (S-303) dihydrochloride, a nucleic acid-targeted alkylator, is an efficient pathogen inactivation agent for blood components containing red blood cells. Amustaline dihydrochloride has three components: an acridine anchor (an intercalator that targets nucleic acids non-covalently), an effector (a bis-alkylator group that reacts with nucleophiles), and a linker (a small flexible carbon chain containing a labile ester bond that hydrolyzes at neutral pH to yield non-reactive breakdown products).
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