2-(Nona-1,7-dien-3,5-diyn-1-YL)furan

Details

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Internal ID 65a449ee-ce86-442e-b059-4717a5a48d6b
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-nona-1,7-dien-3,5-diynylfuran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H10O/c1-2-3-4-5-6-7-8-10-13-11-9-12-14-13/h2-3,8-12H,1H3
InChI Key GRBKWAXRYIITKG-UHFFFAOYSA-N
Popularity 5 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) 13.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.88
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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SCHEMBL28601950
AKOS030230025
DB-050297
NS00067868

2D Structure

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2D Structure of 2-(Nona-1,7-dien-3,5-diyn-1-YL)furan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.7973 79.73%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Plasma membrane 0.3375 33.75%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8919 89.19%
OATP1B3 inhibitior + 0.9683 96.83%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8877 88.77%
P-glycoprotein inhibitior - 0.9494 94.94%
P-glycoprotein substrate - 0.9400 94.00%
CYP3A4 substrate - 0.6211 62.11%
CYP2C9 substrate + 0.8123 81.23%
CYP2D6 substrate - 0.7933 79.33%
CYP3A4 inhibition - 0.9703 97.03%
CYP2C9 inhibition - 0.7899 78.99%
CYP2C19 inhibition - 0.5630 56.30%
CYP2D6 inhibition - 0.9397 93.97%
CYP1A2 inhibition + 0.5950 59.50%
CYP2C8 inhibition - 0.8467 84.67%
CYP inhibitory promiscuity + 0.6998 69.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6517 65.17%
Carcinogenicity (trinary) Danger 0.6328 63.28%
Eye corrosion + 0.9001 90.01%
Eye irritation + 0.9600 96.00%
Skin irritation + 0.8170 81.70%
Skin corrosion + 0.5500 55.00%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5445 54.45%
Micronuclear - 0.5900 59.00%
Hepatotoxicity - 0.5109 51.09%
skin sensitisation + 0.7387 73.87%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.6520 65.20%
Acute Oral Toxicity (c) III 0.6111 61.11%
Estrogen receptor binding + 0.6986 69.86%
Androgen receptor binding - 0.8398 83.98%
Thyroid receptor binding - 0.5812 58.12%
Glucocorticoid receptor binding - 0.6315 63.15%
Aromatase binding - 0.4890 48.90%
PPAR gamma - 0.5777 57.77%
Honey bee toxicity - 0.9322 93.22%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity - 0.4623 46.23%

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 89.50% 94.73%
CHEMBL2039 P27338 Monoamine oxidase B 89.35% 92.51%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.16% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.48% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.40% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 85.47% 91.49%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.45% 96.00%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 83.47% 96.42%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.38% 90.24%

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.
Atractylodes lancea

Cross-Links

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PubChem 171429
LOTUS LTS0255006
wikiData Q105015711