Elsamitrucin

Elsamitrucin
Clinical data
Other namesElsamicin A
ATC code
  • none
Identifiers
  • 10-[3-(3-Amino-5-hydroxy-4-methoxy-6-methyltetrahydropyran-2-yloxy)-4,5-dihydroxy-4,6-dimethyltetrahydropyran-2-yloxy]-6-hydroxy-1-methylbenzo[h]chromeno[5,4,3-cde]chromene-5,12-dione
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC33H35NO13
Molar mass653.637 g·mol−1
3D model (JSmol)
  • Cc1ccc2c3c1c(=O)oc4c3c(c(c5c4c(ccc5)O[C@H]6[C@@H]([C@@]([C@H]([C@H](O6)C)O)(C)O)O[C@@H]7[C@@H]([C@H]([C@H]([C@H](O7)C)O)OC)N)O)c(=O)o2
  • InChI=1S/C33H35NO13/c1-11-9-10-16-19-17(11)29(38)46-25-18-14(24(36)21(20(19)25)30(39)44-16)7-6-8-15(18)45-32-28(33(4,40)27(37)13(3)43-32)47-31-22(34)26(41-5)23(35)12(2)42-31/h6-10,12-13,22-23,26-28,31-32,35-37,40H,34H2,1-5H3/t12-,13-,22-,23+,26-,27+,28+,31-,32+,33+/m1/s1
  • Key:MGQRRMONVLMKJL-KWJIQSIXSA-N
  (verify)

Elsamitrucin (elsamicin A) is a drug used in chemotherapy.[1] Elsamitrucin is chemically related to chartreusin.[2]

References

  1. ^ Barceló F, Portugal J (October 2004). "Elsamicin A binding to DNA. A comparative thermodynamic characterization". FEBS Letters. 576 (1–2): 68–72. Bibcode:2004FEBSL.576...68B. doi:10.1016/j.febslet.2004.08.063. PMID 15474012.
  2. ^ Portugal, Jose (2003). "Chartreusin, Elsamicin a and Related Anti-Cancer Antibiotics". Current Medicinal Chemistry. Anti-Cancer Agents. 3 (6): 411–420. doi:10.2174/1568011033482215. PMID 14529449.


Stub icon

This antineoplastic or immunomodulatory drug article is a stub. You can help Wikipedia by expanding it.