3-[(S)-methylsulfinyl]propan-1-amine

Details

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Internal ID fb579bac-a46f-4090-b856-cae1b23efcbd
Taxonomy Organosulfur compounds > Sulfoxides
IUPAC Name 3-[(S)-methylsulfinyl]propan-1-amine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H11NOS/c1-7(6)4-2-3-5/h2-5H2,1H3/t7-/m0/s1
InChI Key COPMQUUNXNNQJO-ZETCQYMHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C4H11NOS
Molecular Weight 121.20 g/mol
Exact Mass 121.05613515 g/mol
Topological Polar Surface Area (TPSA) 62.30 Ų
XlogP -1.30
Atomic LogP (AlogP) -0.29
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-[(S)-methylsulfinyl]propan-1-amine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9636 96.36%
Caco-2 + 0.7926 79.26%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Lysosomes 0.9405 94.05%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.9680 96.80%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9305 93.05%
P-glycoprotein inhibitior - 0.9827 98.27%
P-glycoprotein substrate - 0.8893 88.93%
CYP3A4 substrate - 0.7099 70.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4009 40.09%
CYP3A4 inhibition - 0.8639 86.39%
CYP2C9 inhibition - 0.8836 88.36%
CYP2C19 inhibition - 0.8606 86.06%
CYP2D6 inhibition - 0.8976 89.76%
CYP1A2 inhibition - 0.7770 77.70%
CYP2C8 inhibition - 0.9681 96.81%
CYP inhibitory promiscuity - 0.9716 97.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6096 60.96%
Carcinogenicity (trinary) Non-required 0.7039 70.39%
Eye corrosion + 0.5000 50.00%
Eye irritation + 0.8277 82.77%
Skin irritation - 0.5521 55.21%
Skin corrosion + 0.5936 59.36%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7715 77.15%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.7561 75.61%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.5196 51.96%
Acute Oral Toxicity (c) III 0.5317 53.17%
Estrogen receptor binding - 0.9281 92.81%
Androgen receptor binding - 0.8809 88.09%
Thyroid receptor binding - 0.8952 89.52%
Glucocorticoid receptor binding - 0.8220 82.20%
Aromatase binding - 0.9096 90.96%
PPAR gamma - 0.8746 87.46%
Honey bee toxicity - 0.9117 91.17%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity - 0.9705 97.05%

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 92.77% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.77% 96.95%
CHEMBL4581 P52732 Kinesin-like protein 1 86.59% 93.18%
CHEMBL3038469 P24941 CDK2/Cyclin A 82.63% 91.38%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.71% 91.11%

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.
Iberis amara

Cross-Links

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PubChem 51534039
LOTUS LTS0199959
wikiData Q104967208