Sebacic Acid

Details

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Internal ID 1cae3fc6-46cc-48b7-b066-3681cc106e08
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name decanedioic acid
SMILES (Canonical) C(CCCCC(=O)O)CCCC(=O)O
SMILES (Isomeric) C(CCCCC(=O)O)CCCC(=O)O
InChI InChI=1S/C10H18O4/c11-9(12)7-5-3-1-2-4-6-8-10(13)14/h1-8H2,(H,11,12)(H,13,14)
InChI Key CXMXRPHRNRROMY-UHFFFAOYSA-N
Popularity 502 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O4
Molecular Weight 202.25 g/mol
Exact Mass 202.12050905 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.28
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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DECANEDIOIC ACID
111-20-6
1,8-Octanedicarboxylic acid
1,10-Decanedioic acid
Sebacinsaure
Decanedicarboxylic acid
n-Decanedioic acid
Acide sebacique
Sebacinsaeure
USAF HC-1
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Sebacic Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6806 68.06%
Caco-2 + 0.5228 52.28%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8984 89.84%
OATP2B1 inhibitior - 0.8454 84.54%
OATP1B1 inhibitior + 0.9620 96.20%
OATP1B3 inhibitior + 0.9623 96.23%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9087 90.87%
P-glycoprotein inhibitior - 0.9676 96.76%
P-glycoprotein substrate - 0.9928 99.28%
CYP3A4 substrate - 0.7996 79.96%
CYP2C9 substrate + 0.6532 65.32%
CYP2D6 substrate - 0.8621 86.21%
CYP3A4 inhibition - 0.9600 96.00%
CYP2C9 inhibition - 0.9390 93.90%
CYP2C19 inhibition - 0.9762 97.62%
CYP2D6 inhibition - 0.9729 97.29%
CYP1A2 inhibition - 0.9046 90.46%
CYP2C8 inhibition - 0.9924 99.24%
CYP inhibitory promiscuity - 0.9927 99.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8035 80.35%
Carcinogenicity (trinary) Non-required 0.7514 75.14%
Eye corrosion + 0.8498 84.98%
Eye irritation + 0.9861 98.61%
Skin irritation - 0.8721 87.21%
Skin corrosion - 0.9639 96.39%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.9278 92.78%
Respiratory toxicity + 0.9667 96.67%
Reproductive toxicity - 0.8950 89.50%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.6209 62.09%
Acute Oral Toxicity (c) IV 0.6448 64.48%
Estrogen receptor binding - 0.8366 83.66%
Androgen receptor binding - 0.9322 93.22%
Thyroid receptor binding - 0.8294 82.94%
Glucocorticoid receptor binding - 0.7133 71.33%
Aromatase binding - 0.7793 77.93%
PPAR gamma + 0.5812 58.12%
Honey bee toxicity - 0.9874 98.74%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.7418 74.18%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 2.8 nM
Potency
via Super-PRED
CHEMBL1293235 P02545 Prelamin-A/C 5 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3060 Q9Y345 Glycine transporter 2 91.31% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 90.44% 83.82%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 88.14% 92.26%
CHEMBL2581 P07339 Cathepsin D 83.51% 98.95%
CHEMBL1781 P11387 DNA topoisomerase I 82.34% 97.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.23% 91.11%

Cross-Links

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PubChem 5192
NPASS NPC118968
LOTUS LTS0251393
wikiData Q413454