U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C22H23N3O4
Molecular Weight 393.4357
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ERLOTINIB

SMILES

COCCOC1=CC2=C(C=C1OCCOC)C(NC3=CC(=CC=C3)C#C)=NC=N2

InChI

InChIKey=AAKJLRGGTJKAMG-UHFFFAOYSA-N
InChI=1S/C22H23N3O4/c1-4-16-6-5-7-17(12-16)25-22-18-13-20(28-10-8-26-2)21(29-11-9-27-3)14-19(18)23-15-24-22/h1,5-7,12-15H,8-11H2,2-3H3,(H,23,24,25)

HIDE SMILES / InChI

Molecular Formula C22H23N3O4
Molecular Weight 393.4357
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:26:04 UTC 2023
Edited
by admin
on Fri Dec 15 16:26:04 UTC 2023
Record UNII
J4T82NDH7E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ERLOTINIB
EMA EPAR   INN   MI   VANDF   WHO-DD  
INN  
Official Name English
N-(3-ETHYNYLPHENYL)-6,7-BIS(2-METHOXYETHOXY)QUINAZOLIN-4-AMINE
Systematic Name English
CP-358774
Code English
RG-1415
Code English
ERLOTINIB [EMA EPAR]
Common Name English
R-1415
Code English
Erlotinib [WHO-DD]
Common Name English
CP-35877401
Code English
ERLOTINIB [MI]
Common Name English
erlotinib [INN]
Common Name English
ERLOTINIB [VANDF]
Common Name English
4-QUINAZOLINAMINE, N-(3-ETHYNYLPHENYL)-6,7-BIS(2-METHOXYETHOXY)-
Systematic Name English
CP-358,774
Code English
Classification Tree Code System Code
NCI_THESAURUS C2167
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
NDF-RT N0000175605
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
WHO-VATC QL01XE03
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
WHO-ATC L01XE03
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
LIVERTOX NBK548407
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
NCI_THESAURUS C129825
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
NDF-RT N0000175076
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
EMA ASSESSMENT REPORTS TARCEVA (AUTHORIZED: PANCREATIC NEOPLASMS)
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
EMA ASSESSMENT REPORTS TARCEVA (AUTHORISED: CARCINOMA, NON-SMALL-CELL LUNG)
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
Code System Code Type Description
DRUG BANK
DB00530
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
DAILYMED
J4T82NDH7E
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
CAS
183321-74-6
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
ChEMBL
CHEMBL553
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
IUPHAR
4920
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
NCI_THESAURUS
C65530
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
INN
8133
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
SMS_ID
100000089519
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
DRUG CENTRAL
1045
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
MERCK INDEX
m5000
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID8046454
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
CHEBI
53509
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
HSDB
8082
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
MESH
C400278
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
LACTMED
Erlotinib
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
CHEBI
114785
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
WIKIPEDIA
ERLOTINIB
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
FDA UNII
J4T82NDH7E
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
RXCUI
337525
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY RxNorm
EVMPD
SUB16423MIG
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
PUBCHEM
176870
Created by admin on Fri Dec 15 16:26:04 UTC 2023 , Edited by admin on Fri Dec 15 16:26:04 UTC 2023
PRIMARY
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