Name: Canthin-6-one - Moligand™, ≥98% , CAS No.479-43-6
Brand: Aladdin Scientific
SKU: C695264
Availability: InStock

Canthin-6-one - Moligand™, ≥98% , CAS No.479-43-6

CAS: 479-43-6 Cat. No.: C695264 Summenformel: C₁₄H₈N₂O Molekulargewicht: 220.23 PubChem CID: 97176

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QUALITÄT & REINHEIT Moligand™ ? ≥98%

Synonyms

6H-Indolo[3,2,1-de][1,5]naphthyridin-6-one

Storage

Protected from light,Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Übersicht Spezifikationen Produkteigenschaften Namen und Kennungen Erweiterte Daten Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Lösungsrechner Bewertungen

Übersicht

Canthin-6-one displays a wide range of biological activities, such as antimycobacterial activity.

Spezifikationen

Synonyme

6H-Indolo[3,2,1-de][1,5]naphthyridin-6-one

Spezifikationen & Reinheit

Moligand™, ≥98%

Storage

Protected from light,Store at -20°C,Argon charged

Verschickt in

Ice chest + Ice pads

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Note

Moligand™

Reinheit

≥98%

Produkteigenschaften

ALogP

2.4

Namen und Kennungen

Kanonisches Lächeln

C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3

IUPAC Name

1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one

InChIKey

ZERVJPYNQLONEK-UHFFFAOYSA-N

INCHI

1S/C14H8N2O/c17-13-6-5-11-14-10(7-8-15-11)9-3-1-2-4-12(9)16(13)14/h1-8H

Isomere SMILES

C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3

PubChem CID

97176

Molekulargewicht

220.23

Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Alkaloids and derivatives
  - Klasse Indolonaphthyridine alkaloids

Kingdom	Organic compounds
Superclass	Alkaloids and derivatives
Klasse	Indolonaphthyridine alkaloids
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Indolonaphthyridine alkaloids
Alternative Parents	Beta carbolines Naphthyridines Indolizines Indoles Pyridinones Benzenoids Pyrroles Heteroaromatic compounds Lactams Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Diazanaphthalene - Naphthyridine - Indole - Indole or derivatives - Indolizine - Pyrrolopyridine - Pyridinone - Pyridine - Benzenoid - Heteroaromatic compound - Pyrrole - Lactam - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Beschreibung	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	organic heterotetracyclic compound - indole alkaloid - enone
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. DOI: 10.1186/s13321-016-0174-y

3D-Struktur

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AKT1 Tchem Serine/threonine-protein kinase AKT (9192 Activities)

Discover Target: AKT1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Calu-3 (339 Activities)

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CCRF-CEM (65223 Activities)

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DU-145 (51482 Activities)

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HCT-8 (3484 Activities)

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HT-29 (80576 Activities)

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MCF7 (126967 Activities)

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MRC5 (9203 Activities)

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NHDF (1164 Activities)

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PC-3 (62116 Activities)

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ADR5000 cell line (115 Activities)

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A549 (127892 Activities)

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HepG2 (196354 Activities)

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Jurkat (10389 Activities)

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KB (17409 Activities)

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HeLa (62764 Activities)

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HCC1395 (122 Activities)

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Zugehörige Ziele (nicht menschlich)

Ptpn1 Protein-tyrosine phosphatase 1B (270 Activities)

Discover Target: Ptpn1

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Pseudomonas aeruginosa (123386 Activities)

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Pseudomonas fluorescens (1630 Activities)

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Ralstonia solanacearum (520 Activities)

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Staphylococcus aureus (210822 Activities)

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Escherichia coli (133304 Activities)

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Bacillus subtilis (32866 Activities)

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Mycobacterium (258 Activities)

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Mycolicibacterium fortuitum (1335 Activities)

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Mycolicibacterium phlei (631 Activities)

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Saccharomyces cerevisiae (19171 Activities)

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Enterococcus faecalis (29875 Activities)

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Bacillus cereus (7522 Activities)

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Mycolicibacterium smegmatis (8003 Activities)

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Aspergillus fumigatus (16427 Activities)

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Entamoeba histolytica (2676 Activities)

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Plasmodium falciparum (966862 Activities)

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Cryptococcus neoformans (21258 Activities)

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Candida albicans (78123 Activities)

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CHO (4503 Activities)

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Vero (26788 Activities)

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C6 (2371 Activities)

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NIH3T3 (5395 Activities)

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Trichophyton mentagrophytes (4846 Activities)

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Gabrp GABA-A receptor; anion channel (5731 Activities)

Discover Target: Gabrp

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Wirkungsmechanismen

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemische und physikalische Eigenschaften

Empfindlichkeit	light & Moisture & heat & air sensitive
Molekulargewicht	220.230 g/mol
XLogP3	2.400
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	220.064 Da
Monoisotopic Mass	220.064 Da
Topological Polar Surface Area	34.900 Å²
Heavy Atom Count	17
Formal Charge	0
Complexity	378.000
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

Lösungsrechner

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Canthin-6-one - Moligand™, ≥98% , CAS No.479-43-6

Übersicht

Spezifikationen

Erweiterte Daten

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Reconstitution Calculator

Kundenbewertungen

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