Methyl sec-butyl disulfide

Details

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Internal ID 2448a7ac-1587-4b09-964e-9b343d379425
Taxonomy Organosulfur compounds > Organic disulfides > Dialkyldisulfides
IUPAC Name 2-(methyldisulfanyl)butane
SMILES (Canonical) CCC(C)SSC
SMILES (Isomeric) CCC(C)SSC
InChI InChI=1S/C5H12S2/c1-4-5(2)7-6-3/h5H,4H2,1-3H3
InChI Key QTWVOHZEDPQFTP-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C5H12S2
Molecular Weight 136.30 g/mol
Exact Mass 136.03804273 g/mol
Topological Polar Surface Area (TPSA) 50.60 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.80
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Methyl sec-butyl disulphide
3-Methyl-4,5-dithiahexane
2-Butylmethyldisulfid
sec-Butyl methyl disulfide
Disulfide, sec-butyl methyl
67421-87-8
SCHEMBL18133318
Disulfide, methyl 1-methylpropyl
QTWVOHZEDPQFTP-UHFFFAOYSA-N

2D Structure

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2D Structure of Methyl sec-butyl disulfide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.6669 66.69%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.4731 47.31%
OATP2B1 inhibitior - 0.8629 86.29%
OATP1B1 inhibitior + 0.9368 93.68%
OATP1B3 inhibitior + 0.9440 94.40%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9394 93.94%
P-glycoprotein inhibitior - 0.9824 98.24%
P-glycoprotein substrate - 0.9609 96.09%
CYP3A4 substrate - 0.7538 75.38%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7426 74.26%
CYP3A4 inhibition - 0.8689 86.89%
CYP2C9 inhibition - 0.7505 75.05%
CYP2C19 inhibition - 0.8120 81.20%
CYP2D6 inhibition - 0.8483 84.83%
CYP1A2 inhibition - 0.7014 70.14%
CYP2C8 inhibition - 0.9867 98.67%
CYP inhibitory promiscuity - 0.6651 66.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.5986 59.86%
Eye corrosion + 0.7586 75.86%
Eye irritation + 0.9543 95.43%
Skin irritation + 0.6311 63.11%
Skin corrosion - 0.9121 91.21%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8071 80.71%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.6677 66.77%
skin sensitisation + 0.7701 77.01%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.7034 70.34%
Acute Oral Toxicity (c) III 0.5363 53.63%
Estrogen receptor binding - 0.8699 86.99%
Androgen receptor binding - 0.8985 89.85%
Thyroid receptor binding - 0.8267 82.67%
Glucocorticoid receptor binding - 0.9481 94.81%
Aromatase binding - 0.8322 83.22%
PPAR gamma - 0.8916 89.16%
Honey bee toxicity - 0.8882 88.82%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9128 91.28%

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
CHEMBL221 P23219 Cyclooxygenase-1 87.15% 90.17%
CHEMBL2581 P07339 Cathepsin D 87.04% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.75% 97.25%
CHEMBL2885 P07451 Carbonic anhydrase III 85.28% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.05% 96.09%
CHEMBL4072 P07858 Cathepsin B 84.01% 93.67%

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.
Ferula assa-foetida
Ferula fukanensis
Ferula sinkiangensis

Cross-Links

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PubChem 522263
NPASS NPC252152
LOTUS LTS0185604
wikiData Q105227961