CHEBI:34954 - (S)-ropivacaine hydrochloride hydrate

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ChEBI Name (S)-ropivacaine hydrochloride hydrate
ChEBI ASCII Name (S)-ropivacaine hydrochloride hydrate
Definition The monohydrate form of (S)-ropivacaine hydrochloride.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C17H29ClN2O2
Net Charge 0
Average Mass 328.87700
Monoisotopic Mass 328.19176
InChI InChI=1S/C17H26N2O.ClH.H2O/c1-4-11-19-12-6-5-10-15(19)17(20)18-16-13(2)8-7-9-14(16)3;;/h7-9,15H,4-6,10-12H2,1-3H3,(H,18,20);1H;1H2/t15-;;/m0../s1
SMILES O.[Cl-].CCC[NH+]1CCCC[C@H]1C(=O)Nc1c(C)cccc1C
Roles Classification
Application(s): local anaesthetic
Any member of a group of drugs that reversibly inhibit the propagation of signals along nerves. Wide variations in potency, stability, toxicity, water-solubility and duration of action determine the route used for administration, e.g. topical, intravenous, epidural or spinal block.
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ChEBI Ontology
Outgoing (S)-ropivacaine hydrochloride hydrate (CHEBI:34954) has part (S)-ropivacaine hydrochloride (anhydrous) (CHEBI:60803)
(S)-ropivacaine hydrochloride hydrate (CHEBI:34954) has role local anaesthetic (CHEBI:36333)
(S)-ropivacaine hydrochloride hydrate (CHEBI:34954) is a hydrate (CHEBI:35505)
(2S)-2-[(2,6-dimethylphenyl)carbamoyl]-1-propylpiperidinium chloride—water(1/1)
(2S)-N-(2,6-dimethylphenyl)-1-propylpiperidine-2-carboxamide hydrochloride—water (1/1)
Synonyms Sources
(S)-(−)-1-propyl-2',6'-pipecoloxylidine hydrochloride monohydrate ChemIDplus
(S)-(−)-1-propylpiperidine-2-carboxylic acid (2,6-dimethylphenyl)amide hydrochloride monohydrate ChemIDplus
(S)-ropivacaine hydrochloride monohydrate ChEBI
L-N-(2,6-dimethylphenyl)-1-propyl-2-piperidinocarboxamide hydrochloride monohydrate ChEBI
L-ropivacaine hydrochloride monohydrate ChEBI
ropivacaine hydrochloride ChemIDplus
ropivacaine hydrochloride hydrate ChemIDplus
ropivacaine hydrochloride monohydrate ChemIDplus
Brand Name Source
Naropin DrugBank
Manual Xrefs Databases
DB00296 DrugBank
WO2009044404 Patent
View more database links
Registry Numbers Types Sources
132112-35-7 CAS Registry Number KEGG DRUG
132112-35-7 CAS Registry Number ChemIDplus
5421768 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
18179827 PubMed citation Europe PMC
18374550 PubMed citation Europe PMC
18754438 PubMed citation Europe PMC
18812844 PubMed citation Europe PMC
19128713 PubMed citation Europe PMC
19501560 PubMed citation Europe PMC
21428705 PubMed citation Europe PMC
Last Modified
25 July 2011