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· · COA & SDS available for every product · Same-day shipping on in-stock items MAP855 - Moligand™ , Inhibitor of mitogen-activated protein kinase kinase 1, CAS No.M611729, Inhibitor of mitogen-activated protein kinase kinase 1
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. Synonyms
compound 30;MAP-855
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Why this grade Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships 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.
Specifications Synonyms
compound 30;MAP-855
Specifications & Purity
Moligand™
Mechanism of action
Inhibitor of mitogen-activated protein kinase kinase 1
Names and Identifiers Canonical Smiles Cc1nc2cnc3cc(c(cc3c2n1[C@H]1CCN(C[C@@H]1F)C(=O)CO)c1ccc(cc1Cl)Oc1ncccn1)F IUPAC Name 1-[(3S,4S)-4-[8-(2-chloro-4-pyrimidin-2-yloxyphenyl)-7-fluoro-2-methylimidazo[4,5-c]quinolin-1-yl]-3-fluoropiperidin-1-yl]-2-hydroxyethanone InChIKey WZZBNLYBHUDSHF-DHLKQENFSA-N INCHI 1S/C28H23ClF2N6O3/c1-15-35-24-12-34-23-11-21(30)18(17-4-3-16(9-20(17)29)40-28-32-6-2-7-33-28)10-19(23)27(24)37(15)25-5-8-36(13-22(25)31)26(39)14-38/h2-4,6-7,9-12,22,25,38H,5,8,13-14H2,1H3/t22-,25-/m0/s1 Isomeric SMILES CC1=NC2=C(N1[C@H]3CCN(C[C@@H]3F)C(=O)CO)C4=CC(=C(C=C4N=C2)F)C5=C(C=C(C=C5)OC6=NC=CC=N6)Cl PubChem CID 90647159
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 Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Quinolines and derivatives Subclass Phenylquinolines Intermediate Tree Nodes Not available Direct Parent Phenylquinolines Alternative Parents Imidazoquinolines Diarylethers Haloquinolines Imidazo-[4,5-c]pyridines N-acylpiperidines Phenol ethers Phenoxy compounds Chlorobenzenes Aryl fluorides N-substituted imidazoles Aryl chlorides Pyridines and derivatives Pyrimidines and pyrimidine derivatives Tertiary carboxylic acid amides Heteroaromatic compounds Azacyclic compounds Hydrocarbon derivatives Alkyl fluorides Organic oxides Carbonyl compounds Organochlorides Organofluorides Organonitrogen compounds Primary alcohols Molecular Framework Aromatic heteropolycyclic compounds Substituents Phenylquinoline - Imidazoquinoline - Haloquinoline - Diaryl ether - N-acyl-piperidine - Imidazopyridine - Imidazo-[4,5-c]pyridine - Phenoxy compound - Phenol ether - Halobenzene - Chlorobenzene - N-substituted imidazole - Aryl chloride - Aryl fluoride - Aryl halide - Pyrimidine - Pyridine - Benzenoid - Piperidine - Monocyclic benzene moiety - Heteroaromatic compound - Imidazole - Azole - Tertiary carboxylic acid amide - Carboxamide group - Azacycle - Carboxylic acid derivative - Ether - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Organofluoride - Alcohol - Carbonyl group - Organochloride - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Alkyl fluoride - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as phenylquinolines. These are heterocyclic compounds containing a quinoline moiety substituted with a phenyl group. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Solution Calculators Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Reviews Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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