Pinselin

Details

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Internal ID 3e46624d-bdb5-4a3b-954b-6529bbe9351f
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name methyl 2,8-dihydroxy-6-methyl-9-oxoxanthene-1-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H12O6/c1-7-5-9(18)12-11(6-7)22-10-4-3-8(17)13(16(20)21-2)14(10)15(12)19/h3-6,17-18H,1-2H3
InChI Key TWQNCGDOHUNFFU-UHFFFAOYSA-N
Popularity 25 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O6
Molecular Weight 300.26 g/mol
Exact Mass 300.06338810 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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476-53-9
9H-Xanthene-1-carboxylic acid, 2,8-dihydroxy-6-methyl-9-oxo-, methyl ester
65E7H52E97
UNII-65E7H52E97
CASSIOLLIN
CHEMBL4064859
CHEBI:68229
DTXSID10197213
TWQNCGDOHUNFFU-UHFFFAOYSA-N
Q27136722
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Pinselin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9386 93.86%
Caco-2 + 0.5218 52.18%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7850 78.50%
OATP2B1 inhibitior - 0.7065 70.65%
OATP1B1 inhibitior + 0.8927 89.27%
OATP1B3 inhibitior + 0.9681 96.81%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7177 71.77%
P-glycoprotein inhibitior - 0.6437 64.37%
P-glycoprotein substrate - 0.9152 91.52%
CYP3A4 substrate + 0.5158 51.58%
CYP2C9 substrate - 0.5626 56.26%
CYP2D6 substrate - 0.8850 88.50%
CYP3A4 inhibition - 0.9023 90.23%
CYP2C9 inhibition - 0.5608 56.08%
CYP2C19 inhibition - 0.8999 89.99%
CYP2D6 inhibition - 0.8731 87.31%
CYP1A2 inhibition + 0.6393 63.93%
CYP2C8 inhibition + 0.4519 45.19%
CYP inhibitory promiscuity - 0.7292 72.92%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.6484 64.84%
Eye corrosion - 0.9792 97.92%
Eye irritation + 0.7766 77.66%
Skin irritation - 0.7269 72.69%
Skin corrosion - 0.9702 97.02%
Ames mutagenesis + 0.7136 71.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6653 66.53%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.6785 67.85%
skin sensitisation - 0.9660 96.60%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.4658 46.58%
Acute Oral Toxicity (c) II 0.5724 57.24%
Estrogen receptor binding + 0.8194 81.94%
Androgen receptor binding + 0.8154 81.54%
Thyroid receptor binding - 0.6002 60.02%
Glucocorticoid receptor binding + 0.8907 89.07%
Aromatase binding + 0.6802 68.02%
PPAR gamma + 0.7369 73.69%
Honey bee toxicity - 0.9438 94.38%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.9569 95.69%

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 97.59% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 92.80% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 92.36% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 91.45% 93.65%
CHEMBL2581 P07339 Cathepsin D 91.32% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.43% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.59% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.31% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.01% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.99% 94.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.66% 94.80%
CHEMBL2535 P11166 Glucose transporter 82.39% 98.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.96% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.37% 94.45%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.37% 94.42%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.33% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Senna occidentalis

Cross-Links

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PubChem 5377796
LOTUS LTS0246656
wikiData Q27136722