6266-66-6

6266-66-6 structure

Name: 2-indol-3-yl-4-oxo-4-phenylbutanoic acid
Chemical Name: 2-(1H-Indol-3-yl)-4-oxo-4-phenyl-butyric acid
CAS Number: 6266-66-6
Molecular Formula: C₁₈H₁₅NO₃
Molecular Weight: 293.31700
Catalog: Biochemical Amino acids and their derivatives Leucine derivative
Create Date: 2019-01-01 14:38:52
Modify Date: 2024-01-31 10:58:11
PEO-IAA is an indole-3-acetic acid (IAA) antagonist. PEO-IAA is an auxin antagonist that binds to transport inhibitor response 1/auxin signaling F-box proteins (TIR1/AFBs).

Name	2-(1H-Indol-3-yl)-4-oxo-4-phenyl-butyric acid
Synonyms	2-(1H-indol-3-yl)-4-oxo-4-phenylbutanoic acid

Description	PEO-IAA is an indole-3-acetic acid (IAA) antagonist. PEO-IAA is an auxin antagonist that binds to transport inhibitor response 1/auxin signaling F-box proteins (TIR1/AFBs).
Related Catalog	Signaling Pathways >> Others >> Others Research Areas >> Others
In Vitro	PEO-IAA is also an α-alkyl-IAA, and shows more potent anti-auxin activity in auxin-responsive gene expression and in the cell division and elongation pathway that is mediated via SCFTIR1/AFBs. PEO-IAA suppresses not only the expression of an auxin-responsive ZmSAUR2 gene, but also gravitropic curvature. PEO-IAA blocks the auxin response in Arabidopsis, rice, moss and maize[1].
References	[1]. Nishimura T, et al. Differential downward stream of auxin synthesized at the tip has a key role in gravitropic curvature via TIR1/AFBs-mediated auxin signaling pathways. Plant Cell Physiol. 2009 Nov;50(11):1874-85.

HS Code	2933990090
Summary	2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%