(3S,4S,5R)-3-Amino-4,5-dimethyloxolan-2-one

Details

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Internal ID 305ecec3-3404-43f3-9f92-267d96e1e947
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acid esters
IUPAC Name (3S,4S,5R)-3-amino-4,5-dimethyloxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H11NO2/c1-3-4(2)9-6(8)5(3)7/h3-5H,7H2,1-2H3/t3-,4-,5+/m1/s1
InChI Key DXLUNIWVHZZSPK-WDCZJNDASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11NO2
Molecular Weight 129.16 g/mol
Exact Mass 129.078978594 g/mol
Topological Polar Surface Area (TPSA) 52.30 Ų
XlogP 0.20
Atomic LogP (AlogP) -0.10
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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(3S,4S,5R)-3-Amino-4,5-dimethyloxolan-2-one
(3S,4S,5R)-3-Amino-4,5-dimethyldihydrofuran-2(3H)-one
Arabinonicacid,2-amino-2,3,5-trideoxy-3-methyl-,gamma-lactone(9CI)
SCHEMBL14420269
AKOS006341383

2D Structure

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2D Structure of (3S,4S,5R)-3-Amino-4,5-dimethyloxolan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 - 0.7971 79.71%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.6829 68.29%
OATP2B1 inhibitior - 0.8639 86.39%
OATP1B1 inhibitior + 0.9551 95.51%
OATP1B3 inhibitior + 0.9577 95.77%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9500 95.00%
P-glycoprotein inhibitior - 0.9778 97.78%
P-glycoprotein substrate - 0.9217 92.17%
CYP3A4 substrate - 0.7172 71.72%
CYP2C9 substrate + 0.6027 60.27%
CYP2D6 substrate - 0.8106 81.06%
CYP3A4 inhibition - 0.9437 94.37%
CYP2C9 inhibition - 0.9319 93.19%
CYP2C19 inhibition - 0.8697 86.97%
CYP2D6 inhibition - 0.9407 94.07%
CYP1A2 inhibition - 0.7074 70.74%
CYP2C8 inhibition - 0.9936 99.36%
CYP inhibitory promiscuity - 0.9215 92.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.5012 50.12%
Eye corrosion - 0.8763 87.63%
Eye irritation + 0.7558 75.58%
Skin irritation - 0.6768 67.68%
Skin corrosion - 0.8815 88.15%
Ames mutagenesis - 0.5537 55.37%
Human Ether-a-go-go-Related Gene inhibition - 0.8233 82.33%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation - 0.8774 87.74%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.7533 75.33%
Acute Oral Toxicity (c) III 0.4628 46.28%
Estrogen receptor binding - 0.8409 84.09%
Androgen receptor binding - 0.8449 84.49%
Thyroid receptor binding - 0.8429 84.29%
Glucocorticoid receptor binding - 0.8491 84.91%
Aromatase binding - 0.7605 76.05%
PPAR gamma - 0.8795 87.95%
Honey bee toxicity - 0.8628 86.28%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.8746 87.46%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.56% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.28% 97.09%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.05% 94.42%

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.
Quararibea funebris

Cross-Links

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PubChem 10630882
LOTUS LTS0248919
wikiData Q104991068