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Details

Stereochemistry ACHIRAL
Molecular Formula C22H24BrFN4O2
Molecular Weight 475.354
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VANDETANIB

SMILES

COC1=CC2=C(C=C1OCC3CCN(C)CC3)N=CN=C2NC4=CC=C(Br)C=C4F

InChI

InChIKey=UHTHHESEBZOYNR-UHFFFAOYSA-N
InChI=1S/C22H24BrFN4O2/c1-28-7-5-14(6-8-28)12-30-21-11-19-16(10-20(21)29-2)22(26-13-25-19)27-18-4-3-15(23)9-17(18)24/h3-4,9-11,13-14H,5-8,12H2,1-2H3,(H,25,26,27)

HIDE SMILES / InChI

Molecular Formula C22H24BrFN4O2
Molecular Weight 475.354
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 16:02:00 UTC 2023
Edited
by admin
on Fri Dec 15 16:02:00 UTC 2023
Record UNII
YO460OQ37K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VANDETANIB
DASH   INN   JAN   MART.   MI   ORANGE BOOK   USAN   VANDF   WHO-DD  
INN   USAN  
Official Name English
GNF-PF-2188
Code English
VANDETANIB [VANDF]
Common Name English
VANDETANIB [MART.]
Common Name English
NSC-744325
Code English
CAPRELSA
Brand Name English
vandetanib [INN]
Common Name English
NSC-760766
Code English
ZD6474
Code English
N-(4-Bromo-2-fluorophenyl)-6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinazolin-4-amine
Systematic Name English
VANDETANIB [USAN]
Common Name English
VANDETANIB [JAN]
Common Name English
VANDETANIB [MI]
Common Name English
VANDETANIB [ORANGE BOOK]
Common Name English
4-QUINAZOLINAMINE, N-(4-BROMO-2-FLUOROPHENYL)-6-METHOXY-7-((1-METHYL-4- PIPERIDINYL)METHOXY)-
Systematic Name English
ZD-64
Code English
ZACTIMA
Brand Name English
ZD-6474
Code English
Vandetanib [WHO-DD]
Common Name English
Classification Tree Code System Code
EMA ASSESSMENT REPORTS CAPRELSA (AUTHORIZED: THYROID NEOPLASMS)
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
LIVERTOX NBK548169
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
NDF-RT N0000175605
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
NCI_THESAURUS C1742
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
NCI_THESAURUS C2167
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
EU-Orphan Drug EU/3/05/344
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
WHO-ATC L01XE12
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
NCI_THESAURUS C93259
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
FDA ORPHAN DRUG 211005
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
WHO-VATC QL01XE12
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
Code System Code Type Description
IUPHAR
5717
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
NDF-RT
N0000185503
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY P-Glycoprotein Inhibitors [MoA]
EVMPD
SUB29174
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
ChEMBL
CHEMBL24828
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
NSC
744325
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
USAN
SS-07
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
DRUG CENTRAL
4178
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
NDF-RT
N0000187061
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY Organic Cation Transporter 2 Inhibitors [MoA]
NCI_THESAURUS
C2737
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
CAS
443913-73-3
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
HSDB
8198
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
DAILYMED
YO460OQ37K
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
WIKIPEDIA
Vandetanib
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
NSC
760766
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
INN
8365
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
EPA CompTox
DTXSID1046681
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
MERCK INDEX
m11387
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY Merck Index
LACTMED
Vandetanib
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
DRUG BANK
DB05294
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
PUBCHEM
3081361
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
SMS_ID
100000090715
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
CHEBI
49960
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
FDA UNII
YO460OQ37K
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
RXCUI
1098413
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY RxNorm
MESH
C452423
Created by admin on Fri Dec 15 16:02:00 UTC 2023 , Edited by admin on Fri Dec 15 16:02:00 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
TRANSPORTER -> SUBSTRATE
METABOLIC ENZYME -> SUBSTRATE
METABOLIC ENZYME -> SUBSTRATE
TRANSPORTER -> INHIBITOR
TARGET -> INHIBITOR
TARGET -> INHIBITOR
TARGET -> INHIBITOR
IC50
TARGET -> INHIBITOR RESISTANT
IC50
EXCRETED UNCHANGED
Within a 21-day collection period after a single dose of 14C-vandetanib, approximately 69% was recovered with 44% in feces and 25% in urine.
FECAL
TRANSPORTER -> INHIBITOR
EXCRETED UNCHANGED
Within a 21-day collection period after a single dose of 14C-vandetanib, approximately 69% was recovered with 44% in feces and 25% in urine.
URINE
BINDER->LIGAND
BINDING
TARGET -> INHIBITOR
METABOLIC ENZYME -> SUBSTRATE
TARGET -> INHIBITOR RESISTANT
IC50
TARGET -> INHIBITOR
Related Record Type Details
METABOLITE INACTIVE -> PARENT
FECAL; PLASMA; URINE
METABOLITE ACTIVE -> PARENT
MAJOR
FECAL; PLASMA; URINE
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Volume of Distribution PHARMACOKINETIC
Tmax PHARMACOKINETIC
Biological Half-life PHARMACOKINETIC