Nigrolineaxanthone L

Details

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Internal ID ae6f4431-7077-4eb1-ba59-9f3ce01b87c6
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 5,10-dihydroxy-7-(3-hydroxy-3-methylbutyl)-2,2-dimethyl-3,4-dihydropyrano[3,2-b]xanthen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H26O6/c1-22(2,27)9-7-12-5-6-14(24)21-17(12)20(26)18-16(28-21)11-15-13(19(18)25)8-10-23(3,4)29-15/h5-6,11,24-25,27H,7-10H2,1-4H3
InChI Key HLNUCGLHJITDDH-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C23H26O6
Molecular Weight 398.40 g/mol
Exact Mass 398.17293854 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.16
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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CHEMBL463924

2D Structure

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2D Structure of Nigrolineaxanthone L

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9746 97.46%
Caco-2 - 0.5751 57.51%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7327 73.27%
OATP2B1 inhibitior + 0.5733 57.33%
OATP1B1 inhibitior + 0.9034 90.34%
OATP1B3 inhibitior + 0.9186 91.86%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5284 52.84%
P-glycoprotein inhibitior - 0.5301 53.01%
P-glycoprotein substrate - 0.6384 63.84%
CYP3A4 substrate + 0.6312 63.12%
CYP2C9 substrate - 0.5940 59.40%
CYP2D6 substrate - 0.8170 81.70%
CYP3A4 inhibition - 0.9152 91.52%
CYP2C9 inhibition - 0.8752 87.52%
CYP2C19 inhibition - 0.8512 85.12%
CYP2D6 inhibition - 0.8637 86.37%
CYP1A2 inhibition - 0.5429 54.29%
CYP2C8 inhibition + 0.6503 65.03%
CYP inhibitory promiscuity - 0.8894 88.94%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6492 64.92%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.5946 59.46%
Skin irritation - 0.7275 72.75%
Skin corrosion - 0.9173 91.73%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5978 59.78%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.6288 62.88%
skin sensitisation - 0.8048 80.48%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.8490 84.90%
Acute Oral Toxicity (c) III 0.7170 71.70%
Estrogen receptor binding + 0.7658 76.58%
Androgen receptor binding + 0.7935 79.35%
Thyroid receptor binding + 0.5947 59.47%
Glucocorticoid receptor binding + 0.8459 84.59%
Aromatase binding + 0.7525 75.25%
PPAR gamma + 0.8850 88.50%
Honey bee toxicity - 0.7697 76.97%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8863 88.63%

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 99.92% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.30% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.81% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 93.56% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.53% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.51% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.11% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.59% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.18% 94.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.85% 90.71%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.89% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.38% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.45% 96.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.23% 92.62%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 81.16% 92.68%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.76% 99.23%
CHEMBL4208 P20618 Proteasome component C5 80.21% 90.00%

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 11749894
LOTUS LTS0143339
wikiData Q105030232