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Merck
CN

A4659

Adenosine 5′-monophosphate sodium salt

from equine muscle, crystalline, suitable for cell culture

Synonym(s):

5′-Adenylic acid, A-5′-P, AMP

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About This Item

Empirical Formula (Hill Notation):
C10H14N5O7P · xNa+ · yH2O
CAS Number:
Molecular Weight:
347.22 (anhydrous free acid basis)
UNSPSC Code:
12352200
PubChem Substance ID:
eCl@ss:
32160414
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biological source

equine muscle

assay

99-100%

form

crystalline

technique(s)

cell culture | mammalian: suitable

storage temp.

−20°C

SMILES string

NC1=NC=NC2=C1N=CN2[C@H]3[C@H](O)[C@H](O)[C@]((COP(O)(O)=O)([H])O3.C.

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Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Shudong Liu et al.
PloS one, 10(5), e0124951-e0124951 (2015-05-02)
Our previous study found that thyroid-stimulating hormone promoted sterol regulatory element-binding protein-2 (SREBP-2) expression and suppressed AMP-activated protein kinase (AMPK) activity in the liver, but it was unclear whether there was a direct link between TSH, AMPK and SREBP-2. Here
Misaki Kawanishi et al.
Biomedical chromatography : BMC, 29(9), 1309-1316 (2015-01-28)
Monitoring of pharmacodynamics in addition to pharmacokinetics is one of strategies to individualize mycophenolate mofetil therapy. The purpose of this study was to develop sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods for evaluation of the pharmacokinetics and pharmacodynamics of mycophenolic

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