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Mitomycins

Several of the naturally occurring indoles also have clinical importance. The dimeric vinca alkaloid vincristine and closely related compounds were among the first of the anti-mitotic class of chemotherapeutic agents for cancer[14]. The mitomycins[15] and derivatives of ellipticine[16] are other examples of compounds having anti-tumour activity. Reserpine, while not now a major drug, was one of the first compounds to show beneficial effects in treatment of mental disorders[17]... [Pg.2]

Aziridines occur naturally in the form of mitomycins (Table 3), which have antibiotic activity (1,449). Mytomycin C is used clinically as one of the most effective agents in the chemotherapy of cancer (450). [Pg.13]

Analogous chemistry with 2,3-dibromo-l,4-naphthoquiaone [13243-65-7] (102) has been used ia the synthesis of mitomycin antibiotics for example, (103) [72866-63-8]h.2iS been obtained ia 91% yield (102). [Pg.416]

Mitochondrial monoamine oxidase, 1, 253 Mitomycin synthesis, 7, 658, 659 Mitomycin-A, 7, 93 Mitomycin-B, 7, 93 Mitomycin-C, 7, 93 as antitumor drug, 4, 374 Mixed function oxidases, 1, 224 Mobam... [Pg.703]

A 3-acetoxypropyl group was used to protect an aziridine — NH group during the synthesis of mitomycins A and C acetyl, benzoyl, ethoxycarbonyl, and methoxymethyl groups were unsatisfactory. ... [Pg.363]

Leptosins D-F (258a-c, Scheme 39) [94JCS(P1)1859] were isolated by Takahashi and co-workers from the culture of a strain of Leptosphaeria sp. as cytotoxic substances against the P388 lymphocytic leukemia cell line comparable to that of mitomycin C. Utilizing the nucleophilic substitution reaction of 1-hydroxytryptamines, a simple methodology for the synthesis of core structures of leptosins has been developed (2000H1255). [Pg.139]

Figure 11.16 Chromatograms of plasma samples obtained by using SPE-SFC with super-aitical desorption of the SPE cartridge (a) blank plasma (20 p.1), UV detection at 215 nm (b) blank plasma (20 p.1), UV detection at 360 nm (c) plasma (1 ml) containing 20 ng mitomycin C (MMC), UV detection at 360 nm. Reprinted from Journal of Chromatography, 454, W. M. A. Niessen et al., Phase-system switching as an on-line sample pretreatment in the bioanalysis of mitomycin C using supercritical fluid cliromatography, pp. 243-251, copyright 1988, with permission from Elsevier Science. Figure 11.16 Chromatograms of plasma samples obtained by using SPE-SFC with super-aitical desorption of the SPE cartridge (a) blank plasma (20 p.1), UV detection at 215 nm (b) blank plasma (20 p.1), UV detection at 360 nm (c) plasma (1 ml) containing 20 ng mitomycin C (MMC), UV detection at 360 nm. Reprinted from Journal of Chromatography, 454, W. M. A. Niessen et al., Phase-system switching as an on-line sample pretreatment in the bioanalysis of mitomycin C using supercritical fluid cliromatography, pp. 243-251, copyright 1988, with permission from Elsevier Science.
W. M. A. Niessen, R J. M. Bergers, U. R. Tjaden and J. van der Greef, Phase-system switclring as an on-line sample preti eatment in the bioanalysis of mitomycin C using supercritical fluid clrromatogi aphy , 7. Chromatogr. 454 243-251 (1988). [Pg.300]

Mitomycin Mitomycin C Ametycine Mutamycin Mytomycin C Mutamycin Mitomycin C... [Pg.1033]

The commercial production of mitomycin involves the preparation of mitomycin-containing broths by culturing a mitomycin-producing organism, e.g. Streptomyces caespitosus, in suitable media as described at length In the literature. At the end of the fermentation cycle the whole broth is usually centrifuged, filtered or otherwise treated to separate the solids (mycelia) from the supernatant which contains substantially all of the antibiotic activity. [Pg.1033]

Microorganisms, by fermentation (cont d) Streptomyces caespitosus Mitomycin... [Pg.1608]

The antitumor antibiotic mitomycin C functions by forming cross-links in DNA chains. [Pg.970]

Microwaves, electromagnetic spectrum and. 419 Mincralocorticoid, 1083 Minor groove (DNA), 1104-1105 Mitomycin C, structure of, 970 Mixed aldol reaction, 885-886 requirements for. 885-886 Mixed Claisen condensation reaction, 890-891... [Pg.1306]


See other pages where Mitomycins is mentioned: [Pg.638]    [Pg.638]    [Pg.638]    [Pg.638]    [Pg.638]    [Pg.638]    [Pg.14]    [Pg.476]    [Pg.158]    [Pg.435]    [Pg.437]    [Pg.445]    [Pg.445]    [Pg.93]    [Pg.93]    [Pg.535]    [Pg.549]    [Pg.102]    [Pg.233]    [Pg.258]    [Pg.394]    [Pg.94]    [Pg.95]    [Pg.340]    [Pg.340]    [Pg.54]    [Pg.577]    [Pg.284]    [Pg.1032]    [Pg.1033]    [Pg.1606]    [Pg.1672]    [Pg.1718]    [Pg.1719]    [Pg.1720]    [Pg.970]   
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5 -fluorouracil/mitomycin

Ametycine - Mitomycin

Ansamycins, Mitomycins, and Pactamycin

Anthracyclines Mitomycin

Antibiotics mitomycin

Anticancer drugs mitomycin

Antitumor agents mitomycin

Biology and Therapeutics of the Mitomycins

Cancer mitomycin

Cellular Mitomycin

Chemotherapeutic agents mitomycin

Chemotherapy mitomycin

Danishefsky synthesis of mitomycins

Doxorubicin Mitomycin

Easy Construction of a Tricyclic Indole Related to the Mitomycins

Kishi synthesis of mitomycins

MUTAMYCIN®, mitomycin

Microbial Mitomycin

Mitomycin A

Mitomycin C

Mitomycin C in plasma

Mitomycin C, structure

Mitomycin Kishi synthesis

Mitomycin Tamoxifen

Mitomycin Vinblastine

Mitomycin Vinca alkaloids

Mitomycin Vindesine

Mitomycin Vinorelbine

Mitomycin X-ray crystal analysis

Mitomycin adverse effects

Mitomycin antitumor natural product

Mitomycin as anticancer drug

Mitomycin extravasation

Mitomycin from Streptomyces caespitosu

Mitomycin from Streptomyces caespitosus

Mitomycin gastric cancer

Mitomycin lung cancer

Mitomycin mutagenic activity

Mitomycin nephrotoxicity

Mitomycin pharmacokinetics

Mitomycin precursors

Mitomycin prodrugs

Mitomycin rearrangement

Mitomycin skeleton

Mitomycin synthesis

Mitomycin synthesisof

Mitomycin via Baeyer-Villiger reaction

Mitomycin, A and

Mitomycin-resistant tumors

Mitomycine

Mitomycins and Related Natural Products

Mitomycins biosynthesis

Mitomycins nucleus

Mitomycins reductive activation

Mitomycins structure

Mitomycins via Peterson methylenation

Mitomycins, bioactivity

NADPH mitomycin

Of mitomycin

Streptomyces caespitosus [Mitomycins

Streptomyces caespitosus mitomycins A-C from

Streptomyces verticillatus [Mitomycins

Streptovaricins and Mitomycins

Thrombocytopenia mitomycin therapy

X-ray analysis of mitomycin

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