2-Azaniumyl-5-methylsulfanylpentanoate

Details

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Internal ID a3af9c91-97cd-4912-8462-9e7f4b541008
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name 2-azaniumyl-5-methylsulfanylpentanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H13NO2S/c1-10-4-2-3-5(7)6(8)9/h5H,2-4,7H2,1H3,(H,8,9)
InChI Key SFSJZXMDTNDWIX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H13NO2S
Molecular Weight 163.24 g/mol
Exact Mass 163.06669983 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP -1.40
Atomic LogP (AlogP) -1.51
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Azaniumyl-5-methylsulfanylpentanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9514 95.14%
Caco-2 - 0.8316 83.16%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.7083 70.83%
OATP2B1 inhibitior - 0.8418 84.18%
OATP1B1 inhibitior + 0.9430 94.30%
OATP1B3 inhibitior + 0.9303 93.03%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9499 94.99%
P-glycoprotein inhibitior - 0.9871 98.71%
P-glycoprotein substrate - 0.8368 83.68%
CYP3A4 substrate - 0.5942 59.42%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.8327 83.27%
CYP3A4 inhibition - 0.9862 98.62%
CYP2C9 inhibition - 0.9432 94.32%
CYP2C19 inhibition - 0.9406 94.06%
CYP2D6 inhibition - 0.9292 92.92%
CYP1A2 inhibition - 0.7781 77.81%
CYP2C8 inhibition - 0.9813 98.13%
CYP inhibitory promiscuity - 0.9783 97.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.6871 68.71%
Eye corrosion - 0.8006 80.06%
Eye irritation - 0.8871 88.71%
Skin irritation + 0.5000 50.00%
Skin corrosion + 0.6024 60.24%
Ames mutagenesis - 0.8178 81.78%
Human Ether-a-go-go-Related Gene inhibition - 0.8154 81.54%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8222 82.22%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.6343 63.43%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.5325 53.25%
Acute Oral Toxicity (c) III 0.5698 56.98%
Estrogen receptor binding - 0.9269 92.69%
Androgen receptor binding - 0.8762 87.62%
Thyroid receptor binding - 0.8009 80.09%
Glucocorticoid receptor binding - 0.8821 88.21%
Aromatase binding - 0.8555 85.55%
PPAR gamma - 0.6983 69.83%
Honey bee toxicity - 0.9203 92.03%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.6832 68.32%

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 95.15% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.80% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.36% 99.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.83% 93.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.72% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.09% 96.95%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.99% 92.29%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.92% 100.00%

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.
Armoracia rusticana
Brassica oleracea

Cross-Links

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PubChem 25203616
NPASS NPC143914