SU-5614 - ≥98%(HPLC) , CAS No.1055412-47-9

CAS: 1055412-47-9 Cat. No.: S131847 Formule: C15H13ClN2O Poids moléculaire: 272.73 Numéro CE: 686-026-9 PubChem CID: 6536806
DISPONIBLE À COMMANDE
GRADE & PURITY ≥98%(HPLC)
Synonyms
AC-36026 | BDBM50415432 | EX-A821 | (Z)-5-Chloro-3-((3,5-dimethyl-1H-pyrrol-2-yl)methylene)indolin-2-one | PLAFIBRIDE [MART.] | 5-CHLORO-3-(3,5-DIMETHYL-1H-PYRROL-2-YLMETHYLENE)-1,3-DIHYDRO-INDOL-2-ONE | 5-chloro-3-(3,5-dimethyl-1h-pyrrol-2-ylmethylene)-1
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
★
Size
Allemagne (EU)
USA*
Price
Qty
5mg
S131847-5mg
—
3 En stock
8,59€
10mg
S131847-10mg
—
3 En stock
9,46€
25mg
S131847-25mg
—
3 En stock

14,66€

22,47€
Enregistrer 7,81 € (34.75%)
50mg
S131847-50mg
—
3 En stock

26,81€

40,70€
Enregistrer 13,88 € (34.12%)
100mg
S131847-100mg
Sur commande · 8–12 semaines

46,77€

70,20€
Enregistrer 23,43 € (33.37%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads 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.

Vue d’ensemble

(Z)-SU5614 is a potent FLT3 inhibitor and selectively induces growth arrest, apoptosis, and cell cycle arrest in Ba/F3 and AML cell lines expressing a constitutively activated FLT3.

Specifications

Synonymes
AC-36026 | BDBM50415432 | EX-A821 | (Z)-5-Chloro-3-((3,5-dimethyl-1H-pyrrol-2-yl)methylene)indolin-2-one | PLAFIBRIDE [MART.] | 5-CHLORO-3-(3,5-DIMETHYL-1H-PYRROL-2-YLMETHYLENE)-1,3-DIHYDRO-INDOL-2-ONE | 5-chloro-3-(3,5-dimethyl-1h-pyrrol-2-ylmethylene)-1
Spécifications et pureté
≥98%(HPLC)
Mécanismes biochimiques et physiologiques
SU5614 is a FMS-like tyrosine kinase 3 (FLT3) inhibitor; selective inhibitor of VEGF and PDGF receptor tyrosine kinases.
Conditions de stockage de stockage
Store at -20°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Pureté
≥98%(HPLC)
Noms et identifiants
Pubchem Sid504764274
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504764274
Sourires canoniquesCC1=CC(=C(N1)C=C2C3=C(C=CC(=C3)Cl)NC2=O)C
IUPAC Name(3Z)-5-chloro-3-[(3,5-dimethyl-1H-pyrrol-2-yl)methylidene]-1H-indol-2-one
InChIKeyXLBQNZICMYZIQT-GHXNOFRVSA-N
INCHI1S/C15H13ClN2O/c1-8-5-9(2)17-14(8)7-12-11-6-10(16)3-4-13(11)18-15(12)19/h3-7,17H,1-2H3,(H,18,19)/b12-7-
Isomères SMILES CC1=CC(=C(N1)/C=C\2/C3=C(C=CC(=C3)Cl)NC2=O)C
WGK Allemagne 3
PubChem CID 6536806
Poids moléculaire 272.73

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
ClasseIndoles and derivatives
SubclassIndolines
Intermediate Tree Nodes Not available
Direct ParentIndolines
Alternative Parents Substituted pyrroles  Benzenoids  Aryl chlorides  Heteroaromatic compounds  Secondary carboxylic acid amides  Lactams  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Dihydroindole - Aryl chloride - Aryl halide - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Carboxamide group - Lactam - Secondary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Organonitrogen compound - Organochloride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Organooxygen compound - Organic nitrogen 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 organochlorine compound - oxindole - pyrroles
Structure 3D
Modèle de structure chimique interactif





Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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.

5 results found

Lot NumberCertificate TypeDateArticle
L2209635Certificate of AnalysisOct 28, 2022 S131847
L2209636Certificate of AnalysisOct 28, 2022 S131847
L2209637Certificate of AnalysisOct 28, 2022 S131847
L2209638Certificate of AnalysisOct 28, 2022 S131847
L2209639Certificate of AnalysisOct 28, 2022 S131847
Propriétés chimiques et physiques
Poids moléculaire272.730 g/mol
XLogP33.100
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count1
Rotatable Bond Count1
Exact Mass272.072 Da
Monoisotopic Mass272.072 Da
Topological Polar Surface Area44.900 Ų
Heavy Atom Count19
Formal Charge0
Complexity409.000
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
Calculateurs de solution
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