Isopropyl propyl disulfide

Details

Top
Internal ID 82d04f46-0230-4095-9208-b6f368627ceb
Taxonomy Organosulfur compounds > Organic disulfides > Dialkyldisulfides
IUPAC Name 1-(propan-2-yldisulfanyl)propane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H14S2/c1-4-5-7-8-6(2)3/h6H,4-5H2,1-3H3
InChI Key YCBVTHJPQCNICU-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H14S2
Molecular Weight 150.30 g/mol
Exact Mass 150.05369279 g/mol
Topological Polar Surface Area (TPSA) 50.60 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
33672-51-4
Isopropyl propyl disulphide
Disulfide, isopropyl propyl
Disulfide, 1-methylethyl propyl
1-(propan-2-yldisulfanyl)propane
Disulfide,1-methylethyl propyl
EINECS 251-628-9
Propyl isopropyl disulfide
2-isopropyldisulfanylpropane
2-methyl-3,4-dithiaheptane
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Isopropyl propyl disulfide

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 + 0.8262 82.62%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Lysosomes 0.4123 41.23%
OATP2B1 inhibitior - 0.8562 85.62%
OATP1B1 inhibitior + 0.9473 94.73%
OATP1B3 inhibitior + 0.9436 94.36%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9376 93.76%
P-glycoprotein inhibitior - 0.9807 98.07%
P-glycoprotein substrate - 0.9178 91.78%
CYP3A4 substrate - 0.7508 75.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7426 74.26%
CYP3A4 inhibition - 0.8277 82.77%
CYP2C9 inhibition - 0.7619 76.19%
CYP2C19 inhibition - 0.8195 81.95%
CYP2D6 inhibition - 0.8446 84.46%
CYP1A2 inhibition - 0.6792 67.92%
CYP2C8 inhibition - 0.9897 98.97%
CYP inhibitory promiscuity - 0.6819 68.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.5801 58.01%
Eye corrosion + 0.8965 89.65%
Eye irritation + 0.9858 98.58%
Skin irritation + 0.5332 53.32%
Skin corrosion - 0.9183 91.83%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7388 73.88%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.7516 75.16%
skin sensitisation + 0.7744 77.44%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6788 67.88%
Estrogen receptor binding - 0.8994 89.94%
Androgen receptor binding - 0.9336 93.36%
Thyroid receptor binding - 0.7298 72.98%
Glucocorticoid receptor binding - 0.9034 90.34%
Aromatase binding - 0.9064 90.64%
PPAR gamma - 0.8558 85.58%
Honey bee toxicity - 0.8697 86.97%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9509 95.09%

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
CHEMBL2581 P07339 Cathepsin D 91.66% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.73% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 85.45% 87.45%
CHEMBL226 P30542 Adenosine A1 receptor 81.51% 95.93%
CHEMBL221 P23219 Cyclooxygenase-1 80.93% 90.17%

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 cepa

Cross-Links

Top
PubChem 118529
NPASS NPC3423