3-Hydroxy-4-methylidene-3-octa-2,4,6-trienoyloxolan-2-one

Details

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Internal ID 8950b33b-91b5-4180-94ff-07d1f47848df
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 3-hydroxy-4-methylidene-3-octa-2,4,6-trienoyloxolan-2-one
SMILES (Canonical) CC=CC=CC=CC(=O)C1(C(=C)COC1=O)O
SMILES (Isomeric) CC=CC=CC=CC(=O)C1(C(=C)COC1=O)O
InChI InChI=1S/C13H14O4/c1-3-4-5-6-7-8-11(14)13(16)10(2)9-17-12(13)15/h3-8,16H,2,9H2,1H3
InChI Key XJTTZELYOODEAA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O4
Molecular Weight 234.25 g/mol
Exact Mass 234.08920892 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.09
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 3-Hydroxy-4-methylidene-3-octa-2,4,6-trienoyloxolan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9287 92.87%
Caco-2 - 0.5896 58.96%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8089 80.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9239 92.39%
OATP1B3 inhibitior + 0.9574 95.74%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6634 66.34%
P-glycoprotein inhibitior - 0.9545 95.45%
P-glycoprotein substrate - 0.9425 94.25%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9047 90.47%
CYP3A4 inhibition - 0.9639 96.39%
CYP2C9 inhibition - 0.8167 81.67%
CYP2C19 inhibition - 0.8661 86.61%
CYP2D6 inhibition - 0.9488 94.88%
CYP1A2 inhibition - 0.8019 80.19%
CYP2C8 inhibition - 0.9339 93.39%
CYP inhibitory promiscuity - 0.9256 92.56%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8871 88.71%
Carcinogenicity (trinary) Non-required 0.5825 58.25%
Eye corrosion - 0.9119 91.19%
Eye irritation - 0.5210 52.10%
Skin irritation - 0.5836 58.36%
Skin corrosion - 0.7892 78.92%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8254 82.54%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.7928 79.28%
skin sensitisation - 0.7555 75.55%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.6627 66.27%
Acute Oral Toxicity (c) III 0.5469 54.69%
Estrogen receptor binding - 0.5753 57.53%
Androgen receptor binding - 0.5066 50.66%
Thyroid receptor binding - 0.5708 57.08%
Glucocorticoid receptor binding - 0.5573 55.73%
Aromatase binding + 0.6953 69.53%
PPAR gamma - 0.6347 63.47%
Honey bee toxicity - 0.9254 92.54%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9010 90.10%

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 92.64% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.67% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.17% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.91% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.54% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.77% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 80.82% 91.19%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139588633
LOTUS LTS0118219
wikiData Q104201057