Methyl n-hexyl disulfide

Details

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Internal ID 13a4c3b2-8e8e-4df0-813f-d19207836b6f
Taxonomy Organosulfur compounds > Organic disulfides > Dialkyldisulfides
IUPAC Name 1-(methyldisulfanyl)hexane
SMILES (Canonical) CCCCCCSSC
SMILES (Isomeric) CCCCCCSSC
InChI InChI=1S/C7H16S2/c1-3-4-5-6-7-9-8-2/h3-7H2,1-2H3
InChI Key WZUAZKYWEVGSEC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H16S2
Molecular Weight 164.30 g/mol
Exact Mass 164.06934286 g/mol
Topological Polar Surface Area (TPSA) 50.60 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.58
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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64580-52-5
Disulfide, hexyl methyl
Hexyl methyl disulfide
1-(Methyldisulfanyl)hexane #
SCHEMBL3380906
DTXSID50336780
WZUAZKYWEVGSEC-UHFFFAOYSA-N

2D Structure

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2D Structure of Methyl n-hexyl disulfide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9874 98.74%
Caco-2 + 0.9323 93.23%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.5227 52.27%
OATP2B1 inhibitior - 0.8436 84.36%
OATP1B1 inhibitior + 0.9352 93.52%
OATP1B3 inhibitior + 0.9436 94.36%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9409 94.09%
P-glycoprotein inhibitior - 0.9810 98.10%
P-glycoprotein substrate - 0.8273 82.73%
CYP3A4 substrate - 0.6558 65.58%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7426 74.26%
CYP3A4 inhibition - 0.9411 94.11%
CYP2C9 inhibition - 0.8493 84.93%
CYP2C19 inhibition - 0.8602 86.02%
CYP2D6 inhibition - 0.8698 86.98%
CYP1A2 inhibition - 0.6949 69.49%
CYP2C8 inhibition - 0.8862 88.62%
CYP inhibitory promiscuity - 0.7883 78.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.7262 72.62%
Eye corrosion + 0.9077 90.77%
Eye irritation + 0.9876 98.76%
Skin irritation + 0.5063 50.63%
Skin corrosion - 0.9600 96.00%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6566 65.66%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.7560 75.60%
skin sensitisation + 0.7673 76.73%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.8114 81.14%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.7363 73.63%
Acute Oral Toxicity (c) III 0.6695 66.95%
Estrogen receptor binding - 0.8991 89.91%
Androgen receptor binding - 0.8224 82.24%
Thyroid receptor binding - 0.6512 65.12%
Glucocorticoid receptor binding - 0.9105 91.05%
Aromatase binding - 0.9180 91.80%
PPAR gamma - 0.8508 85.08%
Honey bee toxicity - 0.9832 98.32%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.8121 81.21%
Fish aquatic toxicity + 0.9841 98.41%

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
CHEMBL230 P35354 Cyclooxygenase-2 95.67% 89.63%
CHEMBL240 Q12809 HERG 93.23% 89.76%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.46% 92.08%
CHEMBL2581 P07339 Cathepsin D 90.59% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.47% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.64% 91.81%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 88.32% 85.94%
CHEMBL2885 P07451 Carbonic anhydrase III 88.26% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.25% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.26% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.97% 99.17%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 80.45% 96.00%
CHEMBL2996 Q05655 Protein kinase C delta 80.22% 97.79%

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.
Rosa canina

Cross-Links

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PubChem 536236
LOTUS LTS0215927
wikiData Q82104150