Unii-L3Z7U4N28P

Details

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Internal ID 232f32dd-8ef6-4bb1-a043-bdffccd51ada
Taxonomy Hydrocarbon derivatives > Tropones > Tropolones
IUPAC Name 2,3,4,5-tetrahydroxybenzo[7]annulen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H8O5/c12-6-3-1-2-5-4-7(13)10(15)11(16)8(5)9(6)14/h1-4,13,15-16H,(H,12,14)
InChI Key WDGFFVCWBZVLCE-UHFFFAOYSA-N
Popularity 415 references in papers

Physical and Chemical Properties

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Molecular Formula C11H8O5
Molecular Weight 220.18 g/mol
Exact Mass 220.03717335 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.02
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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CCRIS 8139
3tiy
EINECS 209-324-9
NSC 35676
BRN 1978265
PURPUROGALLIN [MI]
4-08-00-03456 (Beilstein Handbook Reference)
BIDD:ER0545
orb1307831
MSK181025
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Unii-L3Z7U4N28P

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9593 95.93%
Caco-2 - 0.6699 66.99%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.5694 56.94%
OATP2B1 inhibitior - 0.7131 71.31%
OATP1B1 inhibitior + 0.9338 93.38%
OATP1B3 inhibitior + 0.9615 96.15%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9395 93.95%
P-glycoprotein inhibitior - 0.9692 96.92%
P-glycoprotein substrate - 0.9801 98.01%
CYP3A4 substrate - 0.6615 66.15%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7555 75.55%
CYP3A4 inhibition - 0.5950 59.50%
CYP2C9 inhibition - 0.8655 86.55%
CYP2C19 inhibition - 0.8940 89.40%
CYP2D6 inhibition - 0.8994 89.94%
CYP1A2 inhibition + 0.6212 62.12%
CYP2C8 inhibition - 0.8139 81.39%
CYP inhibitory promiscuity - 0.8487 84.87%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5645 56.45%
Eye corrosion - 0.9606 96.06%
Eye irritation + 0.9843 98.43%
Skin irritation + 0.8095 80.95%
Skin corrosion - 0.8131 81.31%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8840 88.40%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.7354 73.54%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.5936 59.36%
Acute Oral Toxicity (c) III 0.6031 60.31%
Estrogen receptor binding + 0.5487 54.87%
Androgen receptor binding + 0.5937 59.37%
Thyroid receptor binding + 0.6260 62.60%
Glucocorticoid receptor binding + 0.8753 87.53%
Aromatase binding - 0.5244 52.44%
PPAR gamma + 0.7044 70.44%
Honey bee toxicity - 0.9659 96.59%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9528 95.28%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.86% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.37% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.18% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.47% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 90.23% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.87% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.86% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 85.84% 94.73%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.35% 93.03%
CHEMBL1255126 O15151 Protein Mdm4 80.25% 90.20%

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 5281571
LOTUS LTS0148225
wikiData Q7261541