Mechlorethamine: (explain/give the following) a. Class b. Mechanism c. Pharmacokinetics d. Therapeutic use e. adverse effects
a. Alkylating agent (nitrogen mustard) b. Type I. Bifunctional alkylating agent: produces cross-links in DNA. c. IV. No CNS penetration. Highly reactive. Disappears from blood in seconds to minutes d. Hodgkin’s and non-hodgkin’s lymphoma e. nausea/vomiting, myelosuppression, mild alopecia
Name three alkylating agent antineoplastic drugs
Name two vinca alkaloid antineoplastic drugs
Name five antimetabolite antineoplastic drugs
Name one taxane antineoplastic drug
Name four antiestrogenic antineoplastic drugs and the sub-class of each
Name one corticosteroid antineoplastic drug
Name one atypical alkylating agent antineoplastic drug
Name one metal complex used as an antineoplastic drug
Name one monoclonal antibody used as an antineoplastic drug
Name two antibiotic agents used as antineoplastic drugs
Name one epipodphyllotoxin used as an antineoplastic drug
Name one BRM used as an antineoplastic drug
Mechlorethamine: mechanism of action
Type I (nitrogen mustard). Bifunctional alkylating agent: produces cross-links.
Cyclophosphamide: mechanism of action
Type III (nitrogen mustard). Prodrug activated in liver by CYP450 → active compound phosphoramide mustard acts as akylating agent. Acrolein (byproduct) causes bladder toxicity
Mechanism of action: carmustine (BCNU)
alkylating agent. produces cross-links in DNA
Mechanism of action: Methotrexate
antimetabolite:
Binds to DHFR → blocks formation to FH4 → blocks purine and pyrimidine synthesis
Mechanism of action: 5-fluorouracil (5-FU)
antimetabolite
Pyrimidine analog → activated to FUTP → inhibits RNA synthesis
Pyrimidine analog → activated to FdUMP → interferes with thymidylate synthase → inhibit DNA synthesis
Mechanism of action: cytarabine (Ara-C)
antimetabolite
Pyrimidine (cytadine) analog → competes for phosphorylation of cytidine → also competes with cytidine for incorporation into DNA → causes chain termination
Mechanism of action: mercaptopurine
antimetabolite
Purine analog → converted in cells (by HGPRT) to ribonucleotide that inhibits purine synthesis. Further converted and misincorporated into DNA and RNA
Mechanism of action: hydroxyurea
antimetabolite
Substituted urea → inhibits ribonucleotide reductase → blocks conversion to dNTPs → prevents DNA synthesis → arrests cell at G1-S interface
Mechanism of action: vinblastine
vinca alkaloid
Binds tubulin → prevents formation of microtubules and mitotic spindle
Mechanism of action: vincristine
vinca alkaloid
Binds tubulin → prevents formation of microtubules and mitotic spindle