4-Methyl-1,2-dithiacyclopentene

Details

Top
Internal ID b6696aea-b92a-404e-9eba-c0b48e928ded
Taxonomy Organoheterocyclic compounds > Dithioles > 1,2-dithioles
IUPAC Name 4-methyl-3H-dithiole
SMILES (Canonical) CC1=CSSC1
SMILES (Isomeric) CC1=CSSC1
InChI InChI=1S/C4H6S2/c1-4-2-5-6-3-4/h2H,3H2,1H3
InChI Key UHYMACQSUPLYEZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C4H6S2
Molecular Weight 118.20 g/mol
Exact Mass 117.99109254 g/mol
Topological Polar Surface Area (TPSA) 50.60 Ų
XlogP 0.80
Atomic LogP (AlogP) 2.29
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
4-methyl-1,2-dithiacyclopentene

2D Structure

Top
2D Structure of 4-Methyl-1,2-dithiacyclopentene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 + 0.7668 76.68%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.9286 92.86%
Subcellular localzation Lysosomes 0.4455 44.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9682 96.82%
OATP1B3 inhibitior + 0.9486 94.86%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9124 91.24%
P-glycoprotein inhibitior - 0.9798 97.98%
P-glycoprotein substrate - 0.9794 97.94%
CYP3A4 substrate - 0.7454 74.54%
CYP2C9 substrate - 0.6106 61.06%
CYP2D6 substrate - 0.8068 80.68%
CYP3A4 inhibition - 0.8909 89.09%
CYP2C9 inhibition - 0.6358 63.58%
CYP2C19 inhibition - 0.5901 59.01%
CYP2D6 inhibition - 0.7828 78.28%
CYP1A2 inhibition - 0.6001 60.01%
CYP2C8 inhibition - 0.9898 98.98%
CYP inhibitory promiscuity + 0.7369 73.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.4348 43.48%
Eye corrosion + 0.5078 50.78%
Eye irritation + 0.9832 98.32%
Skin irritation + 0.5860 58.60%
Skin corrosion - 0.5943 59.43%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7458 74.58%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.7948 79.48%
skin sensitisation + 0.5070 50.70%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6634 66.34%
Estrogen receptor binding - 0.9398 93.98%
Androgen receptor binding - 0.9145 91.45%
Thyroid receptor binding - 0.8752 87.52%
Glucocorticoid receptor binding - 0.8355 83.55%
Aromatase binding - 0.8761 87.61%
PPAR gamma - 0.8444 84.44%
Honey bee toxicity - 0.9675 96.75%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9473 94.73%

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
CHEMBL3492 P49721 Proteasome Macropain subunit 83.68% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.42% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.59% 96.09%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.24% 85.30%

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
Aniba megaphylla
Berberis integerrima
Calocedrus decurrens
Digitalis sceptrum
Herbertus sakuraii
Nauclea latifolia
Orthopappus angustifolius
Scurrula parasitica

Cross-Links

Top
PubChem 5319597
NPASS NPC292090