Page last updated: 2024-09-20

sebacic acid

Description

sebacic acid : An alpha,omega-dicarboxylic acid that is the 1,8-dicarboxy derivative of octane. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID5192
CHEMBL ID1232164
CHEBI ID41865
SCHEMBL ID3977
MeSH IDM0057150

Synonyms (88)

Synonym
sebacinsaure [german]
ccris 2290
brn 1210591
einecs 203-845-5
n-decanedioic acid
nsc 19492
ai3-09127
acide sebacique [french]
CHEMBL1232164
NCI60_001628
ipomic acid
LMFA01170006
iponic acid
1,10-decanedioic acid
nsc19492 ,
nsc-19492
1,8-octanedicarboxylic acid
usaf hc-1
wln: qv8vq
decanedicarboxylic acid
sebacic acid
C08277
111-20-6
decanedioic acid
sebacic acid, 94%
CHEBI:41865 ,
sebacinsaeure
1,8-dicarboxyoctane
1L6Y
1I8J
1L6S
sebacic acid, 99%
NCGC00164361-01
NCIOPEN2_008624
sebacic acid, >=95.0% (gc)
301CFA7E-7155-4D51-BD2F-EB921428B436
DB07645
AKOS000120056
NCGC00164361-02
tox21_303263
dtxsid7026867 ,
NCGC00257150-01
dtxcid806867
cas-111-20-6
tox21_201778
NCGC00259327-01
BBL011473
26776-29-4
STL146585
unii-97an39ictc
4-02-00-02078 (beilstein handbook reference)
ec 203-845-5
sebacinsaure
acide sebacique
97an39ictc ,
sebacic acid [mi]
sebacic acid [inci]
fema no. 4943
sebacic acid [mart.]
S5732
octane-1,8-dicarboxylic acid
SCHEMBL3977
seracic acid
Q-201703
FT-0696757
mfcd00004440
GS-6713
sebacicacid
1,8-octanedicarboxylate
4-oxodecanedioate
1,10-decanedioate
dicarboxylic acid c10
n-decanedioate
HY-W014787
CS-W015503
Q413454
EN300-19796
disodium-sebacate
CCG-266598
NCGC00164361-03
1,8-octanedicarboxylic acid; decanedioic acid; octane-1,8-dicarboxylic acid
A894762
poly(sebacic anhydride)
BP-27864
Z104475420
1,8-octanedcarboxylic acid
decanedioc acid
sebacic acid (mart.)

Roles (2)

RoleDescription
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
alpha,omega-dicarboxylic acid
dicarboxylic fatty acid
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (10)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
RAR-related orphan receptor gammaMus musculus (house mouse)Potency4.88050.006038.004119,952.5996AID1159523
AR proteinHomo sapiens (human)Potency27.44490.000221.22318,912.5098AID1259247
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency27.44490.001022.650876.6163AID1224893
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency4.88050.003041.611522,387.1992AID1159555
retinoid X nuclear receptor alphaHomo sapiens (human)Potency55.21670.000817.505159.3239AID1159527
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency19.46170.001530.607315,848.9004AID1259401; AID1259403
estrogen nuclear receptor alphaHomo sapiens (human)Potency19.47290.000229.305416,493.5996AID1259248; AID743075
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, Porphobilinogen SynthaseEscherichia coliIC50 (µMol)39.000039.000039.000039.0000AID977608
Chain A, Porphobilinogen SynthaseEscherichia coliIC50 (µMol)129.500039.0000129.5000220.0000AID977608
Chain A, Porphobilinogen SynthaseEscherichia coliIC50 (µMol)129.500039.0000129.5000220.0000AID977608
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (26)

Assay IDTitleYearJournalArticle
AID1635113Upregulation of HDAC1 inhibition-mediated histone H3 acetylation-induced extracellular SOD expression in human THP1 cells at 1 mM after 12 hrs by chromatin immunoprecipitation method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635108Inhibition of HDAC1 in human THP1 cells assessed as increase in histone H4 acetylation level at 1 mM after 12 hrs by Western blot analysis relative to control2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635115Effect on HDAC2 mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635117Effect on HDAC8 mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635119Effect on HDAC5 mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635121Effect on HDAC7 mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635105Upregulation of HDAC1 inhibition/ERK signalling activation-mediated extracellular SOD mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635124Inhibition of HDAC activity in human THP1 cells at 1 mM preincubated for 1 hr followed by substrate addition measured after 2 hrs by fluorescence assay relative to control2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635118Effect on HDAC4 mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635112Upregulation of HDAC1 inhibition-mediated histone H4 acetylation-induced extracellular SOD expression in human THP1 cells at 1 mM after 12 hrs by chromatin immunoprecipitation method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635104Upregulation of HDAC1 inhibition/ERK signalling activation-mediated extracellular SOD protein expression in human THP1 cells at 1 mM after 24 hrs by ELISA2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635120Effect on HDAC6 mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635103Upregulation of Mn SOD mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635122Effect on HDAC9 mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635109Inhibition of HDAC1 in human THP1 cells assessed as increase in histone H3 acetylation level at 1 mM after 12 hrs by Western blot analysis relative to control2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635102Effect on Cu/Zn SOD mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635123Effect on HDAC10 mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635116Effect on HDAC3 mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635139Inhibition of recombinant HDAC1 catalytic domain (unknown origin) using HDAC substrate at 1 mM preincubated for 1 hr followed by substrate addition measured after 30 mins by fluorescence assay relative to control2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID1635114Effect on HDAC1 mRNA expression in human THP1 cells at 1 mM after 24 hrs by RT-PCR method2016Journal of natural products, Apr-22, Volume: 79, Issue:4
Royal Jelly Constituents Increase the Expression of Extracellular Superoxide Dismutase through Histone Acetylation in Monocytic THP-1 Cells.
AID977608Experimentally measured binding affinity data (IC50) for protein-ligand complexes derived from PDB2002The Journal of biological chemistry, May-31, Volume: 277, Issue:22
Species-specific inhibition of porphobilinogen synthase by 4-oxosebacic acid.
AID1811Experimentally measured binding affinity data derived from PDB2002The Journal of biological chemistry, May-31, Volume: 277, Issue:22
Species-specific inhibition of porphobilinogen synthase by 4-oxosebacic acid.
AID1745855NCATS anti-infectives library activity on the primary C. elegans qHTS viability assay2023Disease models & mechanisms, 03-01, Volume: 16, Issue:3
In vivo quantitative high-throughput screening for drug discovery and comparative toxicology.
AID1745854NCATS anti-infectives library activity on HEK293 viability as a counter-qHTS vs the C. elegans viability qHTS2023Disease models & mechanisms, 03-01, Volume: 16, Issue:3
In vivo quantitative high-throughput screening for drug discovery and comparative toxicology.
AID977608Experimentally measured binding affinity data (IC50) for protein-ligand complexes derived from PDB2001Biochemistry, Jul-27, Volume: 40, Issue:28
Mechanistic basis for suicide inactivation of porphobilinogen synthase by 4,7-dioxosebacic acid, an inhibitor that shows dramatic species selectivity.
AID1811Experimentally measured binding affinity data derived from PDB2001Biochemistry, Jul-27, Volume: 40, Issue:28
Mechanistic basis for suicide inactivation of porphobilinogen synthase by 4,7-dioxosebacic acid, an inhibitor that shows dramatic species selectivity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (145)

TimeframeStudies, This Drug (%)All Drugs %
pre-199023 (15.86)18.7374
1990's32 (22.07)18.2507
2000's39 (26.90)29.6817
2010's43 (29.66)24.3611
2020's8 (5.52)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 (%)
Trials3 (1.92%)5.53%
Reviews2 (1.28%)6.00%
Case Studies3 (1.92%)4.05%
Observational0 (0.00%)0.25%
Other148 (94.87%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research Highlights

Safety/Toxicity (2)

ArticleYear
Poly(sebacic acid-co-ricinoleic acid) biodegradable carrier for paclitaxel: in vitro release and in vivo toxicity.
Journal of biomedical materials research. Part A, Apr-01, Volume: 69, Issue: 1
2004
Toxicity of disodium sebacate.
Drugs under experimental and clinical research, Volume: 16, Issue: 10
1990
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Pharmacokinetics (1)

ArticleYear
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioavailability (1)

ArticleYear
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]