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· · COA & SDS available for every product · Same-day shipping on in-stock items Home By Target/Pathway/Disease By Disease (DOID) Genetic diseases monogenic disease (DOID:0050177) N-[3-[3-cyano-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-yl]-1H-indol-5-yl]acetamide - Moligand™ , Inhibitor of dual specificity tyrosine phosphorylation regulated kinase 2;Inhibitor of glycogen synthase kinase 3 beta;Inhibitor of homeodomain interact, Inhibitor of dual specificity tyrosine phosphorylation regulated kinase 2;Inhibitor of glycogen synthase kinase 3 beta;Inhibitor of homeodomain interacting protein kinase 2 N-[3-[3-cyano-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-yl]-1H-indol-5-yl]acetamide - Moligand™ , Inhibitor of dual specificity tyrosine phosphorylation regulated kinase 2;Inhibitor of glycogen synthase kinase 3 beta;Inhibitor of homeodomain interact, Inhibitor of dual specificity tyrosine phosphorylation regulated kinase 2;Inhibitor of glycogen synthase kinase 3 beta;Inhibitor of homeodomain interacting protein kinase 2
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.
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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 Specifications & Purity
Moligand™
Mechanism of action
Inhibitor of dual specificity tyrosine phosphorylation regulated kinase 2;Inhibitor of glycogen synthase kinase 3 beta;Inhibitor of homeodomain interacting protein kinase 2
Names and Identifiers Canonical Smiles N#Cc1cnn2c1nc(cc2NC1CC1)c1c[nH]c2c1cc(cc2)NC(=O)C InChIKey UZZGMJZTCZOSGC-UHFFFAOYSA-N INCHI 1S/C20H17N7O/c1-11(28)24-14-4-5-17-15(6-14)16(10-22-17)18-7-19(25-13-2-3-13)27-20(26-18)12(8-21)9-23-27/h4-7,9-10,13,22,25H,2-3H2,1H3,(H,24,28) Isomeric SMILES CC(=O)NC1=CC2=C(C=C1)NC=C2C3=NC4=C(C=NN4C(=C3)NC5CC5)C#N PubChem CID 136254272
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 Pyrazolopyrimidines Subclass Pyrazolo[1,5-a]pyrimidines Intermediate Tree Nodes Not available Direct Parent Pyrazolo[1,5-a]pyrimidines Alternative Parents N-acetylarylamines Indoles Aminopyrimidines and derivatives Substituted pyrroles Benzenoids Pyrazoles Heteroaromatic compounds Acetamides Secondary carboxylic acid amides Nitriles Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Amines Molecular Framework Aromatic heteropolycyclic compounds Substituents Indole - N-acetylarylamine - Indole or derivatives - Pyrazolo[1,5-a]pyrimidine - N-arylamide - Aminopyrimidine - Pyrimidine - Substituted pyrrole - Benzenoid - Azole - Pyrazole - Pyrrole - Heteroaromatic compound - Acetamide - Carboxamide group - Secondary carboxylic acid amide - Nitrile - Carbonitrile - Carboxylic acid derivative - Azacycle - Organic oxide - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Cyanide - Organic oxygen compound - Hydrocarbon derivative - Amine - Carbonyl group - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as pyrazolo[1,5-a]pyrimidines. These are aromatic heterocyclic compounds containing a pyrazolo[3,4-d]pyrimidine ring system, which consists of a pyrazole ring fused to and sharing exactly one nitrogen atom with a pyrimidine ring. 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) 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.
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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.
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