Page last updated: 2024-12-07

4-methylcyclophosphamide

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

4-methylcyclophosphamide is an alkylating agent with anti-cancer properties. It is a prodrug that is metabolized to an active form, 4-hydroxycyclophosphamide, which is a potent inhibitor of DNA synthesis. 4-methylcyclophosphamide is used to treat a variety of cancers, including leukemia, lymphoma, and multiple myeloma. It is also used to suppress the immune system in patients with autoimmune diseases. 4-methylcyclophosphamide is typically administered intravenously or orally. Common side effects include nausea, vomiting, hair loss, and bone marrow suppression. In research, 4-methylcyclophosphamide is studied for its potential to treat a variety of conditions, including cancer, autoimmune diseases, and viral infections. It is also being investigated as a potential agent for tissue regeneration and stem cell therapy.'

4-methylcyclophosphamide: RN given refers to cpd without isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID119485
SCHEMBL ID17899474
MeSH IDM0063380

Synonyms (14)

Synonym
4-methylcyclophosphamide
2h-1,3,2-oxazaphosphorin-2-amine, n,n-bis(2-chloroethyl)tetrahydro-4-methyl-, 2-oxide
b 699
2h-1,3,2-oxazaphosphorine, tetrahydro-2-(bis(2-chloroethyl)amino)-4-methyl-, 2-oxide
tetrahydro-2-(bis(2-chloroethyl)amino)-4-methyl-2h-1,3,2-oxazaphosphorine 2-oxide
57604-37-2
2h-1,2-oxazaphosphorin-2-amine, n,n-bis(2-chloroethyl)tetrahydro-4-methyl-, 2-oxide, trans-
nsc-241532
nsc241532
52663-82-8
SCHEMBL17899474
2-[bis(2-chloroethyl)amino]-4-methyl-1,3,2lambda~5~-oxazaphosphinan-2-one
DTXSID60967089
n,n-bis(2-chloroethyl)-4-methyl-2-oxo-1,3,2lambda5-oxazaphosphinan-2-amine

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"Cyclophosphamide (CP) is selectively toxic to avian and mammalian B lymphocytes, but the mechanisms of action are incompletely understood."( Cytogenetic mechanisms in the selective toxicity of cyclophosphamide analogs and metabolites towards avian embryonic B lymphocytes in vivo.
Bloom, SE; Colvin, OM; Wilmer, JL, 1992
)
0.28
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (60.00)18.7374
1990's2 (40.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.60

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.60 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.39 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.60)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]