2-(4,5-dimethoxy-6-methylsulfanyl-1,2,3-benzotrithiol-7-yl)-N,N-dimethylethanamine

Details

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Internal ID d4c9bed2-ab3d-4858-bd82-6eb84d4714ea
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenethylamines
IUPAC Name 2-(4,5-dimethoxy-6-methylsulfanyl-1,2,3-benzotrithiol-7-yl)-N,N-dimethylethanamine
SMILES (Canonical) CN(C)CCC1=C2C(=C(C(=C1SC)OC)OC)SSS2
SMILES (Isomeric) CN(C)CCC1=C2C(=C(C(=C1SC)OC)OC)SSS2
InChI InChI=1S/C13H19NO2S4/c1-14(2)7-6-8-11(17-5)9(15-3)10(16-4)13-12(8)18-20-19-13/h6-7H2,1-5H3
InChI Key VDPRVSQPQCVGDF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H19NO2S4
Molecular Weight 349.60 g/mol
Exact Mass 349.02986354 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 4.29
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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BDBM50466813

2D Structure

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2D Structure of 2-(4,5-dimethoxy-6-methylsulfanyl-1,2,3-benzotrithiol-7-yl)-N,N-dimethylethanamine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9856 98.56%
Caco-2 + 0.7610 76.10%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.4687 46.87%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.8713 87.13%
OATP1B3 inhibitior + 0.9377 93.77%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8721 87.21%
P-glycoprotein inhibitior - 0.8102 81.02%
P-glycoprotein substrate - 0.7710 77.10%
CYP3A4 substrate + 0.6121 61.21%
CYP2C9 substrate + 0.5764 57.64%
CYP2D6 substrate + 0.6466 64.66%
CYP3A4 inhibition - 0.6484 64.84%
CYP2C9 inhibition - 0.6801 68.01%
CYP2C19 inhibition - 0.6199 61.99%
CYP2D6 inhibition - 0.6759 67.59%
CYP1A2 inhibition + 0.5117 51.17%
CYP2C8 inhibition - 0.8536 85.36%
CYP inhibitory promiscuity - 0.5079 50.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6210 62.10%
Eye corrosion - 0.9714 97.14%
Eye irritation - 0.6103 61.03%
Skin irritation - 0.7354 73.54%
Skin corrosion - 0.8758 87.58%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5060 50.60%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.5683 56.83%
skin sensitisation - 0.7970 79.70%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.7894 78.94%
Acute Oral Toxicity (c) III 0.5195 51.95%
Estrogen receptor binding - 0.6210 62.10%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.7556 75.56%
Glucocorticoid receptor binding - 0.5082 50.82%
Aromatase binding - 0.6159 61.59%
PPAR gamma - 0.6860 68.60%
Honey bee toxicity - 0.6381 63.81%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9044 90.44%

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 94.94% 96.09%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 93.84% 92.68%
CHEMBL240 Q12809 HERG 87.82% 89.76%
CHEMBL2581 P07339 Cathepsin D 86.08% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.69% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.46% 99.17%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 84.33% 95.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.80% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.47% 94.00%

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 9997973
LOTUS LTS0087519
wikiData Q105284316