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· · COA & SDS available for every product · Same-day shipping on in-stock items 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 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 (
Specifications & Purity
Moligand™, ≥98%(HPLC)
Biochemical and Physiological Mechanisms
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
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Activator of K v7.4
Names and Identifiers Pubchem Sid 504762463 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504762463 Canonical Smiles 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) Isomeric SMILES CC1=CC(=C(C(=C1)C)NC(=O)C2CC3CCC2C3)C WGK Germany 3 Molecular Weight 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 Class 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Solvent:DMSO, Max Conc. mg/mL: 12.87, Max Conc. mM: 50; Solvent:ethanol, Max Conc. mg/mL: 12.87, Max Conc. mM: 50 Molecular Weight 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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