WARNING: This product is for research use only, not for human or veterinary use.
MedKoo CAT#: 597618
Description: Dansylmethionine is a common cosubstrate involved in methyl group transfers, transsulfuration, and aminopropylation. Although these anabolic reactions occur throughout the body, most SAM-e is produced and consumed in the liver. More than 40 methyl transfers from SAM-e are known, to various substrates such as nucleic acids, proteins, lipids and secondary metabolites. It is made from adenosine triphosphate (ATP) and methionine by methionine adenosyltransferase.
MedKoo Cat#: 597618
Chemical Formula: C17H22N2O4S2
Exact Mass: 382.1021
Molecular Weight: 382.49
Elemental Analysis: C, 53.38; H, 5.80; N, 7.32; O, 16.73; S, 16.76
Synonym: Dansylmethionine; Dansyl-met; Dansyl methionine;
IUPAC/Chemical Name: ((5-(dimethylamino)naphthalen-1-yl)sulfonyl)-L-methionine
InChi Key: ADWOYRHKFIZWFB-AWEZNQCLSA-N
InChi Code: InChI=1S/C17H22N2O4S2/c1-19(2)15-8-4-7-13-12(15)6-5-9-16(13)25(22,23)18-14(17(20)21)10-11-24-3/h4-9,14,18H,10-11H2,1-3H3,(H,20,21)/t14-/m0/s1
SMILES Code: CSCC[C@@H](C(O)=O)NS(=O)(C1=C2C=CC=C(N(C)C)C2=CC=C1)=O
1: Atamna IZ, Issaq HJ, Muschik GM, Janini GM. Optimization of resolution in capillary zone electrophoresis: combined effect of applied voltage and buffer concentration. J Chromatogr. 1991 Dec 27;588(1-2):315-20. PubMed PMID: 1818085.
2: Ding GS, Liu Y, Cong RZ, Wang JD. Chiral separation of enantiomers of amino acid derivatives by high-performance liquid chromatography on a norvancomycin-bonded chiral stationary phase. Talanta. 2004 Apr 19;62(5):997-1003. doi: 10.1016/j.talanta.2003.10.032. PubMed PMID: 18969391.