Oxetin

Details

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Internal ID b91d2e4a-3d97-405b-89a9-b5280995eef8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Sugar amino acids and derivatives > Oxetane amino acids and derivatives
IUPAC Name (2R,3S)-3-aminooxetane-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H7NO3/c5-2-1-8-3(2)4(6)7/h2-3H,1,5H2,(H,6,7)/t2-,3+/m0/s1
InChI Key UTIYGJDWWLIDQY-STHAYSLISA-N
Popularity 13 references in papers

Physical and Chemical Properties

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Molecular Formula C4H7NO3
Molecular Weight 117.10 g/mol
Exact Mass 117.042593085 g/mol
Topological Polar Surface Area (TPSA) 72.60 Ų
XlogP -3.10
Atomic LogP (AlogP) -1.20
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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94818-85-6
(2R,3S)-3-aminooxetane-2-carboxylic acid
rel-(2R,3S)-3-aminooxetane-2-carboxylic acid
198563-29-0
(2R-cis)-3-Amino-2-oxetanecarboxylic acid
2-Oxetanecarboxylic acid, 3-amino-, (2R-cis)-
SCHEMBL2554290
DTXSID60241634
3-amino-2-oxetane carboxylic acid
(2r,3s)-3-amino-2-oxetane carboxylic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Oxetin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7771 77.71%
Caco-2 - 0.9335 93.35%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.5271 52.71%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.9780 97.80%
OATP1B3 inhibitior + 0.9261 92.61%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9614 96.14%
P-glycoprotein inhibitior - 0.9880 98.80%
P-glycoprotein substrate - 0.9806 98.06%
CYP3A4 substrate - 0.7323 73.23%
CYP2C9 substrate - 0.6243 62.43%
CYP2D6 substrate - 0.8004 80.04%
CYP3A4 inhibition - 0.9553 95.53%
CYP2C9 inhibition - 0.8545 85.45%
CYP2C19 inhibition - 0.8315 83.15%
CYP2D6 inhibition - 0.9157 91.57%
CYP1A2 inhibition - 0.8585 85.85%
CYP2C8 inhibition - 0.9435 94.35%
CYP inhibitory promiscuity - 0.9755 97.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.6910 69.10%
Eye corrosion - 0.9682 96.82%
Eye irritation - 0.6456 64.56%
Skin irritation - 0.6859 68.59%
Skin corrosion - 0.8313 83.13%
Ames mutagenesis + 0.6853 68.53%
Human Ether-a-go-go-Related Gene inhibition - 0.7820 78.20%
Micronuclear + 0.6574 65.74%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8910 89.10%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.8047 80.47%
Acute Oral Toxicity (c) III 0.5389 53.89%
Estrogen receptor binding - 0.9119 91.19%
Androgen receptor binding - 0.7839 78.39%
Thyroid receptor binding - 0.8661 86.61%
Glucocorticoid receptor binding - 0.8691 86.91%
Aromatase binding - 0.8739 87.39%
PPAR gamma - 0.8154 81.54%
Honey bee toxicity - 0.8634 86.34%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity - 0.9532 95.32%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 89.39% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.53% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 85.24% 83.82%
CHEMBL340 P08684 Cytochrome P450 3A4 84.63% 91.19%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 82.77% 82.05%

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 93506
LOTUS LTS0233033
wikiData Q76009684