Di((2H3)methyl) sulphide

Details

Top
Internal ID 960654df-3c9b-4ec4-9543-4638e85d9203
Taxonomy Organosulfur compounds > Thioethers > Dialkylthioethers
IUPAC Name trideuterio(trideuteriomethylsulfanyl)methane
SMILES (Canonical) CSC
SMILES (Isomeric) [2H]C([2H])([2H])SC([2H])([2H])[2H]
InChI InChI=1S/C2H6S/c1-3-2/h1-2H3/i1D3,2D3
InChI Key QMMFVYPAHWMCMS-WFGJKAKNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C2H6S
Molecular Weight 68.17 g/mol
Exact Mass 68.05668184 g/mol
Topological Polar Surface Area (TPSA) 25.30 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.98
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
Dimethyl sulfide-d6
Di((2H3)methyl) sulphide
trideuterio(trideuteriomethylsulfanyl)methane
EINECS 213-133-6
1,1'-Thiobismethane-d3 (Dimethyl Sulfide-d6)
Di[(2H3)methyl] sulphide
(Methyl sulfide)-d6
Hexadeuterodimethyl sulfide
Di(2H3)methyl sulfide
DIMETHYL-D6 SULFIDE
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Di((2H3)methyl) sulphide

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9700 97.00%
Caco-2 - 0.5649 56.49%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.6157 61.57%
OATP2B1 inhibitior - 0.8691 86.91%
OATP1B1 inhibitior + 0.9749 97.49%
OATP1B3 inhibitior + 0.9570 95.70%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9525 95.25%
P-glycoprotein inhibitior - 0.9747 97.47%
P-glycoprotein substrate - 0.9914 99.14%
CYP3A4 substrate - 0.7981 79.81%
CYP2C9 substrate - 0.7912 79.12%
CYP2D6 substrate - 0.7804 78.04%
CYP3A4 inhibition - 0.9762 97.62%
CYP2C9 inhibition - 0.8496 84.96%
CYP2C19 inhibition - 0.8781 87.81%
CYP2D6 inhibition - 0.9485 94.85%
CYP1A2 inhibition - 0.8392 83.92%
CYP2C8 inhibition - 0.9875 98.75%
CYP inhibitory promiscuity - 0.8913 89.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5483 54.83%
Carcinogenicity (trinary) Non-required 0.6210 62.10%
Eye corrosion + 0.9522 95.22%
Eye irritation + 0.9070 90.70%
Skin irritation + 0.6781 67.81%
Skin corrosion - 0.9529 95.29%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6658 66.58%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.8625 86.25%
skin sensitisation + 0.8994 89.94%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.6012 60.12%
Nephrotoxicity + 0.7127 71.27%
Acute Oral Toxicity (c) III 0.8130 81.30%
Estrogen receptor binding - 0.8611 86.11%
Androgen receptor binding - 0.9514 95.14%
Thyroid receptor binding - 0.8375 83.75%
Glucocorticoid receptor binding - 0.8905 89.05%
Aromatase binding - 0.8782 87.82%
PPAR gamma - 0.8428 84.28%
Honey bee toxicity - 0.6813 68.13%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity - 0.4304 43.04%

Targets

Top

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
No predicted targets yet!

Plants that contains it

Top
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.
Allium sativum
Cistanche deserticola
Sagittaria sagittifolia

Cross-Links

Top
PubChem 2724139
NPASS NPC110511