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· · COA & SDS available for every product · Same-day shipping on in-stock items Nigakinone - Moligand™,≥98% , CAS No.18110-86-6
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% Synonyms
PGFKZUOYIFDMQJ-UHFFFAOYSA-N | 6H-Indolo(3,2,1-de)(1,5)naphthyridin-6-one, 5-hydroxy-4-methoxy- | HMS2269C08 | MLS000574953 | J7E73434D2 | 6H-Indolo[3,2,1-de][1,5]naphthyridin-6-one, 5-hydroxy-4-methoxy- | AC-34395 | 4-Methoxy-5-hydroxycanthin-6-one | E806
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™,≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,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.
Overview Nigakinone is one of the most abundant alkaloids responsible for the major pharmacological activities of Kumu.
Form:Solid
Specifications Synonyms
PGFKZUOYIFDMQJ-UHFFFAOYSA-N | 6H-Indolo(3, 2, 1-de)(1, 5)naphthyridin-6-one, 5-hydroxy-4-methoxy- | HMS2269C08 | MLS000574953 | J7E73434D2 | 6H-Indolo[3, 2, 1-de][1, 5]naphthyridin-6-one, 5-hydroxy-4-methoxy- | AC-34395 | 4-Methoxy-5-hydroxycanthin-6-one | E806
Specifications & Purity
Moligand™, ≥98%
Biochemical and Physiological Mechanisms
Nigakinone is one of the most abundant alkaloids responsible for the major pharmacological activities of Kumu.
Storage
Protected from light, Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles COC1=C(C(=O)N2C3=CC=CC=C3C4=C2C1=NC=C4)O IUPAC Name 3-hydroxy-4-methoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one InChIKey PGFKZUOYIFDMQJ-UHFFFAOYSA-N INCHI 1S/C15H10N2O3/c1-20-14-11-12-9(6-7-16-11)8-4-2-3-5-10(8)17(12)15(19)13(14)18/h2-7,18H,1H3 Isomeric SMILES COC1=C(C(=O)N2C3=CC=CC=C3C4=C2C1=NC=C4)O PubChem CID 5320161 Molecular Weight 266.25
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 Alkaloids and derivatives Class Indolonaphthyridine alkaloids Subclass Not available Intermediate Tree Nodes Not available Direct Parent Indolonaphthyridine alkaloids Alternative Parents Beta carbolines Naphthyridines Indoles Indolizines Alkyl aryl ethers Pyridinones Hydroxypyridines Benzenoids Vinylogous esters Pyrroles Heteroaromatic compounds Lactams Azacyclic compounds Hydrocarbon derivatives Organopnictogen compounds Organonitrogen compounds Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Diazanaphthalene - Naphthyridine - Indole - Indole or derivatives - Indolizine - Pyrrolopyridine - Alkyl aryl ether - Hydroxypyridine - Pyridinone - Pyridine - Benzenoid - Heteroaromatic compound - Vinylogous ester - Pyrrole - Lactam - Azacycle - Ether - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as indolonaphthyridine alkaloids. These are a numerous and relatively straightforward subgroup of the b-carbolines, e.g. Canthin-6-one, in which an additional C3 unit is attached between C-1 and the indole nitrogen to form an additional ring. The group includes a few dimeric examples, such as Haplophytine. External Descriptors beta-carbolines 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 DMSO : 8.33 mg/mL (31.29 mM; Need ultrasonic) Sensitivity Moisture sensitive.；Light sensitive Molecular Weight 266.250 g/mol XLogP3 2.000 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 1 Exact Mass 266.069 Da Monoisotopic Mass 266.069 Da Topological Polar Surface Area 64.400 Ų Heavy Atom Count 20 Formal Charge 0 Complexity 476.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 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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