Propanethial S-oxide, (1Z)-

Details

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Internal ID 7dc71469-b323-4f9d-b134-5985461954ea
Taxonomy Organosulfur compounds > Thiocarbonyl compounds > Thioaldehydes > Thioaldehyde s-oxides
IUPAC Name 1-sulfinylpropane
SMILES (Canonical) CCC=S=O
SMILES (Isomeric) CCC=S=O
InChI InChI=1S/C3H6OS/c1-2-3-5-4/h3H,2H2,1H3
InChI Key BAZSXBOAXJLRNH-UHFFFAOYSA-N
Popularity 72 references in papers

Physical and Chemical Properties

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Molecular Formula C3H6OS
Molecular Weight 90.15 g/mol
Exact Mass 90.01393598 g/mol
Topological Polar Surface Area (TPSA) 18.10 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.41
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Thiopropanal S-oxide
1-sulfinylpropane
Z-Propanethial S-oxide
E-Propanethial S-oxide
Propanethial S-oxide Z-isomer
32157-29-2
Propanethial S-oxide, Z-
Propanethial S-oxide E-isomer
Propanethial, S-oxide, (1Z)-
Syn-Propanethial-S-oxide
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Propanethial S-oxide, (1Z)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9872 98.72%
Caco-2 + 0.7407 74.07%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.5787 57.87%
OATP2B1 inhibitior - 0.8713 87.13%
OATP1B1 inhibitior + 0.9507 95.07%
OATP1B3 inhibitior + 0.9495 94.95%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8829 88.29%
P-glycoprotein inhibitior - 0.9853 98.53%
P-glycoprotein substrate - 0.9893 98.93%
CYP3A4 substrate - 0.7728 77.28%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7004 70.04%
CYP3A4 inhibition - 0.9606 96.06%
CYP2C9 inhibition - 0.7809 78.09%
CYP2C19 inhibition - 0.7852 78.52%
CYP2D6 inhibition - 0.9094 90.94%
CYP1A2 inhibition - 0.6901 69.01%
CYP2C8 inhibition - 0.9859 98.59%
CYP inhibitory promiscuity - 0.7451 74.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6782 67.82%
Carcinogenicity (trinary) Non-required 0.5940 59.40%
Eye corrosion + 0.9509 95.09%
Eye irritation + 0.9935 99.35%
Skin irritation + 0.6258 62.58%
Skin corrosion - 0.7288 72.88%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7695 76.95%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.6949 69.49%
skin sensitisation + 0.7755 77.55%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.6046 60.46%
Acute Oral Toxicity (c) III 0.5250 52.50%
Estrogen receptor binding - 0.9246 92.46%
Androgen receptor binding - 0.9334 93.34%
Thyroid receptor binding - 0.8609 86.09%
Glucocorticoid receptor binding - 0.8904 89.04%
Aromatase binding - 0.8992 89.92%
PPAR gamma - 0.7936 79.36%
Honey bee toxicity - 0.8326 83.26%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.5096 50.96%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.66% 96.09%
CHEMBL2581 P07339 Cathepsin D 84.04% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.30% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 80.08% 94.73%

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.
Allium cepa
Nelumbo nucifera
Stephania rotunda

Cross-Links

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PubChem 441491
NPASS NPC188920