5-(Dimethylamino)-6,7-dimethoxy-8-(methyldisulfanyl)-3,4-dihydroisothiochromen-1-one

Details

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Internal ID b7f4c764-8ec8-41ba-a235-b243f3bf2662
Taxonomy Organoheterocyclic compounds > Isothiochromanes
IUPAC Name 5-(dimethylamino)-6,7-dimethoxy-8-(methyldisulfanyl)-3,4-dihydroisothiochromen-1-one
SMILES (Canonical) CN(C)C1=C(C(=C(C2=C1CCSC2=O)SSC)OC)OC
SMILES (Isomeric) CN(C)C1=C(C(=C(C2=C1CCSC2=O)SSC)OC)OC
InChI InChI=1S/C14H19NO3S3/c1-15(2)10-8-6-7-20-14(16)9(8)13(21-19-5)12(18-4)11(10)17-3/h6-7H2,1-5H3
InChI Key BAKJMSAZZKUWJW-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H19NO3S3
Molecular Weight 345.50 g/mol
Exact Mass 345.05270699 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.57
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(Dimethylamino)-6,7-dimethoxy-8-(methyldisulfanyl)-3,4-dihydroisothiochromen-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9407 94.07%
Caco-2 + 0.6450 64.50%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7468 74.68%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.9493 94.93%
OATP1B3 inhibitior + 0.9412 94.12%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8985 89.85%
P-glycoprotein inhibitior - 0.8146 81.46%
P-glycoprotein substrate - 0.7845 78.45%
CYP3A4 substrate + 0.5995 59.95%
CYP2C9 substrate - 0.7984 79.84%
CYP2D6 substrate - 0.7189 71.89%
CYP3A4 inhibition + 0.8185 81.85%
CYP2C9 inhibition - 0.5573 55.73%
CYP2C19 inhibition + 0.6601 66.01%
CYP2D6 inhibition - 0.7950 79.50%
CYP1A2 inhibition + 0.7344 73.44%
CYP2C8 inhibition - 0.9098 90.98%
CYP inhibitory promiscuity + 0.8249 82.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.5499 54.99%
Eye corrosion - 0.9768 97.68%
Eye irritation - 0.7027 70.27%
Skin irritation - 0.7778 77.78%
Skin corrosion - 0.9216 92.16%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4901 49.01%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8400 84.00%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.6090 60.90%
Acute Oral Toxicity (c) III 0.6487 64.87%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.5765 57.65%
Thyroid receptor binding + 0.7791 77.91%
Glucocorticoid receptor binding + 0.6029 60.29%
Aromatase binding - 0.6217 62.17%
PPAR gamma - 0.6939 69.39%
Honey bee toxicity - 0.7332 73.32%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9084 90.84%

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 92.29% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.42% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.00% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.63% 91.11%
CHEMBL1871 P10275 Androgen Receptor 81.88% 96.43%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.84% 90.08%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.70% 94.00%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 81.27% 95.53%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.00% 99.23%

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 14759718
LOTUS LTS0266249
wikiData Q104922259