7-amino-6-(3,7-dimethylocta-2,6-dienyl)-1,1-dioxo-3,4-dihydro-2H-1lambda6,4-benzothiazine-5,8-dione

Details

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Internal ID be5705e7-f873-49ae-a980-750bee5a3110
Taxonomy Organoheterocyclic compounds > Benzothiazines
IUPAC Name 7-amino-6-(3,7-dimethylocta-2,6-dienyl)-1,1-dioxo-3,4-dihydro-2H-1lambda6,4-benzothiazine-5,8-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H24N2O4S/c1-11(2)5-4-6-12(3)7-8-13-14(19)17(22)18-15(16(13)21)20-9-10-25(18,23)24/h5,7,20H,4,6,8-10,19H2,1-3H3
InChI Key DJHHKWSCPIBQME-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H24N2O4S
Molecular Weight 364.50 g/mol
Exact Mass 364.14567842 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 1.66
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-amino-6-(3,7-dimethylocta-2,6-dienyl)-1,1-dioxo-3,4-dihydro-2H-1lambda6,4-benzothiazine-5,8-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9473 94.73%
Caco-2 + 0.4908 49.08%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.3300 33.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9037 90.37%
OATP1B3 inhibitior + 0.9355 93.55%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8409 84.09%
P-glycoprotein inhibitior - 0.4905 49.05%
P-glycoprotein substrate - 0.5413 54.13%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8197 81.97%
CYP3A4 inhibition - 0.5454 54.54%
CYP2C9 inhibition - 0.7204 72.04%
CYP2C19 inhibition - 0.6859 68.59%
CYP2D6 inhibition - 0.8465 84.65%
CYP1A2 inhibition - 0.7351 73.51%
CYP2C8 inhibition - 0.9021 90.21%
CYP inhibitory promiscuity - 0.8510 85.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.5567 55.67%
Eye corrosion - 0.9779 97.79%
Eye irritation - 0.9394 93.94%
Skin irritation - 0.7519 75.19%
Skin corrosion - 0.9041 90.41%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3830 38.30%
Micronuclear + 0.8000 80.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8249 82.49%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.6235 62.35%
Acute Oral Toxicity (c) III 0.6060 60.60%
Estrogen receptor binding + 0.6132 61.32%
Androgen receptor binding + 0.6279 62.79%
Thyroid receptor binding + 0.5568 55.68%
Glucocorticoid receptor binding + 0.5457 54.57%
Aromatase binding - 0.5523 55.23%
PPAR gamma + 0.7766 77.66%
Honey bee toxicity - 0.8662 86.62%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9284 92.84%

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
CHEMBL2581 P07339 Cathepsin D 95.65% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.52% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.31% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.58% 94.45%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 90.18% 93.10%
CHEMBL255 P29275 Adenosine A2b receptor 90.00% 98.59%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.21% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 85.57% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.61% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 80.86% 95.93%

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 73060483
LOTUS LTS0179086
wikiData Q105212243