8-Methyl-5-oxo-nonanoic acid

Details

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Internal ID d0632877-3e99-437e-842e-eb1b37491aef
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name 8-methyl-5-oxononanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O3/c1-8(2)6-7-9(11)4-3-5-10(12)13/h8H,3-7H2,1-2H3,(H,12,13)
InChI Key CVTYGALEXWGUJW-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O3
Molecular Weight 186.25 g/mol
Exact Mass 186.125594432 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.25
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-Methyl-5-oxo-nonanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9773 97.73%
Caco-2 + 0.7863 78.63%
Blood Brain Barrier + 0.5830 58.30%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.9017 90.17%
OATP2B1 inhibitior - 0.8315 83.15%
OATP1B1 inhibitior + 0.9389 93.89%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9416 94.16%
P-glycoprotein inhibitior - 0.9674 96.74%
P-glycoprotein substrate - 0.9136 91.36%
CYP3A4 substrate - 0.6607 66.07%
CYP2C9 substrate + 0.6594 65.94%
CYP2D6 substrate - 0.8782 87.82%
CYP3A4 inhibition - 0.9612 96.12%
CYP2C9 inhibition - 0.8902 89.02%
CYP2C19 inhibition - 0.9511 95.11%
CYP2D6 inhibition - 0.9626 96.26%
CYP1A2 inhibition - 0.7486 74.86%
CYP2C8 inhibition - 0.9920 99.20%
CYP inhibitory promiscuity - 0.9813 98.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6915 69.15%
Carcinogenicity (trinary) Non-required 0.7781 77.81%
Eye corrosion + 0.8756 87.56%
Eye irritation + 0.9655 96.55%
Skin irritation - 0.6767 67.67%
Skin corrosion - 0.9163 91.63%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7282 72.82%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6429 64.29%
skin sensitisation + 0.5673 56.73%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.7257 72.57%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.6685 66.85%
Acute Oral Toxicity (c) III 0.8432 84.32%
Estrogen receptor binding - 0.9377 93.77%
Androgen receptor binding - 0.9192 91.92%
Thyroid receptor binding - 0.7854 78.54%
Glucocorticoid receptor binding - 0.7954 79.54%
Aromatase binding - 0.8684 86.84%
PPAR gamma - 0.7984 79.84%
Honey bee toxicity - 0.9765 97.65%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity + 0.9182 91.82%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.54% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.22% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 94.17% 83.82%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 93.84% 92.26%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.70% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 87.98% 90.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.25% 93.56%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 86.18% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.73% 96.47%
CHEMBL1907 P15144 Aminopeptidase N 83.86% 93.31%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 132543963
LOTUS LTS0189446
wikiData Q103818096