Page last updated: 2024-12-05

suberic acid

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

Description

Suberic acid, also known as octanedioic acid, is a dicarboxylic acid with the formula HOOC(CH2)6COOH. It is a white, crystalline solid that is soluble in water. Suberic acid is found naturally in some plants, such as cork oak. It is also a byproduct of the oxidation of fats and oils. Suberic acid has a variety of industrial uses, including the production of plasticizers, resins, and lubricants. It is also used as a food additive and in the manufacture of pharmaceuticals. Suberic acid is being studied for its potential use in the treatment of a variety of diseases, including cancer, diabetes, and Alzheimer's disease. Research is ongoing to further understand the potential benefits and risks of suberic acid.'

suberic acid: used in plastics industry; inhibits activity of some enzymes; RN given refers to parent cpd; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

suberic acid : An alpha,omega-dicarboxylic acid that is the 1,6-dicarboxy derivative of hexane. [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 CID10457
CHEMBL ID1162491
CHEBI ID9300
SCHEMBL ID3301
MeSH IDM0047477

Synonyms (70)

Synonym
BIDD:ER0503
nsc53777
nsc-53777
nsc-25952
hexamethylenedicarboxylic acid
NSC25952 ,
LMFA01170001
octanedioic acid
1,8-octanedioic acid
suberic acid
505-48-6
1,6-hexanedicarboxylic acid
cork acid
C08278
suberic acid, 98%
NCGC00164012-01
68937-72-4
1,6-dicarboxyhexane
oktandisaeure
korksaeure
CHEBI:9300 ,
suberinsaeure
octane-1,8-dioic acid
S-9000
932D754A-EE85-46C7-A95B-A93A3DC1EC61
octanedioic acid suberic acid
BMSE000378
FT-0655538
kork acid
O0023
CHEMBL1162491
STK801855
AKOS000119018
NCGC00164012-02
NCGC00258085-01
tox21_200531
cas-505-48-6
dtxcid101644
dtxsid8021644 ,
BBL009289
einecs 273-084-1
nsc 25952
unii-6u7y4m9c1h
6u7y4m9c1h ,
ai3-52672
einecs 208-010-9
AM20100233
S6220
AB00376809-03
SCHEMBL3301
suberic acid [mi]
mfcd00004428
SY004501
STR03966
CS-W016016
F1905-7049
suberic acid, purum, >=98.0% (t)
AC7522
korksaure
hexamethylenedicarboxylate
1,6-hexanedicarboxylate
1,8-octanedioate
octane-1,8-dioate
HY-W015300
NCGC00164012-03
octane-1,8-dioic aid
Q899074
EN300-19300
BP-27862
Z104473456

Research Excerpts

Compound-Compound Interactions

ExcerptReferenceRelevance
" Moreover, more information can be provided on the evaluation of toxicity of phorate using metabonomics combined with clinical chemistry."( Metabonomics evaluation of urine from rats administered with phorate under long-term and low-level exposure by ultra-performance liquid chromatography-mass spectrometry.
Guo, L; Hou, Y; Sun, C; Sun, X; Xu, W; Zeng, Y; Zhao, X, 2014
)
0.4

Dosage Studied

ExcerptRelevanceReference
" Four chemicals (L-Arg, L-Leu-L-Leu-OH, L-Leu-L-Ile-OH and suberic acid) induced behavioral avoidance in toad tadpoles at some (but not all) dosage levels, so we then exposed toad larvae to these chemicals over the entire period of larval development."( The Effects of Conspecific Alarm Cues on Larval Cane Toads (Rhinella marina).
Capon, RJ; Crossland, MR; Salim, AA; Shine, R, 2019
)
0.76
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
[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 (5)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
RAR-related orphan receptor gammaMus musculus (house mouse)Potency77.66370.006038.004119,952.5996AID1159521
farnesoid X nuclear receptorHomo sapiens (human)Potency19.68240.375827.485161.6524AID743220
thyroid hormone receptor beta isoform aHomo sapiens (human)Potency0.01260.010039.53711,122.0200AID588547
[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)
Solute carrier family 22 member 20Mus musculus (house mouse)Ki1,126.01001.10006.67899.1201AID360149
Solute carrier family 22 member 6Mus musculus (house mouse)Ki33.99220.40745.02179.4000AID360150
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (3)

Assay IDTitleYearJournalArticle
AID360151Ratio of pKi for mouse Oat1 expressed in Xenopus oocytes to pKi for mouse Oat6 expressed in Xenopus oocytes2007The Journal of biological chemistry, Aug-17, Volume: 282, Issue:33
Structural variation governs substrate specificity for organic anion transporter (OAT) homologs. Potential remote sensing by OAT family members.
AID360149Inhibition of mouse Oat6-mediated [3H]ES uptake in Xenopus oocytes after 1 hr2007The Journal of biological chemistry, Aug-17, Volume: 282, Issue:33
Structural variation governs substrate specificity for organic anion transporter (OAT) homologs. Potential remote sensing by OAT family members.
AID360150Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hr2007The Journal of biological chemistry, Aug-17, Volume: 282, Issue:33
Structural variation governs substrate specificity for organic anion transporter (OAT) homologs. Potential remote sensing by OAT family members.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (46)

TimeframeStudies, This Drug (%)All Drugs %
pre-199016 (34.78)18.7374
1990's10 (21.74)18.2507
2000's9 (19.57)29.6817
2010's10 (21.74)24.3611
2020's1 (2.17)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 44.68

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 Index44.68 (24.57)
Research Supply Index3.91 (2.92)
Research Growth Index4.46 (4.65)
Search Engine Demand Index66.41 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (44.68)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (2.08%)5.53%
Reviews1 (2.08%)6.00%
Case Studies3 (6.25%)4.05%
Observational0 (0.00%)0.25%
Other43 (89.58%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]