SIB-1893
SIB-1893 | |
| 식별자 | |
|---|---|
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| CAS 번호 | |
| 펍켐 CID | |
| 켐스파이더 | |
| 유니 | |
| 켐벨 | |
| 화학 및 물리적 데이터 | |
| 공식 | C14H13N |
| 어금질량 | 195.265 g·190−1 |
| 3D 모델(JSmol) | |
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 (이게 뭐야?) (iii) | |
SIB-1893은 과학 연구에 사용된 약물로, 메타방성 글루탐산 수용체 하위형 mGluR의5 선택적 길항제 역할을 하는 최초의 화합물 중 하나이다.[1]항경련제 및 신경보호 효과가 있으며 글루타민제 방출을 감소시킨다.[2][3]또한 mGluR의4 포지티브 알로스테릭 모듈레이터 역할을 하는 것으로 밝혀졌다.[4]
참조
- ^ Varney MA, Cosford ND, Jachec C, Rao SP, Sacaan A, Lin FF, Bleicher L, Santori EM, Flor PJ, Allgeier H, Gasparini F, Kuhn R, Hess SD, Veliçelebi G, Johnson EC (July 1999). "SIB-1757 and SIB-1893: selective, noncompetitive antagonists of metabotropic glutamate receptor type 5". The Journal of Pharmacology and Experimental Therapeutics. 290 (1): 170–81. PMID 10381773.
- ^ Chapman AG, Nanan K, Williams M, Meldrum BS (July 2000). "Anticonvulsant activity of two metabotropic glutamate group I antagonists selective for the mGlu5 receptor: 2-methyl-6-(phenylethynyl)-pyridine (MPEP), and (E)-6-methyl-2-styryl-pyridine (SIB 1893)". Neuropharmacology. 39 (9): 1567–74. doi:10.1016/S0028-3908(99)00242-7. PMID 10854901.
- ^ Wang SJ, Sihra TS (June 2004). "Noncompetitive metabotropic glutamate5 receptor antagonist (E)-2-methyl-6-styryl-pyridine (SIB1893) depresses glutamate release through inhibition of voltage-dependent Ca2+ entry in rat cerebrocortical nerve terminals (synaptosomes)". The Journal of Pharmacology and Experimental Therapeutics. 309 (3): 951–8. doi:10.1124/jpet.103.064881. PMID 14982967.
- ^ Mathiesen JM, Svendsen N, Bräuner-Osborne H, Thomsen C, Ramirez MT (March 2003). "Positive allosteric modulation of the human metabotropic glutamate receptor 4 (hmGluR4) by SIB-1893 and MPEP". British Journal of Pharmacology. 138 (6): 1026–30. doi:10.1038/sj.bjp.0705159. PMC 1573757. PMID 12684257.
