Nitrate is a polyatomic ion with the chemical formula NO−3. Salts containing this ion are called nitrates. Nitrates are common components of fertilizers and explosives. Almost all inorganic nitrates are soluble in water. An example of an insoluble nitrate is bismuth oxynitrate.
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InChI=1S/C9H15N5O3/c1-3(15)6(16)4-2-11-7-5(12-4)8(17)14-9(10)13-7/h3-4,6,12,15-16H,2H2,1H3,(H4,10,11,13,14,17)/t3-,4+,6-/m0/s1 |
FNKQXYHWGSIFBK-RPDRRWSUSA-N |
[H][C@@]1(CNc2nc(N)[nH]c(=O)c2N1)[C@@H](O)[C@H](C)O |
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human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via 5,6,7,8-tetrahydrobiopterin )
cofactor
An organic molecule or ion (usually a metal ion) that is required by an enzyme for its activity. It may be attached either loosely (coenzyme) or tightly (prosthetic group).
coenzyme
A low-molecular-weight, non-protein organic compound participating in enzymatic reactions as dissociable acceptor or donor of chemical groups or electrons.
(via 5,6,7,8-tetrahydrobiopterin )
prosthetic group
A tightly bound, specific nonpolypeptide unit in a protein determining and involved in its biological activity.
(via 5,6,7,8-tetrahydrobiopterin )
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diagnostic agent
A substance administered to aid diagnosis of a disease.
nutraceutical
A product in capsule, tablet or liquid form that provide essential nutrients, such as a vitamin, an essential mineral, a protein, an herb, or similar nutritional substance.
(via 5,6,7,8-tetrahydrobiopterin )
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View more via ChEBI Ontology
(6R)-2-amino-6-[(1R,2S)-1,2-dihydroxypropyl]-5,6,7,8-tetrahydropteridin-4(3H)-one
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sapropterin
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ChemIDplus
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sapropterina
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ChemIDplus
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sapropterinum
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ChemIDplus
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(−)-(6R)-2-amino-6-((1R,2S)-1,2-dihydroxypropyl)-5,6,7,8-tetrahydro-4(3H)-pteridinone
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ChemIDplus
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(6R)-L-erythro-5,6,7,8-tetrahydrobiopterin
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UniProt
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(6R)-L-erythro-tetrahydrobiopterin
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ChEBI
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2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)-pteridinone
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KEGG COMPOUND
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5,6,7,8-Tetrahydrobiopterin
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KEGG COMPOUND
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6R-5,6,7,8-tetrahydrobiopterin
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ChemIDplus
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6R-BH4
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ChEBI
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6R-L-5,6,7,8-tetrahydrobiopterin
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ChemIDplus
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R-THBP
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ChEBI
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tetrahydrobiopterin
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DrugBank
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2612
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DrugCentral
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C00018229
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KNApSAcK
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C00272
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KEGG COMPOUND
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CPD-14053
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MetaCyc
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D08505
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KEGG DRUG
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DB00360
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DrugBank
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EP191335
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Patent
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H4B
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PDBeChem
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HMDB0000787
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HMDB
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Sapropterin
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Wikipedia
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US4713454
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Patent
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View more database links |
17528-72-2
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CAS Registry Number
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KEGG COMPOUND
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27070-47-9
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CAS Registry Number
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ChemIDplus
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4699705
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Reaxys Registry Number
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Reaxys
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10333495
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PubMed citation
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SUBMITTER
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1297822
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PubMed citation
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Europe PMC
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16510994
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PubMed citation
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SUBMITTER
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19627172
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PubMed citation
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Europe PMC
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21466737
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PubMed citation
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Europe PMC
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21646032
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PubMed citation
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Europe PMC
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22110560
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PubMed citation
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Europe PMC
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22112818
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PubMed citation
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Europe PMC
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22310224
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PubMed citation
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Europe PMC
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22388642
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PubMed citation
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Europe PMC
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22391997
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PubMed citation
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Europe PMC
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22575621
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PubMed citation
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Europe PMC
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22832064
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PubMed citation
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Europe PMC
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23235653
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PubMed citation
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Europe PMC
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23266371
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PubMed citation
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Europe PMC
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23430527
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PubMed citation
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Europe PMC
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23430545
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PubMed citation
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Europe PMC
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23436109
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PubMed citation
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Europe PMC
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23462988
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PubMed citation
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Europe PMC
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23690520
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PubMed citation
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Europe PMC
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23705856
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PubMed citation
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Europe PMC
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23712020
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Europe PMC
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23743404
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PubMed citation
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Europe PMC
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4004257
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PubMed citation
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Europe PMC
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