(2E)-2-[(4aR,5R,8S)-5-hydroxy-4a,8-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-ylidene]propanal

Details

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Internal ID 9c5c4262-67f9-4cda-a67c-426ffaac1ff8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2E)-2-[(4aR,5R,8S)-5-hydroxy-4a,8-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-ylidene]propanal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-10-4-5-14(17)15(3)7-6-12(8-13(10)15)11(2)9-16/h8-10,14,17H,4-7H2,1-3H3/b12-11+/t10-,14+,15+/m0/s1
InChI Key QATFWOVEOOADOD-XZPHSAEASA-N
Popularity 2 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 2.00
Atomic LogP (AlogP) 3.02
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E)-2-[(4aR,5R,8S)-5-hydroxy-4a,8-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-ylidene]propanal

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 + 0.8073 80.73%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7387 73.87%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.9202 92.02%
OATP1B3 inhibitior + 0.9829 98.29%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.8000 80.00%
BSEP inhibitior - 0.6141 61.41%
P-glycoprotein inhibitior - 0.9468 94.68%
P-glycoprotein substrate - 0.7487 74.87%
CYP3A4 substrate + 0.6104 61.04%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8355 83.55%
CYP3A4 inhibition - 0.8078 80.78%
CYP2C9 inhibition - 0.8485 84.85%
CYP2C19 inhibition - 0.6387 63.87%
CYP2D6 inhibition - 0.9443 94.43%
CYP1A2 inhibition - 0.8568 85.68%
CYP2C8 inhibition - 0.7188 71.88%
CYP inhibitory promiscuity - 0.9009 90.09%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4818 48.18%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.9683 96.83%
Skin irritation + 0.6572 65.72%
Skin corrosion - 0.9665 96.65%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5273 52.73%
skin sensitisation + 0.5068 50.68%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.8256 82.56%
Acute Oral Toxicity (c) III 0.8609 86.09%
Estrogen receptor binding - 0.7012 70.12%
Androgen receptor binding + 0.5318 53.18%
Thyroid receptor binding - 0.6127 61.27%
Glucocorticoid receptor binding - 0.6205 62.05%
Aromatase binding - 0.5790 57.90%
PPAR gamma - 0.6078 60.78%
Honey bee toxicity - 0.8857 88.57%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9832 98.32%

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 95.89% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.25% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.76% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.76% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.61% 98.95%
CHEMBL1871 P10275 Androgen Receptor 81.29% 96.43%
CHEMBL5028 O14672 ADAM10 80.90% 97.50%

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.
Gymnanthemum myrianthum

Cross-Links

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PubChem 162907933
LOTUS LTS0221566
wikiData Q105217587