추천 제품
![(S)-(−)-9,10-Difluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid 97%](/deepweb/assets/sigmaaldrich/product/structures/177/773/83bb0da1-8f11-4fd8-8f74-d32b5f43f2ab/640/83bb0da1-8f11-4fd8-8f74-d32b5f43f2ab.png)
![1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) >95% in F+ active](/deepweb/assets/sigmaaldrich/product/structures/206/487/53d52ee5-ef71-4e9a-9bc8-938b68b98d5d/640/53d52ee5-ef71-4e9a-9bc8-938b68b98d5d.png)
분석
97%
mp
320-322 °C (lit.)
SMILES string
CC1COc2c(F)c(F)cc3C(=O)C(=CN1c23)C(O)=O
InChI
1S/C13H9F2NO4/c1-5-4-20-12-9(15)8(14)2-6-10(12)16(5)3-7(11(6)17)13(18)19/h2-3,5H,4H2,1H3,(H,18,19)
InChI key
NVKWWNNJFKZNJO-UHFFFAOYSA-N
유전자 정보
human ... CSNK2A1(1457)
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
(S)-(-)-9,10-Difluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid may be used in the preparation of the following:
- kynurenine aminotransferase II (KAT II) inhibitor, [(S)-(-)-9-(4-aminopiperazine-1-yl)-8-fluoro-3-methyl-6-oxo-2,3,5,6-tetrahydro-4H-1-oxa-3a-aza-phenalene-5-carboxylic acid]
- fused-ring derivatives
- N-desmethyllevofloxacin
신호어
Warning
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
On the relationship between the two branches of the kynurenine pathway in the rat brain in vivo.
Amori L, et al.
Journal of Neurochemistry, 109(2), 316-325 (2009)
7-Piperazinylquinolones with methylene-bridged nitrofuran scaffold as new antibacterial agents.
Emami S, et al.
Medicinal Chemistry Research, 22(12), 5940-5947 (2013)
Andriy G Golub et al.
Journal of medicinal chemistry, 49(22), 6443-6450 (2006-10-27)
Due to the emerging role of protein kinase CK2 as a molecule that participates not only in the development of some cancers but also in viral infections and inflammatory failures, small organic inhibitors of CK2, besides application in scientific research
Muhammad Malik et al.
Antimicrobial agents and chemotherapy, 54(12), 5214-5221 (2010-09-22)
Quinolones rapidly kill bacteria by two mechanisms, one that requires protein synthesis and one that does not. The latter, which is measured as lethal action in the presence of the protein synthesis inhibitor chloramphenicol, is enhanced by N-1 cyclopropyl and
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