9-Thiophen-2-ylnona-4,6-dien-8-yn-3-ol

Details

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Internal ID 9ace8679-8beb-4426-bbc8-21856161244b
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 9-thiophen-2-ylnona-4,6-dien-8-yn-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14OS/c1-2-12(14)8-5-3-4-6-9-13-10-7-11-15-13/h3-5,7-8,10-12,14H,2H2,1H3
InChI Key CMHULBAPTPMGOV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14OS
Molecular Weight 218.32 g/mol
Exact Mass 218.07653624 g/mol
Topological Polar Surface Area (TPSA) 48.50 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9-Thiophen-2-ylnona-4,6-dien-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 + 0.9943 99.43%
Caco-2 - 0.6127 61.27%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.3737 37.37%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8491 84.91%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7981 79.81%
P-glycoprotein inhibitior - 0.9629 96.29%
P-glycoprotein substrate - 0.9040 90.40%
CYP3A4 substrate - 0.5984 59.84%
CYP2C9 substrate + 0.5916 59.16%
CYP2D6 substrate - 0.7502 75.02%
CYP3A4 inhibition - 0.9034 90.34%
CYP2C9 inhibition - 0.5591 55.91%
CYP2C19 inhibition + 0.5887 58.87%
CYP2D6 inhibition - 0.8711 87.11%
CYP1A2 inhibition - 0.5209 52.09%
CYP2C8 inhibition - 0.8075 80.75%
CYP inhibitory promiscuity + 0.7630 76.30%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Danger 0.3966 39.66%
Eye corrosion - 0.7300 73.00%
Eye irritation - 0.6435 64.35%
Skin irritation + 0.5562 55.62%
Skin corrosion - 0.7542 75.42%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4749 47.49%
Micronuclear - 0.8015 80.15%
Hepatotoxicity - 0.5912 59.12%
skin sensitisation + 0.7570 75.70%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.8244 82.44%
Acute Oral Toxicity (c) III 0.5926 59.26%
Estrogen receptor binding - 0.5473 54.73%
Androgen receptor binding - 0.7139 71.39%
Thyroid receptor binding - 0.5218 52.18%
Glucocorticoid receptor binding - 0.5357 53.57%
Aromatase binding + 0.6448 64.48%
PPAR gamma - 0.6459 64.59%
Honey bee toxicity - 0.8975 89.75%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity - 0.3644 36.44%

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 95.65% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.47% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 91.13% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.03% 91.11%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 83.33% 96.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.15% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.73% 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 85195426
LOTUS LTS0262932
wikiData Q104964556