4-Hydroxy-5-methylidene-3-tetradec-11-enylideneoxolan-2-one

Details

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Internal ID eccc81bc-ee5a-4cd7-aa8f-904feb15f937
Taxonomy Organoheterocyclic compounds > Tetrahydrofurans
IUPAC Name 4-hydroxy-5-methylidene-3-tetradec-11-enylideneoxolan-2-one
SMILES (Canonical) CCC=CCCCCCCCCCC=C1C(C(=C)OC1=O)O
SMILES (Isomeric) CCC=CCCCCCCCCCC=C1C(C(=C)OC1=O)O
InChI InChI=1S/C19H30O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-17-18(20)16(2)22-19(17)21/h4-5,15,18,20H,2-3,6-14H2,1H3
InChI Key CRBJARGKRKVWKY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H30O3
Molecular Weight 306.40 g/mol
Exact Mass 306.21949481 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 5.80
Atomic LogP (AlogP) 4.82
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-5-methylidene-3-tetradec-11-enylideneoxolan-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 + 0.9732 97.32%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6575 65.75%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.8017 80.17%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.6851 68.51%
P-glycoprotein inhibitior - 0.6607 66.07%
P-glycoprotein substrate - 0.8879 88.79%
CYP3A4 substrate + 0.5160 51.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8653 86.53%
CYP3A4 inhibition - 0.8115 81.15%
CYP2C9 inhibition - 0.7770 77.70%
CYP2C19 inhibition - 0.5885 58.85%
CYP2D6 inhibition - 0.9145 91.45%
CYP1A2 inhibition - 0.6035 60.35%
CYP2C8 inhibition - 0.8645 86.45%
CYP inhibitory promiscuity - 0.6671 66.71%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5524 55.24%
Eye corrosion - 0.8777 87.77%
Eye irritation + 0.5796 57.96%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.8896 88.96%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7741 77.41%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.6575 65.75%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6977 69.77%
Acute Oral Toxicity (c) III 0.6905 69.05%
Estrogen receptor binding + 0.5616 56.16%
Androgen receptor binding - 0.6221 62.21%
Thyroid receptor binding + 0.6788 67.88%
Glucocorticoid receptor binding + 0.5657 56.57%
Aromatase binding - 0.6008 60.08%
PPAR gamma + 0.7518 75.18%
Honey bee toxicity - 0.9461 94.61%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.5262 52.62%
Fish aquatic toxicity + 0.9647 96.47%

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
CHEMBL2581 P07339 Cathepsin D 96.06% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.50% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.42% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.30% 91.11%
CHEMBL1829 O15379 Histone deacetylase 3 84.86% 95.00%
CHEMBL3401 O75469 Pregnane X receptor 82.16% 94.73%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 81.38% 96.37%

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.
Lindera glauca

Cross-Links

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PubChem 163029000
LOTUS LTS0141564
wikiData Q104968429