83657-17-4
83657-17-4
Chemical Structure
Uniconazole-P
- CAS No.: 83657-17-4
- Formula:C15H18ClN3O
- Molecular Weight:291.78
IUPAC Name: (S,E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol
InChIKey: YNWVFADWVLCOPU-MAUPQMMJSA-N
SMILES: ClC(C=C1)=CC=C1/C=C(N2C=NC=N2)\[C@@H](O)C(C)(C)C
Biological Activity: Uniconazole-P is a potent competitive inhibitor of Arabidopsis CYP707A3 with an IC50 of 68 nM and a Ki of 8.0 nM. Uniconazole-P inhibits ent-kaurene oxidase, blocking gibberellin biosynthesis via reduced ent-kaurene to ent-kaurenoic acid oxidation. Uniconazole-P inhibits plant growth[1][2][3][4].
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Uniconazole-P | Uniconazole-P is a potent competitive inhibitor of Arabidopsis CYP707A3 with an IC50 of 68 nM and a Ki of 8.0 nM. Uniconazole-P inhibits ent-kaurene oxidase, blocking gibberellin biosynthesis via reduced ent-kaurene to ent-kaurenoic acid oxidation. Uniconazole-P inhibits plant growth. | |||||||||||||||||||||
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References
- [1]. Saito S, et al. A plant growth retardant, uniconazole, is a potent inhibitor of ABA catabolism in Arabidopsis. Biosci Biotechnol Biochem. 2006;70(7):1731-1739. [Content Brief]
- [2]. Kojima K, et al. Effects of Uniconazole-P on Abscission and Endogenous ABA, IAA, and GA-like Substances Levels of Satsuma Mandarin Fruitlet. Biosci Biotechnol Biochem. 1996;60(5):901-902. [Content Brief]
- [3]. Jiang S, et al. Role of GA3, GA4 and uniconazole-P in controlling gravitropism and tension wood formation in Fraxinus mandshurica Rupr. var. japonica Maxim. seedlings. J Integr Plant Biol. 2008;50(1):19-28. [Content Brief]
- [4]. Inada S, et al. Regulation of elongation growth by gibberellin in root segments of Lemna minor. Plant Cell Physiol. 2000;41(8):932-939. [Content Brief]
