Indolo[3,2-b]carbazole - Moligand™, ≥98% , Agonist of Aryl hydrocarbon receptor, CAS No.241-55-4, Agonist of Aryl hydrocarbon receptor

CAS: 241-55-4 Cat. No.: I395944 Peso molecular: 254.29

GRADE & PURITY Moligand™, ≥98%

Synonyms

indolo[3,2-b]carbazole|241-55-4|Indolo(3,2-b)carbazole|ICZ-carbazole|SCHEMBL550600|GTPL10046|DTXSID70178826|HLVSZSQYBQCBQG-UHFFFAOYSA-N|AKOS015840848|OL10030|OL10032|A878005

Storage

Room temperature

Shipped In

Normal

Descripción general

Product Application：

Indolo[3,2-b]carbazol-2-ol is a derivative of Indolo[3,2-b]carbazole (CAS# 241-55-4), which have been studied for their electronic properties as a potential n-type organic semiconductor.

Specifications

Sinónimos

indolo[3, 2-b]carbazole | 241-55-4 | Indolo(3, 2-b)carbazole | ICZ-carbazole | SCHEMBL550600 | GTPL10046 | DTXSID70178826 | HLVSZSQYBQCBQG-UHFFFAOYSA-N | AKOS015840848 | OL10030 | OL10032 | A878005

Especificaciones y pureza

Moligand™, ≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Grado

Moligand™

Tipo de acción

AGONIST

Mecanismo de acción

Agonist of Aryl hydrocarbon receptor

Pureza

≥98%

Nombres e identificadores

• Sonrisas canónicas: C1=CC=C2C(=C1)C3=CC4=NC5=CC=CC=C5C4=CC3=N2
• IUPAC Name: indolo[3,2-b]carbazole
• InChIKey: HLVSZSQYBQCBQG-UHFFFAOYSA-N
• INCHI: 1S/C18H10N2/c1-3-7-15-11(5-1)13-9-18-14(10-17(13)19-15)12-6-2-4-8-16(12)20-18/h1-10H
• Isómeros SMILES: C1=CC=C2C(=C1)C3=CC4=NC5=CC=CC=C5C4=CC3=N2
• Peso molecular: 254.29
• Reaxy-Rn: 790807
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=790807&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Indoles and derivatives
      • Subclass Carbazoles
        • Level5 Pyrrolocarbazoles
          • Level6 Indolocarbazoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Indoles and derivatives
• Subclass: Carbazoles
• Intermediate Tree Nodes: Pyrrolocarbazoles
• Direct Parent: Indolocarbazoles
• Alternative Parents: Indoles Benzenoids Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Indolocarbazole - Indole - Benzenoid - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as indolocarbazoles. These are polycyclic aromatic compounds containing an indole fused to a carbazole.
• 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.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (humanos)

AHR Tclin Aryl hydrocarbon receptor (1 Activities)

Discover Target: AHR

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Propiedades químicas y físicas

• Peso molecular: 254.300 g/mol
• XLogP3: 3.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 254.084 Da
• Monoisotopic Mass: 254.084 Da
• Topological Polar Surface Area: 24.700 Ų
• Heavy Atom Count: 20
• Formal Charge: 0
• Complexity: 526.000
• 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