ChemicalBook--->CAS DataBase List--->211096-49-0

211096-49-0

211096-49-0 Structure

211096-49-0 Structure
IdentificationBack Directory
[Name]

GSK-CXCR2
[CAS]

211096-49-0
[Synonyms]

GSK-CXCR2
SB 265610
SB265610 >=98% (HPLC)
N-(2-Bromophenyl)-N'-(7-cyano-1H-benzotriazol-4-yl)urea
Urea, N-(2-bromophenyl)-N'-(4-cyano-1H-benzotriazol-7-yl)-
1-(2-Bromophenyl)-3-(4-cyano-1H-benzo[d] [1,2,3]triazol-7-yl)urea
[Molecular Formula]

C14H9BrN6O
[MDL Number]

MFCD09971124
[MOL File]

211096-49-0.mol
[Molecular Weight]

357.16
Chemical PropertiesBack Directory
[Boiling point ]

527.0±45.0 °C(Predicted)
[density ]

1.77±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: soluble15mg/mL, clear
[form ]

powder
[pka]

6.13±0.40(Predicted)
[color ]

white to light brown
[InChI]

1S/C14H9BrN6O/c15-9-3-1-2-4-10(9)17-14(22)18-11-6-5-8(7-16)12-13(11)20-21-19-12/h1-6H,(H2,17,18,22)(H,19,20,21)
[InChIKey]

SEDUMQWZEOMXSO-UHFFFAOYSA-N
[SMILES]

Brc1ccccc1NC(=O)Nc2ccc(C#N)c3nn[nH]c23
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Hazard InformationBack Directory
[Uses]

SB 265610 is an anti-tumor pharmaceutical developed to act as an antagonist to cysteine-amino acid-cysteine (CXC) chemokines receptor 2 antagonist.
[Biological Activity]

Potent CXCR2 antagonist that inhibits CINC-1-mediated but not C5a-mediated Ca 2+ mobilization (IC 50 values are 3.4 and 6800 nM respectively). Inhibits CINC-induced chemotaxis and attenuates neutrophil accumulation in inflammatory lung injury in vivo .
[Biochem/physiol Actions]

SB265610 is a potent and selective CXCR2 chemokine receptor antagonist. It has a Kd = 2.5 nM.
[in vivo]

SB-265610 (2 mg/kg/day; i.p.; daily; for two weeks) treatment significantly inhibits the recruitment of Gr-1+CD11b+ cells to the mammary adenocarcinoma with Tgfbr2 deletion but not the control tumors[3].

Animal Model:MMTV-PyVmT/Tgfbr2MGKO and MMTV-PyVmT/Tgfbr2flox/flox tumors from donor mice[3]
Dosage:2 mg/kg/day
Administration:Intraperitoneal injection; daily; for two weeks
Result:Significantly inhibited the recruitment of Gr-1+CD11b+ cells to the mammary adenocarcinoma.
[IC 50]

CXCR2
[storage]

Store at RT
Spectrum DetailBack Directory
[Spectrum Detail]

GSK-CXCR2(211096-49-0)1HNMR
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