4-Chlorocurvularin

Details

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Internal ID f455cde0-347a-40de-9fd9-721cd9939738
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name methyl 4-chloro-3,8-dihydroxy-6-methyl-9-oxoxanthene-1-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H11ClO6/c1-6-3-8(18)12-10(4-6)23-15-11(14(12)20)7(16(21)22-2)5-9(19)13(15)17/h3-5,18-19H,1-2H3
InChI Key BXKPUIOJODIKCJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H11ClO6
Molecular Weight 334.71 g/mol
Exact Mass 334.0244158 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.11
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Chlorocurvularin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9613 96.13%
Caco-2 + 0.7532 75.32%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5215 52.15%
OATP2B1 inhibitior - 0.7065 70.65%
OATP1B1 inhibitior + 0.8520 85.20%
OATP1B3 inhibitior + 0.9058 90.58%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5594 55.94%
P-glycoprotein inhibitior - 0.7698 76.98%
P-glycoprotein substrate - 0.8577 85.77%
CYP3A4 substrate + 0.5709 57.09%
CYP2C9 substrate - 0.5686 56.86%
CYP2D6 substrate - 0.8874 88.74%
CYP3A4 inhibition - 0.8789 87.89%
CYP2C9 inhibition + 0.6900 69.00%
CYP2C19 inhibition - 0.7992 79.92%
CYP2D6 inhibition - 0.8570 85.70%
CYP1A2 inhibition + 0.5975 59.75%
CYP2C8 inhibition + 0.5242 52.42%
CYP inhibitory promiscuity - 0.6201 62.01%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8293 82.93%
Carcinogenicity (trinary) Danger 0.4961 49.61%
Eye corrosion - 0.9753 97.53%
Eye irritation + 0.6343 63.43%
Skin irritation - 0.7128 71.28%
Skin corrosion - 0.9465 94.65%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6886 68.86%
Micronuclear + 0.7874 78.74%
Hepatotoxicity + 0.7690 76.90%
skin sensitisation - 0.9317 93.17%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.5727 57.27%
Acute Oral Toxicity (c) III 0.4127 41.27%
Estrogen receptor binding + 0.8806 88.06%
Androgen receptor binding + 0.7773 77.73%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.9165 91.65%
Aromatase binding + 0.6644 66.44%
PPAR gamma + 0.8491 84.91%
Honey bee toxicity - 0.9137 91.37%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9864 98.64%

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 98.30% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 95.30% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.50% 94.45%
CHEMBL2581 P07339 Cathepsin D 91.38% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.31% 94.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.42% 81.11%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.94% 94.42%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 85.61% 92.29%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.58% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.97% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 84.23% 91.49%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.22% 93.65%
CHEMBL3194 P02766 Transthyretin 83.55% 90.71%
CHEMBL340 P08684 Cytochrome P450 3A4 82.68% 91.19%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.54% 96.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.19% 89.34%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.51% 94.80%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.29% 96.90%
CHEMBL4208 P20618 Proteasome component C5 80.43% 90.00%
CHEMBL2535 P11166 Glucose transporter 80.17% 98.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.12% 90.71%

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 146683968
LOTUS LTS0255764
wikiData Q104948051