4-(2-Methylsulfanyl-1,3-thiazol-5-yl)phenol

Details

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Internal ID e3a7e03c-f898-49e0-8ff7-3ec4a72d30c7
Taxonomy Organosulfur compounds > Thioethers > Aryl thioethers
IUPAC Name 4-(2-methylsulfanyl-1,3-thiazol-5-yl)phenol
SMILES (Canonical) CSC1=NC=C(S1)C2=CC=C(C=C2)O
SMILES (Isomeric) CSC1=NC=C(S1)C2=CC=C(C=C2)O
InChI InChI=1S/C10H9NOS2/c1-13-10-11-6-9(14-10)7-2-4-8(12)5-3-7/h2-6,12H,1H3
InChI Key FKDOJSGVPRNHQH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H9NOS2
Molecular Weight 223.30 g/mol
Exact Mass 223.01255626 g/mol
Topological Polar Surface Area (TPSA) 86.70 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.24
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(2-Methylsulfanyl-1,3-thiazol-5-yl)phenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.7416 74.16%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7389 73.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9507 95.07%
OATP1B3 inhibitior + 0.9477 94.77%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7859 78.59%
P-glycoprotein inhibitior - 0.9646 96.46%
P-glycoprotein substrate - 0.8934 89.34%
CYP3A4 substrate - 0.6026 60.26%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.7719 77.19%
CYP3A4 inhibition - 0.8595 85.95%
CYP2C9 inhibition + 0.6800 68.00%
CYP2C19 inhibition + 0.7398 73.98%
CYP2D6 inhibition - 0.9009 90.09%
CYP1A2 inhibition + 0.8841 88.41%
CYP2C8 inhibition + 0.8180 81.80%
CYP inhibitory promiscuity + 0.8571 85.71%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8931 89.31%
Carcinogenicity (trinary) Non-required 0.4708 47.08%
Eye corrosion - 0.9761 97.61%
Eye irritation + 0.8239 82.39%
Skin irritation - 0.6361 63.61%
Skin corrosion - 0.8600 86.00%
Ames mutagenesis - 0.7137 71.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6790 67.90%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.7177 71.77%
skin sensitisation - 0.8243 82.43%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5250 52.50%
Acute Oral Toxicity (c) III 0.5565 55.65%
Estrogen receptor binding + 0.8215 82.15%
Androgen receptor binding + 0.6907 69.07%
Thyroid receptor binding - 0.4942 49.42%
Glucocorticoid receptor binding + 0.7474 74.74%
Aromatase binding + 0.9103 91.03%
PPAR gamma + 0.6776 67.76%
Honey bee toxicity - 0.9063 90.63%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity - 0.5000 50.00%

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
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 97.14% 93.10%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 95.64% 97.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.34% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.29% 96.09%
CHEMBL2487 P05067 Beta amyloid A4 protein 89.35% 96.74%
CHEMBL2581 P07339 Cathepsin D 88.36% 98.95%
CHEMBL242 Q92731 Estrogen receptor beta 88.13% 98.35%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 87.56% 93.24%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.51% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.21% 86.33%
CHEMBL2093869 P05106 Integrin alpha-IIb/beta-3 86.13% 95.42%
CHEMBL3401 O75469 Pregnane X receptor 85.79% 94.73%
CHEMBL2535 P11166 Glucose transporter 83.09% 98.75%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 81.68% 92.29%
CHEMBL1907 P15144 Aminopeptidase N 81.24% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.58% 99.17%

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 11831064
LOTUS LTS0193070
wikiData Q104996528