LC3-mHTT-IN-AN1 - ≥97%, cis–trans isomerism mixture , CAS No.486443-73-6

CAS: 486443-73-6 Cat. No.: L420033 Molecular Weight: 411.04
AVAILABLE TO ORDER
GRADE & PURITY ≥97% cis–trans isomerism mixture
Synonyms
AN1;5-Bromo-3-[(3-bromo-4,5-dihydroxyphenyl)methylene]-1,3-dihydro-2H-indol-2-one;mHTT-LC3 linker AN1;(Z)-5-bromo-3-(3-bromo-4,5-dihydroxybenzylidene)indolin-2-one
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5mg
L420033-5mg
3

$49.90

$74.90
Save $25.00 (33.38%)
25mg
L420033-25mg
2

$187.90

$281.90
Save $94.00 (33.35%)
50mg
L420033-50mg
2

$198.90

$298.90
Save $100.00 (33.46%)
100mg
L420033-100mg
2

$313.90

$470.90
Save $157.00 (33.34%)
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Why this grade

≥97%, cis–trans isomerism mixture for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

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

Specifications

Synonyms
AN1;5-Bromo-3-[(3-bromo-4, 5-dihydroxyphenyl)methylene]-1, 3-dihydro-2H-indol-2-one;mHTT-LC3 linker AN1;(Z)-5-bromo-3-(3-bromo-4, 5-dihydroxybenzylidene)indolin-2-one
Specifications & Purity
≥97%, cis–trans isomerism mixture
Biochemical and Physiological Mechanisms
AN1 is a brain blood barrier penetrant agent that tether LC3 and mHTT and targets mHTT for autophagosome degradation. AN1 significantly lower mHTT in cortices of HD mice, in cells from patients with Huntington′s disease, and neurons derived from induced p
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥97%
Names and Identifiers
Pubchem Sid504760630
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504760630
Canonical SmilesC1=CC2=C(C=C1Br)C(=CC3=CC(=C(C(=C3)Br)O)O)C(=O)N2
IUPAC Name(3Z)-5-bromo-3-[(3-bromo-4,5-dihydroxyphenyl)methylidene]-1H-indol-2-one
InChIKeyGPKLWRHHVIBYEO-KMKOMSMNSA-N
INCHI1S/C15H9Br2NO3/c16-8-1-2-12-9(6-8)10(15(21)18-12)3-7-4-11(17)14(20)13(19)5-7/h1-6,19-20H,(H,18,21)/b10-3-
Isomeric SMILES C1=CC2=C(C=C1Br)/C(=C/C3=CC(=C(C(=C3)Br)O)O)/C(=O)N2
Molecular Weight 411.04
Reaxy-Rn 35432673
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=35432673&ln=

Documentation

📋 Safety Data Sheet (SDS)

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

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✅ Certificate of Analysis (COA)

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

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassIndoles and derivatives
SubclassIndolines
Intermediate Tree Nodes Not available
Direct ParentIndolines
Alternative Parents Catechols  O-bromophenols  M-bromophenols  1-hydroxy-2-unsubstituted benzenoids  1-hydroxy-4-unsubstituted benzenoids  Bromobenzenes  Aryl bromides  Secondary carboxylic acid amides  Lactams  Azacyclic compounds  Organic oxides  Carbonyl compounds  Organobromides  Organonitrogen compounds  Hydrocarbon derivatives  Organopnictogen compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Dihydroindole - Catechol - 3-halophenol - 2-halophenol - 3-bromophenol - 2-bromophenol - Bromobenzene - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Halobenzene - Phenol - Aryl bromide - Aryl halide - Monocyclic benzene moiety - Benzenoid - Secondary carboxylic acid amide - Lactam - Carboxamide group - Azacycle - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organohalogen compound - Organobromide - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as indolines. These are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot NumberCertificate TypeDateItem
K2209751Certificate of AnalysisAug 12, 2025 L420033
K2209762Certificate of AnalysisAug 12, 2025 L420033
K2209763Certificate of AnalysisAug 12, 2025 L420033
K2209764Certificate of AnalysisAug 12, 2025 L420033
Chemical and Physical Properties
SolubilityDMSO: 2 mg/mL, clear
Molecular Weight411.040 g/mol
XLogP33.600
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass410.893 Da
Monoisotopic Mass408.895 Da
Topological Polar Surface Area69.600 Ų
Heavy Atom Count21
Formal Charge0
Complexity456.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Solution Calculators
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