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Mitomycin C, cell culture reagent, 2 mg
Key Features and Details
Mitomycin C
SYNONYMS: Ametycin; 7-Amino-9-a-methoxymitosane; Mit-C; Mitocin-C; Mitomycinum; Mutamycin; Azirizino[2', 3': 3,4] pyrrolo [1,2-a] indole 4,7-dione-6-amino-1,1a, 2, 8, 8a, 8b-hexahydro- 8- (hydroxymethyl) 8a-methoxy-5-methyl carbamate
CAS: #
50-07-7
MOLECULAR FORMULA: C15H18N4O5
MOLECULAR WEIGHT: 334.332 g/mol
BEILSTEIN REGISTRY No.: 7231816
EC No: 200-008-6
MDL No: MFCD00078109
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PRODUCT DESCRIPTION
Mitomycin C
Application Notes
Mitomycin C is the most widely used as Mitomycin antibiotics because it is the least toxic and with the most potent antitumor activity. It has extraordinarily strong activity against Ehrlich ascites tumor cells.It also possesses strong bactericidal action against Gram-positive and Gram-negative organisms and acid-fact bacilli. Mitomycin C is used to generate mitotically inactive feeder cells used in cell culture systems, such as mitotically inactive fibroblast used in embryonic stem cell (ESC) systems.
Usage Statement
Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department.
Key Applications
Generate mitotically inactive feeder cells
SPECIFICATIONS
SKU: 0219453202
Base Catalog Number: 19453202
Alternate Names: Ametycin; 7-Amino-9-a-methoxymitosane; Mit-C; Mitocin-C; Mitomycinum; Mutamycin; Azirizino[2', 3': 3,4] pyrrolo [1,2-a] indole 4,7-dione-6-amino-1,1a, 2, 8, 8a, 8b-hexahydro- 8- (hydroxymethyl) 8a-methoxy-5-methyl carbamate
Beilstein Registration No
: 7231816
Biochemical Physiological 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.
Boiling Point
: 534 °C
CAS
: #
50-07-7
EC No
: 200-008-6
Grade
: Cell Culture
Hazard Statements
: H302-H351
MDL No
: MFCD00078109
Melting Point
: Above 680° F (EPA, 1998)
Molecular Formula
: C15H18N4O5
Molecular Weight
: 334.332 g/mol
RTECS No
: CN0700000
Safety Symbol
: GHS07, GHS08
Solubility
: Soluble (NTP, 1992)
