S49076 - ≥97% , CAS No.1265965-22-7

CAS: 1265965-22-7 Cat. No.: S414003 Formula: C22H22N4O4S Molecular Weight: 438.5 PubChem CID: 49870909
AVAILABLE TO ORDER
GRADE & PURITY ≥97%
Synonyms
1265965-22-7 | s8404 | 65ZUU7MATU | HY-12965 | CID 49870909 | S-49076(Free base) | 3-((3-((4-((4-Morpholinyl)methyl)-1H-pyrrol-2-yl)methylene)-2-oxo-2,3-dihydro-1H-indol-5-yl)methyl)-1,3-thiazolidine-2,4-dione | BS-14862 | BDBM50172080 | CCG-269111 | 2,4-
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Size
Germany (EU)
USA*
Price
Qty
5mg
S414003-5mg
—
3 In stock
€87.55
10mg
S414003-10mg
—
3 In stock
€142.22
50mg
S414003-50mg
—
3 In stock
€491.92
Enter a quantity for the sizes you want to add.
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Why this grade

≥97% 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.

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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.

Overview

Information

S49076 is a novel, potent inhibitor ofMet (c-Met),AXL/MER, andFGFR1/2/3with IC50 values below 20 nmol/L.


Targets

Met (Cell-free assay); Mer (Cell-free assay); Axl (Cell-free assay); FGFR3 (Cell-free assay); FGFR2 (Cell-free assay) 16457,1 nM; 2 nM; 7 nM; 15 nM; 17 nM


In vitro

S49076 potently blocks cellular phosphorylation of MET, AXL, and FGFRs and inhibits downstream signaling in vitro and in vivo. In cell models, S49076 inhibits the proliferation of MET- and FGFR2-dependent gastric cancer cells, blocks MET-driven migration of lung carcinoma cells, and inhibits colony formation of hepatocarcinoma cells expressing FGFR1/2 and AXL. S49076 inhibits viability, motility, and three-dimensional colony formation of cancer cells expressing MET, AXL, or FGFRs.


In vivo

S49076 shows marked antitumor activity in MET- and FGFR-dependent tumor xenografts at well-tolerated doses. S49076 has high distribution to tumors, in which the half-life for the dose of 3.125 mg/kg is approximately 7 hours versus less than 2 hours in the blood. At doses of 6.25 mg/kg and higher, more than 50% inhibition of MET phosphorylation is retained at 16 hours. S49076 is also active in a bevacizumab-resistant model and totally inhibits the growth of colon carcinoma xenografts in association with bevacizumab.


Cell Research(from reference)

Cell lines:GTL-16 and SNU-16 cell lines 

Incubation Time:96 h or 120 h 

Specifications

Synonyms
1265965-22-7 | s8404 | 65ZUU7MATU | HY-12965 | CID 49870909 | S-49076(Free base) | 3-((3-((4-((4-Morpholinyl)methyl)-1H-pyrrol-2-yl)methylene)-2-oxo-2,3-dihydro-1H-indol-5-yl)methyl)-1,3-thiazolidine-2,4-dione | BS-14862 | BDBM50172080 | CCG-269111 | 2,4-
Specifications & Purity
≥97%
Biochemical and Physiological Mechanisms
S49076 is a novel, potent inhibitor of Met (c-Met), AXL/MER, and FGFR1/2/3 with IC50 values below 20 nmol/L.
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%
Product Properties
alogp1.882
hbd_count2
rotatable_bond5
Names and Identifiers
Pubchem Sid504770959
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504770959
Canonical SmilesC1COCCN1CC2=CNC(=C2)C=C3C4=C(C=CC(=C4)CN5C(=O)CSC5=O)NC3=O
IUPAC Name3-[[(3Z)-3-[[4-(morpholin-4-ylmethyl)-1H-pyrrol-2-yl]methylidene]-2-oxo-1H-indol-5-yl]methyl]-1,3-thiazolidine-2,4-dione
InChIKeyAREYWCZYVPSHGS-NVMNQCDNSA-N
INCHI1S/C22H22N4O4S/c27-20-13-31-22(29)26(20)12-14-1-2-19-17(8-14)18(21(28)24-19)9-16-7-15(10-23-16)11-25-3-5-30-6-4-25/h1-2,7-10,23H,3-6,11-13H2,(H,24,28)/b18-9-
Isomeric SMILES C1COCCN1CC2=CNC(=C2)/C=C\3/C4=C(C=CC(=C4)CN5C(=O)CSC5=O)NC3=O
PubChem CID 49870909
Molecular Weight 438.5

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
ClassIndoles and derivatives
SubclassIndolines
Intermediate Tree Nodes Not available
Direct ParentIndolines
Alternative Parents Aralkylamines  Thiazolidinediones  Benzenoids  Substituted pyrroles  Morpholines  Dicarboximides  Heteroaromatic compounds  Amino acids and derivatives  Trialkylamines  Thiocarbamic acid derivatives  Secondary carboxylic acid amides  Lactams  Dialkyl ethers  Azacyclic compounds  Oxacyclic compounds  Hydrocarbon derivatives  Carbonyl compounds  Organic oxides  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Dihydroindole - Aralkylamine - Thiazolidinedione - Morpholine - Oxazinane - Substituted pyrrole - Benzenoid - Dicarboximide - Heteroaromatic compound - Pyrrole - Thiazolidine - Amino acid or derivatives - Carboxamide group - Lactam - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Thiocarbamic acid derivative - Ether - Oxacycle - Azacycle - Carboxylic acid derivative - Dialkyl ether - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Amine - 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





Associated Targets(Human)
AXL Tchem Tyrosine-protein kinase receptor UFO (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Mechanisms of Action
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.

3 results found

Lot NumberCertificate TypeDateItem
J2214091Certificate of AnalysisApr 03, 2026 S414003
J2214092Certificate of AnalysisApr 03, 2026 S414003
J2214114Certificate of AnalysisApr 03, 2026 S414003
Chemical and Physical Properties
SolubilitySolubility (25°C) In vitro DMSO: 87 mg/mL (198.4 mM); Water: Insoluble; Ethanol: Insoluble;
dmso_mg_max_solubility87
dmso_mM_max_solubility198.4036488
water_mg_max_solubility<1
Molecular Weight438.500 g/mol
XLogP31.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count5
Exact Mass438.136 Da
Monoisotopic Mass438.136 Da
Topological Polar Surface Area120.000 Ų
Heavy Atom Count31
Formal Charge0
Complexity769.000
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
Reviews

Customer Reviews

Frequently Asked Questions

What is the purity of this product?
This product is supplied at ≥97% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
How should this product be stored?
Store at ?20 °C. Freezer storage is required to maintain the specified shelf life.
How is this product shipped?
This product ships in an insulated container with ice pads. Unpack on arrival and transfer it to the storage condition stated above.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 1265965-22-7, the molecular formula is C22H22N4O4S, and the molecular weight is 438.5 g/mol. InChIKey AREYWCZYVPSHGS-NVMNQCDNSA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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