5,6-Dimethoxy-4,7-bis(4-methoxyphenyl)-1,3-benzothiazole

Details

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Internal ID d7c00b28-e97f-47e5-a249-4ca89be3c2b4
Taxonomy Benzenoids > Benzene and substituted derivatives > Terphenyls > P-terphenyls
IUPAC Name 5,6-dimethoxy-4,7-bis(4-methoxyphenyl)-1,3-benzothiazole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H21NO4S/c1-25-16-9-5-14(6-10-16)18-20-23(29-13-24-20)19(22(28-4)21(18)27-3)15-7-11-17(26-2)12-8-15/h5-13H,1-4H3
InChI Key HHZHOMXMQXTDKX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H21NO4S
Molecular Weight 407.50 g/mol
Exact Mass 407.11912932 g/mol
Topological Polar Surface Area (TPSA) 78.10 Ų
XlogP 5.50
Atomic LogP (AlogP) 5.66
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,6-Dimethoxy-4,7-bis(4-methoxyphenyl)-1,3-benzothiazole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 + 0.6424 64.24%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7129 71.29%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.9494 94.94%
OATP1B3 inhibitior + 0.9362 93.62%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9315 93.15%
P-glycoprotein inhibitior + 0.8424 84.24%
P-glycoprotein substrate - 0.9358 93.58%
CYP3A4 substrate + 0.5073 50.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6697 66.97%
CYP3A4 inhibition + 0.8358 83.58%
CYP2C9 inhibition + 0.6019 60.19%
CYP2C19 inhibition + 0.8962 89.62%
CYP2D6 inhibition - 0.7528 75.28%
CYP1A2 inhibition + 0.8867 88.67%
CYP2C8 inhibition + 0.6179 61.79%
CYP inhibitory promiscuity + 0.9546 95.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9108 91.08%
Carcinogenicity (trinary) Non-required 0.3803 38.03%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.6594 65.94%
Skin irritation - 0.8342 83.42%
Skin corrosion - 0.9585 95.85%
Ames mutagenesis + 0.5839 58.39%
Human Ether-a-go-go-Related Gene inhibition + 0.8070 80.70%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8813 88.13%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.4534 45.34%
Acute Oral Toxicity (c) III 0.5705 57.05%
Estrogen receptor binding + 0.9148 91.48%
Androgen receptor binding + 0.8685 86.85%
Thyroid receptor binding + 0.8356 83.56%
Glucocorticoid receptor binding + 0.9300 93.00%
Aromatase binding + 0.8085 80.85%
PPAR gamma + 0.7811 78.11%
Honey bee toxicity - 0.9326 93.26%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.8100 81.00%
Fish aquatic toxicity + 0.9028 90.28%

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 94.52% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.43% 94.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 92.67% 85.30%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.16% 99.15%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.33% 95.50%
CHEMBL4208 P20618 Proteasome component C5 90.28% 90.00%
CHEMBL2243 O00519 Anandamide amidohydrolase 90.15% 97.53%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 88.47% 96.47%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.39% 86.92%
CHEMBL1907 P15144 Aminopeptidase N 88.07% 93.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.85% 96.00%
CHEMBL211 P08172 Muscarinic acetylcholine receptor M2 86.33% 94.97%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 85.44% 93.24%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 85.39% 92.68%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.59% 86.33%
CHEMBL2487 P05067 Beta amyloid A4 protein 84.33% 96.74%
CHEMBL235 P37231 Peroxisome proliferator-activated receptor gamma 83.88% 95.39%
CHEMBL244 P00742 Coagulation factor X 82.90% 98.41%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.13% 95.56%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.93% 80.96%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.39% 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 76331182
LOTUS LTS0174879
wikiData Q105028688