| Name | cytochrome P450 (protein family or complex) |
|---|---|
| Synonyms | cytochrome P450; cytochrome P 450; CYP450; CYP 450 |
| Name | trinexapac |
|---|---|
| CAS | 4-(cyclopropylhydroxymethylene)-3,5-dioxocyclohexanecarboxylic acid |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 19581023 | Villa-Ruano N, Betancourt-Jimenez MG, Lozoya-Gloria E: Biosynthesis of uterotonic diterpenes from Montanoa tomentosa (zoapatle). J Plant Physiol. 2009 Dec 15;166(18):1961-7. Epub 2009 Jul 5. Our results suggest the biosynthetic conversion of KA into GF by a putative cytochrome P450-like desaturase. |
2(0,0,0,2) | Details |
| 15012200 | Rademacher W: GROWTH RETARDANTS: Effects on Biosynthesis and Other Metabolic Pathways. Annu Rev Plant Physiol Plant Mol Biol. 2000 Jun;51:501-531. These retardants block cytochrome P450-dependent monooxygenases, thereby inhibiting oxidation of ent-kaurene into ent-kaurenoic acid. (c) Structural mimics of which is the co-substrate of dioxygenases that catalyze late steps of GA formation. Acylcyclohexanediones, e.g. prohexadione-Ca and trinexapac-ethyl and daminozide, block particularly 3ss-hydroxylation, thereby inhibiting the formation of highly active GAs from inactive precursors, and (d) 16,17-Dihydro-GA5 and related structures act most likely by mimicking the GA precursor substrate of the same dioxygenases. |
1(0,0,0,1) | Details |