Nigrolineaxanthone R

Details

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Internal ID 52a7c3e5-e152-4622-bc02-cf38bb3a94a6
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 5,10-dihydroxy-12-(3-hydroxy-3-methylbutyl)-2,2-dimethyl-3,4-dihydropyrano[3,2-b]xanthen-6-one
SMILES (Canonical) CC1(CCC2=C(C3=C(C(=C2O1)CCC(C)(C)O)OC4=C(C3=O)C=CC=C4O)O)C
SMILES (Isomeric) CC1(CCC2=C(C3=C(C(=C2O1)CCC(C)(C)O)OC4=C(C3=O)C=CC=C4O)O)C
InChI InChI=1S/C23H26O6/c1-22(2,27)10-8-14-19-13(9-11-23(3,4)29-19)18(26)16-17(25)12-6-5-7-15(24)20(12)28-21(14)16/h5-7,24,26-27H,8-11H2,1-4H3
InChI Key DBKLPARCLDNAEQ-UHFFFAOYSA-N
Popularity 1 reference 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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CHEMBL511567

2D Structure

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2D Structure of Nigrolineaxanthone R

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9776 97.76%
Caco-2 + 0.5638 56.38%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7711 77.11%
OATP2B1 inhibitior - 0.7044 70.44%
OATP1B1 inhibitior + 0.8725 87.25%
OATP1B3 inhibitior + 0.8995 89.95%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6163 61.63%
P-glycoprotein inhibitior - 0.4886 48.86%
P-glycoprotein substrate - 0.5282 52.82%
CYP3A4 substrate + 0.6748 67.48%
CYP2C9 substrate - 0.5940 59.40%
CYP2D6 substrate - 0.8170 81.70%
CYP3A4 inhibition - 0.9243 92.43%
CYP2C9 inhibition - 0.9045 90.45%
CYP2C19 inhibition - 0.8636 86.36%
CYP2D6 inhibition - 0.8958 89.58%
CYP1A2 inhibition - 0.5954 59.54%
CYP2C8 inhibition + 0.5868 58.68%
CYP inhibitory promiscuity - 0.9185 91.85%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6820 68.20%
Eye corrosion - 0.9914 99.14%
Eye irritation + 0.6640 66.40%
Skin irritation - 0.7445 74.45%
Skin corrosion - 0.9311 93.11%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4762 47.62%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.8287 82.87%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.8734 87.34%
Acute Oral Toxicity (c) III 0.6737 67.37%
Estrogen receptor binding + 0.7195 71.95%
Androgen receptor binding + 0.7395 73.95%
Thyroid receptor binding + 0.6268 62.68%
Glucocorticoid receptor binding + 0.8329 83.29%
Aromatase binding + 0.7095 70.95%
PPAR gamma + 0.8698 86.98%
Honey bee toxicity - 0.7626 76.26%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9362 93.62%

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 99.63% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.70% 93.99%
CHEMBL2581 P07339 Cathepsin D 97.18% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.49% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.78% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.91% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 92.02% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.94% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 91.49% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.78% 86.33%
CHEMBL2996 Q05655 Protein kinase C delta 90.75% 97.79%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.14% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.09% 94.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.43% 90.08%
CHEMBL233 P35372 Mu opioid receptor 84.53% 97.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.43% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.73% 95.89%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 83.51% 97.33%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 82.11% 96.39%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 81.77% 96.37%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.67% 85.30%
CHEMBL2535 P11166 Glucose transporter 80.02% 98.75%

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 11315494
LOTUS LTS0124328
wikiData Q104974520