5-(5-But-3-en-1-ynylthiophen-2-yl)penta-2,4-diyn-1-ol

Details

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Internal ID 395500fc-4d82-4127-bfd9-6fcf4ee17fbc
Taxonomy Organoheterocyclic compounds > Thiophenes > 2,5-disubstituted thiophenes
IUPAC Name 5-(5-but-3-en-1-ynylthiophen-2-yl)penta-2,4-diyn-1-ol
SMILES (Canonical) C=CC#CC1=CC=C(S1)C#CC#CCO
SMILES (Isomeric) C=CC#CC1=CC=C(S1)C#CC#CCO
InChI InChI=1S/C13H8OS/c1-2-3-7-12-9-10-13(15-12)8-5-4-6-11-14/h2,9-10,14H,1,11H2
InChI Key RLALQOADNWLBKM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H8OS
Molecular Weight 212.27 g/mol
Exact Mass 212.02958605 g/mol
Topological Polar Surface Area (TPSA) 48.50 Ų
XlogP 2.70
Atomic LogP (AlogP) 1.63
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(5-But-3-en-1-ynylthiophen-2-yl)penta-2,4-diyn-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.5374 53.74%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.3584 35.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9159 91.59%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8217 82.17%
P-glycoprotein inhibitior - 0.9594 95.94%
P-glycoprotein substrate - 0.9507 95.07%
CYP3A4 substrate - 0.6448 64.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8017 80.17%
CYP3A4 inhibition - 0.8265 82.65%
CYP2C9 inhibition - 0.7187 71.87%
CYP2C19 inhibition - 0.5378 53.78%
CYP2D6 inhibition - 0.8688 86.88%
CYP1A2 inhibition - 0.5452 54.52%
CYP2C8 inhibition - 0.7337 73.37%
CYP inhibitory promiscuity + 0.6987 69.87%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6817 68.17%
Carcinogenicity (trinary) Danger 0.4394 43.94%
Eye corrosion + 0.6351 63.51%
Eye irritation - 0.8842 88.42%
Skin irritation + 0.6446 64.46%
Skin corrosion + 0.5443 54.43%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7253 72.53%
Micronuclear - 0.7341 73.41%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.6683 66.83%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.6474 64.74%
Acute Oral Toxicity (c) II 0.4788 47.88%
Estrogen receptor binding - 0.7551 75.51%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6027 60.27%
Aromatase binding + 0.7449 74.49%
PPAR gamma + 0.7445 74.45%
Honey bee toxicity - 0.8586 85.86%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.8742 87.42%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.67% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.62% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.74% 96.09%
CHEMBL4578 Q14680 Maternal embryonic leucine zipper kinase 86.37% 81.58%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.47% 86.92%

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.
Lawrencella rosea

Cross-Links

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PubChem 14262758
LOTUS LTS0223516
wikiData Q105239733