Determine the necessary mass, volume, or concentration for preparing a solution.
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Moligand™, ≥99% 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.
Information
Ulixertinib (BVD-523) Ulixertinib (BVD-523, VRT752271) is a potent and reversible ERK1/ERK2 inhibitor with IC50 of <0.3 nM for ERK2. Phase 1.
Targets
ERK1 ; ERK2 ; <0.3 nM
In vitro
In an A375 melanoma cell line containing a b-RAFV600E mutation, Ulixertinib reduces the levels of phosphorylated ERK2 (pERK) and of the phosphorylation of the downstream kinase RSK (pRSK) with IC50 of 4.1/0.14 μM, respectively. Ulixertinib also inhibits A375 cell proliferation with IC50 of 180 nM.
Cell Research(from reference)
Cell lines:A375 cells
Concentrations:~30 μM
Incubation Time:72 h
| ALogP | 4.266 |
|---|---|
| Recuento HBD | 4 |
| Enlace rotable | 7 |
| Pubchem Sid | 488197679 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488197679 |
| Sonrisas canónicas | CC(C)NC1=NC=C(C(=C1)C2=CNC(=C2)C(=O)NC(CO)C3=CC(=CC=C3)Cl)Cl |
| IUPAC Name | N-[(1S)-1-(3-chlorophenyl)-2-hydroxyethyl]-4-[5-chloro-2-(propan-2-ylamino)pyridin-4-yl]-1H-pyrrole-2-carboxamide |
| InChIKey | KSERXGMCDHOLSS-LJQANCHMSA-N |
| INCHI | 1S/C21H22Cl2N4O2/c1-12(2)26-20-8-16(17(23)10-25-20)14-7-18(24-9-14)21(29)27-19(11-28)13-4-3-5-15(22)6-13/h3-10,12,19,24,28H,11H2,1-2H3,(H,25,26)(H,27,29)/t19-/m1/s1 |
| Isómeros SMILES | CC(C)NC1=NC=C(C(=C1)C2=CNC(=C2)C(=O)N[C@H](CO)C3=CC(=CC=C3)Cl)Cl |
| PubChem CID | 11719003 |
| Peso molecular | 433.33 |
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 | Carboxylic acid derivatives |
| Intermediate Tree Nodes | Carboxylic acid amides |
| Direct Parent | 2-heteroaryl carboxamides |
| Alternative Parents | Pyrrole carboxamides Aminopyridines and derivatives Chlorobenzenes Secondary alkylarylamines Imidolactams Substituted pyrroles Aryl chlorides Heteroaromatic compounds Amino acids and derivatives Secondary carboxylic acid amides Azacyclic compounds Primary alcohols Organopnictogen compounds Organochlorides Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | 2-heteroaryl carboxamide - Pyrrole-2-carboxamide - Pyrrole-2-carboxylic acid or derivatives - Aminopyridine - Chlorobenzene - Halobenzene - Secondary aliphatic/aromatic amine - Imidolactam - Benzenoid - Substituted pyrrole - Aryl chloride - Aryl halide - Pyridine - Monocyclic benzene moiety - Heteroaromatic compound - Pyrrole - Secondary carboxylic acid amide - Amino acid or derivatives - Azacycle - Organoheterocyclic compound - Secondary amine - Organopnictogen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organooxygen compound - Amine - Primary alcohol - Organic nitrogen compound - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as 2-heteroaryl carboxamides. These are compounds containing a heteroaromatic ring that carries a carboxamide group. |
| 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 | Jan 19, 2026 | U413857 | |
| Certificate of Analysis | Jan 19, 2026 | U413857 | |
| Certificate of Analysis | Jan 19, 2026 | U413857 | |
| Certificate of Analysis | Jan 19, 2026 | U413857 | |
| Certificate of Analysis | Jan 19, 2026 | U413857 | |
| Certificate of Analysis | Jan 19, 2026 | U413857 | |
| Certificate of Analysis | Jan 19, 2026 | U413857 | |
| Certificate of Analysis | Jan 19, 2026 | U413857 | |
| Certificate of Analysis | Jan 19, 2026 | U413857 | |
| Certificate of Analysis | Jan 19, 2026 | U413857 | |
| Certificate of Analysis | Jan 19, 2026 | U413857 | |
| Certificate of Analysis | Jan 19, 2026 | U413857 | |
| Certificate of Analysis | Jan 19, 2026 | U413857 |
| Solubilidad | Solubility (25°C) In vitro DMSO: 86 mg/mL (198.46 mM); Ethanol: 43 mg/mL (99.23 mM); Water: Insoluble; |
|---|---|
| DMSO (mg/ml) Solubilidad máxima | 86 |
| DMSO (mM) Solubilidad máxima | 198.4630651 |
| Agua (mg/ml) Solubilidad máxima | <1 |
| Peso molecular | 433.300 g/mol |
| XLogP3 | 4.100 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 7 |
| Exact Mass | 432.112 Da |
| Monoisotopic Mass | 432.112 Da |
| Topological Polar Surface Area | 90.000 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 539.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| 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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