Acetic acid (2,2':5',2''-terthiophen-5-yl)methyl ester

Details

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Internal ID 9fa87472-1e2d-4631-9677-710e6def8246
Taxonomy Organoheterocyclic compounds > Bi- and oligothiophenes
IUPAC Name [5-(5-thiophen-2-ylthiophen-2-yl)thiophen-2-yl]methyl acetate
SMILES (Canonical) CC(=O)OCC1=CC=C(S1)C2=CC=C(S2)C3=CC=CS3
SMILES (Isomeric) CC(=O)OCC1=CC=C(S1)C2=CC=C(S2)C3=CC=CS3
InChI InChI=1S/C15H12O2S3/c1-10(16)17-9-11-4-5-14(19-11)15-7-6-13(20-15)12-3-2-8-18-12/h2-8H,9H2,1H3
InChI Key CGONEINYOMPEIT-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H12O2S3
Molecular Weight 320.50 g/mol
Exact Mass 319.99994314 g/mol
Topological Polar Surface Area (TPSA) 111.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 5.27
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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Acetic acid (2,2':5',2''-terthiophen-5-yl)methyl ester

2D Structure

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2D Structure of Acetic acid (2,2':5',2''-terthiophen-5-yl)methyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.7895 78.95%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9128 91.28%
OATP1B3 inhibitior + 0.9414 94.14%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7614 76.14%
P-glycoprotein inhibitior - 0.8595 85.95%
P-glycoprotein substrate - 0.9717 97.17%
CYP3A4 substrate - 0.5568 55.68%
CYP2C9 substrate - 0.5888 58.88%
CYP2D6 substrate - 0.8745 87.45%
CYP3A4 inhibition - 0.9680 96.80%
CYP2C9 inhibition - 0.6341 63.41%
CYP2C19 inhibition - 0.5847 58.47%
CYP2D6 inhibition - 0.8483 84.83%
CYP1A2 inhibition - 0.5242 52.42%
CYP2C8 inhibition - 0.6027 60.27%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7517 75.17%
Carcinogenicity (trinary) Non-required 0.5829 58.29%
Eye corrosion - 0.7547 75.47%
Eye irritation - 0.6145 61.45%
Skin irritation - 0.6110 61.10%
Skin corrosion - 0.9346 93.46%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4307 43.07%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.7302 73.02%
skin sensitisation - 0.6003 60.03%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.5914 59.14%
Acute Oral Toxicity (c) III 0.6536 65.36%
Estrogen receptor binding + 0.8987 89.87%
Androgen receptor binding + 0.7006 70.06%
Thyroid receptor binding - 0.5980 59.80%
Glucocorticoid receptor binding + 0.6450 64.50%
Aromatase binding + 0.6944 69.44%
PPAR gamma - 0.5885 58.85%
Honey bee toxicity - 0.9546 95.46%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5105 51.05%
Fish aquatic toxicity + 0.9701 97.01%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.18% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.05% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 91.52% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.72% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.68% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.65% 95.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.81% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.46% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 82.61% 95.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.51% 95.56%
CHEMBL4208 P20618 Proteasome component C5 81.34% 90.00%

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
Ephedra intermedia
Garcinia lucida

Cross-Links

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PubChem 5321832
NPASS NPC213063
LOTUS LTS0063704
wikiData Q104957966