Topotecan

Topotecan
Systematic (IUPAC) name
(S)-10-[(dimethylamino)methyl]-4-ethyl-4,9-
dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]
quinoline-3,14(4H,12H)-dione monohydrochloride
Clinical data
Trade names Hycamtin
AHFS/Drugs.com monograph
MedlinePlus a610007
Pregnancy cat. D (Au, U.S.)
Legal status ℞-only (U.S.), POM (UK)
Routes Intravenous infusion, oral
Pharmacokinetic data
Bioavailability 31.4 % in humans [1][2]
Protein binding 35%
Metabolism Hepatic
Half-life 2-3 hours
Excretion Renal
Identifiers
CAS number 123948-87-8 N 119413-54-6 (hydrochloride)
ATC code L01XX17
PubChem CID 60700
DrugBank APRD00687
ChemSpider 54705 Y
UNII 7M7YKX2N15 Y
KEGG D08618 Y
ChEMBL CHEMBL84 Y
Chemical data
Formula C23H23N3O5 •HCl 
Mol. mass 457.9 g/mol
SMILES eMolecules & PubChem
 N(what is this?)  (verify)

Topotecan hydrochloride (trade name Hycamtin) is a chemotherapy agent that is a topoisomerase I inhibitor. It is the water-soluble derivative of camptothecin. It is used to treat ovarian cancer and lung cancer, as well as other cancer types.

After GlaxoSmithKline received final FDA approval for Hycamtin Capsules on October 15, 2007, Topotecan is the first topoisomerase inhibitor for oral use.

Contents

Indications (Approved uses)

Experimental use

Administration

IV, oral.

Mode of action

Hycamtin or topotecan is a semi-synthetic derivative of camptothecin. Camptothecin is a natural product extracted from the bark of the tree Camptotheca acuminata. Topoisomerase-I is a nuclear enzyme that relieves torsional strain in DNA by opening single strand breaks. Once topoisomerase-I creates a single strand break, the DNA can rotate in front of the advancing replication fork. Topotecan intercalates between DNA bases. This intercalation disrupts the DNA duplication machinery when it reaches a site where topotecan is intercalated. This disruption prevents DNA replication, and ultimately leads to cell death. Mammalian cells cannot efficiently repair these double strand breaks.[6] This process leads to breaks in the DNA strand resulting in apoptosis.

Side effects

Generic versions

Two generic versions have been approved in EU, and in Nov 2010 the US FDA approved a generic version.[7]

See also

References

External links