9-Thiophen-2-ylnon-6-en-8-yn-3-ol

Details

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Internal ID 060ff508-4547-4585-8da1-49e632c343ee
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 9-thiophen-2-ylnon-6-en-8-yn-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H16OS/c1-2-12(14)8-5-3-4-6-9-13-10-7-11-15-13/h3-4,7,10-12,14H,2,5,8H2,1H3
InChI Key BDOXYFSAWLGAAI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16OS
Molecular Weight 220.33 g/mol
Exact Mass 220.09218630 g/mol
Topological Polar Surface Area (TPSA) 48.50 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.21
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9-Thiophen-2-ylnon-6-en-8-yn-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.5401 54.01%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.3474 34.74%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.8556 85.56%
OATP1B3 inhibitior + 0.9329 93.29%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8164 81.64%
P-glycoprotein inhibitior - 0.9612 96.12%
P-glycoprotein substrate - 0.8592 85.92%
CYP3A4 substrate - 0.5802 58.02%
CYP2C9 substrate + 0.5916 59.16%
CYP2D6 substrate - 0.7502 75.02%
CYP3A4 inhibition - 0.7554 75.54%
CYP2C9 inhibition - 0.6292 62.92%
CYP2C19 inhibition + 0.5243 52.43%
CYP2D6 inhibition - 0.8413 84.13%
CYP1A2 inhibition + 0.5833 58.33%
CYP2C8 inhibition - 0.8872 88.72%
CYP inhibitory promiscuity + 0.7326 73.26%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Danger 0.4036 40.36%
Eye corrosion - 0.8412 84.12%
Eye irritation - 0.7746 77.46%
Skin irritation + 0.5444 54.44%
Skin corrosion - 0.8279 82.79%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6603 66.03%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.5503 55.03%
skin sensitisation + 0.6451 64.51%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.8335 83.35%
Acute Oral Toxicity (c) III 0.5927 59.27%
Estrogen receptor binding - 0.5129 51.29%
Androgen receptor binding - 0.6956 69.56%
Thyroid receptor binding - 0.5069 50.69%
Glucocorticoid receptor binding - 0.6033 60.33%
Aromatase binding - 0.5808 58.08%
PPAR gamma - 0.5260 52.60%
Honey bee toxicity - 0.9164 91.64%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.8996 89.96%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.31% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.34% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 93.27% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.21% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.32% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 84.98% 94.73%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 83.10% 85.94%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 82.96% 96.42%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.73% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 82.68% 95.93%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.61% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.55% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.71% 96.00%

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.
Cota tinctoria

Cross-Links

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PubChem 162889859
LOTUS LTS0183735
wikiData Q104924544