10-Hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-5-one

Details

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Internal ID 4cafb9eb-2c7e-439f-b5c5-561beb663bd0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O2/c1-6-15(5,17)11-7-8-13(4)14(16)10-9-12(2)3/h6,8-9,17H,1,7,10-11H2,2-5H3
InChI Key MUORSVLFTLIZJO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.58
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 10-Hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.6619 66.19%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5104 51.04%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.9129 91.29%
OATP1B3 inhibitior + 0.9285 92.85%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.4937 49.37%
P-glycoprotein inhibitior - 0.9383 93.83%
P-glycoprotein substrate - 0.9414 94.14%
CYP3A4 substrate - 0.5276 52.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8715 87.15%
CYP3A4 inhibition - 0.8294 82.94%
CYP2C9 inhibition - 0.8285 82.85%
CYP2C19 inhibition - 0.8419 84.19%
CYP2D6 inhibition - 0.9352 93.52%
CYP1A2 inhibition - 0.6995 69.95%
CYP2C8 inhibition - 0.9344 93.44%
CYP inhibitory promiscuity - 0.9003 90.03%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6702 67.02%
Eye corrosion - 0.7536 75.36%
Eye irritation + 0.8708 87.08%
Skin irritation + 0.7941 79.41%
Skin corrosion - 0.9180 91.80%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5917 59.17%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5483 54.83%
skin sensitisation + 0.8722 87.22%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.8087 80.87%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.5288 52.88%
Acute Oral Toxicity (c) III 0.8604 86.04%
Estrogen receptor binding - 0.8025 80.25%
Androgen receptor binding - 0.7552 75.52%
Thyroid receptor binding - 0.7506 75.06%
Glucocorticoid receptor binding - 0.6484 64.84%
Aromatase binding - 0.6540 65.40%
PPAR gamma + 0.7371 73.71%
Honey bee toxicity - 0.8444 84.44%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.8627 86.27%

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
CHEMBL3401 O75469 Pregnane X receptor 92.01% 94.73%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 88.42% 91.24%
CHEMBL2581 P07339 Cathepsin D 85.17% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.69% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.07% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.42% 99.17%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.03% 91.07%

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.
Artemisia douglasiana
Pentzia incana

Cross-Links

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PubChem 86073347
LOTUS LTS0148852
wikiData Q105172596