CHEBI:4911 - etoposide

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ChEBI Name etoposide ChEBI ID CHEBI:4911 Stars This entity has been manually annotated by the ChEBI Team. Supplier Information ChemicalBook:CB7852707, eMolecules:475071, ZINC000005224354 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Ethylene glycol (IUPAC name: ethane-1,2-diol) is an organic compound (a vicinal diol) with the formula (CH2OH)2. It is mainly used for two purposes: as a raw material in the manufacture of polyester fibers and for antifreeze formulations. It is an odorless, colorless, flammable, viscous liquid. It has a sweet taste, but is toxic in high concentrations. This molecule has been observed in outer space. Read full article at Wikipedia Formula C29H32O13 Net Charge 0 Average Mass 588.55660 Monoisotopic Mass 588.18429 InChI InChI=1S/C29H32O13/c1-11-36-9-20-27(40-11)24(31)25(32)29(41-20)42-26-14-7-17-16(38-10-39-17)6-13(14)21(22-15(26)8-37-28(22)33)12-4-18(34-2)23(30)19(5-12)35-3/h4-7,11,15,20-22,24-27,29-32H,8-10H2,1-3H3/t11-,15+,20-,21-,22+,24-,25-,26-,27-,29+/m1/s1 InChIKey VJJPUSNTGOMMGY-MRVIYFEKSA-N SMILES [H][C@]12COC(=O)[C@]1([H])[C@H](c1cc(OC)c(O)c(OC)c1)c1cc3OCOc3cc1[C@H]2O[C@@H]1O[C@@H]2CO[C@@H](C)O[C@H]2[C@H](O)[C@H]1O Roles Classification Biological Role(s): DNA synthesis inhibitor Any substance that inhibits the synthesis of DNA. Application(s): antineoplastic agent A substance that inhibits or prevents the proliferation of neoplasms. View more via ChEBI Ontology ChEBI Ontology Outgoing etoposide (CHEBI:4911) has functional parent 4'-demethylepipodophyllotoxin (CHEBI:74422) etoposide (CHEBI:4911) has functional parent podophyllotoxin (CHEBI:50305) etoposide (CHEBI:4911) has role antineoplastic agent (CHEBI:35610) etoposide (CHEBI:4911) has role DNA synthesis inhibitor (CHEBI:59517) etoposide (CHEBI:4911) is a β-D-glucoside (CHEBI:22798) etoposide (CHEBI:4911) is a furonaphthodioxole (CHEBI:50307) etoposide (CHEBI:4911) is a organic heterotetracyclic compound (CHEBI:38163) IUPAC Name (5S,5aR,8aR,9R)-9-(4-hydroxy-3,5-dimethoxyphenyl)-8-oxo-5,5a,6,8,8a,9-hexahydrofuro[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yl 4,6-O-[(1R)-ethylidene]-β-D-glucopyranoside INNs Sources etoposide ChemIDplus Etoposido ChemIDplus etoposidum ChemIDplus Synonyms Sources (−)-etoposide DrugBank 4'-Demethylepipodophyllotoxin 9-(4,6-O-(R)-ethylidene-beta-D-glucopyranoside) ChemIDplus 4-demethylepipodophyllotoxin β-D-ethylideneglucoside ChemIDplus 9-((4,6-O-Ethylidine-beta-D-glucopyranosyl)oxy)-5,8,8a,9-tetrahydro-5-(4-hydroxy-3,4-dimethyloxyphenyl)furo(3',4'':6,7)naptho-(2,3-d)-1,3-dioxol-6(5aH)-one ChemIDplus Etoposide KEGG COMPOUND trans-Etoposide DrugBank VP-16 KEGG COMPOUND Brand Names Sources Eposin DrugBank Etopophos DrugBank Lastet DrugBank Toposar DrugBank Vepesid DrugBank Manual Xrefs Databases 1112 DrugCentral C01576 KEGG COMPOUND D00125 KEGG DRUG DB00773 DrugBank Etoposide Wikipedia LSM-6348 LINCS US3524844 Patent View more database links Registry Numbers Types Sources 33419-42-0 CAS Registry Number KEGG COMPOUND 33419-42-0 CAS Registry Number ChemIDplus Last Modified 22 February 2017