L-m-Tyrosine

Details

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Internal ID e0a4669a-9a77-482b-a131-d5a76639e55e
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Phenylalanine and derivatives
IUPAC Name (2S)-2-amino-3-(3-hydroxyphenyl)propanoic acid
SMILES (Canonical) C1=CC(=CC(=C1)O)CC(C(=O)O)N
SMILES (Isomeric) C1=CC(=CC(=C1)O)C[C@@H](C(=O)O)N
InChI InChI=1S/C9H11NO3/c10-8(9(12)13)5-6-2-1-3-7(11)4-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m0/s1
InChI Key JZKXXXDKRQWDET-QMMMGPOBSA-N
Popularity 426 references in papers

Physical and Chemical Properties

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Molecular Formula C9H11NO3
Molecular Weight 181.19 g/mol
Exact Mass 181.07389321 g/mol
Topological Polar Surface Area (TPSA) 83.60 Ų
XlogP -2.40
Atomic LogP (AlogP) 0.35
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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587-33-7
3-HYDROXY-L-PHENYLALANINE
Meta-Tyrosine
(S)-2-amino-3-(3-hydroxyphenyl)propanoic acid
3-tyrosine
3-Hydroxyphenylalanine
m-Tyrosine
L-META-TYROSINE
m-L-Tyrosine
(2S)-2-amino-3-(3-hydroxyphenyl)propanoic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of L-m-Tyrosine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 - 0.5417 54.17%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5454 54.54%
OATP2B1 inhibitior - 0.8628 86.28%
OATP1B1 inhibitior + 0.9563 95.63%
OATP1B3 inhibitior + 0.9538 95.38%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8734 87.34%
P-glycoprotein inhibitior - 0.9951 99.51%
P-glycoprotein substrate - 0.9020 90.20%
CYP3A4 substrate - 0.7262 72.62%
CYP2C9 substrate - 0.6404 64.04%
CYP2D6 substrate - 0.7186 71.86%
CYP3A4 inhibition - 0.9213 92.13%
CYP2C9 inhibition - 0.9805 98.05%
CYP2C19 inhibition - 0.9214 92.14%
CYP2D6 inhibition - 0.9678 96.78%
CYP1A2 inhibition - 0.9656 96.56%
CYP2C8 inhibition - 0.7399 73.99%
CYP inhibitory promiscuity - 0.9697 96.97%
UGT catelyzed + 0.5362 53.62%
Carcinogenicity (binary) - 0.5835 58.35%
Carcinogenicity (trinary) Non-required 0.7152 71.52%
Eye corrosion - 0.9969 99.69%
Eye irritation + 0.7726 77.26%
Skin irritation - 0.7082 70.82%
Skin corrosion - 0.8612 86.12%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8038 80.38%
Micronuclear + 0.7674 76.74%
Hepatotoxicity - 0.5310 53.10%
skin sensitisation + 0.6666 66.66%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.8729 87.29%
Acute Oral Toxicity (c) III 0.6362 63.62%
Estrogen receptor binding - 0.9412 94.12%
Androgen receptor binding - 0.6298 62.98%
Thyroid receptor binding - 0.8231 82.31%
Glucocorticoid receptor binding - 0.6469 64.69%
Aromatase binding - 0.9189 91.89%
PPAR gamma - 0.5735 57.35%
Honey bee toxicity - 0.9697 96.97%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.5853 58.53%

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
CHEMBL2581 P07339 Cathepsin D 96.94% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.96% 96.09%
CHEMBL236 P41143 Delta opioid receptor 94.23% 99.35%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.50% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.44% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.14% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.03% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 88.15% 90.20%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.57% 99.15%
CHEMBL233 P35372 Mu opioid receptor 87.49% 97.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.11% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 85.81% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.65% 95.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.96% 94.62%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.82% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.69% 97.21%
CHEMBL2535 P11166 Glucose transporter 81.13% 98.75%

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.
Karwinskia parvifolia

Cross-Links

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PubChem 6950578
NPASS NPC30324