(2S)-2-amino-3-methylidenepent-4-enoic acid

Details

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Internal ID 15ca26fd-8de4-424b-86dd-b2e86ecb23f1
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids > L-alpha-amino acids
IUPAC Name (2S)-2-amino-3-methylidenepent-4-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H9NO2/c1-3-4(2)5(7)6(8)9/h3,5H,1-2,7H2,(H,8,9)/t5-/m0/s1
InChI Key JLPKOKKVYNEOES-YFKPBYRVSA-N
Popularity 2 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) 63.30 Ų
XlogP -1.50
Atomic LogP (AlogP) 0.14
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-2-amino-3-methylidenepent-4-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 - 0.8180 81.80%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.5680 56.80%
OATP2B1 inhibitior - 0.8629 86.29%
OATP1B1 inhibitior + 0.9651 96.51%
OATP1B3 inhibitior + 0.9473 94.73%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9635 96.35%
P-glycoprotein inhibitior - 0.9866 98.66%
P-glycoprotein substrate - 0.9897 98.97%
CYP3A4 substrate - 0.7597 75.97%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.8156 81.56%
CYP3A4 inhibition - 0.8754 87.54%
CYP2C9 inhibition - 0.8999 89.99%
CYP2C19 inhibition - 0.9315 93.15%
CYP2D6 inhibition - 0.9181 91.81%
CYP1A2 inhibition - 0.9103 91.03%
CYP2C8 inhibition - 0.9800 98.00%
CYP inhibitory promiscuity - 0.9695 96.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5574 55.74%
Carcinogenicity (trinary) Non-required 0.6333 63.33%
Eye corrosion - 0.9159 91.59%
Eye irritation + 0.9188 91.88%
Skin irritation - 0.6600 66.00%
Skin corrosion - 0.8691 86.91%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9141 91.41%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.8625 86.25%
skin sensitisation - 0.8511 85.11%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.4720 47.20%
Acute Oral Toxicity (c) III 0.6007 60.07%
Estrogen receptor binding - 0.9385 93.85%
Androgen receptor binding - 0.7999 79.99%
Thyroid receptor binding - 0.7573 75.73%
Glucocorticoid receptor binding - 0.8800 88.00%
Aromatase binding - 0.7869 78.69%
PPAR gamma - 0.7447 74.47%
Honey bee toxicity - 0.7950 79.50%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity - 0.4826 48.26%

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 97.74% 83.82%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 91.39% 82.05%
CHEMBL5251 Q06187 Tyrosine-protein kinase BTK 87.75% 98.51%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.77% 96.09%
CHEMBL233 P35372 Mu opioid receptor 83.39% 97.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.54% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 82.30% 91.19%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.66% 91.11%

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 24796332
LOTUS LTS0024657
wikiData Q105130982