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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

Safinamide 분자 구조식

식별자 및 물리적 특성

CAS No.133865-89-1
분자식C17H19FN2O2
평균 분자량302.34 g/mol
단동위원소 질량302.14305607 g/mol
SMILESC[C@H](NCc1ccc(OCc2cccc(F)c2)cc1)C(N)=O
InChIKeyNEMGRZFTLSKBAP-LBPRGKRZSA-N
PubChem CID131682
ChEMBLCHEMBL396778
ChEBICHEBI:134718
EC No.603-772-2
DTXSIDDTXSID601010282

화학 및 물리적 성질

XLogP2.2
극성 표면적64.4
수소 결합 공여자 수2
수소 결합 수용자 수4
회전 가능 결합 수7
무거운 원자 수22
형식 전하0
복잡도346
의약품Pharmaceuticals -> Nervous system -> Anti-parkinson drugsPharmaceuticals -> Listed in ZINC15
Human DrugsBreastfeedingLactationAntiparkinson AgentsMonoamine Oxidase InhibitorsFDA approved drugs -> Active ingredientEMA approved medicines: Human medicine
녹는점208-212°
끓는 점476.7±40.0 °C(Predicted)
밀도1.189±0.06 g/cm3(Predicted)
저장 조건under inert gas (nitrogen or Argon) at 2–8 °C
용해도DMSO에 용해됩니다(최대 50mg/ml).
물리적 상태고체
pKa(산도 계수)16.03±0.50(Predicted)
색상하얀색
Merck14,8315
안정성최대 3개월 동안 -20°의 DMSO에 보관
InChIInChI=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
InChIKeyNEMGRZFTLSKBAP-LBPRGKRZSA-N
SMILESC(N)(=O)[C@@H](NCC1=CC=C(OCC2=CC=CC(F)=C2)C=C1)C

안전 및 규제

GHS 분류DangerH301 (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.
규제 정보Status: Active Update: 02-08-2019 https://echa.europa.eu/registration-dossier/-/registered-dossier/21292
Hazard Classes and CategoriesAcute Tox. 3 (90.5%)
HepatotoxicitySafinamide 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.
Effects During Pregnancy and Lactation◉ Summary of Use during Lactation
RTECS 번호TX1457385
관세 코드2924.29.7790

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.