S-Methyl-L-methionine

Details

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Internal ID 1bbbdd57-4edc-4383-bdb8-ea17e0318970
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Methionine and derivatives
IUPAC Name [(3S)-3-amino-3-carboxypropyl]-dimethylsulfanium
SMILES (Canonical) C[S+](C)CCC(C(=O)O)N
SMILES (Isomeric) C[S+](C)CC[C@@H](C(=O)O)N
InChI InChI=1S/C6H13NO2S/c1-10(2)4-3-5(7)6(8)9/h5H,3-4,7H2,1-2H3/p+1/t5-/m0/s1
InChI Key YDBYJHTYSHBBAU-YFKPBYRVSA-O
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C6H14NO2S+
Molecular Weight 164.25 g/mol
Exact Mass 164.07452486 g/mol
Topological Polar Surface Area (TPSA) 64.30 Ų
XlogP -3.00
Atomic LogP (AlogP) -0.33
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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6708-35-6
CHEBI:17728
[(3S)-3-amino-3-carboxypropyl]-dimethylsulfanium
Cabagin
CHEMBL540394
METHIOSULFONIUM
NCGC00167557-01
L-Methionine methylsulfonium
CHEMBL45024
SCHEMBL149475
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of S-Methyl-L-methionine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8762 87.62%
Caco-2 - 0.8599 85.99%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.7500 75.00%
OATP2B1 inhibitior - 0.8457 84.57%
OATP1B1 inhibitior + 0.9682 96.82%
OATP1B3 inhibitior + 0.9409 94.09%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9609 96.09%
P-glycoprotein inhibitior - 0.9847 98.47%
P-glycoprotein substrate - 0.9707 97.07%
CYP3A4 substrate - 0.7263 72.63%
CYP2C9 substrate + 0.5939 59.39%
CYP2D6 substrate - 0.8050 80.50%
CYP3A4 inhibition - 0.9763 97.63%
CYP2C9 inhibition - 0.9131 91.31%
CYP2C19 inhibition - 0.9219 92.19%
CYP2D6 inhibition - 0.9416 94.16%
CYP1A2 inhibition - 0.8404 84.04%
CYP2C8 inhibition - 0.9933 99.33%
CYP inhibitory promiscuity - 0.9941 99.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6904 69.04%
Carcinogenicity (trinary) Non-required 0.7330 73.30%
Eye corrosion - 0.9127 91.27%
Eye irritation - 0.5608 56.08%
Skin irritation - 0.6856 68.56%
Skin corrosion - 0.5817 58.17%
Ames mutagenesis - 0.8628 86.28%
Human Ether-a-go-go-Related Gene inhibition - 0.7642 76.42%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.8386 83.86%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.6623 66.23%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6940 69.40%
Acute Oral Toxicity (c) III 0.5274 52.74%
Estrogen receptor binding - 0.9402 94.02%
Androgen receptor binding - 0.8867 88.67%
Thyroid receptor binding - 0.8762 87.62%
Glucocorticoid receptor binding - 0.9064 90.64%
Aromatase binding - 0.9396 93.96%
PPAR gamma - 0.8951 89.51%
Honey bee toxicity - 0.9834 98.34%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.9400 94.00%
Fish aquatic toxicity - 0.7213 72.13%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.80% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.83% 96.09%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 90.14% 92.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.74% 99.17%
CHEMBL2581 P07339 Cathepsin D 86.56% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.49% 96.95%
CHEMBL1907 P15144 Aminopeptidase N 80.56% 93.31%

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 145692
LOTUS LTS0198786
wikiData Q27102563