POD

9-HYDROXY-5-(3,4,5-TRIMETHOXYPHENYL)-5,8,8A,9-TETRAHYDROFURO[3',4':6,7]NAPHTHO[2,3-D][1,3]DIOXOL-6(5AH)-ONE



Chemical Component Summary

Name9-HYDROXY-5-(3,4,5-TRIMETHOXYPHENYL)-5,8,8A,9-TETRAHYDROFURO[3',4':6,7]NAPHTHO[2,3-D][1,3]DIOXOL-6(5AH)-ONE
SynonymsPODOPHYLLOTOXIN
Identifiersn/a
FormulaC22 H22 O8
Molecular Weight414.405
TypeNON-POLYMER
Isomeric SMILESCOc1cc(cc(c1OC)OC)[C@@H]2c3cc4c(cc3[C@@H]([C@@H]5C2C(=O)OC5)O)OCO4
InChIInChI=1S/C22H22O8/c1-25-16-4-10(5-17(26-2)21(16)27-3)18-11-6-14-15(30-9-29-14)7-12(11)20(23)13-8-28-22(24)19(13)18/h4-7,13,18-20,23H,8-9H2,1-3H3/t13-,18+,19-,20-/m0/s1
InChIKeyYJGVMLPVUAXIQN-XVVDYKMHSA-N

Chemical Details

Formal Charge0
Atom Count52
Chiral Atom Count4
Bond Count56
Aromatic Bond Count12

Drug Info: DrugBank

DrugBank IDDB01179 
NamePodofilox
Groups approved
DescriptionA lignan found in podophyllin resin from the roots of podophyllum plants. It is a potent spindle poison, toxic if taken internally, and has been used as a cathartic. It is very irritating to skin and mucous membranes, has keratolytic actions, has been used to treat warts and keratoses, and may have antineoplastic properties, as do some of its congeners and derivatives.
Synonyms
  • Podofilox
  • PPT
  • (−)-podophyllotoxin
  • Podophyllinic acid lactone
  • Podophyllotoxin
Brand Names
  • Podofilox
  • Condylox (podofilox)Topical Solution 0.5%
  • Condyline
  • Condylox
  • Wartec
IndicationFor treatment of external genital warts (<i>Condyloma acuminatum</i>).
Categories
  • Antimitotic Agents
  • Antineoplastic Agents, Phytogenic
  • Antiviral Agents
  • Benzene Derivatives
  • Benzyl Compounds
ATC-CodeD06BB04
CAS number518-28-5

Drug Targets

NameTarget SequencePharmacological ActionActions
Tubulin alpha-4A chainMRECISVHVGQAGVQMGNACWELYCLEHGIQPDGQMPSDKTIGGGDDSFT...unknowninhibitor
Tubulin beta chainMREIVHIQAGQCGNQIGAKFWEVISDEHGIDPTGTYHGDSDLQLDRISVY...unknowninhibitor
DNA topoisomerase 2-alphaMEVSPLQPVNENMQVNKIKKNEDAKKRLSVERIYQKKTQLEHILLRPDTY...unknowninhibitor
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS. Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682

Related Resource References

Resource NameReference
Pharos CHEMBL61
PubChem 10607
ChEMBL CHEMBL61
ChEBI CHEBI:50305