4-(5-Pent-3-en-1-ynylthiophen-2-yl)but-3-yn-1-ol

Details

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Internal ID 6a10dcdc-fe24-4cf7-ac01-95429082b7a2
Taxonomy Organoheterocyclic compounds > Thiophenes > 2,5-disubstituted thiophenes
IUPAC Name 4-(5-pent-3-en-1-ynylthiophen-2-yl)but-3-yn-1-ol
SMILES (Canonical) CC=CC#CC1=CC=C(S1)C#CCCO
SMILES (Isomeric) CC=CC#CC1=CC=C(S1)C#CCCO
InChI InChI=1S/C13H12OS/c1-2-3-4-7-12-9-10-13(15-12)8-5-6-11-14/h2-3,9-10,14H,6,11H2,1H3
InChI Key ASXSXWBTTYQRGL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12OS
Molecular Weight 216.30 g/mol
Exact Mass 216.06088618 g/mol
Topological Polar Surface Area (TPSA) 48.50 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.41
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(5-Pent-3-en-1-ynylthiophen-2-yl)but-3-yn-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 + 0.9921 99.21%
Caco-2 - 0.7032 70.32%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.4261 42.61%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8573 85.73%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7896 78.96%
P-glycoprotein inhibitior - 0.9734 97.34%
P-glycoprotein substrate - 0.8958 89.58%
CYP3A4 substrate - 0.5997 59.97%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate - 0.7737 77.37%
CYP3A4 inhibition - 0.7683 76.83%
CYP2C9 inhibition - 0.7021 70.21%
CYP2C19 inhibition - 0.5629 56.29%
CYP2D6 inhibition - 0.8748 87.48%
CYP1A2 inhibition - 0.5752 57.52%
CYP2C8 inhibition - 0.8745 87.45%
CYP inhibitory promiscuity + 0.6426 64.26%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Danger 0.4414 44.14%
Eye corrosion - 0.5621 56.21%
Eye irritation - 0.7894 78.94%
Skin irritation + 0.6104 61.04%
Skin corrosion - 0.7729 77.29%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4559 45.59%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.5880 58.80%
skin sensitisation + 0.6022 60.22%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.4844 48.44%
Acute Oral Toxicity (c) III 0.6261 62.61%
Estrogen receptor binding - 0.5343 53.43%
Androgen receptor binding - 0.5597 55.97%
Thyroid receptor binding - 0.5410 54.10%
Glucocorticoid receptor binding + 0.7732 77.32%
Aromatase binding + 0.7403 74.03%
PPAR gamma + 0.5203 52.03%
Honey bee toxicity - 0.9337 93.37%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.6403 64.03%

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 90.84% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.66% 96.09%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 87.28% 96.42%
CHEMBL2581 P07339 Cathepsin D 83.04% 98.95%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.64% 90.24%
CHEMBL221 P23219 Cyclooxygenase-1 80.51% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.00% 86.33%

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.
Echinops pappii

Cross-Links

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PubChem 162925954
LOTUS LTS0195466
wikiData Q104918169