Page last updated: 2024-11-12

fi-700

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

Description

FI-700: FLT3 inhibitor that selectively suppresses the growth of leukemia cells with FLT3 mutations; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID11517444
CHEMBL ID486332
MeSH IDM0514848

Synonyms (9)

Synonym
CHEMBL486332
866883-79-6
n548ap3gtf ,
fi-700
2,4-pyrimidinediamine, 5-(5-(1-piperazinylmethyl)-1,3,4-oxadiazol-2-yl)-n4-propyl-n2-(2-(4-pyridinyl)ethyl)-
unii-n548ap3gtf
5-(5-(piperazin-1-ylmethyl)-1,3,4-oxadiazol-2-yl)-n4-propyl-n2-(2-(pyridin-4-yl)ethyl)pyrimidine-2,4-diamine
Q27284565
5-[5-(piperazin-1-ylmethyl)-1,3,4-oxadiazol-2-yl]-4-n-propyl-2-n-(2-pyridin-4-ylethyl)pyrimidine-2,4-diamine
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (16)

Assay IDTitleYearJournalArticle
AID344776Antitumor activity against human MOLM13 cells xenografted in SCID mouse assessed as minimal regressive tumor volume ratio at 200 mg/kg, po bid treated for 5 days measured after 10 days relative to control2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344782Antitumor activity against human MOLM13 cells xenografted in po dosed SCID mouse assessed as tumor volume ratio administered bid for 5 days2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344768Antiproliferative activity against human HMC1 cells expressing FLT3-delta599 mutant after 72 hrs by WST-1 assay2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344775Antitumor activity against human MOLM13 cells xenografted in SCID mouse assessed as minimal regressive tumor volume ratio at 100 mg/kg, po bid treated for 5 days measured after 4 days relative to control2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344779Toxicity to human MOLM13 cells xenografted SCID mouse assessed as mortality at 50 mg/kg, po bid after 5 days2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344774Antitumor activity against human MOLM13 cells xenografted in SCID mouse assessed as minimal tumor volume ratio at 100 mg/kg, po bid treated for 5 days measured after 10 days relative to control2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344767Metabolic stability in human liver microsomes assessed as intrinsic clearance2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344781Toxicity to human MOLM13 cells xenografted SCID mouse assessed as mortality at 200 mg/kg, po bid after 5 days2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344773Antitumor activity against human MOLM13 cells xenografted in SCID mouse assessed as tumor volume ratio at 200 mg/kg, po bid treated for 5 days measured after 10 days relative to control2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344772Antitumor activity against human MOLM13 cells xenografted in SCID mouse assessed as minimal tumor volume ratio at 100 mg/kg, po bid treated for 5 days measured after 7 days relative to control2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344769Antiproliferative activity against human HMC1 cells expressing FLT-D835Y mutant after 72 hrs by WST-1 assay2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344784Toxicity to human MOLM13 cells xenografted SCID mouse assessed as body weight loss at 200 mg/kg, po bid after 5 days2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344780Toxicity to human MOLM13 cells xenografted SCID mouse assessed as mortality at 100 mg/kg, po bid after 5 days2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344766Antiproliferative activity against human MOLM13 cells after 72 hrs by WST-1 assay2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344783Antitumor activity against human MOLM13 cells xenografted in po dosed SCID mouse assessed as regression tumor volume ratio administered bid for 5 days2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
AID344770Antiproliferative activity against human ML1 cells after 72 hrs by WST-1 assay2008Bioorganic & medicinal chemistry letters, Oct-15, Volume: 18, Issue:20
Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (50.00)29.6817
2010's3 (50.00)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: 48.30

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 strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index48.30 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.37 (4.65)
Search Engine Demand Index73.28 (26.88)
Search Engine Supply Index2.09 (0.95)

This Compound (48.30)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (16.67%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (83.33%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]