| Identification | Back Directory | [Name]
4-IODO-N-[4-METHOXY-3-(4-METHYL-1-PIPERAZINYL)PHENYL]BENZENESULFONAMIDE HYDROCHLORIDE | [CAS]
209480-63-7 | [Synonyms]
SB258585HCl SB 258585 hydrochlor SB 258585 HYDROCHLORIDE Benzenesulfonamide, 4-iodo-N-[4-methoxy-3-(4-methyl-1-piperazinyl)phenyl]- 4-IODO-N-[4-METHOXY-3-(4-METHYL-1-PIPERAZINYL)PHENYL]BENZENESULFONAMIDE HYDROCHLORIDE | [Molecular Formula]
C18H22IN3O3S | [MDL Number]
MFCD06798382 | [MOL File]
209480-63-7.mol | [Molecular Weight]
487.36 |
| Hazard Information | Back Directory | [Uses]
SB 258585 is a selective and potent SR-6 and 5-HT6R antagonist. | [Biological Activity]
Potent and selective 5-HT 6 receptor antagonist (pK i = 8.6); displays > 160-fold selectivity over other 5-HT receptor subtypes. | [References]
[1] WARREN D HIRST. Characterization of [125I]-SB-258585 binding to human recombinant and native 5-HT6 receptors in rat, pig and human brain tissue[J]. British Journal of Pharmacology, 2009, 130 7: 1597-1605. DOI: 10.1038/sj.bjp.0703458 [2] CAROL ROUTLEDGE. Characterization of SB-271046: A potent, selective and orally active 5-HT6 receptor antagonist[J]. British Journal of Pharmacology, 2009, 130 7: 1606-1612. DOI: 10.1038/sj.bjp.0703457 [3] AYAKA TATARA. Modulation of antipsychotic-induced extrapyramidal side effects by medications for mood disorders[J]. Progress in Neuro-Psychopharmacology & Biological Psychiatry, 2012, 38 2: Pages 252-259. DOI: 10.1016/j.pnpbp.2012.04.008 [4] FANNY DUHR. Cdk5 induces constitutive activation of 5-HT6 receptors to promote neurite growth[J]. Nature chemical biology, 2014, 10 7: 590-597. DOI: 10.1038/nchembio.1547 [5] SAKI SHIMIZU. Interaction between anti-Alzheimer and antipsychotic drugs in modulating extrapyramidal motor disorders in mice[J]. Journal of pharmacological sciences, 2015, 127 4: Pages 439-445. DOI: 10.1016/j.jphs.2015.03.004 |
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