2-(4-acetyloxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl)prop-2-enoic acid

Details

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Internal ID baedb969-ddf3-48a5-8a0b-96a92b636f38
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name 2-(4-acetyloxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl)prop-2-enoic acid
SMILES (Canonical) CC1=C2CC(CC(C2(CCC1)C)OC(=O)C)C(=C)C(=O)O
SMILES (Isomeric) CC1=C2CC(CC(C2(CCC1)C)OC(=O)C)C(=C)C(=O)O
InChI InChI=1S/C17H24O4/c1-10-6-5-7-17(4)14(10)8-13(11(2)16(19)20)9-15(17)21-12(3)18/h13,15H,2,5-9H2,1,3-4H3,(H,19,20)
InChI Key SJYHSBXOBJXDKM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H24O4
Molecular Weight 292.40 g/mol
Exact Mass 292.16745924 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(4-acetyloxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl)prop-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9869 98.69%
Caco-2 + 0.7540 75.40%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8362 83.62%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.8234 82.34%
OATP1B3 inhibitior - 0.2946 29.46%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.7521 75.21%
BSEP inhibitior - 0.8583 85.83%
P-glycoprotein inhibitior - 0.7855 78.55%
P-glycoprotein substrate - 0.9247 92.47%
CYP3A4 substrate + 0.6113 61.13%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9014 90.14%
CYP3A4 inhibition - 0.6439 64.39%
CYP2C9 inhibition - 0.8811 88.11%
CYP2C19 inhibition - 0.9108 91.08%
CYP2D6 inhibition - 0.9414 94.14%
CYP1A2 inhibition + 0.5563 55.63%
CYP2C8 inhibition - 0.6210 62.10%
CYP inhibitory promiscuity - 0.9438 94.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9643 96.43%
Carcinogenicity (trinary) Non-required 0.6530 65.30%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.7157 71.57%
Skin irritation + 0.6647 66.47%
Skin corrosion - 0.9618 96.18%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5202 52.02%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.6875 68.75%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.7668 76.68%
Acute Oral Toxicity (c) III 0.8662 86.62%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.5121 51.21%
Thyroid receptor binding - 0.5940 59.40%
Glucocorticoid receptor binding - 0.4735 47.35%
Aromatase binding - 0.5205 52.05%
PPAR gamma + 0.7115 71.15%
Honey bee toxicity - 0.8246 82.46%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5455 54.55%
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 95.85% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.26% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.58% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 88.05% 91.19%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.45% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.14% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.66% 99.23%
CHEMBL2581 P07339 Cathepsin D 82.49% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.23% 82.69%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.92% 85.14%

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.
Ajania fruticulosa
Artemisia biennis

Cross-Links

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PubChem 13855809
LOTUS LTS0022659
wikiData Q105254639