Camalexin - ≥98% , CAS No.135531-86-1

CAS: 135531-86-1 Cat. No.: C412537 Fórmula: C₁₁H₈N₂S Peso molecular: 200.26 Número CE: 808-542-7

GRADE & PURITY ≥98%

Synonyms

AS-16652 | Q19903715 | 1H-indole, 3-(2-thiazolyl)- | QY3Z69LA99 | 3-thiazol-2'-yl-indole | 3-(thiazol-2-yl)indole | AKOS030257626 | 3-(Thiazol-2-yl)-1H-indole | SCHEMBL343413 | 2-(1H-indol-3-yl)-1,3-thiazole | 3-(2-Thiazolyl)-1H-indole | HY-119502 | Camal

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Visão geral

Camalexin is a phytoalexin isolated from Camelina sativa (Cruciferae) with antibacterial, antifungal, antiproliferative and anticancer activities. Camalexin can induce reactive oxygen species (ROS) production。

Information

Camalexin Camalexin, a phytoalexin isolated from Camelina sativa and Arabidopsis (Cruciferae), can induce reactive oxygen species (ROS) production. Camalexin has antibacterial, antifungal, antiproliferative and anticancer activities.

Specifications

Sinónimos

AS-16652 | Q19903715 | 1H-indole, 3-(2-thiazolyl)- | QY3Z69LA99 | 3-thiazol-2'-yl-indole | 3-(thiazol-2-yl)indole | AKOS030257626 | 3-(Thiazol-2-yl)-1H-indole | SCHEMBL343413 | 2-(1H-indol-3-yl)-1,3-thiazole | 3-(2-Thiazolyl)-1H-indole | HY-119502 | Camal

Especificações e pureza

≥98%

Mecanismos bioquímicos e fisiológicos

Camalexin, a phytoalexin isolated from Camelina sativa and Arabidopsis (Cruciferae), can induce reactive oxygen species (ROS) production. Camalexin has antibacterial, antifungal, antiproliferative and anticancer activities.

Condições de armazenamento de armazenamento

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.

Pureza

≥98%

Nomes e identificadores

• Pubchem Sid: 528772256
• Sorrisos canónicos: C1=CC=C2C(=C1)C(=CN2)C3=NC=CS3
• IUPAC Name: 2-(1H-indol-3-yl)-1,3-thiazole
• InChIKey: IYODIJVWGPRBGQ-UHFFFAOYSA-N
• INCHI: 1S/C11H8N2S/c1-2-4-10-8(3-1)9(7-13-10)11-12-5-6-14-11/h1-7,13H
• SMILES isoméricas: C1=CC=C2C(=C1)C(=CN2)C3=NC=CS3
• WGK Alemanha: 3
• Peso molecular: 200.26
• Reaxy-Rn: 4310041
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4310041&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Indoles and derivatives
      • Subclass Indoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Indoles and derivatives
• Subclass: Indoles
• Intermediate Tree Nodes: Not available
• Direct Parent: Indoles
• Alternative Parents: Substituted pyrroles Benzenoids Thiazoles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Indole - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Thiazole - Pyrrole - Azole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
• Descrição: This compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.
• External Descriptors: an indole-phytolexin

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

Alvos associados (não humanos)

Plenodomus lingam (178 Activities)

Explore this target

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

Mecanismos de ação

Propriedades químicas e físicas

• Solubilidade: Solubility (25°C) In vitro Ethanol: mg/mL
• Peso molecular: 200.260 g/mol
• XLogP3: 2.700
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 200.041 Da
• Monoisotopic Mass: 200.041 Da
• Topological Polar Surface Area: 56.900 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 209.000
• 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