Purpuroine I

Details

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Internal ID 661bf445-fad1-469f-8b3d-57b675dc7ba0
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Tyrosine and derivatives
IUPAC Name (2R)-3-(3-bromo-4-hydroxy-5-iodophenyl)-2-(trimethylazaniumyl)propanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H15BrINO3/c1-15(2,3)10(12(17)18)6-7-4-8(13)11(16)9(14)5-7/h4-5,10H,6H2,1-3H3,(H-,16,17,18)/t10-/m1/s1
InChI Key JRMILWBTUZMVEQ-SNVBAGLBSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H15BrINO3
Molecular Weight 428.06 g/mol
Exact Mass 426.92800 g/mol
Topological Polar Surface Area (TPSA) 60.40 Ų
XlogP 3.50
Atomic LogP (AlogP) 1.13
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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CHEMBL2204073
BDBM50486140

2D Structure

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2D Structure of Purpuroine I

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6463 64.63%
Caco-2 + 0.6669 66.69%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6600 66.00%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.8145 81.45%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6816 68.16%
P-glycoprotein inhibitior - 0.9729 97.29%
P-glycoprotein substrate - 0.8676 86.76%
CYP3A4 substrate - 0.5715 57.15%
CYP2C9 substrate + 0.5771 57.71%
CYP2D6 substrate - 0.8201 82.01%
CYP3A4 inhibition - 0.9565 95.65%
CYP2C9 inhibition - 0.8212 82.12%
CYP2C19 inhibition - 0.8031 80.31%
CYP2D6 inhibition - 0.8229 82.29%
CYP1A2 inhibition - 0.6031 60.31%
CYP2C8 inhibition + 0.4542 45.42%
CYP inhibitory promiscuity - 0.8643 86.43%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6014 60.14%
Carcinogenicity (trinary) Non-required 0.6240 62.40%
Eye corrosion - 0.9767 97.67%
Eye irritation + 0.8999 89.99%
Skin irritation - 0.7304 73.04%
Skin corrosion - 0.9059 90.59%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6240 62.40%
Micronuclear + 0.5068 50.68%
Hepatotoxicity - 0.6431 64.31%
skin sensitisation - 0.8259 82.59%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8424 84.24%
Acute Oral Toxicity (c) III 0.5132 51.32%
Estrogen receptor binding - 0.6323 63.23%
Androgen receptor binding + 0.6960 69.60%
Thyroid receptor binding - 0.5264 52.64%
Glucocorticoid receptor binding - 0.5881 58.81%
Aromatase binding - 0.7041 70.41%
PPAR gamma + 0.5309 53.09%
Honey bee toxicity - 0.9491 94.91%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9552 95.52%

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 94.68% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.63% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.45% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.37% 94.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 91.37% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.20% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.48% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.16% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 82.57% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.35% 99.15%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 71454037
LOTUS LTS0050400
wikiData Q105133987