[(1S,2R,3R,4aR,5S,8aS)-2-hydroxy-4a,5-dimethyl-7-oxo-3-prop-1-en-2-yl-1,2,3,4,5,6,8,8a-octahydronaphthalen-1-yl] (Z)-3-methylpent-3-enoate

Details

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Internal ID 83f5716c-1589-4bb5-8a96-9ade4e7c1f52
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name [(1S,2R,3R,4aR,5S,8aS)-2-hydroxy-4a,5-dimethyl-7-oxo-3-prop-1-en-2-yl-1,2,3,4,5,6,8,8a-octahydronaphthalen-1-yl] (Z)-3-methylpent-3-enoate
SMILES (Canonical) CC=C(C)CC(=O)OC1C2CC(=O)CC(C2(CC(C1O)C(=C)C)C)C
SMILES (Isomeric) C/C=C(/C)\CC(=O)O[C@H]1[C@H]2CC(=O)C[C@@H]([C@]2(C[C@@H]([C@H]1O)C(=C)C)C)C
InChI InChI=1S/C21H32O4/c1-7-13(4)8-18(23)25-20-17-10-15(22)9-14(5)21(17,6)11-16(12(2)3)19(20)24/h7,14,16-17,19-20,24H,2,8-11H2,1,3-6H3/b13-7-/t14-,16+,17+,19+,20-,21+/m0/s1
InChI Key LHIIDGPAVXFPNB-WWRPENJWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H32O4
Molecular Weight 348.50 g/mol
Exact Mass 348.23005950 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2R,3R,4aR,5S,8aS)-2-hydroxy-4a,5-dimethyl-7-oxo-3-prop-1-en-2-yl-1,2,3,4,5,6,8,8a-octahydronaphthalen-1-yl] (Z)-3-methylpent-3-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9881 98.81%
Caco-2 + 0.7310 73.10%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8126 81.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8442 84.42%
OATP1B3 inhibitior + 0.8082 80.82%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5620 56.20%
P-glycoprotein inhibitior - 0.5728 57.28%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6272 62.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8482 84.82%
CYP3A4 inhibition + 0.6026 60.26%
CYP2C9 inhibition - 0.9089 90.89%
CYP2C19 inhibition - 0.8556 85.56%
CYP2D6 inhibition - 0.9488 94.88%
CYP1A2 inhibition - 0.8785 87.85%
CYP2C8 inhibition - 0.7125 71.25%
CYP inhibitory promiscuity - 0.8978 89.78%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Non-required 0.6729 67.29%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.8631 86.31%
Skin irritation + 0.5222 52.22%
Skin corrosion - 0.9663 96.63%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5469 54.69%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.5415 54.15%
skin sensitisation - 0.6691 66.91%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.5548 55.48%
Acute Oral Toxicity (c) III 0.6270 62.70%
Estrogen receptor binding + 0.7015 70.15%
Androgen receptor binding - 0.6487 64.87%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6606 66.06%
Aromatase binding - 0.5571 55.71%
PPAR gamma - 0.5066 50.66%
Honey bee toxicity - 0.7281 72.81%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 1.0000 100.00%

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 97.56% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.53% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.59% 94.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.04% 89.34%
CHEMBL299 P17252 Protein kinase C alpha 88.33% 98.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.03% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.77% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.21% 96.77%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.91% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 85.86% 90.17%
CHEMBL340 P08684 Cytochrome P450 3A4 85.31% 91.19%
CHEMBL1951 P21397 Monoamine oxidase A 84.72% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.81% 86.33%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.62% 91.24%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.58% 94.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.00% 91.07%
CHEMBL1871 P10275 Androgen Receptor 82.83% 96.43%
CHEMBL1859 O95180 Voltage-gated T-type calcium channel alpha-1H subunit 80.79% 98.57%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.26% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.22% 95.89%

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.
Euryops algoensis

Cross-Links

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PubChem 14890370
LOTUS LTS0120758
wikiData Q105151774