Varacin

Varacin

Names
IUPAC name 2-(6,7-dimethoxy-1,2,3,4,5-benzopentathiepin-9-yl)ethanamine
Identifiers
CAS Number	134029-48-4 Y
3D model (JSmol)	Interactive image
ChemSpider	156044 N
PubChem CID	179269
InChI InChI=1S/C10H13NO2S5/c1-12-7-5-6(3-4-11)9-10(8(7)13-2)15-17-18-16-14-9/h5H,3-4,11H2,1-2H3 N Key: HIKCOAGMCNIBMP-UHFFFAOYSA-N N InChI=1/C10H13NO2S5/c1-12-7-5-6(3-4-11)9-10(8(7)13-2)15-17-18-16-14-9/h5H,3-4,11H2,1-2H3 Key: HIKCOAGMCNIBMP-UHFFFAOYAP
SMILES NCCc2cc(OC)c(OC)c1SSSSSc12
Properties
Chemical formula	C10H13NO2S5
Molar mass	339.540 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Varacin is a bicyclic organosulfur compound originally found in marine Ascidiacea from the Polycitor genus.^[1] It contains an unusual pentathiepin ring which reacts with DNA, and varacin and synthetic analogues have been investigated for their antimicrobial and antitumour properties.^[2][3]

References

1. ↑ Makarieva, T. N.; Stonik, V. A.; Dmitrenok, A. S.; Grebnev, B. B.; Isakov, V. V.; Rebachyk, N. M.; Rashkes, Y. W. (1995). "Varacin and three new marine antimicrobial polysulfides from the far-eastern ascidian Polycitor sp.". Journal of Natural Products. 58 (2): 254–8. PMID 7769392. doi:10.1021/np50116a015. 
2. ↑ Greer, A. (2001). "On the origin of cytotoxicity of the natural product varacin. A novel example of a pentathiepin reaction that provides evidence for a triatomic sulfur intermediate". Journal of the American Chemical Society. 123 (42): 10379–86. PMID 11603989. doi:10.1021/ja016495p. 
3. ↑ Brzostowska, E. M.; Greer, A. (2003). "The role of amine in the mechanism of pentathiepin (polysulfur) antitumor agents". Journal of the American Chemical Society. 125 (2): 396–404. PMID 12517151. doi:10.1021/ja027416s.