2-Phenylethanethiol

Details

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Internal ID 5caa124a-71ec-4208-9942-92bd273f0976
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 2-phenylethanethiol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H10S/c9-7-6-8-4-2-1-3-5-8/h1-5,9H,6-7H2
InChI Key ZMRFRBHYXOQLDK-UHFFFAOYSA-N
Popularity 126 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10S
Molecular Weight 138.23 g/mol
Exact Mass 138.05032149 g/mol
Topological Polar Surface Area (TPSA) 1.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.16
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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4410-99-5
Phenethyl mercaptan
Benzeneethanethiol
2-Phenylethyl mercaptan
Phenylethyl mercaptan
2-phenylethylthiol
2-phenylethylmercaptan
2-phenylethane-1-thiol
2-phenyl-ethanethiol
beta-Phenylethyl mercaptan
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Phenylethanethiol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9897 98.97%
Caco-2 + 0.9239 92.39%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Lysosomes 0.6231 62.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9121 91.21%
OATP1B3 inhibitior + 0.9544 95.44%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9225 92.25%
P-glycoprotein inhibitior - 0.9909 99.09%
P-glycoprotein substrate - 0.9468 94.68%
CYP3A4 substrate - 0.7570 75.70%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4236 42.36%
CYP3A4 inhibition - 0.9115 91.15%
CYP2C9 inhibition - 0.7484 74.84%
CYP2C19 inhibition - 0.5619 56.19%
CYP2D6 inhibition - 0.7960 79.60%
CYP1A2 inhibition + 0.6047 60.47%
CYP2C8 inhibition - 0.7658 76.58%
CYP inhibitory promiscuity + 0.5509 55.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.5953 59.53%
Eye corrosion + 0.9903 99.03%
Eye irritation + 0.9829 98.29%
Skin irritation + 0.9452 94.52%
Skin corrosion + 0.7476 74.76%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7481 74.81%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.7182 71.82%
skin sensitisation + 0.9013 90.13%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7119 71.19%
Acute Oral Toxicity (c) II 0.5602 56.02%
Estrogen receptor binding - 0.8228 82.28%
Androgen receptor binding - 0.7991 79.91%
Thyroid receptor binding - 0.7846 78.46%
Glucocorticoid receptor binding - 0.8333 83.33%
Aromatase binding - 0.8152 81.52%
PPAR gamma - 0.7061 70.61%
Honey bee toxicity - 0.8063 80.63%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.6694 66.94%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.48% 94.62%
CHEMBL2581 P07339 Cathepsin D 91.34% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 86.71% 90.17%
CHEMBL240 Q12809 HERG 84.81% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.62% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.96% 86.33%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.97% 93.81%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.63% 95.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 78126
LOTUS LTS0107858
wikiData Q27280442