3-Hexadeca-7,12-dien-9-ynyl-4-hydroxy-5-methylidenefuran-2-one

Details

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Internal ID f0d9aba7-5af0-4f80-b668-2f0e2f84a715
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name 3-hexadeca-7,12-dien-9-ynyl-4-hydroxy-5-methylidenefuran-2-one
SMILES (Canonical) CCCC=CCC#CC=CCCCCCCC1=C(C(=C)OC1=O)O
SMILES (Isomeric) CCCC=CCC#CC=CCCCCCCC1=C(C(=C)OC1=O)O
InChI InChI=1S/C21H28O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-20(22)18(2)24-21(19)23/h5-6,10-11,22H,2-4,7,12-17H2,1H3
InChI Key VWKCLMGZLXLWGO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H28O3
Molecular Weight 328.40 g/mol
Exact Mass 328.20384475 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.52
H-Bond Acceptor 3
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 3-Hexadeca-7,12-dien-9-ynyl-4-hydroxy-5-methylidenefuran-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 + 0.9764 97.64%
Caco-2 + 0.5101 51.01%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6477 64.77%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.7793 77.93%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8150 81.50%
P-glycoprotein inhibitior - 0.5162 51.62%
P-glycoprotein substrate - 0.8068 80.68%
CYP3A4 substrate + 0.5764 57.64%
CYP2C9 substrate - 0.6086 60.86%
CYP2D6 substrate - 0.8801 88.01%
CYP3A4 inhibition - 0.6976 69.76%
CYP2C9 inhibition - 0.7400 74.00%
CYP2C19 inhibition - 0.5318 53.18%
CYP2D6 inhibition - 0.8933 89.33%
CYP1A2 inhibition - 0.5934 59.34%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.6210 62.10%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5530 55.30%
Eye corrosion - 0.9051 90.51%
Eye irritation - 0.8158 81.58%
Skin irritation - 0.5719 57.19%
Skin corrosion - 0.8726 87.26%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7463 74.63%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.6805 68.05%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.6552 65.52%
Acute Oral Toxicity (c) III 0.5143 51.43%
Estrogen receptor binding - 0.5086 50.86%
Androgen receptor binding - 0.6513 65.13%
Thyroid receptor binding + 0.6661 66.61%
Glucocorticoid receptor binding + 0.5876 58.76%
Aromatase binding - 0.6764 67.64%
PPAR gamma + 0.8567 85.67%
Honey bee toxicity - 0.9028 90.28%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6762 67.62%
Fish aquatic toxicity + 0.9886 98.86%

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 96.11% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 95.76% 89.63%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 94.54% 83.57%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.58% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 93.21% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.97% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.68% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 90.55% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.96% 95.56%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 84.98% 96.37%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.25% 89.34%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.91% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.17% 89.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.03% 92.08%

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.
Achillea lingulata
Aristolochia cymbifera
Aristolochia ringens
Ertela trifolia
Magnolia biondii
Magnolia coco
Magnolia denudata
Piper longum
Piper mullesua
Quassia bidwillii
Stauranthus perforatus
Virola elongata
Virola flexuosa
Virola sebifera
Zanthoxylum armatum

Cross-Links

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PubChem 163033172
LOTUS LTS0011756
wikiData Q105100255