Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 131682생성일: 2026년 10월 27일
Safinamide
(4-((3-fluorobenzyl)oxy)benzyl)-L-alanine · CS-484 · FCE 26743 · SAFINAMID · 603-772-2 · Safinamide · EMD 1195686 · Salfenamide
https://huagongshe.com/ko/chemical/131682
식별자 및 물리적 특성
| CAS No. | 133865-89-1 |
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| 분자식 | C17H19FN2O2 |
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| 평균 분자량 | 302.34 g/mol |
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| 단동위원소 질량 | 302.14305607 g/mol |
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| SMILES | C[C@H](NCc1ccc(OCc2cccc(F)c2)cc1)C(N)=O |
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| InChIKey | NEMGRZFTLSKBAP-LBPRGKRZSA-N |
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| PubChem CID | 131682 |
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| ChEMBL | CHEMBL396778 |
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| ChEBI | CHEBI:134718 |
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| EC No. | 603-772-2 |
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| DTXSID | DTXSID601010282 |
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화학 및 물리적 성질
| XLogP | 2.2 |
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| 극성 표면적 | 64.4 |
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| 수소 결합 공여자 수 | 2 |
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| 수소 결합 수용자 수 | 4 |
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| 회전 가능 결합 수 | 7 |
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| 무거운 원자 수 | 22 |
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| 형식 전하 | 0 |
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| 복잡도 | 346 |
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| 의약품 | Pharmaceuticals -> Nervous system -> Anti-parkinson drugsPharmaceuticals -> Listed in ZINC15 |
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| Human Drugs | BreastfeedingLactationAntiparkinson AgentsMonoamine Oxidase InhibitorsFDA approved drugs -> Active ingredientEMA approved medicines: Human medicine |
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| 녹는점 | 208-212° |
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| 끓는 점 | 476.7±40.0 °C(Predicted) |
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| 밀도 | 1.189±0.06 g/cm3(Predicted) |
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| 저장 조건 | under inert gas (nitrogen or Argon) at 2–8 °C |
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| 용해도 | DMSO에 용해됩니다(최대 50mg/ml). |
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| 물리적 상태 | 고체 |
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| pKa(산도 계수) | 16.03±0.50(Predicted) |
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| 색상 | 하얀색 |
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| Merck | 14,8315 |
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| 안정성 | 최대 3개월 동안 -20°의 DMSO에 보관 |
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| InChI | InChI=1S/C17H19FN2O2/c1-12(17(19)21)20-10-13-5-7-16(8-6-13)22-11-14-3-2-4-15(18)9-14/h2-9,12,20H,10-11H2,1H3,(H2,19,21)/t12-/m0/s1 |
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| InChIKey | NEMGRZFTLSKBAP-LBPRGKRZSA-N |
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| SMILES | C(N)(=O)[C@@H](NCC1=CC=C(OCC2=CC=CC(F)=C2)C=C1)C |
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안전 및 규제
| GHS 분류 | DangerH301 (90.5%): Toxic if swallowed [Danger Acute toxicity, oral]P264, P264+P265, P270, P273, P280, P301+P316, P305+P354+P338, P317, P321, P330, P391, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 42 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies. |
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| 규제 정보 | Status: Active Update: 02-08-2019 https://echa.europa.eu/registration-dossier/-/registered-dossier/21292 |
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| Hazard Classes and Categories | Acute Tox. 3 (90.5%) |
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| Hepatotoxicity | Safinamide has been reported to cause serum enzyme elevations in a small proportion of patients treated long term, although the abnormalities were usually mild and self-limiting and were usually no more frequent than with placebo or comparator agents. Safinamide has not been implicated in cases of acute liver injury, but such instances have been reported with nonspecific MAO inhibitors. |
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| Effects During Pregnancy and Lactation | ◉ Summary of Use during Lactation |
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| RTECS 번호 | TX1457385 |
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| 관세 코드 | 2924.29.7790 |
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용도
역사
Safinamide is an α-aminoamide derivative with a multimodal mechanism of action involving both dopaminergic and non-dopaminergic properties. It increases levels of available dopamine through dopamine reuptake inhibition andMAO-B inhibition. It is a potent and reversible inhibitor of MAO-B, with significantly greater selectivity for MAO-B over MAO-A than selegiline and rasagiline. However, it also has an important and novel mode of action that involves blockade of Na+ channels andmodulation of Ca2+ channels that inhibits glutamate release and therefore may provide a level of cognitive improvement and neuroprotection. Homeostatic interactions between dopamine and glutamate are central to the normal physiology of the basal ganglia. In PD, this relationship is altered, resulting in upregulation of cortico-striatal glutamatergic function in l-dopa-induced dyskinesia. Any drug that can counteract such unbalance in glutamate function is potentially useful in controlling dyskinesias. Safinamide was originated by Farmitalia Carlo Erba, a company that was later purchased by Pharmacia. Newron Pharmaceuticals was established as a spin-off of Pharmacia in 1999 and acquired safinamide rights and intellectual property from Pharmacia Corporation. Newron originally granted Serono exclusive worldwide rights to develop, manufacture, and commercialize safinamide in 2006. However, in October 2011, Merck Serono agreed to return full global rights for safinamide to Newron. Newron then finalized a strategic collaboration and license agreement with Zambon for the worldwide development and commercialization of safinamide.