ADENYLIC ACID
- Product Name
- ADENYLIC ACID
- CAS No.
- 67583-85-1
- Chemical Name
- ADENYLIC ACID
- Synonyms
- 2'(3')-AMP;NSC 210570;ADENYLIC ACID;2'(3')-Adenylic acid;ADENOSINE MONOPHOSPHATE;Adenosine 2'(3')-Phosphate;ADENOSINE 2'-3'-MONOPHOSPHATE;ADENOSIDE-2'(3')-PHOSPHORIC ACID;ADENOSINE-2' AND 3'-MONOPHOSPHATE;ADENOSINE-2'(3')-MONOPHOSPHORIC ACID
- CBNumber
- CB0467614
- Molecular Formula
- C20H28N10O14P2
- Formula Weight
- 694.44
- MOL File
- 67583-85-1.mol
ADENYLIC ACID Property
- storage temp.
- −20°C
- CAS DataBase Reference
- 67583-85-1
Safety
- WGK Germany
- 3
- RTECS
- AU7480300
N-Bromosuccinimide Price
- Product number
- 16062
- Product name
- Adenosine 2''(3'')-monophosphate
- Purity
- ≥95% (mixture of isomers)
- Packaging
- 100 mg
- Price
- $56
- Updated
- 2024/03/01
- Product number
- 16062
- Product name
- Adenosine 2''(3'')-monophosphate
- Purity
- ≥95% (mixture of isomers)
- Packaging
- 250 mg
- Price
- $121
- Updated
- 2024/03/01
- Product number
- 16062
- Product name
- Adenosine 2''(3'')-monophosphate
- Purity
- ≥95% (mixture of isomers)
- Packaging
- 500 mg
- Price
- $229
- Updated
- 2024/03/01
- Product number
- 001666
- Product name
- Adenosine Monophosphate
- Packaging
- 50mg
- Price
- $460
- Updated
- 2021/12/16
ADENYLIC ACID Chemical Properties,Usage,Production
Definition
ChEBI: Adenosine 5'-monophosphate is a purine ribonucleoside 5'-monophosphate having adenine as the nucleobase. It has a role as an EC 3.1.3.11 (fructose-bisphosphatase) inhibitor, an EC 3.1.3.1 (alkaline phosphatase) inhibitor, an adenosine A1 receptor agonist, a nutraceutical, a micronutrient, a fundamental metabolite and a cofactor. It is an adenosine 5'-phosphate and a purine ribonucleoside 5'-monophosphate. It is a conjugate base of an adenosine 5'-monophosphate(1+). It is a conjugate acid of an adenosine 5'-monophosphate(2-).
Agricultural Uses
Adenosine monophosphate (AMP) is a phosphate compound formed by the hydrolysis of covalent bonds of adenosine triphosphate (ATP) molecules (linking to adenosine and 3-phosphate groups by N-glycosidic linkage and phosphodiester bonds respectively), by the process of dephosphorylation.