WARNING: This product is for research use only, not for human or veterinary use.
MedKoo CAT#: 100410
CAS#: 122111-03-9 (HCl)
Description: Gemcitabine hydrochloride is the hydrochloride salt of an analogue of the antimetabolite nucleoside deoxycytidine with antineoplastic activity. Gemcitabine is converted intracellularly to the active metabolites difluorodeoxycytidine di- and triphosphate (dFdCDP, dFdCTP). dFdCDP inhibits ribonucleotide reductase, thereby decreasing the deoxynucleotide pool available for DNA synthesis; dFdCTP is incorporated into DNA, resulting in DNA strand termination and apoptosis.
MedKoo Cat#: 100410
Name: Gemcitabine Hydrochloride
CAS#: 122111-03-9 (HCl)
Chemical Formula: C9H12ClF2N3O4
Exact Mass:
Molecular Weight: 299.66
Elemental Analysis: C, 36.07; H, 4.04; Cl, 11.83; F, 12.68; N, 14.02; O, 21.36
Gemcitabine hydrochloride purity > 98%, is in stock. The same day shipping out after order is received.
Related CAS #: 95058-81-4 (free base) 122111-03-9 (HCl)
Synonym: LY188011; LY-188011; LY 188011; Abbreviations: dFdC; dFdCyd; gemcitabine; Gemzar.
IUPAC/Chemical Name: 4-amino-1-((2R,4R,5R)-3,3-difluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one hydrochloride
InChi Key: OKKDEIYWILRZIA-OSZBKLCCSA-N
InChi Code: InChI=1S/C9H11F2N3O4.ClH/c10-9(11)6(16)4(3-15)18-7(9)14-2-1-5(12)13-8(14)17;/h1-2,4,6-7,15-16H,3H2,(H2,12,13,17);1H/t4-,6-,7-;/m1./s1
SMILES Code: O=C1N=C(N)C=CN1[C@@H]2O[C@H](CO)[C@@H](O)C2(F)F.[H]Cl
The following data is based on the product molecular weight 299.66 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 1.15 mL | 5.76 mL | 11.51 mL |
5 mM | 0.23 mL | 1.15 mL | 2.3 mL |
10 mM | 0.12 mL | 0.58 mL | 1.15 mL |
50 mM | 0.02 mL | 0.12 mL | 0.23 mL |
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5: Kuramitsu Y, Wang Y, Taba K, Suenaga S, Ryozawa S, Kaino S, Sakaida I, Nakamura K. Heat-shock protein 27 plays the key role in gemcitabine-resistance of pancreatic cancer cells. Anticancer Res. 2012 Jun;32(6):2295-9. Review. PubMed PMID: 22641665.
6: Sugita Y, Hirai S, Ishkawa W, Maru N, Shimizu T, Yokota S, Nishi M, Iwamura M, Baba S. [Successful gemcitabine-nedaplatin therapy in a hemodialysis patient with ureteral carcinoma after bilateral nephroureterectomy]. Hinyokika Kiyo. 2012 Mar;58(3):159-63. Review. Japanese. PubMed PMID: 22495045.
7: Elnaggar M, Giovannetti E, Peters GJ. Molecular targets of gemcitabine action: rationale for development of novel drugs and drug combinations. Curr Pharm Des. 2012;18(19):2811-29. Review. PubMed PMID: 22390765.
8: Ying JE, Zhu LM, Liu BX. Developments in metastatic pancreatic cancer: is gemcitabine still the standard? World J Gastroenterol. 2012 Feb 28;18(8):736-45. doi: 10.3748/wjg.v18.i8.736. Review. PubMed PMID: 22371633; PubMed Central PMCID: PMC3286136.
9: Gross-Goupil M, Fourcade A, Blot E, Penel N, Négrier S, Culine S, Chaigneau L, Lesimple T, Priou F, Lortholary A, Kaminsky MC, Provencal J, Voog E, Bouzy J, Laplanche A, Fizazi K. Cisplatin alone or combined with gemcitabine in carcinomas of unknown primary: results of the randomised GEFCAPI 02 trial. Eur J Cancer. 2012 Mar;48(5):721-7. doi: 10.1016/j.ejca.2012.01.011. Epub 2012 Feb 6. Review. PubMed PMID: 22317952.
10: Shelley MD, Jones G, Cleves A, Wilt TJ, Mason MD, Kynaston HG. Intravesical gemcitabine therapy for non-muscle invasive bladder cancer (NMIBC): a systematic review. BJU Int. 2012 Feb;109(4):496-505. doi: 10.1111/j.1464-410X.2011.10880.x. Review. PubMed PMID: 22313502.