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Sigma-Aldrich Ganciclovir. ≥98% (HPLC), viral DNA elongation inhibitor, solid. 50 mg
List Price
$338.72
Your Price
$338.72
Sigma-Aldrich Ganciclovir. ≥98% (HPLC), viral DNA elongation inhibitor, solid. 50 mg - SIAL (Additional S&H Or Hazmat Fees May Apply)
NETA PART:
SIAL-345700-50MG
MFG.PART:
345700-50MG
UNSPSC:
12352200
Manufacturer:
Sigma-Aldrich
Product Name
Ganciclovir, A nucleoside analog structurally related to Acyclovir.
Quality Level
100
description
Merck USA index - 14, 4363
assay
≥98% (HPLC)
form
solid
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze
desiccated
color
white
solubility
0.1 M HCl: 5 mg/mL
shipped in
ambient
General description
A nucleoside analog structurally related to Acyclovir (Cat. No. 114798). Acts as a prodrug that is activated by phosphorylation. Has been used in the study of “suicide” gene therapy in cancer research. Upon expression of a viral suicide gene encoding herpes simplex virus, thymidine kinase (TK), the non-toxic prodrug ganciclovir, is converted to an active phosphorylated analog that can be incorporated into the DNA of replicating eukaryotic cells, causing death of the malignant dividing cell. Causes an irreversible cell cycle arrest at the g2/M checkpoint. Has also been used to study the loss of telomeres and to evaluate sensitivity of viruses to antiviral agents.
A nucleoside analog that is structurally related to Acyclovir (Cat. No. 114798). Acts as a pro-drug that is activated by phosphorylation. It has been used in the study of "suicide gene therapy" in cancer research. Upon expression of a viral suicide gene encoding herpes simplex virus thymidine kinase (TK), the non-toxic pro-drug is converted to the phosphorylated active analog and is incorporated into the DNA of replicating eukaryotic cells, causing death of the dividing malignant cells. Causes an irreversible cell cycle arrest at the g2/M checkpoint. Has also been used to study the loss of telomers and to evaluate the sensitivity of viruses to anti-viral agents.
Biochem/physiol Actions
Cell permeable: yes
Primary Target
Acts as a prodrug that is activated by phosphorylation
Acts as a prodrug that is activated by phosphorylation
Product does not compete with ATP.
Reversible: no
Packaging
Packaged under inert gas
Preparation Note
Following reconstitution aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.
Other Notes
Aghi, M., et Al. 2000. J. Gene Med.2, 148.
Qiao, J., et Al. 2000. Hum. Gene Ther.11, 1569.
Cannon, J.S., et Al. 1999. J. Virol.73, 4786.
Rubsam, L.Z., et Al. 1999. Cancer Res.59, 669.
Sprung, C.N., et Al. 1999. Proc. Natl. Acad. Sci. USA96, 6781.
Yamasaki, H., et Al. 1999. C.R. Acad. Sci. III322, 151.
Halloran, P.J., and Fenton, R.g. 1998. Cancer Res.58, 3855.
Qiao, J., et Al. 2000. Hum. Gene Ther.11, 1569.
Cannon, J.S., et Al. 1999. J. Virol.73, 4786.
Rubsam, L.Z., et Al. 1999. Cancer Res.59, 669.
Sprung, C.N., et Al. 1999. Proc. Natl. Acad. Sci. USA96, 6781.
Yamasaki, H., et Al. 1999. C.R. Acad. Sci. III322, 151.
Halloran, P.J., and Fenton, R.g. 1998. Cancer Res.58, 3855.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Toxicity: Carcinogenic / Teratogenic (D)
pictograms
GHS08
signalword
Danger
hcodes
H340,H361fd
pcodes
P201 - P202 - P280 - P308 + P313 - P405 - P501
Hazard Classifications
Muta. 1B - Repr. 2
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
| SKU | SIAL-345700-50MG |
|---|---|
| Supplier Part Number | 345700-50MG |
| UM | EA |
| UNSPSC | 12352200 |
| Manufacturer | Sigma-Aldrich |
| ProductLine | SIAL |
| Qty | 1 |
| MinOrderQty | 1 |
| Weight | 10.000000 |
| Lead Time | 9 |
| Energy Star | No |
| Green | No |
| Controlled | N |