2-Amino-6-hydroxy-4-methyl-4-hexenoic acid

Details

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Internal ID 26ba10d8-bbd4-48e7-a6ed-6ba36f1fc171
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-6-hydroxy-4-methylhex-4-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H13NO3/c1-5(2-3-9)4-6(8)7(10)11/h2,6,9H,3-4,8H2,1H3,(H,10,11)
InChI Key UHJUDIZEJLVXPU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C7H13NO3
Molecular Weight 159.18 g/mol
Exact Mass 159.08954328 g/mol
Topological Polar Surface Area (TPSA) 83.60 Ų
XlogP -2.70
Atomic LogP (AlogP) -0.27
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Amino-6-hydroxy-4-methyl-4-hexenoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9875 98.75%
Caco-2 - 0.5922 59.22%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.6407 64.07%
OATP2B1 inhibitior - 0.8451 84.51%
OATP1B1 inhibitior + 0.9548 95.48%
OATP1B3 inhibitior + 0.9280 92.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9013 90.13%
P-glycoprotein inhibitior - 0.9883 98.83%
P-glycoprotein substrate - 0.9643 96.43%
CYP3A4 substrate - 0.7111 71.11%
CYP2C9 substrate - 0.5973 59.73%
CYP2D6 substrate - 0.8132 81.32%
CYP3A4 inhibition - 0.9545 95.45%
CYP2C9 inhibition - 0.8861 88.61%
CYP2C19 inhibition - 0.9122 91.22%
CYP2D6 inhibition - 0.8107 81.07%
CYP1A2 inhibition - 0.7808 78.08%
CYP2C8 inhibition - 0.9775 97.75%
CYP inhibitory promiscuity - 0.9509 95.09%
UGT catelyzed - 0.5638 56.38%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.6825 68.25%
Eye corrosion - 0.9409 94.09%
Eye irritation - 0.5940 59.40%
Skin irritation - 0.7151 71.51%
Skin corrosion - 0.6724 67.24%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7633 76.33%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8853 88.53%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.5563 55.63%
Acute Oral Toxicity (c) III 0.5721 57.21%
Estrogen receptor binding - 0.9764 97.64%
Androgen receptor binding - 0.8160 81.60%
Thyroid receptor binding - 0.9158 91.58%
Glucocorticoid receptor binding - 0.9060 90.60%
Aromatase binding - 0.9413 94.13%
PPAR gamma - 0.7773 77.73%
Honey bee toxicity - 0.9794 97.94%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity + 0.7982 79.82%

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 95.22% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 93.83% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.93% 99.17%
CHEMBL2581 P07339 Cathepsin D 85.47% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.11% 96.95%
CHEMBL340 P08684 Cytochrome P450 3A4 81.53% 91.19%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.58% 94.45%

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.
Aesculus californica

Cross-Links

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PubChem 549256
LOTUS LTS0134154
wikiData Q105272925