(2S,4R,6S)-4-butyl-2,6-dimethyl-1,3,5-dithiazinane

Details

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Internal ID bdd4a665-3e8f-4143-a091-57bb589bfde9
Taxonomy Organoheterocyclic compounds > Azacyclic compounds > Dithiazinanes > 1,3,5-dithiazinanes
IUPAC Name (2S,4R,6S)-4-butyl-2,6-dimethyl-1,3,5-dithiazinane
SMILES (Canonical) CCCCC1NC(SC(S1)C)C
SMILES (Isomeric) CCCC[C@@H]1N[C@@H](S[C@@H](S1)C)C
InChI InChI=1S/C9H19NS2/c1-4-5-6-9-10-7(2)11-8(3)12-9/h7-10H,4-6H2,1-3H3/t7-,8-,9+/m0/s1
InChI Key ZGCDSMJNRUXZGG-XHNCKOQMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H19NS2
Molecular Weight 205.40 g/mol
Exact Mass 205.09589196 g/mol
Topological Polar Surface Area (TPSA) 62.60 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.26
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,4R,6S)-4-butyl-2,6-dimethyl-1,3,5-dithiazinane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9920 99.20%
Caco-2 + 0.8020 80.20%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.7230 72.30%
OATP2B1 inhibitior - 0.8450 84.50%
OATP1B1 inhibitior + 0.8948 89.48%
OATP1B3 inhibitior + 0.9410 94.10%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8791 87.91%
P-glycoprotein inhibitior - 0.9689 96.89%
P-glycoprotein substrate - 0.6961 69.61%
CYP3A4 substrate - 0.6176 61.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7724 77.24%
CYP3A4 inhibition - 0.9640 96.40%
CYP2C9 inhibition - 0.7946 79.46%
CYP2C19 inhibition - 0.6933 69.33%
CYP2D6 inhibition - 0.7590 75.90%
CYP1A2 inhibition + 0.6083 60.83%
CYP2C8 inhibition - 0.8636 86.36%
CYP inhibitory promiscuity - 0.7233 72.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6806 68.06%
Eye corrosion - 0.8511 85.11%
Eye irritation - 0.7241 72.41%
Skin irritation - 0.5697 56.97%
Skin corrosion + 0.6775 67.75%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7078 70.78%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.6052 60.52%
skin sensitisation - 0.7007 70.07%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6126 61.26%
Acute Oral Toxicity (c) III 0.5862 58.62%
Estrogen receptor binding - 0.8157 81.57%
Androgen receptor binding - 0.6719 67.19%
Thyroid receptor binding - 0.6054 60.54%
Glucocorticoid receptor binding - 0.8762 87.62%
Aromatase binding - 0.7869 78.69%
PPAR gamma - 0.7678 76.78%
Honey bee toxicity - 0.9556 95.56%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity - 0.4162 41.62%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.31% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.40% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.89% 98.95%
CHEMBL255 P29275 Adenosine A2b receptor 88.48% 98.59%
CHEMBL230 P35354 Cyclooxygenase-2 87.90% 89.63%
CHEMBL299 P17252 Protein kinase C alpha 87.45% 98.03%
CHEMBL2996 Q05655 Protein kinase C delta 87.04% 97.79%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 84.32% 90.24%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.36% 92.08%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.16% 91.81%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.17% 96.95%

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 162979695
LOTUS LTS0120360
wikiData Q105375063