Humuladienone

Details

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Internal ID 02e28b88-b259-4226-b1d4-16987af3e042
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4Z,8Z)-2,6,6,9-tetramethylcycloundeca-4,8-dien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-12-7-8-14(16)13(2)6-5-10-15(3,4)11-9-12/h5,9-10,13H,6-8,11H2,1-4H3/b10-5-,12-9-
InChI Key XWFINABYEHNSEP-CGBKSYCJSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.29
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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(4Z,8Z)-2,6,6,9-tetramethylcycloundeca-4,8-dien-1-one
RefChem:1086727
SCHEMBL30752494
CHEBI:195962
Q67879922

2D Structure

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2D Structure of Humuladienone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.8635 86.35%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5236 52.36%
OATP2B1 inhibitior - 0.8491 84.91%
OATP1B1 inhibitior + 0.9110 91.10%
OATP1B3 inhibitior + 0.8945 89.45%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6645 66.45%
P-glycoprotein inhibitior - 0.9597 95.97%
P-glycoprotein substrate - 0.9048 90.48%
CYP3A4 substrate + 0.5288 52.88%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate - 0.8297 82.97%
CYP3A4 inhibition - 0.8940 89.40%
CYP2C9 inhibition - 0.8700 87.00%
CYP2C19 inhibition - 0.8060 80.60%
CYP2D6 inhibition - 0.9530 95.30%
CYP1A2 inhibition - 0.7138 71.38%
CYP2C8 inhibition - 0.9372 93.72%
CYP inhibitory promiscuity - 0.8847 88.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5107 51.07%
Eye corrosion - 0.9057 90.57%
Eye irritation + 0.7457 74.57%
Skin irritation + 0.7153 71.53%
Skin corrosion - 0.9770 97.70%
Ames mutagenesis - 0.7528 75.28%
Human Ether-a-go-go-Related Gene inhibition - 0.4119 41.19%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.9177 91.77%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6622 66.22%
Acute Oral Toxicity (c) III 0.5558 55.58%
Estrogen receptor binding - 0.9492 94.92%
Androgen receptor binding - 0.8494 84.94%
Thyroid receptor binding - 0.6375 63.75%
Glucocorticoid receptor binding - 0.7607 76.07%
Aromatase binding - 0.7489 74.89%
PPAR gamma - 0.7496 74.96%
Honey bee toxicity - 0.8918 89.18%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9651 96.51%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.99% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.39% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 86.18% 86.00%
CHEMBL2581 P07339 Cathepsin D 84.49% 98.95%
CHEMBL1871 P10275 Androgen Receptor 84.07% 96.43%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.28% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.97% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.25% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.19% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.13% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.01% 96.77%

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.
Helichrysum odoratissimum

Cross-Links

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PubChem 101297706
LOTUS LTS0027071
wikiData Q67879922