Porric acid D

Details

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Internal ID be657a84-29c6-4bd3-9b3e-7625172a3d15
Taxonomy Organoheterocyclic compounds > Benzofurans > Dibenzofurans
IUPAC Name 6,7-dihydroxy-2-methoxy-9-methyldibenzofuran-4-carboxylic acid
SMILES (Canonical) CC1=CC(=C(C2=C1C3=C(O2)C(=CC(=C3)OC)C(=O)O)O)O
SMILES (Isomeric) CC1=CC(=C(C2=C1C3=C(O2)C(=CC(=C3)OC)C(=O)O)O)O
InChI InChI=1S/C15H12O6/c1-6-3-10(16)12(17)14-11(6)8-4-7(20-2)5-9(15(18)19)13(8)21-14/h3-5,16-17H,1-2H3,(H,18,19)
InChI Key ZCQTZTJLYWJXFU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H12O6
Molecular Weight 288.25 g/mol
Exact Mass 288.06338810 g/mol
Topological Polar Surface Area (TPSA) 100.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.01
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Porric acid D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9671 96.71%
Caco-2 - 0.5754 57.54%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7191 71.91%
OATP2B1 inhibitior - 0.6996 69.96%
OATP1B1 inhibitior + 0.9072 90.72%
OATP1B3 inhibitior + 0.8874 88.74%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6248 62.48%
P-glycoprotein inhibitior - 0.8519 85.19%
P-glycoprotein substrate - 0.8726 87.26%
CYP3A4 substrate - 0.5892 58.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8749 87.49%
CYP3A4 inhibition - 0.6589 65.89%
CYP2C9 inhibition - 0.7239 72.39%
CYP2C19 inhibition + 0.5631 56.31%
CYP2D6 inhibition - 0.8050 80.50%
CYP1A2 inhibition + 0.7940 79.40%
CYP2C8 inhibition + 0.4438 44.38%
CYP inhibitory promiscuity + 0.5587 55.87%
UGT catelyzed + 0.5362 53.62%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4318 43.18%
Eye corrosion - 0.9806 98.06%
Eye irritation + 0.7159 71.59%
Skin irritation - 0.7044 70.44%
Skin corrosion - 0.9640 96.40%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7592 75.92%
Micronuclear + 0.9000 90.00%
Hepatotoxicity + 0.5784 57.84%
skin sensitisation - 0.8502 85.02%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7773 77.73%
Acute Oral Toxicity (c) II 0.4632 46.32%
Estrogen receptor binding + 0.6961 69.61%
Androgen receptor binding + 0.6621 66.21%
Thyroid receptor binding - 0.5819 58.19%
Glucocorticoid receptor binding + 0.8876 88.76%
Aromatase binding + 0.5499 54.99%
PPAR gamma + 0.7513 75.13%
Honey bee toxicity - 0.8960 89.60%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9742 97.42%

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 98.90% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.97% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.96% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.55% 94.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 92.64% 94.42%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 91.48% 81.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.85% 85.14%
CHEMBL3194 P02766 Transthyretin 88.73% 90.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.85% 95.50%
CHEMBL3714130 P46095 G-protein coupled receptor 6 87.84% 97.36%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 87.35% 87.67%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.34% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.06% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.63% 99.23%
CHEMBL1811 P34995 Prostanoid EP1 receptor 84.96% 95.71%
CHEMBL3401 O75469 Pregnane X receptor 83.52% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.12% 86.33%
CHEMBL4581 P52732 Kinesin-like protein 1 80.08% 93.18%

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 56953861
LOTUS LTS0004898
wikiData Q75067335