Determine the necessary mass, volume, or concentration for preparing a solution.
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≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C,Argon charged 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.
BGT226 (NVP-BGT226) is a novel class I PI3K/mTOR inhibitor for PI3Kα/β/γ with IC50 of 4 nM/63 nM/38 nM.
A novel dual PI3K/FRAP inhibitor
| Pubchem Sid | 488201818 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488201818 |
| Canonical Smiles | CN1C2=CN=C3C=CC(=CC3=C2N(C1=O)C4=CC(=C(C=C4)N5CCNCC5)C(F)(F)F)C6=CN=C(C=C6)OC.C(=CC(=O)O)C(=O)O |
| IUPAC Name | (Z)-but-2-enedioic acid;8-(6-methoxypyridin-3-yl)-3-methyl-1-[4-piperazin-1-yl-3-(trifluoromethyl)phenyl]imidazo[4,5-c]quinolin-2-one |
| InChIKey | YUXMAKUNSXIEKN-BTJKTKAUSA-N |
| INCHI | 1S/C28H25F3N6O2.C4H4O4/c1-35-24-16-33-22-6-3-17(18-4-8-25(39-2)34-15-18)13-20(22)26(24)37(27(35)38)19-5-7-23(21(14-19)28(29,30)31)36-11-9-32-10-12-36;5-3(6)1-2-4(7)8/h3-8,13-16,32H,9-12H2,1-2H3;1-2H,(H,5,6)(H,7,8)/b;2-1- |
| Isomeric SMILES | CN1C2=CN=C3C=CC(=CC3=C2N(C1=O)C4=CC(=C(C=C4)N5CCNCC5)C(F)(F)F)C6=CN=C(C=C6)OC.C(=C\C(=O)O)\C(=O)O |
| Molecular Weight | 650.6 |
| Reaxy-Rn | 31113942 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=31113942&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 | Organoheterocyclic compounds |
| Class | Quinolines and derivatives |
| Subclass | Imidazoquinolines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Imidazoquinolines |
| Alternative Parents | Phenylpiperazines N-arylpiperazines Phenylimidazoles Trifluoromethylbenzenes Imidazo-[4,5-c]pyridines Aniline and substituted anilines Dialkylarylamines Pyridinones Alkyl aryl ethers Unsaturated fatty acids N-substituted imidazoles Dicarboxylic acids and derivatives Heteroaromatic compounds Ureas Azacyclic compounds Carboxylic acids Dialkylamines Alkyl fluorides Carbonyl compounds Organopnictogen compounds Organofluorides Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Not available |
| Substituents | Imidazoquinoline - Phenylpiperazine - N-arylpiperazine - 1-phenylimidazole - Trifluoromethylbenzene - Imidazopyridine - Imidazo-[4,5-c]pyridine - Tertiary aliphatic/aromatic amine - Aniline or substituted anilines - Dialkylarylamine - Alkyl aryl ether - Pyridinone - Monocyclic benzene moiety - 1,4-diazinane - Dicarboxylic acid or derivatives - N-substituted imidazole - Piperazine - Pyridine - Unsaturated fatty acid - Fatty acyl - Benzenoid - Fatty acid - Azole - Heteroaromatic compound - Imidazole - Urea - Tertiary amine - Carboxylic acid - Carboxylic acid derivative - Azacycle - Secondary amine - Secondary aliphatic amine - Ether - Organic oxide - Organic oxygen compound - Alkyl halide - Alkyl fluoride - Amine - Hydrocarbon derivative - Organohalogen compound - Organofluoride - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Organopnictogen compound - Carbonyl group - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as imidazoquinolines. These are aromatic heterocyclic compounds containing an imidazole ring fused to a quinoline ring system. In some configurations, the imidazole ring shares a nitrogen atom with the quinoline moiety. |
| External Descriptors | maleate salt |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Dec 03, 2025 | N125612 | |
| Certificate of Analysis | Feb 07, 2025 | N125612 | |
| Certificate of Analysis | Feb 07, 2025 | N125612 | |
| Certificate of Analysis | Feb 07, 2025 | N125612 | |
| Certificate of Analysis | Feb 07, 2025 | N125612 | |
| Certificate of Analysis | Feb 07, 2025 | N125612 | |
| Certificate of Analysis | Feb 07, 2025 | N125612 |
| Solubility | DMSO 30 mg/mL Water <1 mg/mL Ethanol <1 mg/mL |
|---|---|
| Sensitivity | Moisture sensitive |
| Molecular Weight | 650.600 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 13 |
| Rotatable Bond Count | 6 |
| Exact Mass | 650.21 Da |
| Monoisotopic Mass | 650.21 Da |
| Topological Polar Surface Area | 148.000 Ų |
| Heavy Atom Count | 47 |
| Formal Charge | 0 |
| Complexity | 992.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 2 |