F9128
5′-(4-Fluorosulfonylbenzoyl)adenosine hydrochloride
동의어(들):
Adenosine-5′-(4-fluorosulfonylbenzoate) hydrochloride, FSBA
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About This Item
실험식(Hill 표기법):
C17H16FN5O7S · HCl
CAS Number:
Molecular Weight:
489.86
Beilstein:
8178939
MDL number:
UNSPSC 코드:
41106305
PubChem Substance ID:
NACRES:
NA.51
생물학적 소스
synthetic (organic)
Quality Level
분석
≥95% (TLC)
양식
powder
solubility
methanol: 50 mg/mL, clear, colorless
저장 온도
−20°C
SMILES string
Cl[H].Nc1ncnc2n(cnc12)[C@@H]3O[C@H](COC(=O)c4ccc(cc4)S(F)(=O)=O)[C@@H](O)[C@H]3O
InChI
1S/C17H16FN5O7S.ClH/c18-31(27,28)9-3-1-8(2-4-9)17(26)29-5-10-12(24)13(25)16(30-10)23-7-22-11-14(19)20-6-21-15(11)23;/h1-4,6-7,10,12-13,16,24-25H,5H2,(H2,19,20,21);1H/t10-,12-,13-,16-;/m1./s1
InChI key
ZUHVYHQVJYIHPN-KHXPSBENSA-N
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애플리케이션
5′-(4-Fluorosulfonylbenzoyl)adenosine (FSBA) is an ATP analog used to study the mechanism of action of wortmannin. FSBA has been used to study vesicular transport in intestinal cells such as Caco-2, and to covalently modify residues in the nucleotide-binding domains (NBDs) of various ATPases, kinases, and other proteins.
5′-(4-Fluorosulfonylbenzoyl)adenosine hydrochloride has been used to incubate with Ime2 (inducer of meiosis 2) to determine the sensitivity of Ime2 to the adenosine triphosphate (ATP) analog 5′-fluorosulfonylbenzoyladenosine (FSBA).
생화학적/생리학적 작용
5′-(4-Fluorosulfonylbenzoyl)adenosine helps to recognize adenosine triphosphate (ATP)-binding sites in kinases due to its reaction with nucleophilic amino acids happening within these motifs.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
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