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

Details

Stereochemistry ABSOLUTE
Molecular Formula C28H30N4O6
Molecular Weight 518.561
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LURTOTECAN

SMILES

CC[C@@]1(O)C(=O)OCC2=C1C=C3N(CC4=C3N=C5C=C6OCCOC6=CC5=C4CN7CCN(C)CC7)C2=O

InChI

InChIKey=RVFGKBWWUQOIOU-NDEPHWFRSA-N
InChI=1S/C28H30N4O6/c1-3-28(35)20-11-22-25-18(14-32(22)26(33)19(20)15-38-27(28)34)17(13-31-6-4-30(2)5-7-31)16-10-23-24(12-21(16)29-25)37-9-8-36-23/h10-12,35H,3-9,13-15H2,1-2H3/t28-/m0/s1

HIDE SMILES / InChI
Lurtotecan is a semisynthetic analog of camptothecin with antineoplastic activity. It is an inhibitor of DNA topoisomerase I. Liposomal formulation of lurtotecan was being studied in the treatment of cancer. Lurtotecan development has been discontinued.

Approval Year

Targets

Targets

PubMed

PubMed

TitleDatePubMed
Modulation of camptothecin analogs in the treatment of cancer: a review.
2001 Feb
Biodistribution of NX211, liposomal lurtotecan, in tumor-bearing mice.
2001 Mar
Gateways to clinical trials.
2005 Dec
Stealth liposomes: review of the basic science, rationale, and clinical applications, existing and potential.
2006
Experimental designs for phase I and phase I/II dose-finding studies.
2006 Mar 13
Tumour-targeted nanomedicines: principles and practice.
2008 Aug 5
Organic anion-transporting polypeptide 1B1 mediates transport of Gimatecan and BNP1350 and can be inhibited by several classic ATP-binding cassette (ABC) B1 and/or ABCG2 inhibitors.
2009 Apr
Patents
Name Type Language
LURTOTECAN
INN  
INN  
Official Name English
(8S)-8-ETHYL-2,3-DIHYDRO-8-HYDROXY-15-((4-METHYL-1-PIPERAZINYL)METHYL)-11H-P-DIOXINO(2,3-G)PYRANO(3',4':6,7)INDOLIZINO(1,2-B)QUINOLINE-9,12(8H,14H)-DIONE
Common Name English
11H-1,4-DIOXINO(2,3-G)PYRANO(3',4':6,7)INDOLIZINO(1,2-B)QUINOLINE-9,12(8H,14H)-DIONE, 8-ETHYL-2,3-DIHYDRO-8-HYDROXY-15-((4-METHYL-1-PIPERAZINYL)METHYL)-, (S)
Common Name English
lurtotecan [INN]
Common Name English
Lurtotecan [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C2843
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
Code System Code Type Description
MESH
C091719
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
PRIMARY
NCI_THESAURUS
C1610
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
PRIMARY
SMS_ID
100000082293
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
PRIMARY
EVMPD
SUB08622MIG
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
PRIMARY
DRUG BANK
DB12222
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
PRIMARY
ChEMBL
CHEMBL305666
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
PRIMARY
PUBCHEM
60956
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
PRIMARY
INN
7402
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
PRIMARY
FDA UNII
4J1L80T08I
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
PRIMARY
WIKIPEDIA
LURTOTECAN
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
PRIMARY
CAS
149882-10-0
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID30164422
Created by admin on Sat Dec 16 17:14:56 GMT 2023 , Edited by admin on Sat Dec 16 17:14:56 GMT 2023
PRIMARY