2-Amino-2-cyclopent-3-en-1-ylacetic acid

Details

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Internal ID 982316a6-6c0f-4721-8b1d-9d4b47a3ce1d
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-cyclopent-3-en-1-ylacetic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H11NO2/c8-6(7(9)10)5-3-1-2-4-5/h1-2,5-6H,3-4,8H2,(H,9,10)
InChI Key RPCCYCFYTTUSNO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C7H11NO2
Molecular Weight 141.17 g/mol
Exact Mass 141.078978594 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP -2.00
Atomic LogP (AlogP) 0.36
H-Bond Acceptor 2
H-Bond Donor 2
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-cyclopent-3-en-1-ylacetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 - 0.8182 81.82%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.5072 50.72%
OATP2B1 inhibitior - 0.8494 84.94%
OATP1B1 inhibitior + 0.9592 95.92%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9149 91.49%
P-glycoprotein inhibitior - 0.9921 99.21%
P-glycoprotein substrate - 0.9807 98.07%
CYP3A4 substrate - 0.7673 76.73%
CYP2C9 substrate + 0.6009 60.09%
CYP2D6 substrate - 0.7886 78.86%
CYP3A4 inhibition - 0.9328 93.28%
CYP2C9 inhibition - 0.9184 91.84%
CYP2C19 inhibition - 0.9355 93.55%
CYP2D6 inhibition - 0.9639 96.39%
CYP1A2 inhibition - 0.9147 91.47%
CYP2C8 inhibition - 0.9780 97.80%
CYP inhibitory promiscuity - 0.9826 98.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.5828 58.28%
Eye corrosion - 0.9449 94.49%
Eye irritation - 0.4776 47.76%
Skin irritation - 0.6566 65.66%
Skin corrosion - 0.7563 75.63%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7756 77.56%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation - 0.8875 88.75%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.8170 81.70%
Acute Oral Toxicity (c) III 0.5852 58.52%
Estrogen receptor binding - 0.9687 96.87%
Androgen receptor binding - 0.7555 75.55%
Thyroid receptor binding - 0.9047 90.47%
Glucocorticoid receptor binding - 0.8065 80.65%
Aromatase binding - 0.8641 86.41%
PPAR gamma - 0.7674 76.74%
Honey bee toxicity - 0.9002 90.02%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.3765 37.65%

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 94.41% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.06% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.44% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 80.97% 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.
Rinorea ilicifolia

Cross-Links

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PubChem 20184469
LOTUS LTS0093621
wikiData Q105242606