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{{short description|Chemical compound}}
{{multiple issues|
{{context|date=April 2014}}
{{one source|date=March 2021}}
}}
{{Drugbox {{Drugbox
| Watchedfields = changed
⚫ | IUPAC_name = 2-(diethylamino)-1-methylethyl (1''S'')-1-hydroxy-1,1'-bi(cyclohexyl)-2-carboxylate
| verifiedrevid = 443791079
⚫ |synonyms = <small>(1''S'')-1-(diethylamino)propan-2-yl 1-hydroxybi(cyclohexane)-2-carboxylate</small>
⚫ | IUPAC_name = 2-(diethylamino)-1-methylethyl (1''S'')-1-hydroxy-1,1'-bi(cyclohexyl)-2-carboxylate
| image = Rociverine.png | image = Rociverine.png
⚫ | CAS_number = 53716-44-2

⚫ | ATC_prefix = A03
<!--Clinical data-->
⚫ | ATC_suffix = AA06
| tradename =
⚫ | PubChem = 68705
| Drugs.com = {{drugs.com|international|rociverine}}
⚫ | DrugBank =
⚫ | pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X -->
⚫ | C=20|H=37|N=1|O=3
⚫ | pregnancy_US = <!-- A / B / C / D / X -->
| molecular_weight = 339.51 g/mol
⚫ | pregnancy_category =
⚫ | bioavailability =
⚫ | legal_AU = <!-- S2, S3, S4, S5, S6, S7, S8, S9 or Unscheduled-->
⚫ | protein_bound =
⚫ | legal_CA = <!-- Schedule I, II, III, IV, V, VI, VII, VIII -->
⚫ | metabolism =
⚫ | legal_UK = <!-- GSL, P, POM, CD, or Class A, B, C -->
⚫ | elimination_half-life =
⚫ | legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V -->
⚫ | excretion =
⚫ | legal_status =
⚫ | pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X -->
⚫ | routes_of_administration =
⚫ | pregnancy_US = <!-- A / B / C / D / X -->

⚫ | pregnancy_category=
<!--Pharmacokinetic data-->
⚫ | legal_AU = <!-- S2, S3, S4, S5, S6, S7, S8, S9 or Unscheduled-->
⚫ | bioavailability =
⚫ | legal_CA = <!-- Schedule I, II, III, IV, V, VI, VII, VIII -->
⚫ | protein_bound =
⚫ | legal_UK = <!-- GSL, P, POM, CD, or Class A, B, C -->
⚫ | metabolism =
⚫ | legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V -->
⚫ | elimination_half-life =
⚫ | legal_status =
⚫ | excretion =
⚫ | routes_of_administration =

<!--Identifiers-->
⚫ | CAS_number = 53716-44-2
⚫ | ATC_prefix = A03
⚫ | ATC_suffix = AA06
⚫ | PubChem = 68705
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
⚫ | DrugBank =
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = VI08KS44V0

<!--Chemical data-->
⚫ | C=20 | H=37 | N=1 | O=3
⚫ | synonyms = <small>(1''S'')-1-(diethylamino)propan-2-yl 1-hydroxybi(cyclohexane)-2-carboxylate</small>
}} }}
{{Unreferenced|date=February 2009}}
'''Rociverine''' is an ].


'''Rociverine''' is an antispasmodic drug used to treat urinary, gastrointestinal and biliary spasms.<ref>{{Cite web |title=Rociverine |url=https://go.drugbank.com/drugs/DB13581}}</ref> It is ] drug.<ref name="pmid582702">{{cite journal | vauthors = Toson G, Schiantarelli P, Murmann W | title = Rociverine, a new antispasmodic agent with balanced neurotropic and myotropic activity | journal = Arzneimittel-Forschung | volume = 28 | issue = 7 | pages = 1130–42 | date = 1978 | pmid = 582702 | doi = | url = }}</ref>
]


The (1R,2R) compound showed 240-fold greater affinity for the muscarinic receptor, but the (1S,2S) compound showed the best selectivity. <ref>{{Cite journal |last=Barbier |first=Pascaline |last2=Renzetti |first2=Anna R. |last3=Turbanti |first3=Luigi |last4=Di Bugno |first4=Cristina |last5=Fornai |first5=Francesco |last6=Vaglini |first6=Francesca |last7=Maggio |first7=Roberto |last8=Corsini |first8=Giovanni U. |date=1995-07 |title=Stereoselective inhibition of muscarinic receptor subtypes by the eight stereoisomers related to rociverine |url=https://linkinghub.elsevier.com/retrieve/pii/0922410695900241 |journal=European Journal of Pharmacology: Molecular Pharmacology |language=en |volume=290 |issue=2 |pages=125–132 |doi=10.1016/0922-4106(95)90024-1}}</ref>
⚫ {{Drugs for functional gastrointestinal disorders}}


==References==
{{Reflist}}


{{pharmacology-stub}}


⚫ {{Drugs for functional gastrointestinal disorders}}
{{Muscarinic acetylcholine receptor modulators}}

]
] ]
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{{gastrointestinal-drug-stub}}

Revision as of 05:45, 27 December 2024

Chemical compound
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Pharmaceutical compound
Rociverine
Clinical data
Other names(1S)-1-(diethylamino)propan-2-yl 1-hydroxybi(cyclohexane)-2-carboxylate
AHFS/Drugs.comInternational Drug Names
ATC code
Identifiers
IUPAC name
  • 2-(diethylamino)-1-methylethyl (1S)-1-hydroxy-1,1'-bi(cyclohexyl)-2-carboxylate
CAS Number
PubChem CID
UNII
CompTox Dashboard (EPA)
ECHA InfoCard100.053.356 Edit this at Wikidata
Chemical and physical data
FormulaC20H37NO3
Molar mass339.520 g·mol
  (verify)

Rociverine is an antispasmodic drug used to treat urinary, gastrointestinal and biliary spasms. It is antimuscarinic drug.

The (1R,2R) compound showed 240-fold greater affinity for the muscarinic receptor, but the (1S,2S) compound showed the best selectivity.

References

  1. "Rociverine".
  2. Toson G, Schiantarelli P, Murmann W (1978). "Rociverine, a new antispasmodic agent with balanced neurotropic and myotropic activity". Arzneimittel-Forschung. 28 (7): 1130–42. PMID 582702.
  3. Barbier, Pascaline; Renzetti, Anna R.; Turbanti, Luigi; Di Bugno, Cristina; Fornai, Francesco; Vaglini, Francesca; Maggio, Roberto; Corsini, Giovanni U. (1995-07). "Stereoselective inhibition of muscarinic receptor subtypes by the eight stereoisomers related to rociverine". European Journal of Pharmacology: Molecular Pharmacology. 290 (2): 125–132. doi:10.1016/0922-4106(95)90024-1. {{cite journal}}: Check date values in: |date= (help)


Drugs for functional gastrointestinal disorders (A03)
Drugs for
functional
bowel
disorders
Antimuscarinics
Tertiary
amino group
Quaternary
ammonium
compounds
Phosphodiesterase
inhibitors
Acting on
serotonin receptors
Other
Belladonna
and derivatives
(antimuscarinics)
Propulsives
Muscarinic acetylcholine receptor modulators
mAChRsTooltip Muscarinic acetylcholine receptors
Agonists
Antagonists
Precursors
(and prodrugs)
See also
Receptor/signaling modulators
Nicotinic acetylcholine receptor modulators
Acetylcholine metabolism/transport modulators
Stub icon

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