L-Sarcolysin
L-Sarcolysin Brand names, L-Sarcolysin Analogs
L-Sarcolysin Brand Names Mixture
- No information avaliable
L-Sarcolysin Chemical_Formula
C13H18Cl2N2O2
L-Sarcolysin RX_link
http://www.rxlist.com/cgi/generic2/melph.htm
L-Sarcolysin fda sheet
L-Sarcolysin msds (material safety sheet)
L-Sarcolysin Synthesis Reference
Sen, A.K., et al.; Indian J.Chem.Sect.B; 22; 9; 939-941(1983)
L-Sarcolysin Molecular Weight
305.2 g/mol
L-Sarcolysin Melting Point
182.5 oC
L-Sarcolysin H2O Solubility
< 0.1 g/100 mL at 22°C
L-Sarcolysin State
Solid
L-Sarcolysin LogP
-0.432
L-Sarcolysin Dosage Forms
Tablet; Solution (for injection)
L-Sarcolysin Indication
For the palliative treatment of multiple myeloma and for the palliation of non-resectable epithelial carcinoma of the ovary.
L-Sarcolysin Pharmacology
Melphalan is an antineoplastic in the class of alkylating agents and is used to treat various forms of cancer. Alkylating agents are so named because of their ability to add alkyl groups to many electronegative groups under conditions present in cells. They stop tumor growth by cross-linking guanine bases in DNA double-helix strands - directly attacking DNA. This makes the strands unable to uncoil and separate. As this is necessary in DNA replication, the cells can no longer divide. In addition, these drugs add methyl or other alkyl groups onto molecules where they do not belong which in turn inhibits their correct utilization by base pairing and causes a miscoding of DNA. Alkylating agents are cell cycle-nonspecific. Alkylating agents work by three different mechanisms all of which achieve the same end result - disruption of DNA function and cell death.
L-Sarcolysin Absorption
Incomplete, variable, 25-89% post oral dose
L-Sarcolysin side effects and Toxicity
Vomiting, ulceration of the mouth, diarrhea, and hemorrhage of the gastrointestinal tract; The principal toxic effect is bone marrow suppression. LD50=11.2 mg/kg (orally in rat)
L-Sarcolysin Patient Information
PATIENT INFORMATION
Patients should be informed that the major toxicities of ALKERAN are related
to bone marrow suppression, hypersensitivity reactions, gastrointestinal
toxicity, and pulmonary toxicity. The major long-term toxicities are related
to infertility and secondary malignancies. Patients should never be allowed
to take the drug without close medical supervision and should be advised to
consult their physician if they experience skin rash, vasculitis, bleeding,
fever, persistent cough, nausea, vomiting, amenorrhea, weight loss, or unusual
lumps/masses. Women of childbearing potential should be advised to avoid
becoming pregnant.
Laboratory Tests: Periodic complete blood counts with differentials should be
performed during the course of treatment with ALKERAN. At least one determination
should be obtained prior to each treatment course. Patients should be observed
closely for consequences of bone marrow suppression, which include severe infections,
bleeding, and symptomatic anemia.
Patients should be informed that the major toxicities of ALKERAN are related
to bone marrow suppression, hypersensitivity reactions, gastrointestinal
toxicity, and pulmonary toxicity. The major long-term toxicities are related
to infertility and secondary malignancies. Patients should never be allowed
to take the drug without close medical supervision and should be advised to
consult their physician if they experience skin rash, vasculitis, bleeding,
fever, persistent cough, nausea, vomiting, amenorrhea, weight loss, or unusual
lumps/masses. Women of childbearing potential should be advised to avoid
becoming pregnant.
Laboratory Tests: Periodic complete blood counts with differentials should be
performed during the course of treatment with ALKERAN. At least one determination
should be obtained prior to each treatment course. Patients should be observed
closely for consequences of bone marrow suppression, which include severe infections,
bleeding, and symptomatic anemia.
L-Sarcolysin Organisms Affected
Humans and other mammals
