L-Phenylalanine, 23

Details

Top
Internal ID ec63635a-1ec6-4a13-ae81-7170c2e010f6
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Phenylalanine and derivatives
IUPAC Name 2-azaniumyl-3-phenylpropanoate
SMILES (Canonical) C1=CC=C(C=C1)CC(C(=O)[O-])[NH3+]
SMILES (Isomeric) C1=CC=C(C=C1)CC(C(=O)[O-])[NH3+]
InChI InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)
InChI Key COLNVLDHVKWLRT-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H11NO2
Molecular Weight 165.19 g/mol
Exact Mass 165.078978594 g/mol
Topological Polar Surface Area (TPSA) 67.80 Ų
XlogP -0.90
Atomic LogP (AlogP) -1.41
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
SCHEMBL23141075
BDBM92701

2D Structure

Top
2D Structure of L-Phenylalanine, 23

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.9312 93.12%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.4481 44.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9577 95.77%
OATP1B3 inhibitior + 0.9570 95.70%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8471 84.71%
P-glycoprotein inhibitior - 0.9945 99.45%
P-glycoprotein substrate - 0.9647 96.47%
CYP3A4 substrate - 0.7362 73.62%
CYP2C9 substrate - 0.6029 60.29%
CYP2D6 substrate - 0.8094 80.94%
CYP3A4 inhibition - 0.9803 98.03%
CYP2C9 inhibition - 0.9682 96.82%
CYP2C19 inhibition - 0.9199 91.99%
CYP2D6 inhibition - 0.8031 80.31%
CYP1A2 inhibition - 0.6286 62.86%
CYP2C8 inhibition - 0.9391 93.91%
CYP inhibitory promiscuity - 0.9277 92.77%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5824 58.24%
Carcinogenicity (trinary) Non-required 0.8053 80.53%
Eye corrosion - 0.9697 96.97%
Eye irritation - 0.7870 78.70%
Skin irritation + 0.7474 74.74%
Skin corrosion - 0.5428 54.28%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8488 84.88%
Micronuclear + 0.6274 62.74%
Hepatotoxicity + 0.5609 56.09%
skin sensitisation - 0.8498 84.98%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7039 70.39%
Acute Oral Toxicity (c) III 0.7310 73.10%
Estrogen receptor binding - 0.9432 94.32%
Androgen receptor binding - 0.7618 76.18%
Thyroid receptor binding - 0.8910 89.10%
Glucocorticoid receptor binding - 0.6220 62.20%
Aromatase binding - 0.8407 84.07%
PPAR gamma - 0.6880 68.80%
Honey bee toxicity - 0.9520 95.20%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity - 0.5515 55.15%

Targets

Top

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 95.99% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.27% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.65% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.28% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.81% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 83.79% 90.17%
CHEMBL1255126 O15151 Protein Mdm4 83.33% 90.20%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.22% 93.81%

Plants that contains it

Top
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.
Allium sativum
Brassica juncea
Centipeda minima
Ginkgo biloba
Lycium barbarum
Pinellia ternata
Sinapis alba
Ziziphus jujuba

Cross-Links

Top
PubChem 57397115
NPASS NPC293628