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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Nigakinone - Moligand™,≥98% , CAS No.18110-86-6
Disponível para encomenda
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.
Visão geral Nigakinone is one of the most abundant alkaloids responsible for the major pharmacological activities of Kumu.
Form:Solid
Specifications Sinónimos
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
Especificações e pureza
Moligand™,≥98%
Mecanismos bioquímicos e fisiológicos
Nigakinone is one of the most abundant alkaloids responsible for the major pharmacological activities of Kumu.
Condições de armazenamento de armazenamento
Protected from light,Store at -20°C
Enviado em
Ice chest + Ice pads
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Nomes e identificadores Sorrisos canónicos 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 SMILES isoméricas COC1=C(C(=O)N2C3=CC=CC=C3C4=C2C1=NC=C4)O PubChem CID 5320161 Peso molecular 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 Classe 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 Descrição 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.
Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Solubilidade DMSO : 8.33 mg/mL (31.29 mM; Need ultrasonic) Sensibilidade Moisture sensitive.；Light sensitive Peso molecular 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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View Moligand™ grade guide →
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