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99% Quality Adenosine Monophosphate with Safe Delivery/ CAS: 61-19-8

  • CAS No.: 61-19-8
  • Purity: 99%
  • Min quantity: 1 Kilograms
  • Price: USD 100~2000/Kilograms
  • Place of Orign: Shenzhen,Guangdong,China
Ms.Cathy Zhang

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  • Product Name.:99% Quality Adenosine Monophosphate with Safe Delivery/ CAS: 61-19-8
  • CAS No: 61-19-8
  • Weight: 347.221222
  • Formula: C10H14N5O7P
  • Melting Point: 178-185 ºC
  • Boiling Point: 798.518°C at 760 mmHg
  • Density: 2.32 g/cm3

Details

99% Quality Adenosine Monophosphate with Safe Delivery/ CAS: 61-19-8

Adenosine MonophosphateSynonyms:5'-Adenylic acid; Adenosine-5'-monophosphoric acid; AMP
Adenosine Monophosphate Molecular Formula :C10H14N5O7P
Adenosine Monophosphate Molecular Weight :347.22
Product Name: Adenosine 5'-monophosphate
Adenosine Monophosphate CAS: 61-19-8
Adenosine Monophosphate EINECS No.: 200-500-0
Adenosine Monophosphate Purity: 99%
Adenosine Monophosphate Appearance White or white crystalline powder
Adenosine Monophosphate Dry weight loss ≤ 6.0%
A250/260 0.76 ~ 0.80
A280/260 0.14 ~ 0.16
Total number of colonies ≤ 1000cfu/g
E. Coli ≤ 40MPN/100g
Mold, yeast ≤ 25cfu/g
Heavy metals (Pb) ≤ 10 ppm
Arsenic ≤ 2 ppm
Pathogenic bacteria NONE

Description:

Dexamethasone is a synthetic corticosteroid with approximately 25 times the anti-inflammatory potency of naturally occurring cortisol. The IUPAC Name of it is (8S,9R,10S,11S,13S,14S,16R,17R)-9-Fluoro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl6,7,8,11,12,14,15, octahydrocyclopenta[a]phenanthren-3-one. Dexamethasone commonly is used in both small- and large-animal veterinary medicine. It may be given by injection, inhalation orally or topically. Preparations for topical use may include other active ingredients such as antibiotics, antifungals or miticides.

Main applications: Infant milk powder, spices and pharmaceutical intermediates

Use: As intermediates of nucleic acid series drug, health food, and biochemical reagents, it's also used to produce Adenosine triphosphate, Cyclic adenosine monophosphate and so on. It has good function on hemangiectasis and bringing blood pressure down.

Adenosine monophosphate (AMP), also known as 5'-adenylic acid, is a nucleotide that is used as a monomer in DNA and RNA. It is an ester of phosphoric acid and the nucleoside adenosine. AMP consists of a phosphate group, the sugar ribose, and the nucleobase adenine. As a substituent it takes the form of the prefix adenylyl-.
AMP can also exist as a cyclic structure known as cyclic AMP (or cAMP). Within certain cells the enzyme adenylate cyclase makes cAMP from ATP, and typically this reaction is regulated by hormones such as glucagon. cAMP plays an important role in intracellular signaling.

Adenosine monophosphate (AMP) deaminase deficiency is a condition that can affect the muscles used for movement (skeletal muscles). People with this condition do not make enough of an enzyme called AMP deaminase. In most people, AMP deaminase deficiency does not cause any symptoms. People who do experience symptoms typically have muscle pain (myalgia) or weakness after exercise or prolonged physical activity. They often get tired more quickly and stay tired longer than would normally be expected. Some affected individuals have more severe symptoms, but it is unclear whether these symptoms are due solely to a lack of AMP deaminase or additional factors. Muscle weakness is typically apparent beginning in childhood or early adulthood.
Researchers have proposed three types of AMP deaminase deficiency, which are distinguished by their symptoms and genetic cause.

AMP deaminase deficiency is one of the most common inherited muscle disorders in white populations, affecting 1 in 50 to 100 people. The prevalence is lower in African Americans, affecting an estimated 1 in 40,000 people, and the condition is even less common in the Japanese population.

This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.

1. Triethanolamine buffer, 0.1M, pH 7.6: 1.86 g TEA HCl in 80 ml distilled water. Adjust to pH 7.6 with 1.0 M NaOH, adjust volume to 100 ml with distilled water.
2. 14mM NADH:10 mg NADH-Na2 with 1 ml distilled water.
3. 16.5 mM ATP: 10 mg NADH-Na2 in 1 ml distilled water.
4. 0.5 M MgSO4/2 M KCl: 1.23 g MgSO4 7 H2O and 1.49 g KCl in 10 ml distilled water.
5. 32 mM Phosphoenolpyruvate: 15 mg PEP-(CHA)3 in 1 ml MgSO4/KCl.
6. LDH, from rabbit muscle: 5 mg protein/ml (550 U/mg).
7. Pyruvate kinase, from rabbit muscle: 10 mg protein/ml (200 U/mg).
8. Myokinase, from rabbit muscle: 5 mg protein/ml (360 U/mg).



99% Quality Adenosine Monophosphate with Safe Delivery/ CAS: 61-19-8

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