Size : | Price | Quantity | |
---|---|---|---|
20 mg | $40.00 | ||
100 mg | $80.00 |
Griseofulvin (126-07-8) is an antifungal antimitotic agent. Induces apoptosis of human germ cell tumor cells via disruption of connexin 43/tubulin association concomitant with enhanced translocation of connexin 43 from the cytoplasm to the nucleus.1 Inhibits the growth of adrenocortical cancer cells in vitro.2 Griseofulvin inhibits centrosome clustering, induces spindle multipolarity, mitotic arrest and cell death in multiple tumor cell lines but not in diploid fibroblasts and keratinocytes with normal centrosome content.3
References/Citations:
1) Mauro et al. (2013), The anti-mitotic drug griseofulvin induces apoptosis of human germ cell tumor cells through a connexin 43-dependent molecular mechanism; Apoptosis, 18 480
2) Bramann et al. (2013), Griseofulvin inhibits the growth of adrenocortical cancer cells in vitro; Horm. Metab. Res., 45 297
3) Rebacz et al. (2007), Identification of griseofulvin as an inhibitor of centrosomal clustering in a phenotype-based screen; Cancer Res., 67 6342
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Griseofulvin (126-07-8) is an antifungal antimitotic agent. Induces apoptosis of human germ cell tumor cells via disruption of connexin 43/tubulin association concomitant with enhanced translocation of connexin 43 from the cytoplasm to the nucleus.1 Inhibits the growth of adrenocortical cancer cells in vitro.2 Griseofulvin inhibits centrosome clustering, induces spindle multipolarity, mitotic arrest and cell death in multiple tumor cell lines but not in diploid fibroblasts and keratinocytes with normal centrosome content.3
References/Citations:
1) Mauro et al. (2013), The anti-mitotic drug griseofulvin induces apoptosis of human germ cell tumor cells through a connexin 43-dependent molecular mechanism; Apoptosis, 18 480
2) Bramann et al. (2013), Griseofulvin inhibits the growth of adrenocortical cancer cells in vitro; Horm. Metab. Res., 45 297
3) Rebacz et al. (2007), Identification of griseofulvin as an inhibitor of centrosomal clustering in a phenotype-based screen; Cancer Res., 67 6342
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