2-(Hepta-1,3,5-triyn-1-yl)-5-phenylthiophene

Details

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Internal ID d2fc703f-68ab-4685-92b2-b712a41f06ec
Taxonomy Organoheterocyclic compounds > Thiophenes > 2,5-disubstituted thiophenes
IUPAC Name 2-hepta-1,3,5-triynyl-5-phenylthiophene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H10S/c1-2-3-4-5-9-12-16-13-14-17(18-16)15-10-7-6-8-11-15/h6-8,10-11,13-14H,1H3
InChI Key UGOYLCMSCJDWIO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H10S
Molecular Weight 246.30 g/mol
Exact Mass 246.05032149 g/mol
Topological Polar Surface Area (TPSA) 28.20 Ų
XlogP 4.80
Atomic LogP (AlogP) 3.79
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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2-(HEPTA-1,3,5-TRIYN-1-YL)-5-PHENYLTHIOPHENE
DTXSID70756002

2D Structure

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2D Structure of 2-(Hepta-1,3,5-triyn-1-yl)-5-phenylthiophene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.7417 74.17%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.5080 50.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9540 95.40%
OATP1B3 inhibitior + 0.9549 95.49%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7127 71.27%
P-glycoprotein inhibitior - 0.9135 91.35%
P-glycoprotein substrate - 0.9185 91.85%
CYP3A4 substrate - 0.6339 63.39%
CYP2C9 substrate - 0.5852 58.52%
CYP2D6 substrate - 0.7759 77.59%
CYP3A4 inhibition - 0.8900 89.00%
CYP2C9 inhibition + 0.5949 59.49%
CYP2C19 inhibition + 0.6777 67.77%
CYP2D6 inhibition - 0.7600 76.00%
CYP1A2 inhibition + 0.5414 54.14%
CYP2C8 inhibition - 0.6586 65.86%
CYP inhibitory promiscuity + 0.8715 87.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6336 63.36%
Carcinogenicity (trinary) Danger 0.4250 42.50%
Eye corrosion - 0.6379 63.79%
Eye irritation + 0.7684 76.84%
Skin irritation + 0.6210 62.10%
Skin corrosion - 0.8866 88.66%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6071 60.71%
Micronuclear - 0.7241 72.41%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation + 0.7518 75.18%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.5823 58.23%
Acute Oral Toxicity (c) III 0.8456 84.56%
Estrogen receptor binding + 0.7431 74.31%
Androgen receptor binding + 0.7516 75.16%
Thyroid receptor binding + 0.5759 57.59%
Glucocorticoid receptor binding + 0.7245 72.45%
Aromatase binding + 0.8304 83.04%
PPAR gamma + 0.8162 81.62%
Honey bee toxicity - 0.9258 92.58%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.9799 97.99%

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
CHEMBL221 P23219 Cyclooxygenase-1 95.91% 90.17%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 94.88% 96.42%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 93.59% 94.62%
CHEMBL2581 P07339 Cathepsin D 93.32% 98.95%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 90.73% 94.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.18% 86.33%
CHEMBL2487 P05067 Beta amyloid A4 protein 89.43% 96.74%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.56% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.73% 95.56%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.07% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.61% 96.09%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 83.69% 94.23%

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.
Coreopsis grandiflora

Cross-Links

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PubChem 71326874
LOTUS LTS0175376
wikiData Q82707929