3-(4-Methoxypent-3-enyl)thiophene

Details

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Internal ID a12371a7-fc6a-46f6-9a2c-cb7786412899
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 3-(4-methoxypent-3-enyl)thiophene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14OS/c1-9(11-2)4-3-5-10-6-7-12-8-10/h4,6-8H,3,5H2,1-2H3
InChI Key ZIWJMUUUGGFRQC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14OS
Molecular Weight 182.28 g/mol
Exact Mass 182.07653624 g/mol
Topological Polar Surface Area (TPSA) 37.50 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.23
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(4-Methoxypent-3-enyl)thiophene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.9432 94.32%
Blood Brain Barrier + 0.9368 93.68%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.4269 42.69%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.9286 92.86%
OATP1B3 inhibitior + 0.9450 94.50%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8536 85.36%
P-glycoprotein inhibitior - 0.9810 98.10%
P-glycoprotein substrate - 0.8435 84.35%
CYP3A4 substrate - 0.5922 59.22%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7143 71.43%
CYP3A4 inhibition - 0.9670 96.70%
CYP2C9 inhibition - 0.8014 80.14%
CYP2C19 inhibition - 0.5148 51.48%
CYP2D6 inhibition - 0.8190 81.90%
CYP1A2 inhibition + 0.5606 56.06%
CYP2C8 inhibition - 0.6204 62.04%
CYP inhibitory promiscuity + 0.8414 84.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7628 76.28%
Carcinogenicity (trinary) Non-required 0.4829 48.29%
Eye corrosion - 0.8110 81.10%
Eye irritation + 0.6251 62.51%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9578 95.78%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4191 41.91%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5724 57.24%
skin sensitisation + 0.6717 67.17%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.7609 76.09%
Acute Oral Toxicity (c) III 0.8316 83.16%
Estrogen receptor binding - 0.8382 83.82%
Androgen receptor binding - 0.8522 85.22%
Thyroid receptor binding - 0.7509 75.09%
Glucocorticoid receptor binding - 0.4723 47.23%
Aromatase binding - 0.5881 58.81%
PPAR gamma - 0.7978 79.78%
Honey bee toxicity - 0.8055 80.55%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.7297 72.97%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.03% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.65% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.24% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 89.99% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.83% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.17% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.29% 86.33%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.73% 90.24%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.45% 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.
Rosa canina

Cross-Links

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PubChem 163190308
LOTUS LTS0247369
wikiData Q105377627