2-(Hexa-3,5-dien-1-YN-1-YL)-5-(prop-1-YN-1-YL)thiophene

Details

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Internal ID 1169a055-1a31-4b79-8aa5-5840150067e4
Taxonomy Organoheterocyclic compounds > Thiophenes > 2,5-disubstituted thiophenes
IUPAC Name 2-hexa-3,5-dien-1-ynyl-5-prop-1-ynylthiophene
SMILES (Canonical) CC#CC1=CC=C(S1)C#CC=CC=C
SMILES (Isomeric) CC#CC1=CC=C(S1)C#CC=CC=C
InChI InChI=1S/C13H10S/c1-3-5-6-7-9-13-11-10-12(14-13)8-4-2/h3,5-6,10-11H,1H2,2H3
InChI Key BTXGXNRHWLHJBS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H10S
Molecular Weight 198.29 g/mol
Exact Mass 198.05032149 g/mol
Topological Polar Surface Area (TPSA) 28.20 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.21
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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DTXSID10822730
2-(HEXA-3,5-DIEN-1-YN-1-YL)-5-(PROP-1-YN-1-YL)THIOPHENE

2D Structure

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2D Structure of 2-(Hexa-3,5-dien-1-YN-1-YL)-5-(prop-1-YN-1-YL)thiophene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.6089 60.89%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.4708 47.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9299 92.99%
OATP1B3 inhibitior + 0.9562 95.62%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8453 84.53%
P-glycoprotein inhibitior - 0.9426 94.26%
P-glycoprotein substrate - 0.9532 95.32%
CYP3A4 substrate - 0.5855 58.55%
CYP2C9 substrate + 1.0000 100.00%
CYP2D6 substrate - 0.7961 79.61%
CYP3A4 inhibition - 0.8756 87.56%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.5917 59.17%
CYP2D6 inhibition - 0.8194 81.94%
CYP1A2 inhibition - 0.5849 58.49%
CYP2C8 inhibition - 0.8723 87.23%
CYP inhibitory promiscuity + 0.8056 80.56%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6317 63.17%
Carcinogenicity (trinary) Danger 0.4188 41.88%
Eye corrosion + 0.8553 85.53%
Eye irritation + 0.6493 64.93%
Skin irritation + 0.7152 71.52%
Skin corrosion - 0.6372 63.72%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5428 54.28%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.7783 77.83%
skin sensitisation + 0.8015 80.15%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5778 57.78%
Acute Oral Toxicity (c) III 0.8170 81.70%
Estrogen receptor binding - 0.7589 75.89%
Androgen receptor binding - 0.5859 58.59%
Thyroid receptor binding + 0.5972 59.72%
Glucocorticoid receptor binding + 0.7068 70.68%
Aromatase binding + 0.7375 73.75%
PPAR gamma + 0.7246 72.46%
Honey bee toxicity - 0.6697 66.97%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.9790 97.90%

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 95.04% 96.42%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.69% 85.30%
CHEMBL3401 O75469 Pregnane X receptor 87.57% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.82% 95.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.33% 93.65%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.87% 93.40%
CHEMBL1951 P21397 Monoamine oxidase A 82.20% 91.49%
CHEMBL2487 P05067 Beta amyloid A4 protein 80.99% 96.74%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.87% 91.11%

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.
Geigeria aspera
Rudbeckia hirta

Cross-Links

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PubChem 71401707
LOTUS LTS0246295
wikiData Q82805398