Drug class
Antineoplastics - Arsenic Compounds
Antineoplastics – Arsenic Compounds is a specialized therapeutic subclass of antineoplastic agents consisting of arsenic-based compounds, primarily represented in clinical practice by arsenic trioxide. Read more about Antineoplastics - Arsenic Compounds
17 drugs in this class 17 manufacturers
Drugs in Antineoplastics - Arsenic Compounds
ARSENIC TRIOXIDE
ARSENIC TRIOXIDE
ARSENIC TRIOXIDE
ARSENIC TRIOXIDE
ARSENIC TRIOXIDE
ARSENIC TRIOXIDE
ARSENIC TRIOXIDE
Antineoplastics – Arsenic Compounds is a specialized therapeutic subclass of antineoplastic agents consisting of arsenic-based compounds, primarily represented in clinical practice by arsenic trioxide.
These agents exert antineoplastic activity by inducing morphological changes, promoting oxidative stress, generating reactive oxygen species, and triggering programmed cell death (apoptosis) in malignant cells.
Additionally, they facilitate the degradation of the pathognomonic promyelocytic leukemia–retinoic acid receptor alpha (PML-RARa) fusion protein, thereby restoring myeloid cell differentiation.
The primary established therapeutic indication for this class is acute promyelocytic leukemia, utilized in both frontline regimens alongside tretinoin and for relapsed or refractory disease.
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rsc.org
Antineoplastics – Arsenic Compounds is a specialized therapeutic subclass of antineoplastic agents consisting of arsenic-based compounds, primarily represented in clinical practice by arsenic trioxide The primary established therapeutic indication for this class is acute promyelocytic leukemia, utilized in both frontline regimens alongside tretinoin and for relapsed or refractory disease
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researchgate.net
Antineoplastics – Arsenic Compounds is a specialized therapeutic subclass of antineoplastic agents consisting of arsenic-based compounds, primarily represented in clinical practice by arsenic trioxide
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plos.org
These agents exert antineoplastic activity by inducing morphological changes, promoting oxidative stress, generating reactive oxygen species, and triggering programmed cell death (apoptosis) in malignant cells
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nih.gov
These agents exert antineoplastic activity by inducing morphological changes, promoting oxidative stress, generating reactive oxygen species, and triggering programmed cell death (apoptosis) in malignant cells Additionally, they facilitate the degradation of the pathognomonic promyelocytic leukemia–retinoic acid receptor alpha (PML-RARα) fusion protein, thereby restoring myeloid cell differentiation
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patsnap.com
These agents exert antineoplastic activity by inducing morphological changes, promoting oxidative stress, generating reactive oxygen species, and triggering programmed cell death (apoptosis) in malignant cells Additionally, they facilitate the degradation of the pathognomonic promyelocytic leukemia–retinoic acid receptor alpha (PML-RARα) fusion protein, thereby restoring myeloid cell differentiation
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cancer.gov
The primary established therapeutic indication for this class is acute promyelocytic leukemia, utilized in both frontline regimens alongside tretinoin and for relapsed or refractory disease
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