5-nona-6,8-dien-2,4-diynylidene-2H-furan

Details

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Internal ID 52eb318a-11fd-4688-bf14-8dcec3b5811e
Taxonomy Organoheterocyclic compounds > Dihydrofurans
IUPAC Name 5-nona-6,8-dien-2,4-diynylidene-2H-furan
SMILES (Canonical) C=CC=CC#CC#CC=C1C=CCO1
SMILES (Isomeric) C=CC=CC#CC#CC=C1C=CCO1
InChI InChI=1S/C13H10O/c1-2-3-4-5-6-7-8-10-13-11-9-12-14-13/h2-4,9-11H,1,12H2
InChI Key VUTHUFKTXIOUJH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H10O
Molecular Weight 182.22 g/mol
Exact Mass 182.073164938 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-nona-6,8-dien-2,4-diynylidene-2H-furan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.6150 61.50%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.3883 38.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9304 93.04%
OATP1B3 inhibitior + 0.9566 95.66%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8157 81.57%
P-glycoprotein inhibitior - 0.9622 96.22%
P-glycoprotein substrate - 0.9163 91.63%
CYP3A4 substrate - 0.5523 55.23%
CYP2C9 substrate + 0.6171 61.71%
CYP2D6 substrate - 0.7845 78.45%
CYP3A4 inhibition - 0.9626 96.26%
CYP2C9 inhibition - 0.8451 84.51%
CYP2C19 inhibition - 0.6327 63.27%
CYP2D6 inhibition - 0.9326 93.26%
CYP1A2 inhibition + 0.5186 51.86%
CYP2C8 inhibition - 0.8397 83.97%
CYP inhibitory promiscuity + 0.6491 64.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6644 66.44%
Carcinogenicity (trinary) Warning 0.3829 38.29%
Eye corrosion + 0.8297 82.97%
Eye irritation - 0.6585 65.85%
Skin irritation + 0.7530 75.30%
Skin corrosion + 0.6671 66.71%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5470 54.70%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.7303 73.03%
skin sensitisation + 0.4901 49.01%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.6949 69.49%
Acute Oral Toxicity (c) II 0.7370 73.70%
Estrogen receptor binding - 0.6686 66.86%
Androgen receptor binding - 0.5617 56.17%
Thyroid receptor binding - 0.5549 55.49%
Glucocorticoid receptor binding + 0.6081 60.81%
Aromatase binding + 0.6100 61.00%
PPAR gamma - 0.5217 52.17%
Honey bee toxicity - 0.6254 62.54%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.3836 38.36%

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
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 94.40% 96.42%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.85% 91.11%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.78% 86.00%
CHEMBL3401 O75469 Pregnane X receptor 81.26% 94.73%

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.
Carlina diae

Cross-Links

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PubChem 163030089
LOTUS LTS0086669
wikiData Q105297415