9-(3,3-Dimethyloxiran-2-yl)-3,7-dimethylnona-2,6-dienoic acid

Details

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Internal ID dbd83d24-573c-4eef-842e-290d6f1d288e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name 9-(3,3-dimethyloxiran-2-yl)-3,7-dimethylnona-2,6-dienoic acid
SMILES (Canonical) CC(=CCCC(=CC(=O)O)C)CCC1C(O1)(C)C
SMILES (Isomeric) CC(=CCCC(=CC(=O)O)C)CCC1C(O1)(C)C
InChI InChI=1S/C15H24O3/c1-11(8-9-13-15(3,4)18-13)6-5-7-12(2)10-14(16)17/h6,10,13H,5,7-9H2,1-4H3,(H,16,17)
InChI Key DIAZNFMKLJLDNM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O3
Molecular Weight 252.35 g/mol
Exact Mass 252.17254462 g/mol
Topological Polar Surface Area (TPSA) 49.80 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.70
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 9-(3,3-Dimethyloxiran-2-yl)-3,7-dimethylnona-2,6-dienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9708 97.08%
Caco-2 + 0.5122 51.22%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7015 70.15%
OATP2B1 inhibitior - 0.8533 85.33%
OATP1B1 inhibitior + 0.8907 89.07%
OATP1B3 inhibitior + 0.9287 92.87%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.5218 52.18%
P-glycoprotein inhibitior - 0.9531 95.31%
P-glycoprotein substrate - 0.9074 90.74%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate + 0.6189 61.89%
CYP2D6 substrate - 0.9088 90.88%
CYP3A4 inhibition - 0.7343 73.43%
CYP2C9 inhibition - 0.6302 63.02%
CYP2C19 inhibition - 0.6651 66.51%
CYP2D6 inhibition - 0.9314 93.14%
CYP1A2 inhibition - 0.5487 54.87%
CYP2C8 inhibition - 0.8666 86.66%
CYP inhibitory promiscuity - 0.8480 84.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8143 81.43%
Carcinogenicity (trinary) Non-required 0.6564 65.64%
Eye corrosion - 0.9576 95.76%
Eye irritation - 0.8639 86.39%
Skin irritation + 0.5725 57.25%
Skin corrosion - 0.9598 95.98%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4929 49.29%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.5694 56.94%
skin sensitisation + 0.7036 70.36%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.5830 58.30%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.5658 56.58%
Acute Oral Toxicity (c) III 0.6014 60.14%
Estrogen receptor binding - 0.7363 73.63%
Androgen receptor binding - 0.5364 53.64%
Thyroid receptor binding - 0.5606 56.06%
Glucocorticoid receptor binding - 0.5579 55.79%
Aromatase binding - 0.6655 66.55%
PPAR gamma + 0.5963 59.63%
Honey bee toxicity - 0.8354 83.54%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9711 97.11%

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 92.88% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.94% 91.11%
CHEMBL2039 P27338 Monoamine oxidase B 86.42% 92.51%
CHEMBL2061 P19793 Retinoid X receptor alpha 84.89% 91.67%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.62% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.78% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 82.82% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 81.92% 94.73%

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 135008
LOTUS LTS0021633
wikiData Q104981086