7-(3-Hydroxyprop-1-en-2-yl)-1,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one

Details

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Internal ID 5eb69950-264a-4955-999d-f41375a14396
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name 7-(3-hydroxyprop-1-en-2-yl)-1,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-10(9-16)12-4-6-15(3)7-5-14(17)11(2)13(15)8-12/h12,16H,1,4-9H2,2-3H3
InChI Key PPEAYEMIWAFAFB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.02
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(3-Hydroxyprop-1-en-2-yl)-1,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.8186 81.86%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6918 69.18%
OATP2B1 inhibitior - 0.8488 84.88%
OATP1B1 inhibitior + 0.9079 90.79%
OATP1B3 inhibitior + 0.9355 93.55%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.6436 64.36%
BSEP inhibitior - 0.5808 58.08%
P-glycoprotein inhibitior - 0.8839 88.39%
P-glycoprotein substrate - 0.8755 87.55%
CYP3A4 substrate + 0.5843 58.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8859 88.59%
CYP3A4 inhibition - 0.7275 72.75%
CYP2C9 inhibition - 0.8695 86.95%
CYP2C19 inhibition - 0.7042 70.42%
CYP2D6 inhibition - 0.9056 90.56%
CYP1A2 inhibition - 0.7282 72.82%
CYP2C8 inhibition - 0.8806 88.06%
CYP inhibitory promiscuity - 0.7973 79.73%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5981 59.81%
Eye corrosion - 0.9857 98.57%
Eye irritation + 0.5626 56.26%
Skin irritation - 0.6006 60.06%
Skin corrosion - 0.9681 96.81%
Ames mutagenesis - 0.7670 76.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5058 50.58%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.6098 60.98%
skin sensitisation - 0.6560 65.60%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.6814 68.14%
Acute Oral Toxicity (c) III 0.8226 82.26%
Estrogen receptor binding - 0.7856 78.56%
Androgen receptor binding - 0.5376 53.76%
Thyroid receptor binding - 0.6495 64.95%
Glucocorticoid receptor binding - 0.6811 68.11%
Aromatase binding - 0.7249 72.49%
PPAR gamma - 0.5987 59.87%
Honey bee toxicity - 0.8847 88.47%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9871 98.71%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.03% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.32% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.45% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.36% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.64% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.39% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.29% 97.09%
CHEMBL1937 Q92769 Histone deacetylase 2 85.57% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.72% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.30% 95.89%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.49% 93.03%
CHEMBL1871 P10275 Androgen Receptor 82.43% 96.43%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.93% 94.45%

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 afra
Artemisia herba-alba
Cestrum parqui

Cross-Links

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PubChem 14021353
LOTUS LTS0033690
wikiData Q105212839