Page last updated: 2024-11-05

acetylshikonin

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

Description

acetylshikonin: from roots of Boraginacea; RN given refers to cpd without isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID479501
SCHEMBL ID219826
MeSH IDM0199747

Synonyms (19)

Synonym
AC-20169
24502-78-1
shikonin, acetyl
acetylshikonin
[(1r)-1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-4-methylpent-3-enyl] acetate
acetyl shikonin
S9257
AKOS015965847
FT-0621835
SCHEMBL219826
(r)-1-(5,8-dihydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-4-methylpent-3-en-1-yl acetate
AC-35023
Q-100314
1-(5,8-dihydroxy-1,4-dioxo-1,4-dihydro-2-naphthalenyl)-4-methyl-3-pentenyl acetate #
mfcd00143538
HY-N2181
CS-0019489
CCG-267808
DTXSID901317360

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" However, only a few studies have reported the adverse effects of acetylshikonin, with respect to reproductive toxicity and genotoxicity."( Pharmacology, toxicity and pharmacokinetics of acetylshikonin: a review.
Bai, J; Cai, M; Dong, X; Ni, J; Wu, H; Yao, Y; You, L; Zeng, Y; Zhang, Z, 2020
)
0.56

Pharmacokinetics

acetylshikonin is associated with a wide distribution and poor absorption. The pharmacokinetic parameters were obtained through the non-compartmental analysis.

ExcerptReferenceRelevance
"To develop and validate a novel precolumn derivatization method for the quantitative determination and pharmacokinetic application of acetylshikonin in macaque monkeys by liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS)."( Quantitative determination of acetylshikonin in macaque monkey blood by LC-ESI-MS/MS after precolumn derivatization with 2-mercaptoethanol and its application in pharmacokinetic study.
Dou, GF; Du, A; Gu, RL; Meng, ZY; Sun, DX; Tian, HF; Wu, ZN; Yuan, D, 2008
)
0.35
" After the administration of acetylshikonin (80 mg/kg, po) in macaque monkeys, the pharmacokinetic parameters were obtained through the non-compartmental analysis, where the area under the concentration-time curve to the last measurable concentration, the terminal elimination halflife, and the mean residual time were 615."( Quantitative determination of acetylshikonin in macaque monkey blood by LC-ESI-MS/MS after precolumn derivatization with 2-mercaptoethanol and its application in pharmacokinetic study.
Dou, GF; Du, A; Gu, RL; Meng, ZY; Sun, DX; Tian, HF; Wu, ZN; Yuan, D, 2008
)
0.35
"The method was validated and applied to the quantitative determination and pharmacokinetic study of acetylshikonin in the blood samples of macaque monkeys."( Quantitative determination of acetylshikonin in macaque monkey blood by LC-ESI-MS/MS after precolumn derivatization with 2-mercaptoethanol and its application in pharmacokinetic study.
Dou, GF; Du, A; Gu, RL; Meng, ZY; Sun, DX; Tian, HF; Wu, ZN; Yuan, D, 2008
)
0.35
" Pharmacokinetic studies demonstrate that acetylshikonin is associated with a wide distribution and poor absorption."( Pharmacology, toxicity and pharmacokinetics of acetylshikonin: a review.
Bai, J; Cai, M; Dong, X; Ni, J; Wu, H; Yao, Y; You, L; Zeng, Y; Zhang, Z, 2020
)
0.56

Compound-Compound Interactions

ExcerptReferenceRelevance
" In this study, we investigated erlotinib in combination with shikonin and 14 shikonin derivatives in parental U87MG and transfected U87MG."( Shikonin and its derivatives inhibit the epidermal growth factor receptor signaling and synergistically kill glioblastoma cells in combination with erlotinib.
Bauer, R; Efferth, T; Kretschmer, N; Zhao, Q, 2015
)
0.42
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (59)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's7 (11.86)18.2507
2000's11 (18.64)29.6817
2010's26 (44.07)24.3611
2020's15 (25.42)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 (1.64%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other60 (98.36%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]