9-Oxononanoic acid

Details

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Internal ID 33741624-ad80-4c8b-adae-285e9bd80981
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name 9-oxononanoic acid
SMILES (Canonical) C(CCCC=O)CCCC(=O)O
SMILES (Isomeric) C(CCCC=O)CCCC(=O)O
InChI InChI=1S/C9H16O3/c10-8-6-4-2-1-3-5-7-9(11)12/h8H,1-7H2,(H,11,12)
InChI Key WLGDDELKYAWBBL-UHFFFAOYSA-N
Popularity 118 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16O3
Molecular Weight 172.22 g/mol
Exact Mass 172.109944368 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.00
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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2553-17-5
9-oxo-nonanoic acid
9-Ketononanoic acid
Nonanoic acid, 9-oxo-
YH3Q8RSX3Z
MFCD05864080
9-OxononanoicAcid
8-formyloctanoic acid
UNII-YH3Q8RSX3Z
AZELAALDEHYDIC ACID
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 9-Oxononanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9310 93.10%
Caco-2 + 0.5230 52.30%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8933 89.33%
OATP2B1 inhibitior - 0.8473 84.73%
OATP1B1 inhibitior + 0.9027 90.27%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9131 91.31%
P-glycoprotein inhibitior - 0.9844 98.44%
P-glycoprotein substrate - 0.9725 97.25%
CYP3A4 substrate - 0.7243 72.43%
CYP2C9 substrate - 0.5790 57.90%
CYP2D6 substrate - 0.8555 85.55%
CYP3A4 inhibition - 0.9613 96.13%
CYP2C9 inhibition - 0.9044 90.44%
CYP2C19 inhibition - 0.9725 97.25%
CYP2D6 inhibition - 0.9742 97.42%
CYP1A2 inhibition - 0.8414 84.14%
CYP2C8 inhibition - 0.9793 97.93%
CYP inhibitory promiscuity - 0.9919 99.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7535 75.35%
Carcinogenicity (trinary) Non-required 0.7172 71.72%
Eye corrosion + 0.9719 97.19%
Eye irritation + 0.9541 95.41%
Skin irritation + 0.5465 54.65%
Skin corrosion - 0.7069 70.69%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6208 62.08%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.6488 64.88%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity - 0.7746 77.46%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.6681 66.81%
Acute Oral Toxicity (c) IV 0.7231 72.31%
Estrogen receptor binding - 0.8872 88.72%
Androgen receptor binding - 0.9310 93.10%
Thyroid receptor binding - 0.8099 80.99%
Glucocorticoid receptor binding - 0.7793 77.93%
Aromatase binding - 0.7415 74.15%
PPAR gamma - 0.5904 59.04%
Honey bee toxicity - 0.9791 97.91%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.6657 66.57%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4040 P28482 MAP kinase ERK2 95.78% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.43% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.23% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.63% 98.95%
CHEMBL1781 P11387 DNA topoisomerase I 86.38% 97.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.44% 91.11%
CHEMBL1829 O15379 Histone deacetylase 3 84.23% 95.00%
CHEMBL221 P23219 Cyclooxygenase-1 82.24% 90.17%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 82.23% 92.26%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.18% 93.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Cynomorium coccineum subsp. songaricum
Patrinia scabiosifolia
Patrinia villosa
Vitis vinifera

Cross-Links

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PubChem 75704
NPASS NPC305693
LOTUS LTS0152632
wikiData Q27147919