n-Butyl crotyl disulfide

Details

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Internal ID 37a0f5a6-c196-4390-b13e-855b538b223f
Taxonomy Organosulfur compounds > Organic disulfides > Dialkyldisulfides
IUPAC Name 1-(but-2-enyldisulfanyl)butane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H16S2/c1-3-5-7-9-10-8-6-4-2/h3,5H,4,6-8H2,1-2H3
InChI Key IIVDKJKEPLNHMD-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16S2
Molecular Weight 176.30 g/mol
Exact Mass 176.06934286 g/mol
Topological Polar Surface Area (TPSA) 50.60 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.74
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of n-Butyl crotyl 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 + 0.9321 93.21%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.4825 48.25%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.8346 83.46%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8475 84.75%
P-glycoprotein inhibitior - 0.9840 98.40%
P-glycoprotein substrate - 0.8650 86.50%
CYP3A4 substrate - 0.6425 64.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7612 76.12%
CYP3A4 inhibition - 0.9026 90.26%
CYP2C9 inhibition - 0.8149 81.49%
CYP2C19 inhibition - 0.8017 80.17%
CYP2D6 inhibition - 0.8652 86.52%
CYP1A2 inhibition - 0.6525 65.25%
CYP2C8 inhibition - 0.9111 91.11%
CYP inhibitory promiscuity - 0.5984 59.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.5981 59.81%
Eye corrosion + 0.9261 92.61%
Eye irritation + 0.9606 96.06%
Skin irritation + 0.5130 51.30%
Skin corrosion - 0.9310 93.10%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6148 61.48%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.7492 74.92%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6370 63.70%
Acute Oral Toxicity (c) III 0.8192 81.92%
Estrogen receptor binding - 0.8866 88.66%
Androgen receptor binding - 0.7589 75.89%
Thyroid receptor binding - 0.5270 52.70%
Glucocorticoid receptor binding - 0.7865 78.65%
Aromatase binding - 0.9216 92.16%
PPAR gamma - 0.4940 49.40%
Honey bee toxicity - 0.9230 92.30%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9950 99.50%

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 96.77% 89.63%
CHEMBL2581 P07339 Cathepsin D 89.53% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.51% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.15% 99.17%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 86.12% 91.81%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.77% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 84.71% 85.94%
CHEMBL1907 P15144 Aminopeptidase N 82.79% 93.31%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 82.78% 96.00%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 81.53% 92.86%
CHEMBL2996 Q05655 Protein kinase C delta 80.14% 97.79%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 129651424
LOTUS LTS0101239
wikiData Q105113778