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Details

Stereochemistry RACEMIC
Molecular Formula C22H33NO3.ClH
Molecular Weight 395.963
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CYCLOMETHYCAINE HYDROCHLORIDE

SMILES

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

InChI

InChIKey=UFWWXJRCWHOHOQ-UHFFFAOYSA-N
InChI=1S/C22H33NO3.ClH/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;/h11-14,18,20H,2-10,15-17H2,1H3;1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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 ( + / - )

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

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Cell to substrate adhesion and spreading: inhibition by cationic anesthetics.
1975 Apr
In vitro release of therapeutically active ingredients from polymer matrixes.
1976 Oct
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 Fri Dec 15 18:45:09 GMT 2023
Edited
by admin
on Fri Dec 15 18:45:09 GMT 2023
Record UNII
2FYK6V755H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CYCLOMETHYCAINE HYDROCHLORIDE
MI  
Common Name English
3-(2-METHYLPIPERIDINO)PROPYL P-(CYCLOHEXYLOXY)BENZOATE HYDROCHLORIDE (1:1)
Common Name English
CYCLOMETHYCAINE HYDROCHLORIDE [MI]
Common Name English
CYCLOMETHYCAINE HCL
Common Name English
BENZOIC ACID, 4-(CYCLOHEXYLOXY)-, 3-(2-METHYL-1-PIPERIDINYL)PROPYL ESTER HYDROCHLORIDE (1:1)
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C245
Created by admin on Fri Dec 15 18:45:09 GMT 2023 , Edited by admin on Fri Dec 15 18:45:09 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID90968463
Created by admin on Fri Dec 15 18:45:09 GMT 2023 , Edited by admin on Fri Dec 15 18:45:09 GMT 2023
PRIMARY
FDA UNII
2FYK6V755H
Created by admin on Fri Dec 15 18:45:09 GMT 2023 , Edited by admin on Fri Dec 15 18:45:09 GMT 2023
PRIMARY
MERCK INDEX
m1098
Created by admin on Fri Dec 15 18:45:09 GMT 2023 , Edited by admin on Fri Dec 15 18:45:09 GMT 2023
PRIMARY Merck Index
PUBCHEM
10838
Created by admin on Fri Dec 15 18:45:09 GMT 2023 , Edited by admin on Fri Dec 15 18:45:09 GMT 2023
PRIMARY
NCI_THESAURUS
C83643
Created by admin on Fri Dec 15 18:45:09 GMT 2023 , Edited by admin on Fri Dec 15 18:45:09 GMT 2023
PRIMARY
CAS
537-61-1
Created by admin on Fri Dec 15 18:45:09 GMT 2023 , Edited by admin on Fri Dec 15 18:45:09 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY