Nigrolineaxanthone A

Details

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Internal ID 9d019328-1853-4523-9338-7a3d91e73699
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 1,5-dihydroxy-4-(3-hydroxy-3-methylbutyl)-3-methoxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H20O6/c1-19(2,23)8-7-10-14(24-3)9-13(21)15-16(22)11-5-4-6-12(20)17(11)25-18(10)15/h4-6,9,20-21,23H,7-8H2,1-3H3
InChI Key BUVUUTYHRGVEBL-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20O6
Molecular Weight 344.40 g/mol
Exact Mass 344.12598835 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.07
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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1,5-Dihydroxy-3-methoxy-4-(3-hydroxy-3-methylbutyl)xanthone
1,5-dihydroxy-4-(3-hydroxy-3-methylbutyl)-3-methoxy-9H-xanthen-9-one
1,8-Dihydroxy-4-(3-hydroxy-3-methyl-butyl)-3-methoxy-xanthen-9-one
9H-xanthen-9-one, 1,5-dihydroxy-4-(3-hydroxy-3-methylbutyl)-3-methoxy-
InChI=1/C19H20O6/c1-19(2,23)8-7-10-14(24-3)9-13(21)15-16(22)11-5-4-6-12(20)17(11)25-18(10)15/h4-6,9,20-21,23H,7-8H2,1-3H

2D Structure

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2D Structure of Nigrolineaxanthone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9838 98.38%
Caco-2 + 0.6634 66.34%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7151 71.51%
OATP2B1 inhibitior - 0.7034 70.34%
OATP1B1 inhibitior + 0.8970 89.70%
OATP1B3 inhibitior + 0.9063 90.63%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6480 64.80%
P-glycoprotein inhibitior - 0.6152 61.52%
P-glycoprotein substrate - 0.5681 56.81%
CYP3A4 substrate + 0.6139 61.39%
CYP2C9 substrate - 0.5940 59.40%
CYP2D6 substrate - 0.8170 81.70%
CYP3A4 inhibition - 0.7904 79.04%
CYP2C9 inhibition - 0.8572 85.72%
CYP2C19 inhibition - 0.8746 87.46%
CYP2D6 inhibition - 0.8815 88.15%
CYP1A2 inhibition + 0.6885 68.85%
CYP2C8 inhibition + 0.6371 63.71%
CYP inhibitory promiscuity - 0.8876 88.76%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6973 69.73%
Eye corrosion - 0.9909 99.09%
Eye irritation + 0.6583 65.83%
Skin irritation - 0.7527 75.27%
Skin corrosion - 0.9406 94.06%
Ames mutagenesis + 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5679 56.79%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8598 85.98%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8342 83.42%
Acute Oral Toxicity (c) III 0.6378 63.78%
Estrogen receptor binding + 0.7981 79.81%
Androgen receptor binding + 0.6839 68.39%
Thyroid receptor binding + 0.6009 60.09%
Glucocorticoid receptor binding + 0.9014 90.14%
Aromatase binding + 0.7392 73.92%
PPAR gamma + 0.9215 92.15%
Honey bee toxicity - 0.7949 79.49%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5051 50.51%
Fish aquatic toxicity + 0.9024 90.24%

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 98.26% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.96% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.67% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.59% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 94.96% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.94% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.72% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.35% 89.00%
CHEMBL2535 P11166 Glucose transporter 90.50% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.84% 99.17%
CHEMBL1937 Q92769 Histone deacetylase 2 86.59% 94.75%
CHEMBL1907 P15144 Aminopeptidase N 86.52% 93.31%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.97% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.26% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.00% 92.62%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.90% 93.65%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.11% 97.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.53% 95.89%

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 5324508
LOTUS LTS0065263
wikiData Q104946354