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Compound InformationSONAR Target prediction
Name:

ADENOSINE PHOSPHATE

Unique Identifier:SPE01500667
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:333.11 g/mol
X log p:1.065  (online calculus)
Lipinksi Failures1
TPSA85.66
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:12
Rotatable Bond Count:4
Canonical Smiles:Nc1ncnc2n(cnc12)C1OC(COP(O)(O)=O)C(O)C1O
Class:alkaloid
Source:widespread in living tissue
Therapeutics:vasodilator, neuromodulator
Generic_name:Adenosine-5--Monophosphate
Chemical_iupac_name:[5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxyphosphonic acid
Drug_type:Experimental
Kegg_compound_id:C00020
Drugbank_id:EXPT00362
Melting_point:183-188 oC
H2o_solubility:Soluble
Logp:-1.6
Cas_registry_number:61-19-8
Drug_category:Dietary supplement; Micronutrient
Indication:For nutritional supplementation, also for treating dietary shortage or imbalance
Pharmacology:Adenosine monophosphate, also known as 5--adenylic acid and abbreviated AMP, is a
nucleotide that is found in RNA. It is an ester of phosphoric acid with the
nucleoside adenosine. AMP consists of the phosphate group, the pentose sugar ribose,
and the nucleobase adenine. AMP is used as a dietary supplement to boost immune
activity, and is also used as a substitute sweetener to aid in the maintenance of a
low-calorie diet.
Mechanism_of_action:Nucleotides such as Adenosine-5--Monophosphate affect a number of immune functions,
including the reversal of malnutrition and starvation-induced immunosuppression, the
enhancement of T-cell maturation and function, the enhancement of natural killer
cell activity, the improvement of delayed cutaneous hypersensitivity, helping
resistance to such infectious agents as Staphylococcus aureus and Candida albicans,
and finally the modulation of T-cell responses toward type 1 CD4 helper lymphocytes
or Th1 cells. Studies have shown that mice fed a nucleotide-free diet have both
impaired humoral and cellular immune responses. The addition of dietary nucleotides
normalizes both types of responses. RNA, a delivery form of nucleotides, and
ribonucleotides were used in these studies. The mechanism of the immune-enhancing
activity of nucleic acids/nucleotides is not clear.
Organisms_affected:Humans and other mammals

Found: 33 active | as graph: single | with analogs 2 3 4 5 6 7 8 9 10  Next >> [33]
Species: 4932
Condition: BY4741-3rd
Replicates: 2
Raw OD Value: r im 0.9200±0.036416
Normalized OD Score: sc h 0.8662±0.0317314
Z-Score: -5.3484±0.998255
p-Value: 0.00000172202
Z-Factor: -5.65929
Fitness Defect: 13.272
Bioactivity Statement: Active
Experimental Conditions
Library:Spectrum_ED
Plate Number and Position:1|F5
Drug Concentration:50.00 nM
OD Absorbance:595 nm
Robot Temperature:30.00 Celcius
Date:2010-08-10 YYYY-MM-DD
Plate CH Control (+):0.09±0.00250
Plate DMSO Control (-):0.9574999999999999±0.01026
Plate Z-Factor:0.9662
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DBLink | Rows returned: 242 3 4 Next >> 
224 [5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxyphosphonic acid
6083 [(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxyphosphonic acid
20712 disodium (2R,3R,4R,5R)-2-(6-aminopurin-9-yl)-5-(phosphonatooxymethyl)oxolane-3,4-diol
26054 sodium (2R,3R,4R,5R)-2-(6-aminopurin-9-yl)-5-[(hydroxy-oxido-phosphoryl)oxymethyl]oxolane-3,4-diol
34768 [(2R,3R,4S,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxyphosphonic acid
37080 potassium (2R,3R,4R,5R)-2-(6-aminopurin-9-yl)-5-[(hydroxy-oxido-phosphoryl)oxymethyl]oxolane-3,4-diol

internal high similarity DBLink | Rows returned: 1
LOPAC 00694 0.9421

active | Cluster 9750 | Additional Members: 25 | Rows returned: 3
Prest466 0.433333333333333
SPE01502238 0.423728813559322
Prest983 0

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