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Organic compounds characterized as anthracene derivatives, and known for their use in cancer chemotherapy; they are commonly extracted from Streptomyces bacterium.
Doxorubicin hydrochloride an anthracycline antibiotic derivative exhibits cytotoxic activity and is widely utilized as an anticancer chemotherapeutic agent Its mechanism involves intercalating into DNA double-strands inhibiting DNA topoisomerase II activity and consequently interrupting replication processes causing DNA damage and altered chromatin structure by histone displacement In biomedical research settings doxorubicin hydrochloride is employed in vitro and in animal models to study therapeutic strategies against hematologic malignancies solid tumors and sarcomas Reported IC50 values vary with cell type and assay conditions typically ranging between approximately 0 1 M to 2 M in various tumor-derived cell models
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Doxorubicin hydrochloride is a cytotoxic anthracycline antibiotic and an anti-cancer chemotherapy agent. It is a potent human DNA topoisomerase I and topoisomerase II inhibitor, reducing basal phosphorylation of AMPK and its downstream target acetyl-CoA carboxylase. It also induces apoptosis and autophagy.
Potent human DNA topoisomerase I and topoisomerase II inhibitor
Reduces basal phosphorylation of AMPK
Induces apoptosis and autophagy
Used in infection and cancer research
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Daunorubicin hydrochloride, also known as Daunomycin, is a potent topoisomerase II inhibitor with significant anti-tumor activity. This anthracycline antibiotic functions by inhibiting DNA and RNA synthesis, leading to the suppression of cancer cell viability. It is recognized for its ability to induce apoptosis and necrosis in target cells.
Potent anti-tumor agent
Inhibits DNA and RNA synthesis
Induces apoptosis and necrosis
Anthracycline antibiotic
Useful in research for various cancers, including leukemia and lymphomas
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Doxorubicin hydrochloride (Hydroxydaunorubicin hydrochloride; ADR), a cytotoxic anthracycline antibiotic, is an anti-cancer chemotherapy agent. It is a potent human DNA topoisomerase I and topoisomerase II inhibitor with IC50s of 0.8 μM and 2.67 μM, respectively. Doxorubicin hydrochloride reduces basal phosphorylation of AMPK and its downstream target acetyl-CoA carboxylase. It also induces apoptosis and autophagy.
Cytotoxic anthracycline antibiotic
Anti-cancer chemotherapy agent
Potent human DNA topoisomerase I and topoisomerase II inhibitor (IC50s of 0.8 μM and 2.67 μM)
Reduces basal phosphorylation of AMPK and its downstream target acetyl-CoA carboxylase
Induces apoptosis and autophagy
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Doxorubicin hydrochloride (Standard) is an analytical standard and cytotoxic anthracycline antibiotic, primarily used as an anti-cancer chemotherapy agent. It functions as a potent human DNA topoisomerase I and topoisomerase II inhibitor, reducing basal phosphorylation of AMPK and its downstream target acetyl-CoA carboxylase, while also inducing apoptosis and autophagy.
Intended for research and analytical applications
Functions as a cytotoxic anthracycline antibiotic
Acts as an anti-cancer chemotherapy agent
Potent human DNA topoisomerase I and II inhibitor
Induces apoptosis and autophagy
Used in qualitative and quantitative research experiments
Suitable for HPLC, GC, and MS applications
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