2-methyl-2-methylsulfanyl-3H-furan

Details

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Internal ID 58dd33b5-4704-42b3-a16d-9ba664d79593
Taxonomy Organosulfur compounds > Thioacetals > Monothioacetals > Monothioketals
IUPAC Name 2-methyl-2-methylsulfanyl-3H-furan
SMILES (Canonical) CC1(CC=CO1)SC
SMILES (Isomeric) CC1(CC=CO1)SC
InChI InChI=1S/C6H10OS/c1-6(8-2)4-3-5-7-6/h3,5H,4H2,1-2H3
InChI Key RLDSVUFVYLJHPZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10OS
Molecular Weight 130.21 g/mol
Exact Mass 130.04523611 g/mol
Topological Polar Surface Area (TPSA) 34.50 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.00
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-methyl-2-methylsulfanyl-3H-furan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9819 98.19%
Caco-2 + 0.8759 87.59%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.3749 37.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9432 94.32%
OATP1B3 inhibitior + 0.9530 95.30%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8783 87.83%
P-glycoprotein inhibitior - 0.9854 98.54%
P-glycoprotein substrate - 0.9716 97.16%
CYP3A4 substrate - 0.6491 64.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7825 78.25%
CYP3A4 inhibition - 0.9635 96.35%
CYP2C9 inhibition - 0.7316 73.16%
CYP2C19 inhibition - 0.6101 61.01%
CYP2D6 inhibition - 0.9093 90.93%
CYP1A2 inhibition - 0.6249 62.49%
CYP2C8 inhibition - 0.9410 94.10%
CYP inhibitory promiscuity - 0.5918 59.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6817 68.17%
Carcinogenicity (trinary) Non-required 0.4744 47.44%
Eye corrosion - 0.6324 63.24%
Eye irritation + 0.8000 80.00%
Skin irritation + 0.5367 53.67%
Skin corrosion - 0.9223 92.23%
Ames mutagenesis - 0.5554 55.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7580 75.80%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.7085 70.85%
skin sensitisation + 0.6742 67.42%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.6876 68.76%
Acute Oral Toxicity (c) III 0.6229 62.29%
Estrogen receptor binding - 0.9036 90.36%
Androgen receptor binding - 0.8710 87.10%
Thyroid receptor binding - 0.9105 91.05%
Glucocorticoid receptor binding - 0.8722 87.22%
Aromatase binding - 0.8623 86.23%
PPAR gamma - 0.8975 89.75%
Honey bee toxicity - 0.9161 91.61%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.4072 40.72%

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
CHEMBL4040 P28482 MAP kinase ERK2 89.39% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.65% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 86.86% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.25% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 84.36% 90.17%

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.
Coffea arabica

Cross-Links

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PubChem 163192713
LOTUS LTS0012938
wikiData Q105239855