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MedKoo product information:
Lomustine
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MedKoo Code#: 100550
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Name:
Lomustine
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CAS#: 13010-47-4
Synonym: Synonym:
Lomustinum. US brand name: CeeNU. Foreign brand names: Belustin;
Belustine; Cecenu; Citostal; Lomeblastin; Lucostin; Lucostine;
Prava. Abbreviation: CCNU. Acronym: CCNU. Code names: RB-1509;
WR-139017. Chemical structure names:
1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea;
Chloroethylcyclo-hexylnitrosourea; N-(2-chloroethyl)-N'-cyclohexyl-N-nitrosourea.
IUPAC/Chemical name:
1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea
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Chemical structure:
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Theoretical analysis
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Chemical Formula: C9H16ClN3O2
Exact Mass: 233.09310
Molecular Weight: 233.69524
m/z: 233.09310 (100.0%), 235.09015 (32.0%),
234.09646 (9.7%), 236.09351 (3.1%), 234.09014 (1.1%)
Elemental Analysis: C, 46.26; H, 6.90; Cl,
15.17; N, 17.98; O, 13.69
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Availability and price:
This agent is
available through custom synthesis. For quotation, question, and order, please send email to
sales@medkoo.com to describe your needs. A representative
will respond your email shortly. We offer significant discount
for larger quantity order.
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Quality control
data:
Product will be shipped with
supporting analytical data.
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Information about this agent
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Lomustine is a nitrosourea with antineoplastic activity. Lomustine
alkylates and crosslinks DNA, thereby inhibiting DNA and RNA
synthesis. This agent also carbamoylates DNA and proteins, resulting
in inhibition of DNA and RNA synthesis and disruption of RNA
processing. Lomustine is lipophilic and crosses the blood-brain
barrier. Check for
active clinical trials or
closed clinical trials using this agent. (NCI
Thesaurus).
CeeNU® (lomustine) (CCNU) is one of the nitrosoureas used in the
treatment of certain neoplastic diseases. It is
1-(2-chloro-ethyl)-3-cyclohexyl-1-nitrosourea. It is a yellow powder
with the empirical formula of C9H16ClN3O2 and a molecular weight of
233.71. CeeNU is soluble in 10% ethanol (0.05 mg per mL) and in
absolute alcohol (70 mg per mL). CeeNU is relatively insoluble in
water ( < 0.05 mg per mL). It is relatively unionized at a
physiological pH. Inactive ingredients in CeeNU Capsules are
magnesium stearate and mannitol.
Although it is generally agreed that CeeNU alkylates
DNA and RNA, it is not cross resistant with other alkylators. As with
other nitrosoureas, it may also inhibit several key enzymatic processes
by carbamoylation of amino acids in proteins. CeeNU may be given orally.
Following oral administration of radioactive CeeNU at doses ranging from
30 mg/m2 to 100 mg/m2, about half of the radioactivity given was
excreted in the urine in the form of degradation products within 24
hours. The serum half-life of the metabolites ranges from 16 hours to 2
days. Tissue levels are comparable to plasma levels at 15 minutes after
intravenous administration. Because of the high lipid solubility and the
relative lack of ionization at physiological pH, CeeNU crosses the
blood-brain barrier quite effectively. Levels of radioactivity in the
CSF are 50% or greater than those measured concurrently in plasma.
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