Hydroxylation-induced migration and retention of tritium on conversion of [4-3H] cinnamic acid to 4-hydroxycinnamic acid by an enzyme from pea seedlings

scientific article published on 01 November 1968

Hydroxylation-induced migration and retention of tritium on conversion of [4-3H] cinnamic acid to 4-hydroxycinnamic acid by an enzyme from pea seedlings is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/0304-4165(68)90178-5
P953full work available at URLhttps://api.elsevier.com/content/article/PII:0304416568901785?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:0304416568901785?httpAccept=text/plain
P698PubMed publication ID5721918

P2093author name stringH. Grisebach
D. W. Russell
E. E. Conn
A. Sutter
P2860cites workLiebigs Annalen der ChemieQ662963
The cinnamic acid 4-hydroxylase of pea seedlingsQ28240931
Hydroxylation-induced migration: the NIH shift. Recent experiments reveal an unexpected and general result of enzymatic hydroxylation of aromatic compoundsQ28258732
L-Phenylalanine ammonia-lyase. I. Purification and molecular size of the enzyme from potato tubersQ47402055
Induction of Phenylalanine Deaminase by Light and its Relation to Chlorogenic Acid Synthesis in Potato Tuber TissueQ83241115
P433issue1
P407language of work or nameEnglishQ1860
P921main subjectbiochemistryQ7094
biophysicsQ7100
cinnamatesQ13468236
P304page(s)210-213
P577publication date1968-11-01
P1433published inBiochimica et Biophysica ActaQ864239
P1476titleHydroxylation-induced migration and retention of tritium on conversion of (4-3H) cinnamic acid to 4-hydroxycinnamic acid by an enzyme from pea seedings
Hydroxylation-induced migration and retention of tritium on conversion of [4-3H] cinnamic acid to 4-hydroxycinnamic acid by an enzyme from pea seedlings
P478volume170

Reverse relations

cites work (P2860)
Q54563707Arene oxides and the NIH shift: the metabolism, toxicity and carcinogenicity of aromatic compounds.
Q69960988Aromatic amino acids in the metabolism of higher plants
Q48009584Formation of phenols from aromatic subtrates by plant and animal mono-oxygenases: The effect of adjacent deuteriums on the magnitude of the NIH shift of tritium
Q40159297Phytoalexins: Enzymology and Molecular Biology