2-(1,3-Butadiynyl)-5-(3-butene-1-ynyl)thiophene

Details

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Internal ID f941a757-795c-47f8-9988-eeef3c0c39f7
Taxonomy Organoheterocyclic compounds > Thiophenes > 2,5-disubstituted thiophenes
IUPAC Name 2-buta-1,3-diynyl-5-but-3-en-1-ynylthiophene
SMILES (Canonical) C=CC#CC1=CC=C(S1)C#CC#C
SMILES (Isomeric) C=CC#CC1=CC=C(S1)C#CC#C
InChI InChI=1S/C12H6S/c1-3-5-7-11-9-10-12(13-11)8-6-4-2/h1,4,9-10H,2H2
InChI Key QVLQCDBLHFENOC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H6S
Molecular Weight 182.24 g/mol
Exact Mass 182.01902136 g/mol
Topological Polar Surface Area (TPSA) 28.20 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.27
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(1,3-Butadiynyl)-5-(3-butene-1-ynyl)thiophene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 + 0.6746 67.46%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.4255 42.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9380 93.80%
OATP1B3 inhibitior + 0.9538 95.38%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8548 85.48%
P-glycoprotein inhibitior - 0.9568 95.68%
P-glycoprotein substrate - 0.9722 97.22%
CYP3A4 substrate - 0.6523 65.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7949 79.49%
CYP3A4 inhibition - 0.9101 91.01%
CYP2C9 inhibition - 0.5484 54.84%
CYP2C19 inhibition + 0.6025 60.25%
CYP2D6 inhibition - 0.8063 80.63%
CYP1A2 inhibition - 0.5652 56.52%
CYP2C8 inhibition - 0.8101 81.01%
CYP inhibitory promiscuity + 0.8314 83.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6317 63.17%
Carcinogenicity (trinary) Danger 0.4160 41.60%
Eye corrosion + 0.8984 89.84%
Eye irritation + 0.6025 60.25%
Skin irritation + 0.7728 77.28%
Skin corrosion - 0.6261 62.61%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6543 65.43%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation + 0.7745 77.45%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.5682 56.82%
Acute Oral Toxicity (c) III 0.6119 61.19%
Estrogen receptor binding - 0.7065 70.65%
Androgen receptor binding - 0.6378 63.78%
Thyroid receptor binding - 0.6281 62.81%
Glucocorticoid receptor binding - 0.4751 47.51%
Aromatase binding + 0.5860 58.60%
PPAR gamma + 0.6468 64.68%
Honey bee toxicity - 0.7812 78.12%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 0.9780 97.80%

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
CHEMBL1951 P21397 Monoamine oxidase A 93.03% 91.49%
CHEMBL2487 P05067 Beta amyloid A4 protein 90.53% 96.74%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 88.73% 96.42%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.44% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.39% 93.40%
CHEMBL221 P23219 Cyclooxygenase-1 81.79% 90.17%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.81% 85.30%

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.
Eclipta prostrata
Eclipta prostrata
Ephedra intermedia
Garcinia lucida

Cross-Links

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PubChem 5315560
NPASS NPC235589
LOTUS LTS0220041
wikiData Q105228744