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2-Fluoro-ATP, also known as 2-fluoroadenosine 5'-triphosphate, is a chemical compound that is structurally similar to adenosine triphosphate (ATP), the primary energy currency of cells. The key difference is the presence of a fluorine atom at the 2' position of the ribose sugar moiety. This modification can significantly alter the compound's properties and interactions within biological systems. 2-Fluoro-ATP is often used in biochemical research to study the effects of ATP on various enzymes and cellular processes, as its unique structure can provide insights into the mechanisms of ATP binding and hydrolysis. It may also have potential applications in the development of drugs targeting ATP-dependent processes, although its use in such contexts would require careful consideration of its biochemical properties and potential side effects.

1492-62-2

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1492-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1492-62-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1492-62:
(6*1)+(5*4)+(4*9)+(3*2)+(2*6)+(1*2)=82
82 % 10 = 2
So 1492-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H15FN5O13P3/c11-10-14-7(12)4-8(15-10)16(2-13-4)9-6(18)5(17)3(27-9)1-26-31(22,23)29-32(24,25)28-30(19,20)21/h2-3,5-6,9,17-18H,1H2,(H,22,23)(H,24,25)(H2,12,14,15)(H2,19,20,21)/t3-,5-,6-,9-/m1/s1

1492-62-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [[(2R,3S,4R,5R)-5-(6-amino-2-fluoropurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

1.2 Other means of identification

Product number -
Other names 2-Fluoro-ATP

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1492-62-2 SDS

1492-62-2Downstream Products

1492-62-2Relevant academic research and scientific papers

Enzymatic synthesis and 19F NMR studies of 2-fluoroadenine- substituted RNA

Scott, Lincoln G.,Geierstanger, Bernhard H.,Williamson, James R.,Hennig, Mirko

, p. 11776 - 11777 (2004)

The production of isotopically labeled RNA remains critical to current NMR structural studies. One approach to obtain simple NMR spectra is to label with a nucleus that is not naturally occurring in RNA. Fluorine-19 can serve as a sensitive site-specific probe upon incorporation into RNA. Here we report the efficient in vitro enzymatic synthesis of 2-fluoroadenosine-5′-triphosphate and its incorporation into the HIV-2 transactivation region (TAR) of RNA by DNA template-directed transcription using phage T7 RNA polymerase. We provide unequivocal evidence for this 19F-substituted base analogue capability to selectively interact with uracil, forming 2F-A-U base pairs in RNA. The introduction of a 2-fluoroadenyl substitution is relatively nonperturbing and provides us with uniquely positioned, sensitive NMR reporter groups to monitor structural changes in the local RNA environment. Copyright

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