Thespesone

Details

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Internal ID 18be6756-43a9-43b1-a251-221d1b761a36
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 9-hydroxy-1,5,8-trimethyl-1,2-dihydrobenzo[e][1]benzofuran-6,7-dione
SMILES (Canonical) CC1COC2=C1C3=C(C(=C2)C)C(=O)C(=O)C(=C3O)C
SMILES (Isomeric) CC1COC2=C1C3=C(C(=C2)C)C(=O)C(=O)C(=C3O)C
InChI InChI=1S/C15H14O4/c1-6-4-9-10(7(2)5-19-9)12-11(6)15(18)14(17)8(3)13(12)16/h4,7,16H,5H2,1-3H3
InChI Key NBWHNPKICLVSGW-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O4
Molecular Weight 258.27 g/mol
Exact Mass 258.08920892 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.55
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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RefChem:189224
85889-26-5
9-hydroxy-1,5,8-trimethyl-1,2-dihydrobenzo[e][1]benzofuran-6,7-dione

2D Structure

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2D Structure of Thespesone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.7577 75.77%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7604 76.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9177 91.77%
OATP1B3 inhibitior + 0.9522 95.22%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8533 85.33%
P-glycoprotein inhibitior - 0.9496 94.96%
P-glycoprotein substrate - 0.8355 83.55%
CYP3A4 substrate - 0.5511 55.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8554 85.54%
CYP3A4 inhibition - 0.7369 73.69%
CYP2C9 inhibition + 0.8249 82.49%
CYP2C19 inhibition + 0.6288 62.88%
CYP2D6 inhibition - 0.8834 88.34%
CYP1A2 inhibition + 0.9386 93.86%
CYP2C8 inhibition - 0.8927 89.27%
CYP inhibitory promiscuity + 0.7174 71.74%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9943 99.43%
Carcinogenicity (trinary) Non-required 0.4939 49.39%
Eye corrosion - 0.9848 98.48%
Eye irritation + 0.7719 77.19%
Skin irritation - 0.6808 68.08%
Skin corrosion - 0.9545 95.45%
Ames mutagenesis + 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7562 75.62%
Micronuclear + 0.6259 62.59%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.5584 55.84%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6301 63.01%
Acute Oral Toxicity (c) III 0.4113 41.13%
Estrogen receptor binding + 0.6639 66.39%
Androgen receptor binding + 0.7628 76.28%
Thyroid receptor binding - 0.6826 68.26%
Glucocorticoid receptor binding - 0.4934 49.34%
Aromatase binding - 0.7017 70.17%
PPAR gamma - 0.5520 55.20%
Honey bee toxicity - 0.9042 90.42%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9923 99.23%

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 96.59% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.88% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.00% 89.00%
CHEMBL2581 P07339 Cathepsin D 91.14% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.53% 93.40%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 89.26% 86.00%
CHEMBL3401 O75469 Pregnane X receptor 87.31% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.85% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.66% 100.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.46% 94.80%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.68% 90.71%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.80% 92.94%

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.
Pilocarpus grandiflorus
Thespesia populnea

Cross-Links

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PubChem 5321934
NPASS NPC95100
LOTUS LTS0256588
wikiData Q105114984