2-Ammonio-4-sulfanylbutanoate

Details

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Internal ID c494e1a3-1a81-4ad2-8c78-7c9bf4a48ae0
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-4-sulfanylbutanoate
SMILES (Canonical) C(CS)C(C(=O)[O-])[NH3+]
SMILES (Isomeric) C(CS)C(C(=O)[O-])[NH3+]
InChI InChI=1S/C4H9NO2S/c5-3(1-2-8)4(6)7/h3,8H,1-2,5H2,(H,6,7)
InChI Key FFFHZYDWPBMWHY-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C4H9NO2S
Molecular Weight 135.19 g/mol
Exact Mass 135.03539970 g/mol
Topological Polar Surface Area (TPSA) 68.80 Ų
XlogP -2.10
Atomic LogP (AlogP) -2.33
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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2-ammonio-4-sulfanylbutanoate
2-azaniumyl-4-sulfanylbutanoate
CHEBI:58065

2D Structure

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2D Structure of 2-Ammonio-4-sulfanylbutanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9420 94.20%
Caco-2 - 0.9433 94.33%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.6460 64.60%
OATP2B1 inhibitior - 0.8429 84.29%
OATP1B1 inhibitior + 0.9526 95.26%
OATP1B3 inhibitior + 0.9410 94.10%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9412 94.12%
P-glycoprotein inhibitior - 0.9902 99.02%
P-glycoprotein substrate - 0.9557 95.57%
CYP3A4 substrate - 0.6947 69.47%
CYP2C9 substrate - 0.6044 60.44%
CYP2D6 substrate - 0.8288 82.88%
CYP3A4 inhibition - 0.9752 97.52%
CYP2C9 inhibition - 0.9117 91.17%
CYP2C19 inhibition - 0.9201 92.01%
CYP2D6 inhibition - 0.9302 93.02%
CYP1A2 inhibition - 0.7865 78.65%
CYP2C8 inhibition - 0.9929 99.29%
CYP inhibitory promiscuity - 0.9206 92.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.7237 72.37%
Eye corrosion - 0.9185 91.85%
Eye irritation - 0.7212 72.12%
Skin irritation - 0.5387 53.87%
Skin corrosion + 0.5157 51.57%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8239 82.39%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.9366 93.66%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6295 62.95%
Acute Oral Toxicity (c) III 0.5556 55.56%
Estrogen receptor binding - 0.9355 93.55%
Androgen receptor binding - 0.8674 86.74%
Thyroid receptor binding - 0.8866 88.66%
Glucocorticoid receptor binding - 0.8240 82.40%
Aromatase binding - 0.8678 86.78%
PPAR gamma - 0.7932 79.32%
Honey bee toxicity - 0.8245 82.45%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity - 0.9338 93.38%

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 91.21% 96.09%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.89% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.92% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 80.29% 83.82%

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.
Nelumbo nucifera
Spinacia oleracea

Cross-Links

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PubChem 49791978
NPASS NPC136476