Ircinin 2

Details

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Internal ID 7c74f653-b226-4e9c-926c-8be6dcd433e5
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (5Z)-5-[(Z,2R)-9-[5-(furan-3-ylmethyl)furan-3-yl]-2,6-dimethylnon-5-enylidene]-4-hydroxy-3-methylfuran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H30O5/c1-17(6-4-8-18(2)12-23-24(26)19(3)25(27)30-23)7-5-9-20-13-22(29-16-20)14-21-10-11-28-15-21/h6,10-13,15-16,18,26H,4-5,7-9,14H2,1-3H3/b17-6-,23-12-/t18-/m1/s1
InChI Key YIWFEASCLZQHBJ-MGPQNOLOSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C25H30O5
Molecular Weight 410.50 g/mol
Exact Mass 410.20932405 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 6.00
Atomic LogP (AlogP) 6.42
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ircinin 2

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9723 97.23%
Caco-2 - 0.5471 54.71%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6643 66.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7694 76.94%
OATP1B3 inhibitior + 0.8814 88.14%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8347 83.47%
P-glycoprotein inhibitior + 0.8480 84.80%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6704 67.04%
CYP2C9 substrate + 1.0000 100.00%
CYP2D6 substrate - 0.8896 88.96%
CYP3A4 inhibition - 0.6293 62.93%
CYP2C9 inhibition - 0.8597 85.97%
CYP2C19 inhibition - 0.6802 68.02%
CYP2D6 inhibition - 0.9183 91.83%
CYP1A2 inhibition - 0.5118 51.18%
CYP2C8 inhibition + 0.5455 54.55%
CYP inhibitory promiscuity - 0.8841 88.41%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8439 84.39%
Carcinogenicity (trinary) Non-required 0.5323 53.23%
Eye corrosion - 0.9849 98.49%
Eye irritation - 0.9222 92.22%
Skin irritation - 0.5667 56.67%
Skin corrosion - 0.9483 94.83%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8633 86.33%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.6075 60.75%
skin sensitisation - 0.8157 81.57%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6726 67.26%
Acute Oral Toxicity (c) III 0.5304 53.04%
Estrogen receptor binding - 0.5725 57.25%
Androgen receptor binding + 0.6329 63.29%
Thyroid receptor binding + 0.5998 59.98%
Glucocorticoid receptor binding + 0.8342 83.42%
Aromatase binding + 0.6831 68.31%
PPAR gamma + 0.7494 74.94%
Honey bee toxicity - 0.7472 74.72%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9903 99.03%

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 97.90% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.53% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.43% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 95.64% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 92.39% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.49% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.97% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.61% 86.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 88.31% 93.00%
CHEMBL4581 P52732 Kinesin-like protein 1 87.32% 93.18%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.57% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.24% 96.09%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 81.20% 95.34%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.83% 93.65%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.83% 95.89%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.77% 96.47%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.44% 93.56%

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 54726397
LOTUS LTS0217307
wikiData Q104397056