(2E,5E)-7-hydroperoxy-1-hydroxy-3,7-dimethylocta-2,5-dien-4-one

Details

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Internal ID 2cd26cbf-4154-4c17-9220-1a11d6fbf24e
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (2E,5E)-7-hydroperoxy-1-hydroxy-3,7-dimethylocta-2,5-dien-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O4/c1-8(5-7-11)9(12)4-6-10(2,3)14-13/h4-6,11,13H,7H2,1-3H3/b6-4+,8-5+
InChI Key XJJPOJYHJBZLMP-HLQBBKRNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O4
Molecular Weight 200.23 g/mol
Exact Mass 200.10485899 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 0.10
Atomic LogP (AlogP) 1.32
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,5E)-7-hydroperoxy-1-hydroxy-3,7-dimethylocta-2,5-dien-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9557 95.57%
Caco-2 + 0.8708 87.08%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7646 76.46%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.9456 94.56%
OATP1B3 inhibitior + 0.9338 93.38%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7498 74.98%
P-glycoprotein inhibitior - 0.9723 97.23%
P-glycoprotein substrate - 0.9306 93.06%
CYP3A4 substrate - 0.5523 55.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8804 88.04%
CYP3A4 inhibition - 0.8182 81.82%
CYP2C9 inhibition - 0.8052 80.52%
CYP2C19 inhibition - 0.7740 77.40%
CYP2D6 inhibition - 0.9010 90.10%
CYP1A2 inhibition - 0.8376 83.76%
CYP2C8 inhibition - 0.9423 94.23%
CYP inhibitory promiscuity - 0.6915 69.15%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5323 53.23%
Carcinogenicity (trinary) Non-required 0.6449 64.49%
Eye corrosion - 0.7722 77.22%
Eye irritation + 0.7574 75.74%
Skin irritation - 0.5142 51.42%
Skin corrosion - 0.7991 79.91%
Ames mutagenesis + 0.6292 62.92%
Human Ether-a-go-go-Related Gene inhibition - 0.6956 69.56%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.4788 47.88%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.8667 86.67%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5624 56.24%
Acute Oral Toxicity (c) III 0.5965 59.65%
Estrogen receptor binding - 0.7336 73.36%
Androgen receptor binding - 0.9060 90.60%
Thyroid receptor binding - 0.8283 82.83%
Glucocorticoid receptor binding - 0.6774 67.74%
Aromatase binding - 0.7965 79.65%
PPAR gamma - 0.8258 82.58%
Honey bee toxicity - 0.8486 84.86%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.7696 76.96%

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 92.29% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 91.27% 89.34%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.52% 94.45%
CHEMBL2581 P07339 Cathepsin D 85.14% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.63% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.76% 86.33%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.67% 80.78%
CHEMBL340 P08684 Cytochrome P450 3A4 80.66% 91.19%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.29% 94.33%

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.
Mosla chinensis
Seriphidium aucheri

Cross-Links

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PubChem 13855814
NPASS NPC190920
LOTUS LTS0215712
wikiData Q105329006