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[[(2R,3R,4S,5S)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
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group of stereoisomers with the chemical formula C₁₀H₁₆N₅O₁₃P₃
Attributes
Values
rdf:type
Item
description
groep van stereo-isomeren
(nl)
група стереоізомерів з хімічною формулою C₁₀H₁₆N₅O₁₃P₃
(uk)
group of stereoisomers with the chemical formula C₁₀H₁₆N₅O₁₃P₃
(en)
rdfs:label
[[(2R,3R,4S,5S)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
(en)
skos:prefLabel
[[(2R,3R,4S,5S)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
(en)
name
[[(2R,3R,4S,5S)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
(en)
isomeric SMILES
wds:Q105378464-CAB76E48-B5FD-4139-A339-7ED0282E331A
isomeric SMILES
Nc1ncnc2c1ncn2[C@H]1O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)[C@H](O)[C@@H]1O
instance of
wds:Q105378464-31F12659-D6C2-4BCA-8DA5-6DCCEFCBDC16
instance of
group of stereoisomers
subclass of
wds:Q105378464-A4BC44E1-77B8-47A1-86EB-484CC971783E
subclass of
purine nucleotides
found in taxon
wds:Q105378464-291F3F57-AAC8-46A3-935B-008D4AD3780C
wds:Q105378464-339509AD-F608-4271-A452-20F01F9277EB
wds:Q105378464-361F1797-71CD-473B-B325-1DE8C14AB545
wds:Q105378464-3957C7E2-B53D-4067-8050-4E2EE60FDAFD
wds:Q105378464-7B19921E-201C-4886-9A51-3E809B0DD9EB
found in taxon
Humulus lupulus
Oryza sativa
Escherichia coli
Arabidopsis thaliana
Phaseolus vulgaris
UniChem compound ID
wds:Q105378464-51E87A2D-6CA4-4656-9EB6-EC77D139B83F
canonical SMILES
wds:Q105378464-D5B14266-A5A3-4E49-A939-070522FE13FF
InChI
wds:Q105378464-52C169FA-E3BF-4B07-8FD6-6DBF1B208D8E
InChIKey
wds:Q105378464-C8C05DCE-2356-43AF-B58F-9C1E00483CBF
chemical formula
wds:Q105378464-E8FF2DB1-F77E-4098-BB06-4BD09E443021
PubChem CID
wds:Q105378464-C384A330-39D1-4312-80E0-0DA25B7BECAE
PubChem CID
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23638216
UniChem compound ID
66972428
canonical SMILES
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC1OC(N2C=NC=3C(=NC=NC32)N)C(O)C1O
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6+,7+,10+/m1/s1
InChIKey
ZKHQWZAMYRWXGA-ASCDQALMSA-N
chemical formula
C₁₀H₁₆N₅O₁₃P₃
PubChem CID
23638216
mass
wds:Q105378464-2D6C0593-AF7F-4642-8916-CE73DC3892B7
mass
506.995745462
(
xsd:decimal
)
is
about
of
https://www.wikidata.org/wiki/Special:EntityData/Q105378464
is
main subject
of
Simultaneous determination of the main metabolites in rice leaves using capillary electrophoresis mass spectrometry and capillary electrophoresis diode array detection
Metabolite Profiling of Root Exudates of Common Bean under Phosphorus Deficiency
Molecular and catalytic properties of Arabidopsis thaliana adenylyl sulfate (APS)-kinase
Trehalose 6-phosphate is indispensable for carbohydrate utilization and growth in Arabidopsis thaliana
Purification and properties of the chloroplastic form of biotin holocarboxylase synthetase from Arabidopsis thaliana overexpressed in Escherichia coli
Biosynthesis of methionine-derived glucosinolates in Arabidopsis thaliana: recombinant expression and characterization of methylthioalkylmalate synthase, the condensing enzyme of the chain-elongation cycle
A protein phosphatase 2C involved in ABA signal transduction in Arabidopsis thaliana.
The role of inorganic phosphate in the development of freezing tolerance and the acclimatization of photosynthesis to low temperature is revealed by the pho mutants of Arabidopsis thaliana
Sugar-induced increases in trehalose 6-phosphate are correlated with redox activation of ADPglucose pyrophosphorylase and higher rates of starch synthesis in Arabidopsis thaliana
Molecular cloning, expression, and characterization of adenylate isopentenyltransferase from hop (Humulus lupulus L.).
The Arabidopsis thylakoid ADP/ATP carrier TAAC has an additional role in supplying plastidic phosphoadenosine 5'-phosphosulfate to the cytosol
Anaerobic Growth Yields of Aerobacter cloacae and Escherichia coli
Arabidopsis chloroplasts dissimilate L-arginine and L-citrulline for use as N source
is
main subject
of
wds:Q44739855-762932A7-FF13-417B-ADCF-7586975CF231
wds:Q30999357-524177B7-BF50-4573-8B14-0A158F0D4755
wds:Q38336366-942200E3-1F01-4780-9B8C-FDA02DEE0B81
wds:Q42407854-26965A39-ABB5-42A5-9116-656D9B6D3246
wds:Q58062372-1F1280F0-8260-466F-AA5A-EEAD8114A04D
wds:Q42110256-94F176BD-0AB1-4579-A7F7-85D2B850BE81
wds:Q72699089-838AF904-4D61-41E5-B8DD-DB9F774BF805
wds:Q33206722-FBD3F932-8F43-474B-A8B6-37FB247CF0F6
wds:Q35144517-07313E1A-40C4-41CA-8591-58E5F6095B02
wds:Q77750984-A2D1B513-F374-4C56-AED6-AC5C7AC61BDE
wds:Q105378463-812B9DF5-945D-4123-B211-519FB9AB9DB1
wds:Q48081852-C910B09F-B841-474D-A1AC-F0B70AF9BBBC
wds:Q85241367-B9385C1E-E4C3-4D39-8DA4-63A0BDC04C8C
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