ent-Diplophyllolide-A

Details

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Internal ID cf439864-6dc6-4faa-bd98-84c77c95fe0b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Eudesmanolides, secoeudesmanolides, and derivatives
IUPAC Name 5,8a-dimethyl-3-methylidene-4,4a,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-2-one
SMILES (Canonical) CC1=CCCC2(C1CC3C(C2)OC(=O)C3=C)C
SMILES (Isomeric) CC1=CCCC2(C1CC3C(C2)OC(=O)C3=C)C
InChI InChI=1S/C15H20O2/c1-9-5-4-6-15(3)8-13-11(7-12(9)15)10(2)14(16)17-13/h5,11-13H,2,4,6-8H2,1,3H3
InChI Key PQRAHHQIYITFCT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O2
Molecular Weight 232.32 g/mol
Exact Mass 232.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.24
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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ent-Diplophyllolide-A
NSC-258633

2D Structure

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2D Structure of ent-Diplophyllolide-A

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 + 0.8605 86.05%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.4574 45.74%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.9134 91.34%
OATP1B3 inhibitior + 0.8789 87.89%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior - 0.9514 95.14%
P-glycoprotein inhibitior - 0.9205 92.05%
P-glycoprotein substrate - 0.8944 89.44%
CYP3A4 substrate + 0.5656 56.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8497 84.97%
CYP3A4 inhibition + 0.5523 55.23%
CYP2C9 inhibition - 0.9611 96.11%
CYP2C19 inhibition + 0.7655 76.55%
CYP2D6 inhibition - 0.9480 94.80%
CYP1A2 inhibition + 0.7986 79.86%
CYP2C8 inhibition - 0.7252 72.52%
CYP inhibitory promiscuity - 0.8134 81.34%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4895 48.95%
Eye corrosion - 0.9844 98.44%
Eye irritation - 0.7596 75.96%
Skin irritation + 0.4937 49.37%
Skin corrosion - 0.9382 93.82%
Ames mutagenesis - 0.7754 77.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4632 46.32%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.6961 69.61%
skin sensitisation + 0.5586 55.86%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.7103 71.03%
Acute Oral Toxicity (c) III 0.7649 76.49%
Estrogen receptor binding - 0.6146 61.46%
Androgen receptor binding - 0.5207 52.07%
Thyroid receptor binding - 0.5933 59.33%
Glucocorticoid receptor binding + 0.5773 57.73%
Aromatase binding - 0.7289 72.89%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.7819 78.19%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9954 99.54%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.31% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.30% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.95% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.07% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.70% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.09% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.99% 95.50%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 84.86% 96.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.70% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.33% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.88% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 80.69% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.35% 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.
Artemisia gmelinii
Chiloscyphus polyanthos
Inula racemosa
Mastigophora diclados
Ratibida mexicana
Tritomaria quinquedentata

Cross-Links

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PubChem 318811
LOTUS LTS0167133
wikiData Q105213393