4-(4,9-dihydroxyundeca-2,10-dien-5,7-diynyl)-2-methyl-2H-furan-5-one

Details

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Internal ID 3e858bce-de16-4478-b9d0-fea305e1d5e9
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 4-(4,9-dihydroxyundeca-2,10-dien-5,7-diynyl)-2-methyl-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H16O4/c1-3-14(17)8-4-5-9-15(18)10-6-7-13-11-12(2)20-16(13)19/h3,6,10-12,14-15,17-18H,1,7H2,2H3
InChI Key ZVNJQANZWXBDCG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O4
Molecular Weight 272.29 g/mol
Exact Mass 272.10485899 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 1.50
Atomic LogP (AlogP) 0.72
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(4,9-dihydroxyundeca-2,10-dien-5,7-diynyl)-2-methyl-2H-furan-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9065 90.65%
Caco-2 - 0.7987 79.87%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7032 70.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8380 83.80%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9225 92.25%
P-glycoprotein inhibitior - 0.9173 91.73%
P-glycoprotein substrate - 0.8764 87.64%
CYP3A4 substrate + 0.5108 51.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8641 86.41%
CYP3A4 inhibition - 0.7104 71.04%
CYP2C9 inhibition - 0.6353 63.53%
CYP2C19 inhibition - 0.6019 60.19%
CYP2D6 inhibition - 0.9236 92.36%
CYP1A2 inhibition - 0.6861 68.61%
CYP2C8 inhibition - 0.8670 86.70%
CYP inhibitory promiscuity + 0.5711 57.11%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8077 80.77%
Carcinogenicity (trinary) Danger 0.4443 44.43%
Eye corrosion - 0.8915 89.15%
Eye irritation - 0.9076 90.76%
Skin irritation - 0.5412 54.12%
Skin corrosion - 0.6898 68.98%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6477 64.77%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.6276 62.76%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.4595 45.95%
Acute Oral Toxicity (c) III 0.5551 55.51%
Estrogen receptor binding + 0.6063 60.63%
Androgen receptor binding - 0.7572 75.72%
Thyroid receptor binding + 0.5412 54.12%
Glucocorticoid receptor binding + 0.7750 77.50%
Aromatase binding + 0.7413 74.13%
PPAR gamma + 0.7068 70.68%
Honey bee toxicity - 0.7169 71.69%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9415 94.15%

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 94.03% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.18% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.32% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.01% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.84% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.86% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.14% 86.33%

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 85397890
LOTUS LTS0152727
wikiData Q105384452