2-Azaniumyl-2-(2-methylidenecyclopropyl)acetate

Details

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Internal ID 28291057-6fec-4c4a-b22c-1171547aa476
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-azaniumyl-2-(2-methylidenecyclopropyl)acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H9NO2/c1-3-2-4(3)5(7)6(8)9/h4-5H,1-2,7H2,(H,8,9)
InChI Key MPIZVHPMGFWKMJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H9NO2
Molecular Weight 127.14 g/mol
Exact Mass 127.063328530 g/mol
Topological Polar Surface Area (TPSA) 67.80 Ų
XlogP -2.20
Atomic LogP (AlogP) -2.08
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Azaniumyl-2-(2-methylidenecyclopropyl)acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9819 98.19%
Caco-2 - 0.9544 95.44%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.4526 45.26%
OATP2B1 inhibitior - 0.8562 85.62%
OATP1B1 inhibitior + 0.9536 95.36%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9502 95.02%
P-glycoprotein inhibitior - 0.9898 98.98%
P-glycoprotein substrate - 0.9276 92.76%
CYP3A4 substrate - 0.6688 66.88%
CYP2C9 substrate - 0.5942 59.42%
CYP2D6 substrate - 0.8309 83.09%
CYP3A4 inhibition - 0.9469 94.69%
CYP2C9 inhibition - 0.8473 84.73%
CYP2C19 inhibition - 0.8178 81.78%
CYP2D6 inhibition - 0.8709 87.09%
CYP1A2 inhibition - 0.7727 77.27%
CYP2C8 inhibition - 0.9812 98.12%
CYP inhibitory promiscuity - 0.8440 84.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6254 62.54%
Carcinogenicity (trinary) Non-required 0.6860 68.60%
Eye corrosion - 0.8021 80.21%
Eye irritation + 0.7859 78.59%
Skin irritation - 0.5791 57.91%
Skin corrosion - 0.7819 78.19%
Ames mutagenesis - 0.7054 70.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8300 83.00%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation - 0.7551 75.51%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.4535 45.35%
Acute Oral Toxicity (c) II 0.5236 52.36%
Estrogen receptor binding - 0.9479 94.79%
Androgen receptor binding - 0.8560 85.60%
Thyroid receptor binding - 0.8448 84.48%
Glucocorticoid receptor binding - 0.8525 85.25%
Aromatase binding - 0.8313 83.13%
PPAR gamma - 0.7771 77.71%
Honey bee toxicity - 0.8609 86.09%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.8794 87.94%

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 89.14% 96.09%
CHEMBL217 P14416 Dopamine D2 receptor 85.61% 95.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.34% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 81.90% 91.19%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.95% 90.71%

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.
Litchi chinensis

Cross-Links

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PubChem 25203707
LOTUS LTS0104638
wikiData Q105169556