SB 452533 - Moligand™, ≥98%(HPLC) , Channel blocker of TRPV1, CAS No.459429-39-1, Channel blocker of TRPV1

CAS: 459429-39-1 Cat. No.: S288655 Summenformel: C₁₈H₂₂BrN₃O Molekulargewicht: 376.29 EG-Nummer: 806-206-4 PubChem CID: 9842609

GRADE & PURITY Moligand™, ≥98%(HPLC)

Synonyms

n-(2-bromophenyl)-n'-[2-[ethyl(3-methylphenyl)amino]ethyl]urea | N-(2-Bromophenyl)-N'-[2-[ethyl(3-methylphenyl)amino]ethyl]-urea | AKOS024457514 | MS-26098 | SB452533 | SB-452533 | N-[2-Bromophenyl]-N'-[2-(N''-ethyl-N''-(3-methylphenyl)amino)ethyl]urea |

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Specifications

Synonyme

n-(2-bromophenyl)-n'-[2-[ethyl(3-methylphenyl)amino]ethyl]urea | N-(2-Bromophenyl)-N'-[2-[ethyl(3-methylphenyl)amino]ethyl]-urea | AKOS024457514 | MS-26098 | SB452533 | SB-452533 | N-[2-Bromophenyl]-N'-[2-(N''-ethyl-N''-(3-methylphenyl)amino)ethyl]urea |

Spezifikationen & Reinheit

Moligand™, ≥98%(HPLC)

Biochemische und physiologische Mechanismen

Potent TRPV1 antagonist against capsaicin (pKb= 7.7), noxious heat and acid-mediated (pIC50= 7.0) receptor activation (pKi= 6.22 at the recombinant hTRPV1 receptor). Exhibits analgesic properties.

Storage

Store at -20°C

Verschickt in

Ice chest + Ice pads

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

Note

Moligand™

Aktionsart

CHANNEL BLOCKER

Mechanismus der Wirkung

Channel blocker of TRPV1

Reinheit

≥98%(HPLC)

Namen und Kennungen

• Pubchem Sid: 504764960
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764960
• Kanonisches Lächeln: CCN(CCNC(=O)NC1=CC=CC=C1Br)C2=CC=CC(=C2)C
• IUPAC Name: 1-(2-bromophenyl)-3-[2-(N-ethyl-3-methylanilino)ethyl]urea
• InChIKey: IFJYEGJUQIBBQV-UHFFFAOYSA-N
• INCHI: 1S/C18H22BrN3O/c1-3-22(15-8-6-7-14(2)13-15)12-11-20-18(23)21-17-10-5-4-9-16(17)19/h4-10,13H,3,11-12H2,1-2H3,(H2,20,21,23)
• Isomere SMILES: CCN(CCNC(=O)NC1=CC=CC=C1Br)C2=CC=CC(=C2)C
• WGK Deutschland: 3
• PubChem CID: 9842609
• Molekulargewicht: 376.29

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Benzene and substituted derivatives
      • Subclass N-phenylureas

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Benzene and substituted derivatives
• Subclass: N-phenylureas
• Intermediate Tree Nodes: Not available
• Direct Parent: N-phenylureas
• Alternative Parents: Dialkylarylamines Aniline and substituted anilines Aminotoluenes Bromobenzenes Aryl bromides Ureas Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: N-phenylurea - Aminotoluene - Aniline or substituted anilines - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Bromobenzene - Halobenzene - Toluene - Aryl bromide - Aryl halide - Urea - Tertiary amine - Amine - Organonitrogen compound - Organobromide - Organohalogen compound - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as n-phenylureas. These are compounds containing a N-phenylurea moiety, which is structurally characterized by a phenyl group linked to one nitrogen atom of a urea group.
• 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

Zugehörige Ziele (menschlich)

TRPV1 Tclin Transient receptor potential cation channel subfamily V member 1 (1 Activities)

Discover Target: TRPV1

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

TRPV1 Tclin Vanilloid receptor (8273 Activities)

Discover Target: TRPV1

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

Liver microsomes (16955 Activities)

Explore this target

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

Zugehörige Ziele (nicht menschlich)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

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

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Solvent:DMSO, Max Conc. mg/mL: 37.63, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 3.76, Max Conc. mM: 10 with gentle warming
• Molekulargewicht: 376.300 g/mol
• XLogP3: 4.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 375.095 Da
• Monoisotopic Mass: 375.095 Da
• Topological Polar Surface Area: 44.400 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 366.000
• 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