2-t-Butylthieno[2,3-b]thiophene

Details

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Internal ID a4a728ca-bfe1-4ad2-9d26-ad8a00a09381
Taxonomy Organoheterocyclic compounds > Thienothiophenes
IUPAC Name 5-tert-butylthieno[2,3-b]thiophene
SMILES (Canonical) CC(C)(C)C1=CC2=C(S1)SC=C2
SMILES (Isomeric) CC(C)(C)C1=CC2=C(S1)SC=C2
InChI InChI=1S/C10H12S2/c1-10(2,3)8-6-7-4-5-11-9(7)12-8/h4-6H,1-3H3
InChI Key JGLLGJAWEFPOHD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12S2
Molecular Weight 196.30 g/mol
Exact Mass 196.03804273 g/mol
Topological Polar Surface Area (TPSA) 56.50 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.26
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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SCHEMBL18876390
JGLLGJAWEFPOHD-UHFFFAOYSA-N
2-tert-Butylthieno[2,3-b]thiophene #

2D Structure

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2D Structure of 2-t-Butylthieno[2,3-b]thiophene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 + 0.7050 70.50%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6032 60.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9568 95.68%
OATP1B3 inhibitior + 0.9542 95.42%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9246 92.46%
P-glycoprotein inhibitior - 0.9734 97.34%
P-glycoprotein substrate - 0.9496 94.96%
CYP3A4 substrate - 0.6608 66.08%
CYP2C9 substrate - 0.7477 74.77%
CYP2D6 substrate - 0.7316 73.16%
CYP3A4 inhibition - 0.8172 81.72%
CYP2C9 inhibition - 0.7861 78.61%
CYP2C19 inhibition - 0.6555 65.55%
CYP2D6 inhibition - 0.7963 79.63%
CYP1A2 inhibition - 0.7221 72.21%
CYP2C8 inhibition - 0.8689 86.89%
CYP inhibitory promiscuity - 0.5514 55.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7017 70.17%
Carcinogenicity (trinary) Warning 0.4192 41.92%
Eye corrosion - 0.8600 86.00%
Eye irritation + 0.9693 96.93%
Skin irritation - 0.5436 54.36%
Skin corrosion - 0.9173 91.73%
Ames mutagenesis - 0.6554 65.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6247 62.47%
Micronuclear - 0.7593 75.93%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.6548 65.48%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.7196 71.96%
Nephrotoxicity - 0.6645 66.45%
Acute Oral Toxicity (c) III 0.7293 72.93%
Estrogen receptor binding - 0.5710 57.10%
Androgen receptor binding - 0.7465 74.65%
Thyroid receptor binding - 0.8024 80.24%
Glucocorticoid receptor binding - 0.7216 72.16%
Aromatase binding - 0.6228 62.28%
PPAR gamma - 0.8867 88.67%
Honey bee toxicity - 0.9382 93.82%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.8900 89.00%
Fish aquatic toxicity + 0.9525 95.25%

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
CHEMBL2581 P07339 Cathepsin D 89.59% 98.95%
CHEMBL2487 P05067 Beta amyloid A4 protein 85.09% 96.74%
CHEMBL3401 O75469 Pregnane X receptor 84.54% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.99% 86.33%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 83.67% 85.30%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.88% 93.65%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.80% 100.00%
CHEMBL3524 P56524 Histone deacetylase 4 80.96% 92.97%

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.
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

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PubChem 602491
NPASS NPC207316