2-Amino-3-but-1-enylsulfinylpropanoic acid

Details

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Internal ID 9e220b2d-d7b5-4f18-836a-eb99647e9ffd
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-amino-3-but-1-enylsulfinylpropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H13NO3S/c1-2-3-4-12(11)5-6(8)7(9)10/h3-4,6H,2,5,8H2,1H3,(H,9,10)
InChI Key SNXJMSVHWSIWAN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H13NO3S
Molecular Weight 191.25 g/mol
Exact Mass 191.06161445 g/mol
Topological Polar Surface Area (TPSA) 99.60 Ų
XlogP -3.00
Atomic LogP (AlogP) 0.07
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Amino-3-but-1-enylsulfinylpropanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9661 96.61%
Caco-2 - 0.7325 73.25%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.4915 49.15%
OATP2B1 inhibitior - 0.8513 85.13%
OATP1B1 inhibitior + 0.8967 89.67%
OATP1B3 inhibitior + 0.9400 94.00%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8957 89.57%
P-glycoprotein inhibitior - 0.9808 98.08%
P-glycoprotein substrate - 0.9399 93.99%
CYP3A4 substrate - 0.7095 70.95%
CYP2C9 substrate - 0.5947 59.47%
CYP2D6 substrate - 0.8463 84.63%
CYP3A4 inhibition - 0.8092 80.92%
CYP2C9 inhibition - 0.8728 87.28%
CYP2C19 inhibition - 0.8791 87.91%
CYP2D6 inhibition - 0.9128 91.28%
CYP1A2 inhibition - 0.8722 87.22%
CYP2C8 inhibition - 0.9456 94.56%
CYP inhibitory promiscuity - 0.9936 99.36%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5096 50.96%
Carcinogenicity (trinary) Non-required 0.6430 64.30%
Eye corrosion - 0.9406 94.06%
Eye irritation - 0.8376 83.76%
Skin irritation - 0.7724 77.24%
Skin corrosion - 0.8721 87.21%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7755 77.55%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8487 84.87%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.8554 85.54%
Acute Oral Toxicity (c) III 0.6231 62.31%
Estrogen receptor binding - 0.9326 93.26%
Androgen receptor binding - 0.8938 89.38%
Thyroid receptor binding - 0.8560 85.60%
Glucocorticoid receptor binding - 0.7559 75.59%
Aromatase binding - 0.8870 88.70%
PPAR gamma - 0.7618 76.18%
Honey bee toxicity - 0.9447 94.47%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.6659 66.59%

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 95.54% 96.09%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 93.69% 92.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 93.18% 96.95%
CHEMBL4040 P28482 MAP kinase ERK2 88.51% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.81% 99.17%
CHEMBL2581 P07339 Cathepsin D 85.52% 98.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.05% 100.00%
CHEMBL236 P41143 Delta opioid receptor 84.35% 99.35%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.40% 97.21%
CHEMBL221 P23219 Cyclooxygenase-1 82.50% 90.17%

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 tripedale

Cross-Links

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PubChem 162891292
LOTUS LTS0187341
wikiData Q105256740