MBQ-167 - 10mM in DMSO , CAS No.2097938-73-1

CAS: 2097938-73-1 Cat. No.: M422545 Summenformel: C₂₂H₁₈N₄ Molekulargewicht: 338.41

GRADE & PURITY 10mM in DMSO

Synonyms

XID93873 | 9H-Carbazole, 9-ethyl-3-(5-phenyl-1H-1,2,3-triazol-1-yl)- | 9-Ethyl-3-(5-phenyl-1H-1,2,3-triazol-1-yl)-9H-carbazole | A16808 | 2097938-73-1 | UNII-RRY5XN588Q | s8749 | RRY5XN588Q | D71171 | MBQ-167 | 1-(9-ethyl-9h-carbazol-3-yl)-5-phenyl-1h-1,2

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Übersicht

Information

MBQ-167 MBQ-167 is a potent and dual inhibitor of Rac and Cdc42 with IC50s of 103 nM and 78 nM respectively, in metastatic breast cancer cells.

Targets

cdc42 (in metastatic breast cancer cells); Rac (in metastatic breast cancer cells) 78 nM; 103 nM

In vitro

MBQ-167 inhibits mammary tumor growth and metastasis in immunocompromised mice by ~90%.

Cell Research(from reference)

Cell lines：MDA-MB-231 cells 

Concentrations：250 or 500 nM 

Incubation Time：24 h 

Specifications

Synonyme

XID93873 | 9H-Carbazole, 9-ethyl-3-(5-phenyl-1H-1,2,3-triazol-1-yl)- | 9-Ethyl-3-(5-phenyl-1H-1,2,3-triazol-1-yl)-9H-carbazole | A16808 | 2097938-73-1 | UNII-RRY5XN588Q | s8749 | RRY5XN588Q | D71171 | MBQ-167 | 1-(9-ethyl-9h-carbazol-3-yl)-5-phenyl-1h-1,2

Spezifikationen & Reinheit

10mM in DMSO

Biochemische und physiologische Mechanismen

MBQ-167 is a potent and dual inhibitor of Rac and Cdc42 with IC50s of 103 nM and 78 nM respectively, in metastatic breast cancer cells.

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

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

Aktionsart

INHIBITOR

Produkteigenschaften

• ALogP: 5.446
• hba_count: 2
• Rotationsfähige Bindung: 3

Namen und Kennungen

• Pubchem Sid: 528765421
• Kanonisches Lächeln: CCN1C2=C(C=C(C=C2)N3C(=CN=N3)C4=CC=CC=C4)C5=CC=CC=C51
• IUPAC Name: 9-ethyl-3-(5-phenyltriazol-1-yl)carbazole
• InChIKey: LJCANTASZGYJLG-UHFFFAOYSA-N
• INCHI: 1S/C22H18N4/c1-2-25-20-11-7-6-10-18(20)19-14-17(12-13-21(19)25)26-22(15-23-24-26)16-8-4-3-5-9-16/h3-15H,2H2,1H3
• Isomere SMILES: CCN1C2=C(C=C(C=C2)N3C(=CN=N3)C4=CC=CC=C4)C5=CC=CC=C51
• Molekulargewicht: 338.41
• Reaxy-Rn: 31253890
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=31253890&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Klasse Indoles and derivatives
      • Subclass Carbazoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Klasse: Indoles and derivatives
• Subclass: Carbazoles
• Intermediate Tree Nodes: Not available
• Direct Parent: Carbazoles
• Alternative Parents: N-alkylindoles Substituted pyrroles Benzene and substituted derivatives Triazoles Heteroaromatic compounds Trialkylamines Propargyl-type 1,3-dipolar organic compounds Enamines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Carbazole - N-alkylindole - Benzenoid - Substituted pyrrole - Monocyclic benzene moiety - Heteroaromatic compound - 1,2,3-triazole - Azole - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Enamine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as carbazoles. These are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.
• 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

Chemische und physikalische Eigenschaften

• DMSO (mg/ml) Maximale Löslichkeit: 68
• DMSO (mM) Maximale Löslichkeit: 200.939688543483
• Wasser (mg/ml) Maximale Löslichkeit: ＜1
• Molekulargewicht: 338.400 g/mol
• XLogP3: 4.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 338.153 Da
• Monoisotopic Mass: 338.153 Da
• Topological Polar Surface Area: 35.600 Ų
• Heavy Atom Count: 26
• Formal Charge: 0
• Complexity: 477.000
• 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