trans-(2R,3S)-1-amino-3-hydroxy-2-methylcyclobutane-1-carboxylic acid

Details

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Internal ID c6b34a8d-50eb-4791-9f96-d9ac031466dd
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name trans-(2R,3S)-1-amino-3-hydroxy-2-methylcyclobutane-1-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H11NO3/c1-3-4(8)2-6(3,7)5(9)10/h3-4,8H,2,7H2,1H3,(H,9,10)/t3-,4-,6?/m0/s1
InChI Key SUFFQWMBPDEZFN-IUJOKSNGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11NO3
Molecular Weight 145.16 g/mol
Exact Mass 145.07389321 g/mol
Topological Polar Surface Area (TPSA) 83.60 Ų
XlogP -3.20
Atomic LogP (AlogP) -0.83
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of trans-(2R,3S)-1-amino-3-hydroxy-2-methylcyclobutane-1-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8929 89.29%
Caco-2 - 0.8999 89.99%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.5071 50.71%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.9745 97.45%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9540 95.40%
P-glycoprotein inhibitior - 0.9915 99.15%
P-glycoprotein substrate - 0.9135 91.35%
CYP3A4 substrate - 0.6451 64.51%
CYP2C9 substrate - 0.5795 57.95%
CYP2D6 substrate - 0.7841 78.41%
CYP3A4 inhibition - 0.9622 96.22%
CYP2C9 inhibition - 0.9121 91.21%
CYP2C19 inhibition - 0.9037 90.37%
CYP2D6 inhibition - 0.9597 95.97%
CYP1A2 inhibition - 0.9067 90.67%
CYP2C8 inhibition - 0.9935 99.35%
CYP inhibitory promiscuity - 0.9852 98.52%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6673 66.73%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.8671 86.71%
Skin irritation - 0.7216 72.16%
Skin corrosion - 0.8281 82.81%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8815 88.15%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.5783 57.83%
skin sensitisation - 0.8026 80.26%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6069 60.69%
Acute Oral Toxicity (c) III 0.6247 62.47%
Estrogen receptor binding - 0.8895 88.95%
Androgen receptor binding - 0.8579 85.79%
Thyroid receptor binding - 0.8624 86.24%
Glucocorticoid receptor binding - 0.8304 83.04%
Aromatase binding - 0.9259 92.59%
PPAR gamma - 0.8371 83.71%
Honey bee toxicity - 0.9611 96.11%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity - 0.8400 84.00%

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 97.50% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 89.63% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.89% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.52% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.59% 95.56%

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.
Ateleia cubensis

Cross-Links

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PubChem 163195285
LOTUS LTS0240895
wikiData Q105260865