4-Chlorocurvularinic acid

Details

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Internal ID b99a9967-5e33-484d-b170-ffb1dc4716bd
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 4-chloro-2,8-dihydroxy-6-methoxycarbonyl-9-oxoxanthene-1-carboxylic acid
SMILES (Canonical) COC(=O)C1=CC(=C2C(=C1)OC3=C(C=C(C(=C3C2=O)C(=O)O)O)Cl)O
SMILES (Isomeric) COC(=O)C1=CC(=C2C(=C1)OC3=C(C=C(C(=C3C2=O)C(=O)O)O)Cl)O
InChI InChI=1S/C16H9ClO8/c1-24-16(23)5-2-7(18)10-9(3-5)25-14-6(17)4-8(19)11(15(21)22)12(14)13(10)20/h2-4,18-19H,1H3,(H,21,22)
InChI Key LYYIYBBOOZELLQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H9ClO8
Molecular Weight 364.69 g/mol
Exact Mass 363.9985949 g/mol
Topological Polar Surface Area (TPSA) 130.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.50
H-Bond Acceptor 7
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 4-Chlorocurvularinic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9322 93.22%
Caco-2 - 0.5591 55.91%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.4717 47.17%
OATP2B1 inhibitior - 0.6911 69.11%
OATP1B1 inhibitior + 0.7565 75.65%
OATP1B3 inhibitior + 0.9100 91.00%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7132 71.32%
P-glycoprotein inhibitior - 0.7770 77.70%
P-glycoprotein substrate - 0.8419 84.19%
CYP3A4 substrate + 0.5817 58.17%
CYP2C9 substrate - 0.5994 59.94%
CYP2D6 substrate - 0.9033 90.33%
CYP3A4 inhibition - 0.6913 69.13%
CYP2C9 inhibition + 0.6217 62.17%
CYP2C19 inhibition - 0.8116 81.16%
CYP2D6 inhibition - 0.8368 83.68%
CYP1A2 inhibition + 0.6196 61.96%
CYP2C8 inhibition + 0.5868 58.68%
CYP inhibitory promiscuity - 0.5263 52.63%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8298 82.98%
Carcinogenicity (trinary) Danger 0.5479 54.79%
Eye corrosion - 0.9736 97.36%
Eye irritation - 0.7064 70.64%
Skin irritation - 0.6686 66.86%
Skin corrosion - 0.9279 92.79%
Ames mutagenesis + 0.5536 55.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6933 69.33%
Micronuclear + 0.8074 80.74%
Hepatotoxicity + 0.6284 62.84%
skin sensitisation - 0.9099 90.99%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.6495 64.95%
Acute Oral Toxicity (c) III 0.5417 54.17%
Estrogen receptor binding + 0.8800 88.00%
Androgen receptor binding + 0.7184 71.84%
Thyroid receptor binding - 0.6026 60.26%
Glucocorticoid receptor binding + 0.7656 76.56%
Aromatase binding + 0.6478 64.78%
PPAR gamma + 0.8554 85.54%
Honey bee toxicity - 0.9326 93.26%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6351 63.51%
Fish aquatic toxicity + 0.9779 97.79%

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 97.28% 91.11%
CHEMBL3194 P02766 Transthyretin 95.31% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 93.22% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.17% 86.33%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 92.99% 94.42%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 92.94% 89.34%
CHEMBL2581 P07339 Cathepsin D 88.21% 98.95%
CHEMBL4208 P20618 Proteasome component C5 88.12% 90.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.09% 81.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.04% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.72% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.40% 94.45%
CHEMBL1811 P34995 Prostanoid EP1 receptor 82.37% 95.71%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 82.31% 87.67%
CHEMBL340 P08684 Cytochrome P450 3A4 82.00% 91.19%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.70% 99.17%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.15% 96.90%

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 146683970
LOTUS LTS0261953
wikiData Q105159670