3-Vinyl-1,2-dithiacyclohex-4-ene

Details

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Internal ID ada17e1e-4776-4ea5-a7bb-7c30d8ae8526
Taxonomy Organoheterocyclic compounds > Dithiins
IUPAC Name 3-ethenyl-3,6-dihydrodithiine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H8S2/c1-2-6-4-3-5-7-8-6/h2-4,6H,1,5H2
InChI Key UQXHSMWBRGWFBK-UHFFFAOYSA-N
Popularity 18 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8S2
Molecular Weight 144.30 g/mol
Exact Mass 144.00674260 g/mol
Topological Polar Surface Area (TPSA) 50.60 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.49
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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62488-52-2
3-vinyl-1,2-dithi-4-ene
3-Ethenyl-1,2-dithi-4-ene
SCHEMBL2928659
1,2-Dithi-4-ene, 3-ethenyl
DTXSID50335470
UQXHSMWBRGWFBK-UHFFFAOYSA-N
3-vinyl-1,2-dithia-4-cyclohexene
3-Vinyl-3,6-dihydro-1,2-dithiine
3-Vinyl-3,6-dihydro-1,2-dithiine #

2D Structure

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2D Structure of 3-Vinyl-1,2-dithiacyclohex-4-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9816 98.16%
Caco-2 + 0.6894 68.94%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.4923 49.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9576 95.76%
OATP1B3 inhibitior + 0.9514 95.14%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9207 92.07%
P-glycoprotein inhibitior - 0.9827 98.27%
P-glycoprotein substrate - 0.9675 96.75%
CYP3A4 substrate - 0.6627 66.27%
CYP2C9 substrate + 0.5994 59.94%
CYP2D6 substrate - 0.7683 76.83%
CYP3A4 inhibition - 0.6751 67.51%
CYP2C9 inhibition - 0.5675 56.75%
CYP2C19 inhibition - 0.5324 53.24%
CYP2D6 inhibition - 0.7620 76.20%
CYP1A2 inhibition + 0.5367 53.67%
CYP2C8 inhibition - 0.9512 95.12%
CYP inhibitory promiscuity + 0.5957 59.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5834 58.34%
Carcinogenicity (trinary) Non-required 0.5702 57.02%
Eye corrosion + 0.7292 72.92%
Eye irritation + 0.9796 97.96%
Skin irritation + 0.7047 70.47%
Skin corrosion + 0.5530 55.30%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7397 73.97%
Micronuclear - 0.6700 67.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.5992 59.92%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.4706 47.06%
Acute Oral Toxicity (c) II 0.6580 65.80%
Estrogen receptor binding - 0.8922 89.22%
Androgen receptor binding - 0.8156 81.56%
Thyroid receptor binding - 0.7971 79.71%
Glucocorticoid receptor binding - 0.7252 72.52%
Aromatase binding - 0.8483 84.83%
PPAR gamma - 0.7496 74.96%
Honey bee toxicity + 0.5664 56.64%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9238 92.38%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.68% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.89% 96.09%

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.
Mansoa alliacea

Cross-Links

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PubChem 525328
LOTUS LTS0080416
wikiData Q82101883