Produktinformation
- 2'-Deoxy-2',2'-difluorocytidine hydrochloride
- 2',2'-Difluoro-2'-deoxycytidine
- 2',2'-Difluoro-2'-deoxycytidine hydrochloride
- 2,2-Difluoro-2-deoxycytidine DDFC
- 2′-Deoxy-2′,2′-difluorocytidine monohydrochloride
- 4-Amino-1-[3,3-difluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-1H-pyrimidin-2-one hydrochloride
- 4-amino-1-(2-deoxy-2,2-difluoropentofuranosyl)pyrimidin-2(1H)-one
- 4-amino-1-(2-deoxy-2,2-difluoropentofuranosyl)pyrimidin-2(1H)-one hydrochloride (1:1)
- Cytidine, 2′-deoxy-2′,2′-difluoro-, hydrochloride (1:1)
- Cytidine, 2′-deoxy-2′,2′-difluoro-, monohydrochloride
- Mehr Synonyme anzeigen
- Gemcitabine HCl
- Gemcitabine hydrochlorid
- Gemcitera
- Gemoral
- Gemsar
- Gemzar
- LY 188011 hydrochloride
Gemcitabine is as a synthetic pyrimidine nucleoside prodrug. The hydrogen atoms on the 2' carbon of deoxycytidine are replaced by fluorine atoms. Gemcitabine works by being incorporated into the DNA of cancer cells during replication and inhibiting DNA synthesis. First gemcitabine is converted into its active form, gemcitabine triphosphate, by cellular enzymes including deoxycytidine kinase (DCK), after it is taken up by cancer cells. The gemcitabine triphosphate interferes with the normal functioning of the enzymes involved in replicating DNA, leading to the termination of DNA synthesis and ultimately, cell death. Gemcitabine is used as a chemotherapy drug used to treat various types of cancer, including pancreatic, lung, breast, and ovarian cancer.
Gemcitabine is part of our Bio-X ™ Range. These products are aimed at life science researchers who need high quality ready to use products for assay development, screening or other R&D work. With a solubility datasheet and convenient vials, all of our Bio-X ™ products are in stock across our global warehouses for rapid delivery and ease of use.
Chemische Eigenschaften
Technische Anfrage zu: 3D-BG164501 Gemcitabine hydrochloride - Bio-X ™
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