2-Amino-3-methylenepentanoic acid

Details

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Internal ID 0f98dd1f-530e-45ff-a2e4-85d6888c823a
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-3-methylidenepentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H11NO2/c1-3-4(2)5(7)6(8)9/h5H,2-3,7H2,1H3,(H,8,9)
InChI Key SBTLHKXSISNXTP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11NO2
Molecular Weight 129.16 g/mol
Exact Mass 129.078978594 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP -1.50
Atomic LogP (AlogP) 0.36
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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SCHEMBL865856
AKOS006341440

2D Structure

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2D Structure of 2-Amino-3-methylenepentanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9889 98.89%
Caco-2 - 0.8348 83.48%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.5251 52.51%
OATP2B1 inhibitior - 0.8432 84.32%
OATP1B1 inhibitior + 0.9608 96.08%
OATP1B3 inhibitior + 0.9383 93.83%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9501 95.01%
P-glycoprotein inhibitior - 0.9821 98.21%
P-glycoprotein substrate - 0.9739 97.39%
CYP3A4 substrate - 0.7686 76.86%
CYP2C9 substrate - 0.5888 58.88%
CYP2D6 substrate - 0.8039 80.39%
CYP3A4 inhibition - 0.8693 86.93%
CYP2C9 inhibition - 0.8260 82.60%
CYP2C19 inhibition - 0.9134 91.34%
CYP2D6 inhibition - 0.9044 90.44%
CYP1A2 inhibition - 0.8766 87.66%
CYP2C8 inhibition - 0.9739 97.39%
CYP inhibitory promiscuity - 0.9209 92.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5426 54.26%
Carcinogenicity (trinary) Non-required 0.5901 59.01%
Eye corrosion - 0.9498 94.98%
Eye irritation + 0.7610 76.10%
Skin irritation - 0.7176 71.76%
Skin corrosion - 0.6304 63.04%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8425 84.25%
Micronuclear + 0.6300 63.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.8221 82.21%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.7539 75.39%
Acute Oral Toxicity (c) III 0.6379 63.79%
Estrogen receptor binding - 0.9299 92.99%
Androgen receptor binding - 0.8581 85.81%
Thyroid receptor binding - 0.8237 82.37%
Glucocorticoid receptor binding - 0.9088 90.88%
Aromatase binding - 0.7846 78.46%
PPAR gamma - 0.6821 68.21%
Honey bee toxicity - 0.9749 97.49%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity + 0.6984 69.84%

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 99.82% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.18% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.91% 96.95%
CHEMBL2581 P07339 Cathepsin D 86.29% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 82.49% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.57% 99.17%

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.
Philadelphus coronarius

Cross-Links

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PubChem 12755839
LOTUS LTS0164206
wikiData Q105249709