Nigrolineaxanthone P

Details

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Internal ID 2edcaef8-d868-403c-9092-f873498f6556
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 2-(3-ethoxy-3-methylbutyl)-1,3,5-trihydroxy-8-(3-hydroxy-3-methylbutyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H32O7/c1-6-31-25(4,5)12-10-15-17(27)13-18-20(21(15)28)22(29)19-14(9-11-24(2,3)30)7-8-16(26)23(19)32-18/h7-8,13,26-28,30H,6,9-12H2,1-5H3
InChI Key CQWFDJXIXDPPCM-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C25H32O7
Molecular Weight 444.50 g/mol
Exact Mass 444.21480336 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.51
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 8

Synonyms

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CHEMBL462706

2D Structure

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2D Structure of Nigrolineaxanthone P

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9716 97.16%
Caco-2 - 0.5977 59.77%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8018 80.18%
OATP2B1 inhibitior + 0.5774 57.74%
OATP1B1 inhibitior + 0.8813 88.13%
OATP1B3 inhibitior + 0.8766 87.66%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.7542 75.42%
BSEP inhibitior + 0.7176 71.76%
P-glycoprotein inhibitior - 0.4706 47.06%
P-glycoprotein substrate - 0.6436 64.36%
CYP3A4 substrate + 0.6026 60.26%
CYP2C9 substrate - 0.5826 58.26%
CYP2D6 substrate - 0.8351 83.51%
CYP3A4 inhibition - 0.5671 56.71%
CYP2C9 inhibition - 0.7030 70.30%
CYP2C19 inhibition - 0.6873 68.73%
CYP2D6 inhibition - 0.9079 90.79%
CYP1A2 inhibition + 0.6668 66.68%
CYP2C8 inhibition + 0.6987 69.87%
CYP inhibitory promiscuity - 0.7875 78.75%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7391 73.91%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.7947 79.47%
Skin irritation - 0.7713 77.13%
Skin corrosion - 0.9589 95.89%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4182 41.82%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.9018 90.18%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7737 77.37%
Acute Oral Toxicity (c) III 0.6107 61.07%
Estrogen receptor binding + 0.8890 88.90%
Androgen receptor binding + 0.8153 81.53%
Thyroid receptor binding + 0.5833 58.33%
Glucocorticoid receptor binding + 0.8275 82.75%
Aromatase binding + 0.7792 77.92%
PPAR gamma + 0.8767 87.67%
Honey bee toxicity - 0.7551 75.51%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9895 98.95%

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 99.29% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 95.06% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.01% 86.33%
CHEMBL2581 P07339 Cathepsin D 94.80% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.99% 94.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 91.84% 89.34%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.76% 96.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.95% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.40% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.84% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.33% 94.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.94% 86.92%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 84.11% 80.78%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.73% 95.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.72% 99.17%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 81.10% 92.68%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.30% 93.65%

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.
Garcinia nigrolineata

Cross-Links

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PubChem 11430697
LOTUS LTS0160243
wikiData Q104968311