2-Amino-2-(2-hydroxycyclopent-3-en-1-yl)acetic acid

Details

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Internal ID 9c0c6174-ea2d-41f2-9add-5ac7314976ac
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-2-(2-hydroxycyclopent-3-en-1-yl)acetic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H11NO3/c8-6(7(10)11)4-2-1-3-5(4)9/h1,3-6,9H,2,8H2,(H,10,11)
InChI Key PEAQTUDKZGSVCV-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C7H11NO3
Molecular Weight 157.17 g/mol
Exact Mass 157.07389321 g/mol
Topological Polar Surface Area (TPSA) 83.60 Ų
XlogP -2.50
Atomic LogP (AlogP) -0.66
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Amino-2-(2-hydroxycyclopent-3-en-1-yl)acetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9501 95.01%
Caco-2 - 0.9512 95.12%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.4794 47.94%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9558 95.58%
OATP1B3 inhibitior + 0.9518 95.18%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9338 93.38%
BSEP inhibitior - 0.9627 96.27%
P-glycoprotein inhibitior - 0.9899 98.99%
P-glycoprotein substrate - 0.9637 96.37%
CYP3A4 substrate - 0.6883 68.83%
CYP2C9 substrate - 0.5979 59.79%
CYP2D6 substrate - 0.7834 78.34%
CYP3A4 inhibition - 0.9335 93.35%
CYP2C9 inhibition - 0.9222 92.22%
CYP2C19 inhibition - 0.8776 87.76%
CYP2D6 inhibition - 0.9543 95.43%
CYP1A2 inhibition - 0.9012 90.12%
CYP2C8 inhibition - 0.9816 98.16%
CYP inhibitory promiscuity - 0.9673 96.73%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8023 80.23%
Carcinogenicity (trinary) Non-required 0.6559 65.59%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.9270 92.70%
Skin irritation - 0.7224 72.24%
Skin corrosion - 0.8859 88.59%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8832 88.32%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.7150 71.50%
skin sensitisation - 0.7594 75.94%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.7308 73.08%
Acute Oral Toxicity (c) III 0.5944 59.44%
Estrogen receptor binding - 0.9209 92.09%
Androgen receptor binding - 0.8903 89.03%
Thyroid receptor binding - 0.8564 85.64%
Glucocorticoid receptor binding - 0.7284 72.84%
Aromatase binding - 0.9388 93.88%
PPAR gamma - 0.7826 78.26%
Honey bee toxicity - 0.8549 85.49%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity - 0.6159 61.59%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.85% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.45% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.23% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 85.73% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.30% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.53% 93.56%
CHEMBL340 P08684 Cytochrome P450 3A4 80.44% 91.19%

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.
Passiflora subpeltata

Cross-Links

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PubChem 71437781
LOTUS LTS0059346
wikiData Q105206846