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피라진카르복스아미드,6-플루오로-3,4-디히드로-3-옥소-(9CI)

6-Fluoro-3-hydroxypyrazine-2-carboxamide

HCID 492405
노트반응

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기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
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기본 정보

CAS
259793-96-9
표준 SMILES
NC(=O)c1nc(F)c[nH]c1=O
InChIKey
ZCGNOVWYSGBHAU-UHFFFAOYSA-N
분자식
C5H4FN3O2
평균 분자량
157.104 g/mol
단동위원소 질량
157.02875459

이름 및 식별자

우선 이름
6-Fluoro-3-hydroxypyrazine-2-carboxamide
IUPAC
6-Fluoro-3-hydroxypyrazine-2-carboxamide
현지명
피라진카르복스아미드,6-플루오로-3,4-디히드로-3-옥소-(9CI)
영어명
Favipiravir
분자식
C5H4FN3O2
분자량
157.1

이름 및 동의어

피라진카르복스아미드,6-플루오로-3,4-디히드로-3-옥소-(9CI)6-Fluoro-3-hydroxypyrazine-2-carboxamideT-7056-fluoro-3,4-dihydro-3-oxo-PyrazinecarboxamideAviganFavipiravi6-fluoro-3,4-dihydro-3-oxo- (9CI)6-Fluoro-3-hydroxy-2-pyrazinecarboxamidePyrazinecarboxamide, 6-fluoro-3,4-dihydro-3-oxo- (9CI)Farapiwe3-Dithian

데이터베이스 식별자

CAS
259793-96-9
PubChem CID
492405
DTXSID
DTXSID60948878
ChEMBL
CHEMBL221722
ChEBI
CHEBI:134722
UNII
EW5GL2X7E0
EC Number
856-840-0
Nikkaji
J1.636.682J

물성

물리화학적 성질

녹는점
151 °C · >151°C (dec.)
밀도
1.78 · 1.78±0.1 g/cm3(Predicted)
저장 조건
2 · under inert gas (nitrogen or Argon) at 2-8°C
용해도
DMSO(30mg/mL), 물(가온 시 12mg/mL)에 용해됨
산도 계수 (pKa)
8.77 · 8.77±0.60(Predicted)
물리적 상태
고체
색상
회백색
안정성
1 · 제공된 대로 구매일로부터 1년 동안 안정적입니다. DMSO 또는 물에 용해된 용액은 -20°에서 최대 3개월 동안 보관할 수 있습니다.
InChI
InChI=1S/C5H4FN3O2/c6-2-1-8-5(11)3(9-2)4(7)10/h1H,(H2,7,10)(H,8,11)
InChIKey
ZCGNOVWYSGBHAU-UHFFFAOYSA-N
SMILES
C1(C(N)=O)=NC(F)=CNC1=O

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

안전 데이터

wgk
WGK 3
Hazard Classifications
Muta. 2Repr. 2
스토리지 클래스
11 - Combustible Solids

화학 및 산업

응용 분야 · 3건

개요Favipiravir, 6-fluoro-3-hydroxypyrazine-2-carboxamide, is a new broad-spectrum antiviral drug targeting RNA-dependent RNA polymerase (RdRp) developed by Japan's Toyama Chemical Pharmaceutical Company. It was approved for marketing in Japan in March 2014 for the treatment of new and recurrent influenza. During the outbreak of the new coronavirus, the results of the Phase I clinical study of the drug published in March 2020 showed that the drug may have the effect of speeding up virus clearance to alleviate the progress of new coronavirus pneumonia.

역사Favipiravir was originally developed in the late 1990s by a company that was later purchased by the Japanese firm Fujifilm as part of its transition from the photo business to healthcare. After being tested against a range of viruses, the drug was approved in Japan in 2014 for emergency use against flu epidemics or to treat new strains of influenza.

용도Favipiravir is used for the treatment of advanced Ebola virus infection in a small animal model. It suppressed the replication of Zaire Ebola virus and prevented a lethal outcome in 100% of the animals. Based on the studies, Favipiravir can be a candidate for the treatment of Ebola hemorrhagic fever. Favipiravir can be used for antiviral treatment of influenza A and B. Studies have shown that in addition to influenza virus, the drug also exhibits good antiviral activity against a variety of RNA viruses, such as Ebola virus, arena virus, Bunia virus, rabies virus and now COVID-19.

상·하류 제품 정보

상류 원료

수산화나트륨3-Aminopyrazine-2-carboxylic acidAminopyrazineMethyl 3-amino-6-bromopyrazine-2-carboxylate메틸6-브로모-3-메톡시피라진-2-카르복실레이트

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추가 설명 · 1건

정의ChEBI: Favipiravir is a member of the class of pyrazines that is pyrazine substituted by aminocarbonyl, hydroxy and fluoro groups at positions 2, 3 and 6, respectively. It is an anti-viral agent that inhibits RNA-dependent RNA polymerase of several RNA viruses and is approved for the treatment of influenza in Japan. It has a role as an antiviral drug, an anticoronaviral agent and an EC 2.7.7.48 (RNA-directed RNA polymerase) inhibitor. It is a primary carboxamide, a hydroxypyrazine and an organofluorine compound.