4,6-Dimethyltetrahydro-1,3-oxazine-2-thione

Details

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Internal ID 4daac5f9-84ca-4ad7-b671-994a2a3fc8f2
Taxonomy Organoheterocyclic compounds > Oxazinanes > 1,3-oxazinanes
IUPAC Name 4,6-dimethyl-1,3-oxazinane-2-thione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H11NOS/c1-4-3-5(2)8-6(9)7-4/h4-5H,3H2,1-2H3,(H,7,9)
InChI Key USYWBVZOBCQVOG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11NOS
Molecular Weight 145.23 g/mol
Exact Mass 145.05613515 g/mol
Topological Polar Surface Area (TPSA) 53.40 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.06
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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4,6-Dimethyl-1,3-oxazinane-2-thione #
4,6-Dimethyltetrahydro-1,3-oxazine-2-thione

2D Structure

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2D Structure of 4,6-Dimethyltetrahydro-1,3-oxazine-2-thione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9832 98.32%
Caco-2 + 0.5782 57.82%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.6106 61.06%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.9510 95.10%
OATP1B3 inhibitior + 0.9468 94.68%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9463 94.63%
P-glycoprotein inhibitior - 0.9750 97.50%
P-glycoprotein substrate - 0.8602 86.02%
CYP3A4 substrate - 0.6861 68.61%
CYP2C9 substrate - 0.5914 59.14%
CYP2D6 substrate - 0.7785 77.85%
CYP3A4 inhibition - 0.9414 94.14%
CYP2C9 inhibition - 0.6857 68.57%
CYP2C19 inhibition - 0.5960 59.60%
CYP2D6 inhibition - 0.9218 92.18%
CYP1A2 inhibition + 0.5238 52.38%
CYP2C8 inhibition - 0.9759 97.59%
CYP inhibitory promiscuity - 0.7117 71.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5759 57.59%
Eye corrosion - 0.9562 95.62%
Eye irritation + 0.7215 72.15%
Skin irritation - 0.6434 64.34%
Skin corrosion - 0.8328 83.28%
Ames mutagenesis + 0.6046 60.46%
Human Ether-a-go-go-Related Gene inhibition - 0.7593 75.93%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.6677 66.77%
skin sensitisation - 0.8281 82.81%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.5841 58.41%
Acute Oral Toxicity (c) III 0.6264 62.64%
Estrogen receptor binding - 0.8703 87.03%
Androgen receptor binding - 0.9247 92.47%
Thyroid receptor binding - 0.8114 81.14%
Glucocorticoid receptor binding - 0.9074 90.74%
Aromatase binding - 0.7530 75.30%
PPAR gamma - 0.8651 86.51%
Honey bee toxicity - 0.8336 83.36%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity - 0.9305 93.05%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 92.78% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.34% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.99% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 82.18% 97.79%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.12% 91.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Cleome chrysantha

Cross-Links

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PubChem 5372777
LOTUS LTS0158419
wikiData Q104667204