5'-P-FLUOROSULFONYL-BENZOYLADENOSINE HYDROCHLORIDE

Product Name
5'-P-FLUOROSULFONYL-BENZOYLADENOSINE HYDROCHLORIDE
CAS No.
78859-42-4
Chemical Name
5'-P-FLUOROSULFONYL-BENZOYLADENOSINE HYDROCHLORIDE
Synonyms
FSBA;5'-FSBA;5'-Fluorosulfonylbenzoyladenosine;5'-p-Fluorosulfonylbenzoyl adenosine;5’-(4-(fluorosulfonyl)benzoyl)adenosine;5'-(4-Fluorosulfonylbenzoyl)adenosine HCI;5'-O-[4-(Fluorosulfonyl)benzoyl]adenosine;5'-(4-Fluorosulfonylbenzoyl)adenosine HCl;5'-P-FLUOROSULFONYL-BENZOYLADENOSINE HYDROCHLORIDE;5'-(4-FLUOROSULFONYLBENZOYL)ADENOSINE HYDROCHLORIDE
CBNumber
CB7671319
Molecular Formula
C17H17ClFN5O7S
Formula Weight
489.86
MOL File
78859-42-4.mol
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5'-P-FLUOROSULFONYL-BENZOYLADENOSINE HYDROCHLORIDE Property

storage temp. 
-20°C
solubility 
methanol: 50 mg/mL, clear, slightly yellow
BRN 
8178939
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Safety

Hazard Codes 
T
Risk Statements 
45-20/21/22-36/37/38
Safety Statements 
53-22-26-36/37/39-45-24/25
WGK Germany 
3
F 
10
HS Code 
29349990
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
F9128
Product name
5′-(4-Fluorosulfonylbenzoyl)adenosine hydrochloride
Packaging
25mg
Price
$547
Updated
2024/03/01
Sigma-Aldrich
Product number
F9128
Product name
5′-(4-Fluorosulfonylbenzoyl)adenosine hydrochloride
Packaging
100mg
Price
$1680
Updated
2024/03/01
Sigma-Aldrich
Product number
F9128
Product name
5′-(4-Fluorosulfonylbenzoyl)adenosine hydrochloride
Packaging
500mg
Price
$6630
Updated
2024/03/01
TRC
Product number
F599218
Product name
5′-(4-Fluorosulfonylbenzoyl)adenosine hydrochloride
Packaging
5mg
Price
$240
Updated
2021/12/16
TRC
Product number
F599218
Product name
5′-(4-Fluorosulfonylbenzoyl)adenosine hydrochloride
Packaging
0.5mg
Price
$45
Updated
2021/12/16
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5'-P-FLUOROSULFONYL-BENZOYLADENOSINE HYDROCHLORIDE Chemical Properties,Usage,Production

Chemical Properties

Off-white powder

Uses

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.

Biochem/physiol Actions

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.

5'-P-FLUOROSULFONYL-BENZOYLADENOSINE HYDROCHLORIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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5'-P-FLUOROSULFONYL-BENZOYLADENOSINE HYDROCHLORIDE Suppliers

China 9 India 1 Switzerland 1 United Kingdom 3 United States 6 Global 20
J & K SCIENTIFIC LTD.
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010-82848833 400-666-7788
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TargetMol Chemicals Inc.
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Energy Chemical
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TargetMol Chemicals Inc.
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marketing@tsbiochem.com
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Suzhou Zhixin Biotechnology Co., Ltd.
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0512-65118909 15162312715
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sales@szzxbio.com
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78859-42-4, 5'-P-FLUOROSULFONYL-BENZOYLADENOSINE HYDROCHLORIDERelated Search:

L-Adenosine Adenosine Tetrahydrofurfuryl benzoate Adenosinehydrochloride 4-(FLUOROSULFONYL)BENZOIC ACID Methyl 4-Mercaptobenzoate Adenine Sulfate (S)-3-AMINO-1,2-DIHYDROXYPROPANE HYDROCHLORIDE Adenine hydrochloride hemihydrate (R)-4-BENZYLOXY-1,2-BUTANEDIOL Adenine hydrochloride P-TOLUENESULFONYL FLUORIDE 5'-P-FLUOROSULFONYL-BENZOYLADENOSINE HYDROCHLORIDE

  • 5’-(4-(fluorosulfonyl)benzoyl)adenosine
  • 5'-P-FLUOROSULFONYL-BENZOYLADENOSINE HYDROCHLORIDE
  • ADENOSINE-5'-(4-FLUOROSULFONYLBENZOATE) HYDROCHLORIDE
  • 5'-(4-FLUOROSULFONYLBENZOYL)ADENOSINE HYDROCHLORIDE
  • FSBA
  • Adenosine-5μ-(4-fluorosulfonylbenzoate) hydrochloride, FSBA
  • 5'-Fluorosulfonylbenzoyladenosine
  • 5'-FSBA
  • 5'-O-[4-(Fluorosulfonyl)benzoyl]adenosine
  • 5'-p-Fluorosulfonylbenzoyl adenosine
  • 5'-(4-Fluorosulfonylbenzoyl)adenosine HCI
  • 5'-(4-Fluorosulfonylbenzoyl)adenosine HCl
  • 78859-42-4
  • C17H16FN5O7SHCl
  • C17H16FN5O7SHCI
  • Nucleoside Analogs
  • Nucleosides, Nucleotides, Oligonucleotides
  • Organic Covalent Modifiers
  • Enzymes, Inhibitors, and Substrates
  • Enzyme Inhibitors
  • Enzyme Inhibitors by Type
  • BioChemical
  • Biochemicals and Reagents