5-Hexa-2,4-diynylidenefuran-2-one

Details

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Internal ID b57558ff-38cc-4b38-a807-069be4b9b8c8
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name 5-hexa-2,4-diynylidenefuran-2-one
SMILES (Canonical) CC#CC#CC=C1C=CC(=O)O1
SMILES (Isomeric) CC#CC#CC=C1C=CC(=O)O1
InChI InChI=1S/C10H6O2/c1-2-3-4-5-6-9-7-8-10(11)12-9/h6-8H,1H3
InChI Key YOTOGBLIOFSWLS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H6O2
Molecular Weight 158.15 g/mol
Exact Mass 158.036779430 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.01
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2739-62-0
DTXSID60295410

2D Structure

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2D Structure of 5-Hexa-2,4-diynylidenefuran-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 + 0.9971 99.71%
Caco-2 + 0.6338 63.38%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5870 58.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9282 92.82%
OATP1B3 inhibitior + 0.9653 96.53%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9310 93.10%
P-glycoprotein inhibitior - 0.9808 98.08%
P-glycoprotein substrate - 0.9682 96.82%
CYP3A4 substrate - 0.5874 58.74%
CYP2C9 substrate - 0.8116 81.16%
CYP2D6 substrate - 0.8833 88.33%
CYP3A4 inhibition - 0.9596 95.96%
CYP2C9 inhibition - 0.8958 89.58%
CYP2C19 inhibition - 0.7293 72.93%
CYP2D6 inhibition - 0.9670 96.70%
CYP1A2 inhibition - 0.6630 66.30%
CYP2C8 inhibition - 0.9711 97.11%
CYP inhibitory promiscuity - 0.6099 60.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7444 74.44%
Carcinogenicity (trinary) Non-required 0.3517 35.17%
Eye corrosion + 0.9252 92.52%
Eye irritation + 0.8914 89.14%
Skin irritation + 0.7455 74.55%
Skin corrosion + 0.5494 54.94%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7948 79.48%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.7266 72.66%
skin sensitisation + 0.6004 60.04%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.8005 80.05%
Acute Oral Toxicity (c) III 0.5296 52.96%
Estrogen receptor binding - 0.9006 90.06%
Androgen receptor binding - 0.6244 62.44%
Thyroid receptor binding - 0.6930 69.30%
Glucocorticoid receptor binding - 0.6691 66.91%
Aromatase binding - 0.6775 67.75%
PPAR gamma - 0.6922 69.22%
Honey bee toxicity - 0.8560 85.60%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity - 0.3625 36.25%

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
CHEMBL3401 O75469 Pregnane X receptor 88.50% 94.73%
CHEMBL2581 P07339 Cathepsin D 87.94% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.04% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.78% 86.33%

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.
Solidago altissima
Solidago canadensis
Solidago petiolaris

Cross-Links

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PubChem 265579
LOTUS LTS0035170
wikiData Q82035337