5-(3-Acetyloxy-7-hydroxy-1,2,4a-trimethyl-5-methylidene-6-oxo-2,3,4,8a-tetrahydronaphthalen-1-yl)-3-methylpent-2-enoic acid

Details

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Internal ID c7dcf007-222c-4095-a0ca-1b97b229d1e0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Quinomethanes > O-quinomethanes
IUPAC Name 5-(3-acetyloxy-7-hydroxy-1,2,4a-trimethyl-5-methylidene-6-oxo-2,3,4,8a-tetrahydronaphthalen-1-yl)-3-methylpent-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H30O6/c1-12(9-19(25)26)7-8-21(5)13(2)17(28-15(4)23)11-22(6)14(3)20(27)16(24)10-18(21)22/h9-10,13,17-18,24H,3,7-8,11H2,1-2,4-6H3,(H,25,26)
InChI Key YEUFKPMMZGYLFU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H30O6
Molecular Weight 390.50 g/mol
Exact Mass 390.20423867 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.98
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(3-Acetyloxy-7-hydroxy-1,2,4a-trimethyl-5-methylidene-6-oxo-2,3,4,8a-tetrahydronaphthalen-1-yl)-3-methylpent-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 + 0.9681 96.81%
Caco-2 + 0.5427 54.27%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7763 77.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8563 85.63%
OATP1B3 inhibitior - 0.2345 23.45%
MATE1 inhibitior - 0.5600 56.00%
OCT2 inhibitior - 0.7021 70.21%
BSEP inhibitior + 0.6966 69.66%
P-glycoprotein inhibitior - 0.4820 48.20%
P-glycoprotein substrate - 0.6406 64.06%
CYP3A4 substrate + 0.6466 64.66%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.9095 90.95%
CYP3A4 inhibition - 0.7097 70.97%
CYP2C9 inhibition - 0.9270 92.70%
CYP2C19 inhibition - 0.9140 91.40%
CYP2D6 inhibition - 0.9129 91.29%
CYP1A2 inhibition - 0.7859 78.59%
CYP2C8 inhibition - 0.6225 62.25%
CYP inhibitory promiscuity - 0.8683 86.83%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Non-required 0.6815 68.15%
Eye corrosion - 0.9931 99.31%
Eye irritation - 0.8693 86.93%
Skin irritation + 0.6028 60.28%
Skin corrosion - 0.9501 95.01%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7046 70.46%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.6295 62.95%
skin sensitisation - 0.6873 68.73%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.6020 60.20%
Acute Oral Toxicity (c) III 0.7138 71.38%
Estrogen receptor binding + 0.5468 54.68%
Androgen receptor binding + 0.5504 55.04%
Thyroid receptor binding + 0.6057 60.57%
Glucocorticoid receptor binding + 0.7151 71.51%
Aromatase binding + 0.6580 65.80%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.7777 77.77%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9959 99.59%

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 98.74% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.96% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.41% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.89% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.39% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.83% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.31% 99.23%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 83.85% 94.08%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.72% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 83.22% 90.17%

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.
Oedera genistifolia

Cross-Links

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PubChem 162923065
LOTUS LTS0207002
wikiData Q105347407