SL-327 - Moligand™, 10mM in DMSO , Inhibitor of mitogen-activated protein kinase kinase 2, CAS No.305350-87-2, Inhibitor of mitogen-activated protein kinase kinase 2

CAS: 305350-87-2 Cat. No.: S423164 Formula: C₁₆H₁₂F₃N₃S Peso molecolare: 335.35 Numero EC: 878-717-0 PubChem CID: 9549284

GRADE & PURITY Moligand™, 10mM in DMSO

Synonyms

CCG-206867 | STL555675 | Benzeneacetonitrile, alpha-[amino[(4-aminophenyl)thio]methylene]-2-(trifluoromethyl)- | HY-15437 | SCHEMBL570318 | BCP05310 | FT-0600361 | Q27084156 | AC-33170 | NCGC00092290-01 | (Z)-3-Amino-3-((4-aminophenyl)thio)-2-(2-(trifluor

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Panoramica

SL327
SL327 was used to study the role of MAPK signaling in interictal spiking and behavior of epileptic rats.¹ It was used to study the effect of estradiol on ERK signaling in mouse dorsal hippocampus.²

Specifications

Sinonimi

CCG-206867 | STL555675 | Benzeneacetonitrile, alpha-[amino[(4-aminophenyl)thio]methylene]-2-(trifluoromethyl)- | HY-15437 | SCHEMBL570318 | BCP05310 | FT-0600361 | Q27084156 | AC-33170 | NCGC00092290-01 | (Z)-3-Amino-3-((4-aminophenyl)thio)-2-(2-(trifluor

Specifiche e purezza

Moligand™, 10mM in DMSO

Meccanismi biochimici e fisiologici

SL-327 is a cell-permeable vinylogous cyanamide that acts as a selective inhibitor of MEK-1 and MEK-2 (IC50 = 0.18 and 0.22 μM respectively). SL-327 has been shown to block hippocampal LTP via inhibition of the MAPK/ERK cascade, which prevents CREB and

Condizioni di conservazione di stoccaggio

Store at -80°C

Spedito in

Dry ice packs + Cold packs

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Moligand™

Tipo di azione

INHIBITOR

Meccanismo d'azione

Inhibitor of mitogen-activated protein kinase kinase 2

Nomi e identificatori

• Pubchem Sid: 528767119
• Sorrisi canonici: C1=CC=C(C(=C1)C(=C(N)SC2=CC=C(C=C2)N)C#N)C(F)(F)F
• IUPAC Name: (Z)-3-amino-3-(4-aminophenyl)sulfanyl-2-[2-(trifluoromethyl)phenyl]prop-2-enenitrile
• InChIKey: JLOXTZFYJNCPIS-FYWRMAATSA-N
• INCHI: 1S/C16H12F3N3S/c17-16(18,19)14-4-2-1-3-12(14)13(9-20)15(22)23-11-7-5-10(21)6-8-11/h1-8H,21-22H2/b15-13+
• Isomeri SMILES: C1=CC=C(C(=C1)/C(=C(\N)/SC2=CC=C(C=C2)N)/C#N)C(F)(F)F
• WGK Germania: 3
• PubChem CID: 9549284
• Peso molecolare: 335.35

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Trifluoromethylbenzenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Trifluoromethylbenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Trifluoromethylbenzenes
• Alternative Parents: Aryl thioethers Aniline and substituted anilines Ketene acetals Sulfenyl compounds Nitriles Primary amines Organofluorides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Trifluoromethylbenzene - Aniline or substituted anilines - Aryl thioether - Ketene acetal or derivatives - Sulfenyl compound - Nitrile - Carbonitrile - Hydrocarbon derivative - Organic nitrogen compound - Primary amine - Organosulfur compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Alkyl fluoride - Amine - Alkyl halide - Cyanide - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as trifluoromethylbenzenes. These are organofluorine compounds that contain a benzene ring substituted with one or more trifluoromethyl groups.
• 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

Obiettivi associati (umani)

MAP2K2 Tclin Dual specificity mitogen-activated protein kinase kinase 2 (1 Activities)

Discover Target: MAP2K2

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

Proprietà chimiche e fisiche

• Sensibilità: Light Sensitive,Air Sensitive,Moisture Sensitive,Heat Sensitive
• Punto di fusione (°C): 128 °C
• Peso molecolare: 335.300 g/mol
• XLogP3: 3.700
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 3
• Exact Mass: 335.07 Da
• Monoisotopic Mass: 335.07 Da
• Topological Polar Surface Area: 101.000 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 487.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1