SUNITINIB

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C22H27FN4O2
Molecular Weight	398.4738
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	1
Charge	0

SHOW SMILES / InChI

Structure of SUNITINIB

Structure Search

SMILES

CCN(CC)CCNC(=O)C1=C(C)NC(\C=C2/C(=O)NC3=C2C=C(F)C=C3)=C1C

InChI

InChIKey=WINHZLLDWRZWRT-ATVHPVEESA-N

InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12-

HIDE SMILES / InChI

Approval Year

Name

Type

Language

SUNITINIB

Official Name

English

SU-011248

Code

English

1H-PYRROLE-3-CARBOXAMIDE, N-(2-(DIETHYLAMINO)ETHYL)-5-((Z)-(5-FLUORO-1,2-DIHYDRO-2-OXO-3H-INDOL-3-YLIDENE)METHYL)-2,4-DIMETHYL-

Systematic Name

English

NSC-736511

Code

English

SU-11248

Code

English

SUNITINIB [VANDF]

Common Name

English

N-(2-(DIETHYLAMINO)ETHYL)-5-((Z)-(5-FLUORO-2-OXO-1,2-DIHYDRO-3H-INDOL-3-YLIDENE)METHYL)-2,4-DIMETHYL-1H-PYRROLE-3-CARBOXAMIDE

Systematic Name

English

NSC-750690

Code

English

SU011248

Code

English

Sunitinib [WHO-DD]

Common Name

English

SUNITINIB [EMA EPAR]

Common Name

English

SUNITINIB [MI]

Common Name

English

sunitinib [INN]

Common Name

English

N-(2-(DIETHYLAMINO)ETHYL)-5-((Z)-(5-FLUORO-1,2-DIHYDRO-2-OXO-3H-INDOL-3-YLIDENE)METHYL)-2,4-DIMETHYL-1H-PYRROLE-3-CARBOXAMIDE

Systematic Name

English

Classification Tree Code System Code

WHO-ATC

L01XE04

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

NDF-RT

N0000175076

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

EMA ASSESSMENT REPORTS

SUTENT (AUTHORIZED: GASTROINTESTINAL STROMAL TUMORS, NEUROENDOCRINE TUMORS, RENAL CELL CARCINOMA)

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

NCI_THESAURUS

C1971

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

NCI_THESAURUS

C129825

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

NDF-RT

N0000175605

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

NCI_THESAURUS

C1967

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

LIVERTOX

NBK548118

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

WHO-VATC

QL01XE04

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

Code System Code Type Description

SMS_ID

100000087970

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

DAILYMED

V99T50803M

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

CHEBI

38940

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

RXCUI

357977

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

RxNorm

MESH

C473478

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

NSC

736511

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

EVMPD

SUB22321

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

EPA CompTox

DTXSID1041134

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

NCI_THESAURUS

C71622

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

HSDB

7932

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

CAS

557795-19-4

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

INN

8646

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

PUBCHEM

5329102

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

LACTMED

Sunitinib

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

ChEMBL

CHEMBL535

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

MERCK INDEX

m10399

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

Merck Index

IUPHAR

5713

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

DRUG BANK

DB01268

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

FDA UNII

V99T50803M

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

NSC

750690

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

WIKIPEDIA

SUNITINIB

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

DRUG CENTRAL

2544

Created by admin on Fri Dec 15 16:27:52 UTC 2023 , Edited by admin on Fri Dec 15 16:27:52 UTC 2023

PRIMARY

ACTIVE MOIETY


					V99T50803M

SUNITINIB

METABOLITE (PARENT)


					XL74DDP8VB

METABOLITE ACTIVE (PARENT)


					42LJ35612R

N-DESETHYLSUNITINIB

METABOLITE INACTIVE (PARENT)


					FH2DP6X8LW

SU-014335

METABOLITE INACTIVE (PARENT)


					4MK76GX29B

METABOLITE INACTIVE (PARENT)


					UZ2R9A2TLL

SUNITINIB N-OXIDE

SALT/SOLVATE (PARENT)


					LVX8N1UT73

Sunitinib Malate

SALT/SOLVATE (PARENT)


					J48Z6FW33H

SUNITINIB HYDROCHLORIDE

SALT/SOLVATE (PARENT)


					T6473Z6HNM

SUNITINIB CYCLAMATE