WARNING: This product is for research use only, not for human or veterinary use.
MedKoo CAT#: 571083
Description: A 20832 is an inhibitor that Inhibits resolvase-promoted site-specific recombination postsynaptically at strand cleavage. It does not inhibit resolvase binding to res, as measured by filter binding, or synapse formation. DNase I analysis in the presence of A20832 indicates that only site I of res is bound by resolvase.
MedKoo Cat#: 571083
Name: A 20832
Chemical Formula: C10H14Cl2O3
Exact Mass: 252.032
Molecular Weight: 253.12
Elemental Analysis: C, 47.45; H, 5.58; Cl, 28.01; O, 18.96
Synonym: A 20832; A20832; A-20832
IUPAC/Chemical Name: 4-Pentenoic acid, 2-acetyl-5,5-dichloro-4-methyl-, ethyl ester
InChi Key: CSIXHPCPUJVRQT-UHFFFAOYSA-N
InChi Code: InChI=1S/C10H14Cl2O3/c1-4-15-10(14)8(7(3)13)5-6(2)9(11)12/h8H,4-5H2,1-3H3
SMILES Code: O=C(OCC)C(C(C)=O)C/C(C)=C(Cl)\Cl
1: Flanagan PM, Finn MC, Fennewald MA. Inhibitor analysis of synapsis by resolvase. J Biol Chem. 1989 Oct 5;264(28):16892-6. PubMed PMID: 2550464.