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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock ML213 - Moligand™, ≥98%(HPLC) , Activator of K v7.4, CAS No.489402-47-3, Activator of K v7.4
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. ≥98%(HPLC) Synonyms
N-(2,4,6-trimethylphenyl)bicyclo[2.2.1]heptane-6-carboxamide | ML213 | ML-213 | MLS003370512 | SMR000514557 | EX-A2551 | s6553 | Q27087011 | STK373915 | CID 3111211 | N-mesitylbicyclo[2.2.1]heptane-2-carboxamide | bicyclo[2.2.1]heptane-2-carboxylic acid (
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥98%(HPLC) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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 Synonymes
N-(2,4,6-trimethylphenyl)bicyclo[2.2.1]heptane-6-carboxamide | ML213 | ML-213 | MLS003370512 | SMR000514557 | EX-A2551 | s6553 | Q27087011 | STK373915 | CID 3111211 | N-mesitylbicyclo[2.2.1]heptane-2-carboxamide | bicyclo[2.2.1]heptane-2-carboxylic acid (
Spécifications et pureté
Moligand™, ≥98%(HPLC)
Mécanismes biochimiques et physiologiques
Selective KV7.2 (KCNQ2) and KV7.4 (KCNQ4) channel opener (EC50values are 230 and 510 nM for KV7.2 and KV7.4 respectively). Displays > 80-fold selectivity against KV7.1, KV7.3 and KV7.5 in a thallium-based fluorescence assay. Hyperpolarizes resting membran
Conditions de stockage de stockage
Store at -20°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Mécanisme d'action
Activator of K v7.4
Noms et identifiants Pubchem Sid 504762463 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504762463 Sourires canoniques CC1=CC(=C(C(=C1)C)NC(=O)C2CC3CCC2C3)C IUPAC Name N-(2,4,6-trimethylphenyl)bicyclo[2.2.1]heptane-2-carboxamide InChIKey SIQGKPGBLYKQBB-UHFFFAOYSA-N INCHI 1S/C17H23NO/c1-10-6-11(2)16(12(3)7-10)18-17(19)15-9-13-4-5-14(15)8-13/h6-7,13-15H,4-5,8-9H2,1-3H3,(H,18,19) Isomères SMILES CC1=CC(=C(C(=C1)C)NC(=O)C2CC3CCC2C3)C WGK Allemagne 3 Poids moléculaire 257.37 Reaxy-Rn 24287972 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=24287972&ln=
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 Lipids and lipid-like molecules Classe Prenol lipids Subclass Monoterpenoids Intermediate Tree Nodes Not available Direct Parent Bicyclic monoterpenoids Alternative Parents Aromatic monoterpenoids Anilides N-arylamides Secondary carboxylic acid amides Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homopolycyclic compounds Substituents Aromatic monoterpenoid - Bicyclic monoterpenoid - Anilide - N-arylamide - Monocyclic benzene moiety - Benzenoid - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Aromatic homopolycyclic compound Description This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. 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.
Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Solubilité Solvent:DMSO, Max Conc. mg/mL: 12.87, Max Conc. mM: 50; Solvent:ethanol, Max Conc. mg/mL: 12.87, Max Conc. mM: 50 Poids moléculaire 257.370 g/mol XLogP3 4.200 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 2 Exact Mass 257.178 Da Monoisotopic Mass 257.178 Da Topological Polar Surface Area 29.100 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 341.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 3 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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