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Details

Stereochemistry ACHIRAL
Molecular Formula C18H30N2O2
Molecular Weight 306.443
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTACAINE

SMILES

CCCCN(CCCC)CCCOC(=O)C1=CC=C(N)C=C1

InChI

InChIKey=HQFWVSGBVLEQGA-UHFFFAOYSA-N
InChI=1S/C18H30N2O2/c1-3-5-12-20(13-6-4-2)14-7-15-22-18(21)16-8-10-17(19)11-9-16/h8-11H,3-7,12-15,19H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C18H30N2O2
Molecular Weight 306.443
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Keratitis from misuse of corneal anesthetics.
1968 Aug 22
Selective dopaminergic vulnerability: 3,4-dihydroxyphenylacetaldehyde targets mitochondria.
2001 Apr 15
Managing patients with local anesthetic complications using alternative methods.
2002 May-Jun
PAMPA - excipient classification gradient map.
2006 Nov
Solubility-excipient classification gradient maps.
2007 Mar
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
The specific activities of two transferases, aspartate-amino-transferase and creatine phosphokinase, are increased by 10(-5) mol/l butacaine
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:24:02 GMT 2023
Edited
by admin
on Fri Dec 15 16:24:02 GMT 2023
Record UNII
Z84S23CGJJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTACAINE
INN   MI   VANDF   WHO-DD  
INN  
Official Name English
BUTACAINE [VANDF]
Common Name English
butacaine [INN]
Common Name English
Butacaine [WHO-DD]
Common Name English
1-PROPANOL, 3-(DIBUTYLAMINO)-, 4-AMINOBENZOATE (ESTER)
Common Name English
BUTACAINE [MI]
Common Name English
NSC-758632
Code English
3-(DIBUTYLAMINO)-1-PROPANOL P-AMINOBENZOATE (ESTER)
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C245
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
CFR 21 CFR 524.1580C
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C87457
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
NSC
758632
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
DRUG BANK
DB11502
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
ECHA (EC/EINECS)
205-734-7
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
MERCK INDEX
m2780
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY Merck Index
FDA UNII
Z84S23CGJJ
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
WIKIPEDIA
BUTACAINE
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
PUBCHEM
2480
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
SMS_ID
100000088471
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
ChEMBL
CHEMBL129529
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
INN
381
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
EPA CompTox
DTXSID3045300
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
EVMPD
SUB05994MIG
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
CAS
149-16-6
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
RXCUI
1829
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY RxNorm
DRUG CENTRAL
3050
Created by admin on Fri Dec 15 16:24:02 GMT 2023 , Edited by admin on Fri Dec 15 16:24:02 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY