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MW 334.33 Da, Purity >99%. Anticancer and antibiotic agent. Crosslinks DNA. Inhibits DNA synthesis and nuclear division. Also induces apoptosis.


Images

Chemical Structure - Mitomycin C (MMC), Anticancer and antibiotic agent (AB120797), expandable thumbnail
  • Functional Studies - Mitomycin C (MMC), Anticancer and antibiotic agent (AB120797), expandable thumbnail

Publications

  • Molecular medicine reports 28:2023
    Improvement of wound healing by capsaicin through suppression of the inflammatory response and amelioration of the repair process.
    Applications:
    Unspecified application
    Reactive species:
    Unspecified reactive species
    Chi-Jung Huang,Chi-Ming Pu,Su-Yi Su,Shih-Lun Lo,Cheng Hung Lee,Yu-Hsiu Yen
    PubMed 37387413
  • Cell journal 25:255-2632023
    Fabrication of Cell-Laden AME-Loaded Collagen-Based Hydrogel Promotes Fibroblast Proliferation and Wound Healing .
    Applications:
    Unspecified application
    Reactive species:
    Unspecified reactive species
    Mohammad Azimi Lamouty,Niloufar Shayan Asl,Abdollah Safari,Marzieh Ebrahimi,Hamed Daemi
    PubMed 37210646

Key facts

CAS number

50-07-7

Purity

> 99%

Form

Solid

Source

Streptomyces sp.

Molecular weight

334.33 Da

Molecular formula

C15H18N4O5

PubChem identifier

5746

Nature

Native

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MW 334.33 Da, Purity >99%. Anticancer and antibiotic agent. Crosslinks DNA. Inhibits DNA synthesis and nuclear division. Also induces apoptosis.

Key facts

Purity

> 99%

Source

Streptomyces sp.

PubChem identifier

5746

Solubility

SOL IN WATER, METHANOL, BUTYL ACETATE, ACETONE, AND CYCLOHEXANONE; SLIGHTLY SOL IN BENZENE, ETHER, AND CARBON TETRACHLORIDE; PRACTICALLY INSOL IN PETROLEUM ETHER.

Biochemical name

Mitomycin

Biological description

Anticancer and antibiotic agent. Crosslinks DNA. Inhibits DNA synthesis and nuclear division. Also induces apoptosis.

Canonical SMILES

CC1=C(C(=O)C2=C(C1=O)N3CC4C(C3(C2COC(=O)N)OC)N4)N

Isomeric SMILES

CC1=C(C(=O)C2=C(C1=O)N3C[C@H]4[C@@H]([C@@]3([C@@H]2COC(=O)N)OC)N4)N

InChI

InChI=1S/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

InChIKey

NWIBSHFKIJFRCO-WUDYKRTCSA-N

IUPAC name

[(4S,6S,7R,8S)-11-amino-7-methoxy-12-methyl-10,13-dioxo-2,5-diazatetracyclo[7.4.0.02,7.04,6]trideca-1(9),11-dien-8-yl]methyl carbamate

Storage

Shipped at conditions

Ambient - Can Ship with Ice

Appropriate long-term storage conditions

+4°C

Storage information

The product can be stored for up to 12 months

Product promise

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2 product images

  • Chemical Structure - Mitomycin C (MMC), Anticancer and antibiotic agent (ab120797), expandable thumbnail

    Chemical Structure - Mitomycin C (MMC), Anticancer and antibiotic agent (ab120797)

    2D chemical structure image of ab120797, Mitomycin C (MMC), Anticancer and antibiotic agent

  • Functional Studies - Mitomycin C (MMC), Anticancer and antibiotic agent (ab120797), expandable thumbnail

    Functional Studies - Mitomycin C (MMC), Anticancer and antibiotic agent (ab120797)

    Functional assays: Caspase 8 (active) FITC Staining Kit (Caspase-8 (active) FITC Staining Kit ab65614)

    Active caspase 8 in control Jurkat cells (10e6/mL) or cells treated for five hours with 10 ug/mL Cyclohexamide (CHX) (Cycloheximide, Protein synthesis inhibitor ab120093) or four hours with 25 ug/mL Mitomycin C (MitoC) (ab120797). Background signal subtracted, duplicates; +/- SD.

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