Cat. No. | Product Name | Target | Signaling Pathways |
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T36705 |
Mitomycin A
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Antibiotic | Microbiology/Virology |
Mitomycin A 是从链霉菌中提取出具有细胞毒性的抗生素,具有抗癌活性和抗肿瘤活性。Mitomycin A 可用于研究实体癌。 | |||
T32429 |
KW 2149
KT6149,KW2149,KW-2149 |
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KW 2149 is a compound derived from mitomycin C. | |||
T26102 |
RM 49
RM49,RM-49 |
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RM 49 is a mitomycin C derivative that has antitumor activity in vitro. | |||
T29487 |
7-N-(4-Hydroxyphenyl)mitomycin C
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7-N-(4-Hydroxyphenyl)mitomycin C is a bioactive chemical. | |||
T80635 | Gentisuric acid | Drug Metabolite | Metabolism |
Gentisuric Acid,作为Aspirin的代谢产物同时也是α-酰胺化单加氧酶(PAM)的底物,可抵御Mitomycin C导致的DNA损伤。 | |||
T68675 |
Porfiromycin
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Porfiromycin is a n N-methyl derivative of the antineoplastic antibiotic mitomycin C isolated from the bacterium Streptomyces ardus and other Streptomyces bacterial species. Bioreduced porfiromycin generates oxygen radicals and alkylates DNA, producing interstrand cross-links and single-strand breaks, thereby inhibiting DNA synthesis. Porfiromycin is preferentially toxic to hypoxic cells. | |||
T36385 |
Ansatrienin A
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Ansatrienin A is an ansamycin antibiotic and antifungal agent first isolated from S. collinus and S. rishiriensis. In fetal rat long bones, it is an inhibitor of parathyroid hormone-induced calcium release (IC50 = 64 nM), which is a measure of bone resorption, and pp60c-srcM kinase (IC50 = 100 nM). It also inhibits TNF-α-induced expression of intercellular adhesion molecule-1 (ICAM-1; IC50 = 570 nM). Early in vitro studies showed that ansatrienin A potentiates the chemotherapeutic action of 5-fl... | |||
T36650 |
Ansatrienin B
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Ansatrienin B is an ansamycin antibiotic and antifungal agent first isolated from S. collinus and S. rishiriensis., In fetal rat long bones, it is an inhibitor of parathyroid hormone-induced calcium release (IC50 = 21 nM), which is a measure of bone resorption, and pp60c-src kinase (IC50 = 50 nM). It is an inhibitor of translation at the protein synthesis stage by specific inhibition of L-leucine incorporation (IC50 = 58 nM in A549 cells). It also inhibits TNF-α-induced expression of intercellul... |