Determine the necessary mass, volume, or concentration for preparing a solution.
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Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
GSK1838705A is a potent IGF-1R inhibitor with IC50 of 2.0 nM, modestly potent to IR and ALK with IC50 of 1.6 nM and 0.5 nM, respectively, and little activity to other protein kinases.
An ATP-competitive inhibitor of IGF-IR, IR, and ALK in various cell lines
| Pubchem Sid | 488200778 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488200778 |
| Sonrisas canónicas | CNC(=O)C1=C(C=CC=C1F)NC2=NC(=NC3=C2C=CN3)NC4=C(C=C5CCN(C5=C4)C(=O)CN(C)C)OC |
| IUPAC Name | 2-[[2-[[1-[2-(dimethylamino)acetyl]-5-methoxy-2,3-dihydroindol-6-yl]amino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]amino]-6-fluoro-N-methylbenzamide |
| InChIKey | HZTYDQRUAWIZRE-UHFFFAOYSA-N |
| INCHI | 1S/C27H29FN8O3/c1-29-26(38)23-17(28)6-5-7-18(23)31-25-16-8-10-30-24(16)33-27(34-25)32-19-13-20-15(12-21(19)39-4)9-11-36(20)22(37)14-35(2)3/h5-8,10,12-13H,9,11,14H2,1-4H3,(H,29,38)(H3,30,31,32,33,34) |
| Isómeros SMILES | CNC(=O)C1=C(C=CC=C1F)NC2=NC(=NC3=C2C=CN3)NC4=C(C=C5CCN(C5=C4)C(=O)CN(C)C)OC |
| WGK Alemania | 3 |
| CAS alternativo | 1116235-97-2 |
| Términos de entrada MeSH | GSK 1838705A;GSK-1838705A;GSK1838705A |
| Peso molecular | 532.57 |
| Reaxy-Rn | 18983141 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=18983141&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Clase | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives |
| Direct Parent | Alpha amino acids and derivatives |
| Alternative Parents | 2-halobenzoic acids and derivatives Benzamides Indoles and derivatives Methoxyanilines Pyrrolo[2,3-d]pyrimidines Anisoles Benzoyl derivatives Aminopyrimidines and derivatives Alkyl aryl ethers Fluorobenzenes Imidolactams Aryl fluorides Vinylogous amides Pyrroles Tertiary carboxylic acid amides Heteroaromatic compounds Vinylogous halides Trialkylamines Secondary carboxylic acid amides Secondary amines Azacyclic compounds Hydrocarbon derivatives Organic oxides Organofluorides Organopnictogen compounds Carbonyl compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Alpha-amino acid or derivatives - 2-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Indole or derivatives - Benzamide - Methoxyaniline - Benzoic acid or derivatives - Anisole - Aniline or substituted anilines - Benzoyl - Alkyl aryl ether - Aminopyrimidine - Halobenzene - Fluorobenzene - Benzenoid - Imidolactam - Monocyclic benzene moiety - Aryl halide - Pyrimidine - Aryl fluoride - Heteroaromatic compound - Vinylogous amide - Vinylogous halide - Tertiary carboxylic acid amide - Pyrrole - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Carboxamide group - Secondary amine - Azacycle - Ether - Organoheterocyclic compound - Organofluoride - Amine - Organic oxygen compound - Carbonyl group - Organopnictogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organohalogen compound - Organic oxide - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. |
| External Descriptors | Not available |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Apr 01, 2026 | G126428 | |
| Certificate of Analysis | Jan 16, 2025 | G126428 | |
| Certificate of Analysis | Jan 16, 2025 | G126428 | |
| Certificate of Analysis | Jan 16, 2025 | G126428 | |
| Certificate of Analysis | Jan 16, 2025 | G126428 | |
| Certificate of Analysis | Jan 16, 2025 | G126428 | |
| Certificate of Analysis | Jan 16, 2025 | G126428 | |
| Certificate of Analysis | Jan 16, 2025 | G126428 | |
| Certificate of Analysis | Jan 16, 2025 | G126428 | |
| Certificate of Analysis | Jan 16, 2025 | G126428 | |
| Certificate of Analysis | Jan 16, 2025 | G126428 | |
| Certificate of Analysis | Dec 12, 2022 | G126428 |
| Solubilidad | Solvent:DMSO, Max Conc. mg/mL: 53.26, Max Conc. mM: 100 |
|---|---|
| Peso molecular | 532.600 g/mol |
| XLogP3 | 3.800 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 8 |
| Exact Mass | 532.235 Da |
| Monoisotopic Mass | 532.235 Da |
| Topological Polar Surface Area | 128.000 Ų |
| Heavy Atom Count | 39 |
| Formal Charge | 0 |
| Complexity | 867.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
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