Page last updated: 2024-11-12

apicidin

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

Description

apicidin: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID124933487
MeSH IDM0268034

Synonyms (1)

Synonym
apicidin

Research Excerpts

Pharmacokinetics

ExcerptReferenceRelevance
" The developed assay method was applied to a pharmacokinetic study after intravenous injection of apicidin in rats at a dose of 1 mg/kg."( Development of a liquid chromatography/electrospray tandem mass spectrometry assay for the quantification of apicidin, a novel histone deacetylase inhibitor, in rat serum: application to a pharmacokinetic study.
Han, JW; Kim, CH; Kim, J; Park, EH; Shin, BS; Yoo, SD; Yoon, CH, 2005
)
0.33
" All concentrations were analyzed using a population pharmacokinetic model with 9 compartments in S-ADAPT."( Population pharmacokinetics of a novel histone deacetylase inhibitor, cyclo{(2S)-2-amino-8-[(aminocarbonyl)hydrazono] decanoyl-1-L-tryptophyl-L-isoleucyl-(2R)-2-piperidinecarbonyl} (SD-2007), and its metabolic conversion to apicidin after intravenous inje
Bulitta, JB; Choi, Y; Hong, DK; Hwang, SW; Kim, HY; Kim, MK; Lee, JB; Lee, MH; Shin, BS; Yoo, SD, 2011
)
0.37
" The population pharmacokinetic model described all profiles well."( Population pharmacokinetics of a novel histone deacetylase inhibitor, cyclo{(2S)-2-amino-8-[(aminocarbonyl)hydrazono] decanoyl-1-L-tryptophyl-L-isoleucyl-(2R)-2-piperidinecarbonyl} (SD-2007), and its metabolic conversion to apicidin after intravenous inje
Bulitta, JB; Choi, Y; Hong, DK; Hwang, SW; Kim, HY; Kim, MK; Lee, JB; Lee, MH; Shin, BS; Yoo, SD, 2011
)
0.37

Bioavailability

Apicidin was poorly absorbed, with the absolute oral bioavailability of 19. After oral administration, the total bioavailability is known to be low (14.5%)

ExcerptReferenceRelevance
" Apicidin was poorly absorbed, with the absolute oral bioavailability of 19."( Pharmacokinetics of a novel histone deacetylase inhibitor, apicidin, in rats.
Cao, D; Chang, HS; Kim, HY; Kim, J; Lee, KC; Park, EH; Ryu, JK; Shin, BS; Yoo, SD; Yoon, CH; Zee, OP, 2006
)
0.33
" After oral administration, the total bioavailability of apicidin is known to be low (14."( Quantitative determination of absorption and first-pass metabolism of apicidin, a potent histone deacetylase inhibitor.
Bulitta, JB; Choi, JH; Joo, SH; Kim, TH; Landersdorfer, CB; Shin, BS; Shin, JC; Shin, S; Weon, KY; Yoo, SD, 2014
)
0.4
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (116)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's2 (1.72)18.2507
2000's60 (51.72)29.6817
2010's48 (41.38)24.3611
2020's6 (5.17)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (0.85%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other116 (99.15%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]