Terpestacin

Terpestacin
Identifiers

3D model (Jmol)	Interactive image
ChemSpider	4976965
PubChem	6475118
InChI InChI=1S/C25H38O4/c1-16-7-6-8-17(2)13-14-25(5)20(11-10-18(3)21(27)12-9-16)22(19(4)15-26)23(28)24(25)29/h7,10,13,19-21,26-28H,6,8-9,11-12,14-15H2,1-5H3/b16-7+,17-13+,18-10+/t19-,20-,21+,25+/m1/s1 Key: UTGBBPSEQPITLF-IXRUDUFRSA-N InChI=1/C25H38O4/c1-16-7-6-8-17(2)13-14-25(5)20(11-10-18(3)21(27)12-9-16)22(19(4)15-26)23(28)24(25)29/h7,10,13,19-21,26-28H,6,8-9,11-12,14-15H2,1-5H3/b16-7+,17-13+,18-10+/t19-,20-,21+,25+/m1/s1 Key: UTGBBPSEQPITLF-IXRUDUFRBX
SMILES C/C/1=C\CC/C(=C/C[C@]2([C@H](C/C=C(/[C@H](CC1)O)\C)C(=C(C2=O)O)[C@H](C)CO)C)/C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Terpestacin^[1] is a fungal metabolite with anticancer activity.

References

↑ Chan, Johann; Jamison, Timothy F. (September 2003). "Synthesis of (−)-Terpestacin via Catalytic, Stereoselective Fragment Coupling: Siccanol Is Terpestacin, Not 11- -Terpestacin". Journal of the American Chemical Society. 125 (38): 11514–11515. doi:10.1021/ja0373925.

Grigoriev PA, Schlegel B, Schmidtke M, Gräfe U (September 2002). "Alteration of membrane polarization by (−)-terpestacin, a biologically active fungal metabolite". Die Pharmazie. 57 (9): 653–4. PMID 12369460.
Park KC, Choi SH (December 2013). "Effects of endostatin and a new drug terpestacin against human neuroblastoma xenograft and cell lines". Pediatric Surgery International. 29 (12): 1327–40. doi:10.1007/s00383-013-3398-1. PMID 24072200.

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