2-Amino-3-methylpent-3-enoic acid

Details

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Internal ID 9f5e68ad-037f-4c40-ba9a-e9d270545df0
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-methylpent-3-enoic acid
SMILES (Canonical) CC=C(C)C(C(=O)O)N
SMILES (Isomeric) CC=C(C)C(C(=O)O)N
InChI InChI=1S/C6H11NO2/c1-3-4(2)5(7)6(8)9/h3,5H,7H2,1-2H3,(H,8,9)
InChI Key WLNGAYXEECPGBD-UHFFFAOYSA-N
Popularity 0 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 -1.70
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-3-methylpent-3-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 + 0.9935 99.35%
Caco-2 - 0.6366 63.66%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.6211 62.11%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.9526 95.26%
OATP1B3 inhibitior + 0.9551 95.51%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9126 91.26%
P-glycoprotein inhibitior - 0.9783 97.83%
P-glycoprotein substrate - 0.9859 98.59%
CYP3A4 substrate - 0.7696 76.96%
CYP2C9 substrate - 0.5969 59.69%
CYP2D6 substrate - 0.8270 82.70%
CYP3A4 inhibition - 0.9124 91.24%
CYP2C9 inhibition - 0.8934 89.34%
CYP2C19 inhibition - 0.9433 94.33%
CYP2D6 inhibition - 0.9064 90.64%
CYP1A2 inhibition - 0.8702 87.02%
CYP2C8 inhibition - 0.9944 99.44%
CYP inhibitory promiscuity - 0.9633 96.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5274 52.74%
Carcinogenicity (trinary) Non-required 0.6338 63.38%
Eye corrosion - 0.9297 92.97%
Eye irritation + 0.7079 70.79%
Skin irritation - 0.6479 64.79%
Skin corrosion - 0.6798 67.98%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8284 82.84%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.9068 90.68%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6110 61.10%
Acute Oral Toxicity (c) III 0.7771 77.71%
Estrogen receptor binding - 0.9280 92.80%
Androgen receptor binding - 0.8689 86.89%
Thyroid receptor binding - 0.8722 87.22%
Glucocorticoid receptor binding - 0.9390 93.90%
Aromatase binding - 0.8462 84.62%
PPAR gamma - 0.8185 81.85%
Honey bee toxicity - 0.9376 93.76%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.9500 95.00%
Fish aquatic toxicity - 0.6277 62.77%

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 94.74% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.85% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 81.17% 91.19%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.35% 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.
Coniogramme intermedia

Cross-Links

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PubChem 85085264
LOTUS LTS0246015
wikiData Q105308093