Lanthionine is a nonproteinogenic amino acid with the chemical formula (HOOC-CH(NH2)-CH2-S-CH2-CH(NH2)-COOH). It is typically formed by a cysteine residue and a dehydrated serine residue. Despite its name, lanthionine does not contain the element lanthanum. |
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InChI=1S/C22H26F3N3OS/c23- 22(24,25) 17- 6- 7- 21- 19(16- 17) 28(18- 4- 1- 2- 5- 20(18) 30- 21) 9- 3- 8- 26- 10- 12- 27(13- 11- 26) 14- 15- 29/h1- 2,4- 7,16,29H,3,8- 15H2 |
PLDUPXSUYLZYBN-UHFFFAOYSA-N |
OCCN1CCN(CCCN2c3ccccc3Sc3ccc(cc23)C(F)(F)F)CC1 |
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Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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anticoronaviral agent
Any antiviral agent which inhibits the activity of coronaviruses.
dopaminergic antagonist
A drug that binds to but does not activate dopamine receptors, thereby blocking the actions of dopamine or exogenous agonists.
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phenothiazine antipsychotic drug
dopaminergic antagonist
A drug that binds to but does not activate dopamine receptors, thereby blocking the actions of dopamine or exogenous agonists.
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View more via ChEBI Ontology
2-(4-{3-[2-(trifluoromethyl)-10H-phenothiazin-10-yl]propyl}piperazin-1-yl)ethan-1-ol
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fluphenazine
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KEGG DRUG
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fluphenazinum
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ChemIDplus
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1-(2-hydroxyethyl)-4-(3-(trifluoromethyl-10-phenothiazinyl)propyl)-piperazine
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ChemIDplus
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10-(3'-(4''-(β-hydroxyethyl)-1''-piperazinyl)-propyl)-3-trifluoromethylphenothiazine
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ChemIDplus
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10-(3-(2-hydroxyethyl)piperazinopropyl)-2-(trifluoromethyl)phenothiazine
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NIST Chemistry WebBook
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2-(4-(3-[2-(trifluoromethyl)-10H-phenothiazin-10-yl]propyl)-1-piperazinyl)ethanol
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NIST Chemistry WebBook
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2-(trifluoromethyl)-10-(3-(1-(β-hydroxyethyl)-4-piperazinyl)propyl)phenothiazine
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ChemIDplus
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4-(3-(-trifluoromethyl-10-phenothiazyl)-propyl)-1-piperazineethanol
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ChemIDplus
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4-(3-(2-(trifluoromethyl)-10H-phenothiazin-10-yl)propyl)-1-piperazineethanol
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ChemIDplus
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4-(3-(2-trifluoromethyl-10-phenothiazyl)-propyl)-1-piperazineethanol
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ChemIDplus
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flufenazina
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ChemIDplus
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Fluorfenazine
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DrugBank
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Fluorophenazine
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DrugBank
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Fluorphenazine
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DrugBank
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Fluphenazine
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KEGG COMPOUND
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Triflumethazine
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DrugBank
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1189506
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Beilstein Registry Number
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Beilstein
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1231182
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Gmelin Registry Number
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Gmelin
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61643
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Reaxys Registry Number
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Reaxys
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69-23-8
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CAS Registry Number
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NIST Chemistry WebBook
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69-23-8
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CAS Registry Number
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ChemIDplus
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13950763
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PubMed citation
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Europe PMC
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16117689
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PubMed citation
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Europe PMC
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1650428
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PubMed citation
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Europe PMC
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16839522
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PubMed citation
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Europe PMC
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25595294
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PubMed citation
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Europe PMC
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5128930
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PubMed citation
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Europe PMC
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