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Adenylyl-(3'-5')-adenylyl-(3'-5')-adenosine, also known as cyclic AMP or cAMP, is a cyclic nucleotide that plays a crucial role in intracellular signaling. It is derived from adenosine triphosphate (ATP) through the action of adenylate cyclase, an enzyme that catalyzes the conversion of ATP to cAMP. cAMP acts as a second messenger within cells, relaying signals from hormones and neurotransmitters to various cellular processes. It binds to proteins called protein kinases, which in turn phosphorylate other proteins, leading to a cascade of events that regulate cellular functions such as metabolism, gene expression, and cell growth. The degradation of cAMP is facilitated by the enzyme phosphodiesterase, which breaks down cAMP into 5'-AMP, thus terminating the signal. This intricate balance between synthesis and degradation ensures that cAMP levels are tightly regulated, allowing for precise control over cellular responses.

917-44-2

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917-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 917-44-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,1 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 917-44:
(5*9)+(4*1)+(3*7)+(2*4)+(1*4)=82
82 % 10 = 2
So 917-44-2 is a valid CAS Registry Number.

917-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Adenosine, adenylyl-(3'→5')-adenylyl-(3'→5')-

1.2 Other means of identification

Product number -
Other names ApApA

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:917-44-2 SDS

917-44-2Upstream product

917-44-2Relevant academic research and scientific papers

Synthesis and structural characterization of diastereomeric isomers of RNA trimer adenylyl(3′-5′)adenylyl(3′-5′)adenosine

Urata, Hidehito,Hara, Hisafumi,Hirata, Yoshihiro,Ohmoto, Norihiko,Akagi, Masao

, p. 2908 - 2917 (2007/10/03)

We have synthesized the diastereomeric isomers of adenylyl(3′- 5′)adenylyl(3′-5′)adenosine (ApApA), and investigated their helical structures and hybridization properties with d-poly(U) by circular dichroism (CD) and UV melting experiments. The configurat

Nucleotides, XVII. Synthesis of Homogeneous Adenosyl-3',5'-oligomers by the Phosphotriester Method

Flockerzi, Dieter,Uhlmann, Eugen,Pfleiderer, Wolfgang

, p. 2018 - 2030 (2007/10/02)

The chemical synthesis of the fully protected trimer 12, the tetramers 11 and 23 as well as the pentamer 14 was achieved in preparative scales starting from the fully blocked adenosine-3'-phosphotriesters 1, 2, and N6-benzoyl-2',3'-bis-O-(tert-

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