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Details

Stereochemistry RACEMIC
Molecular Formula C22H33NO3.H2O4S
Molecular Weight 457.581
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CYCLOMETHYCAINE BISULFATE

SMILES

OS(O)(=O)=O.CC1CCCCN1CCCOC(=O)C2=CC=C(OC3CCCCC3)C=C2

InChI

InChIKey=FEBLWCUYHGPGOW-UHFFFAOYSA-N
InChI=1S/C22H33NO3.H2O4S/c1-18-8-5-6-15-23(18)16-7-17-25-22(24)19-11-13-21(14-12-19)26-20-9-3-2-4-10-20;1-5(2,3)4/h11-14,18,20H,2-10,15-17H2,1H3;(H2,1,2,3,4)

HIDE SMILES / InChI

Molecular Formula C22H33NO3
Molecular Weight 359.5023
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula H2O4S
Molecular Weight 98.078
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Cyclomethycaine (also known as Surfacaine) is a local anesthetic.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
CYCLOMETHYCAINE sulfate.
1957 May 18
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:15:17 GMT 2023
Edited
by admin
on Sat Dec 16 05:15:17 GMT 2023
Record UNII
7323N7T136
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CYCLOMETHYCAINE BISULFATE
Common Name English
3-(2-METHYLPIPERIDINO)PROPYL P-(CYCLOHEXYLOXY)BENZOATE SULFATE (1:1)
Common Name English
BENZOIC ACID, 4-(CYCLOHEXYLOXY)-, 3-(2-METHYL-1-PIPERIDINYL)PROPYL ESTER SULFATE (1:1)
Common Name English
3-(2-METHYLPIPERIDINO)PROPYL 4-CYCLOHEXYLOXYBENZOATE HYDROGEN SULFATE
Systematic Name English
CYCLOMETHYCAINE HYDROGEN SULFATE
Common Name English
CYCLOMETHYCAINE SULFATE [MART.]
Common Name English
Code System Code Type Description
NCI_THESAURUS
C75089
Created by admin on Sat Dec 16 05:15:17 GMT 2023 , Edited by admin on Sat Dec 16 05:15:17 GMT 2023
PRIMARY
PUBCHEM
3084954
Created by admin on Sat Dec 16 05:15:17 GMT 2023 , Edited by admin on Sat Dec 16 05:15:17 GMT 2023
PRIMARY
CAS
50978-10-4
Created by admin on Sat Dec 16 05:15:17 GMT 2023 , Edited by admin on Sat Dec 16 05:15:17 GMT 2023
PRIMARY
FDA UNII
7323N7T136
Created by admin on Sat Dec 16 05:15:17 GMT 2023 , Edited by admin on Sat Dec 16 05:15:17 GMT 2023
PRIMARY
EPA CompTox
DTXSID60965247
Created by admin on Sat Dec 16 05:15:17 GMT 2023 , Edited by admin on Sat Dec 16 05:15:17 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY