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PEO-IAA - 10mM in DMSO , CAS No.6266-66-6

CAS: 6266-66-6 Cat. No.: P425179 Summenformel: C18H15NO3 Molekulargewicht: 293.33 EG-Nummer: 108-405-5 PubChem CID: 235453
COA
PEO-IAA - 10mM in DMSO CAS No(6266-66-6) by Aladdin Scientific
Zu bestellen verfügbar
GRADE & PURITY 10mM in DMSO
Synonyms
(+/-)- -Methoxy- -trifluoromethylphenylacetic acid | Opera_ID_1008 | 2-(1H-Indol-3-yl)-4-oxo-4-phenylbutanoic acid # | 2-indol-3-yl-4-oxo-4-phenylbutanoic acid | AKOS000300600 | 1,2-Benzenediol, 4-[2-(methylamino)ethyl]-hydrochloride | BCP32692 | HMS2637H
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
Deutschland (EU)
USA*
Price
Qty
1ml
P425179-1ml
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1 Auf Lager

143,09€

209,91€
Speichern 66,82 € (31.83%)
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SDS
Safety data
COA
Certificate
DS
Datasheet
SP
Spec sheet
Übersicht Specifications Namen und Kennungen Documentation Advanced Data Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Lösungsrechner Bewertungen
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Information

PEO-IAA (2-(1H-Indol-3-yl)-4-oxo-4-phenyl-butyric acid) is a novel potentauxinantagonist that binds totransport inhibitor response 1/auxin signaling F-box proteins (TIR1/AFBs). PEO-IAA suppresses not only the expression of an auxin-responsive ZmSAUR2 gene, but also gravitropic curvature.

Specifications

Synonyme
(+/-)- -Methoxy- -trifluoromethylphenylacetic acid | Opera_ID_1008 | 2-(1H-Indol-3-yl)-4-oxo-4-phenylbutanoic acid # | 2-indol-3-yl-4-oxo-4-phenylbutanoic acid | AKOS000300600 | 1,2-Benzenediol, 4-[2-(methylamino)ethyl]-hydrochloride | BCP32692 | HMS2637H
Spezifikationen & Reinheit
10mM in DMSO
Storage
Store at -80°C
Verschickt in
Dry ice packs + Cold packs
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Aktionsart
ANTAGONIST
Namen und Kennungen
Pubchem Sid
528766575
Kanonisches Lächeln
C1=CC=C(C=C1)C(=O)CC(C2=CNC3=CC=CC=C32)C(=O)O
IUPAC Name
2-(1H-indol-3-yl)-4-oxo-4-phenylbutanoic acid
InChIKey
SJVMWLJNHPHNPT-UHFFFAOYSA-N
INCHI
1S/C18H15NO3/c20-17(12-6-2-1-3-7-12)10-14(18(21)22)15-11-19-16-9-5-4-8-13(15)16/h1-9,11,14,19H,10H2,(H,21,22)
Isomere SMILES
C1=CC=C(C=C1)C(=O)CC(C2=CNC3=CC=CC=C32)C(=O)O
PubChem CID
235453
Molekulargewicht
293.33

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
KlasseIndoles and derivatives
SubclassIndolyl carboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentIndole-3-acetic acid derivatives
Alternative Parents Alkyl-phenylketones  Butyrophenones  3-alkylindoles  Gamma-keto acids and derivatives  Benzoyl derivatives  Aryl alkyl ketones  Substituted pyrroles  Heteroaromatic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Alkyl-phenylketone - Indole-3-acetic acid derivative - Butyrophenone - 3-alkylindole - Phenylketone - Indole - Benzoyl - Gamma-keto acid - Aryl alkyl ketone - Aryl ketone - Monocyclic benzene moiety - Keto acid - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Ketone - Monocarboxylic acid or derivatives - Azacycle - Carboxylic acid - Carboxylic acid derivative - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as indole-3-acetic acid derivatives. These are compounds containing an acetic acid (or a derivative) linked to the C3 carbon atom of an indole.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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Zugehörige Ziele (nicht menschlich)
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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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NS1 Nonstructural protein 1 (33327 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemische und physikalische Eigenschaften
Molekulargewicht293.300 g/mol
XLogP32.900
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count5
Exact Mass293.105 Da
Monoisotopic Mass293.105 Da
Topological Polar Surface Area70.200 Ų
Heavy Atom Count22
Formal Charge0
Complexity417.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Lösungsrechner
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