Mitomycine c à partir de Streptomyces caespitosus, >=970 mug/mg (USP XXIV), >=970 mug / mg(USP XXIV)

Code: m0440-5mg D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Mitomycin C is produced by a strain of actinomyces, Streptomyces caespitosus. It contains three anticancer moieties, quinine, urethane, and aziridine gro...


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Votre prix
£155.00 5MG

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Mitomycin C is produced by a strain of actinomyces, Streptomyces caespitosus. It contains three anticancer moieties, quinine, urethane, and aziridine groups. It is used to generate mitotically inactive feeder cells in cell culture systems, such as the mitotically inactive fibroblasts used in embryonic stem cell systems.

Biochem/physiol Actions

Mode of Action: This product is an alkylating agent that specifically targets the guanine nucleoside sequence 5′-CpG-3′. It inhibits DNA synthesis by covalently reacting with DNA, forming crosslinks between complementary strands of DNA. This interaction prevents separation of complementary DNA strands, inhibiting DNA replication.Antimicrobial Spectrum: Mitomycin C has strong antitumor activity, especially against Ehrlich ascites tumor cells, and strong bactericidal action against gram-positive and gram-negative bacteria.

Caution

Stock solutions should be filter sterilized and stored at 2-8 °C in the dark. Solutions at pH 6-9 can be stored at 0-5 °C for up to a week, but if a precipitate forms, a fresh solution should be prepared - the precipitated solution has been proven toxic to cells.

General description

Chemical structure: aziridine

Packaging

5, 25 mg in glass bottle

Preparation Note

Mitomycin C is soluble in water at .5 mg/mL, with a pH of 6.0-7.5. It undergoes rapid degradation in acidic solutions with pH﹤6, and is mostly likely to retain activity in solutions with a pH between 6-9.

antibiotic activity spectrumGram-positive bacteria, Gram-negative bacteria
biological sourceStreptomyces caespitosus
colorblue-violet
concentration≥970 µg/mg (USP XXIV)
InChI keyNWIBSHFKIJFRCO-WUDYKRTCSA-N
InChI1S/C15H18N4O5/c1-5-9(16)12(21)8-6(4-24-14(17)22)15(23-2)13-7(18-13)3-19(15)10(8)11(5)20/h6-7,13,18H,3-4,16H2,1-2H3,(H2,17,22)/t6-,7+,13+,15-/m1/s1
mode of actionDNA synthesis | interferes
Quality Level100
SMILES string[H][C@]12CN3C4=C([C@@H](COC(N)=O)[C@@]3(OC)[C@@]1([H])N2)C(=O)C(N)=C(C)C4=O
solubilityH2O: 40 mg/mL, clear to very slightly hazy, colorless, H2O: soluble
storage temp.2-8°C
Code
Description
Unité de vente
Prix annoncé
Qté
Cas Number50-07-7
Hazard Class6.1
Un Number3462
Pack GroupII
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