5-(2,5,5,8a-tetramethyl-7-oxo-4,4a,6,8-tetrahydro-1H-naphthalen-1-yl)-3-methylpent-2-enal

Details

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Internal ID c729e106-0ce8-4649-88c6-b80d88593ba4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 5-(2,5,5,8a-tetramethyl-7-oxo-4,4a,6,8-tetrahydro-1H-naphthalen-1-yl)-3-methylpent-2-enal
SMILES (Canonical) CC1=CCC2C(CC(=O)CC2(C1CCC(=CC=O)C)C)(C)C
SMILES (Isomeric) CC1=CCC2C(CC(=O)CC2(C1CCC(=CC=O)C)C)(C)C
InChI InChI=1S/C20H30O2/c1-14(10-11-21)6-8-17-15(2)7-9-18-19(3,4)12-16(22)13-20(17,18)5/h7,10-11,17-18H,6,8-9,12-13H2,1-5H3
InChI Key VZPRTHXWRBQXOY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O2
Molecular Weight 302.50 g/mol
Exact Mass 302.224580195 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.89
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(2,5,5,8a-tetramethyl-7-oxo-4,4a,6,8-tetrahydro-1H-naphthalen-1-yl)-3-methylpent-2-enal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8728 87.28%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7270 72.70%
OATP2B1 inhibitior - 0.8628 86.28%
OATP1B1 inhibitior + 0.8763 87.63%
OATP1B3 inhibitior + 0.9074 90.74%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.6300 63.00%
P-glycoprotein inhibitior - 0.6615 66.15%
P-glycoprotein substrate - 0.7828 78.28%
CYP3A4 substrate + 0.6057 60.57%
CYP2C9 substrate - 0.8329 83.29%
CYP2D6 substrate - 0.8689 86.89%
CYP3A4 inhibition - 0.7988 79.88%
CYP2C9 inhibition - 0.8409 84.09%
CYP2C19 inhibition - 0.6178 61.78%
CYP2D6 inhibition - 0.9577 95.77%
CYP1A2 inhibition - 0.8751 87.51%
CYP2C8 inhibition - 0.6666 66.66%
CYP inhibitory promiscuity - 0.6935 69.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5686 56.86%
Eye corrosion - 0.9870 98.70%
Eye irritation - 0.9330 93.30%
Skin irritation - 0.5176 51.76%
Skin corrosion - 0.9734 97.34%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7874 78.74%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5571 55.71%
skin sensitisation + 0.8000 80.00%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7903 79.03%
Estrogen receptor binding + 0.6209 62.09%
Androgen receptor binding - 0.6108 61.08%
Thyroid receptor binding + 0.6129 61.29%
Glucocorticoid receptor binding + 0.6452 64.52%
Aromatase binding - 0.6233 62.33%
PPAR gamma - 0.5484 54.84%
Honey bee toxicity - 0.8983 89.83%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9922 99.22%

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 96.06% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.17% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.65% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.90% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.44% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.10% 100.00%
CHEMBL1871 P10275 Androgen Receptor 84.61% 96.43%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.32% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 80.34% 94.73%

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.
Baccharis boliviensis

Cross-Links

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PubChem 163001713
LOTUS LTS0155956
wikiData Q105299920