Nigrolineaxanthone Q

Details

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Internal ID eed77ae3-3801-414b-a089-9149d5efe928
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 6,11-dihydroxy-3,3-dimethyl-5-(3-methylbut-2-enyl)-1,2-dihydropyrano[2,3-c]xanthen-7-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H24O5/c1-12(2)8-9-14-19(26)17-18(25)13-6-5-7-16(24)21(13)27-22(17)15-10-11-23(3,4)28-20(14)15/h5-8,24,26H,9-11H2,1-4H3
InChI Key KNIWDQZUTDLRKZ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O5
Molecular Weight 380.40 g/mol
Exact Mass 380.16237386 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 5.70
Atomic LogP (AlogP) 4.97
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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CHEMBL467408

2D Structure

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2D Structure of Nigrolineaxanthone Q

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9894 98.94%
Caco-2 + 0.5912 59.12%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7745 77.45%
OATP2B1 inhibitior - 0.7071 70.71%
OATP1B1 inhibitior + 0.9097 90.97%
OATP1B3 inhibitior + 0.8874 88.74%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.7786 77.86%
P-glycoprotein inhibitior + 0.6400 64.00%
P-glycoprotein substrate - 0.6402 64.02%
CYP3A4 substrate + 0.6586 65.86%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.8265 82.65%
CYP2C9 inhibition - 0.6357 63.57%
CYP2C19 inhibition - 0.5777 57.77%
CYP2D6 inhibition - 0.8464 84.64%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.5732 57.32%
CYP inhibitory promiscuity - 0.6222 62.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6847 68.47%
Eye corrosion - 0.9923 99.23%
Eye irritation + 0.6707 67.07%
Skin irritation - 0.7211 72.11%
Skin corrosion - 0.9323 93.23%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4898 48.98%
Micronuclear - 0.7200 72.00%
Hepatotoxicity - 0.5299 52.99%
skin sensitisation - 0.7278 72.78%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7874 78.74%
Acute Oral Toxicity (c) III 0.5649 56.49%
Estrogen receptor binding + 0.8000 80.00%
Androgen receptor binding + 0.7245 72.45%
Thyroid receptor binding + 0.5605 56.05%
Glucocorticoid receptor binding + 0.8878 88.78%
Aromatase binding + 0.6279 62.79%
PPAR gamma + 0.9293 92.93%
Honey bee toxicity - 0.7375 73.75%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9907 99.07%

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 99.75% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.44% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.41% 94.45%
CHEMBL2581 P07339 Cathepsin D 97.05% 98.95%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 96.79% 85.30%
CHEMBL1937 Q92769 Histone deacetylase 2 96.44% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.22% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.25% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 92.46% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 91.59% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.92% 99.23%
CHEMBL5103 Q969S8 Histone deacetylase 10 88.62% 90.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.50% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.89% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.46% 95.89%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 82.72% 96.39%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.51% 100.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.59% 95.50%

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 11440392
LOTUS LTS0026885
wikiData Q105143428