nigrolineaxanthone T

Details

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Internal ID 7816b498-ca23-4331-bbf7-8a1aebdb391e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 1,5,6-trihydroxy-4-(3-hydroxy-3-methylbutyl)-3-methoxyxanthen-9-one
SMILES (Canonical) CC(C)(CCC1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3O)O)O)OC)O
SMILES (Isomeric) CC(C)(CCC1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3O)O)O)OC)O
InChI InChI=1S/C19H20O7/c1-19(2,24)7-6-9-13(25-3)8-12(21)14-15(22)10-4-5-11(20)16(23)18(10)26-17(9)14/h4-5,8,20-21,23-24H,6-7H2,1-3H3
InChI Key KWHHTRSOMASIJT-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20O7
Molecular Weight 360.40 g/mol
Exact Mass 360.12090297 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.78
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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CHEMBL565010
1,5,6-trihydroxy-3-methoxy-4-(3-hydroxyl-3-methylbutyl)xanthone
1,5,6-trihydroxy-4-(3-hydroxy-3-methylbutyl)-3-methoxyxanthen-9-one

2D Structure

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2D Structure of nigrolineaxanthone T

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9713 97.13%
Caco-2 + 0.5103 51.03%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7185 71.85%
OATP2B1 inhibitior - 0.5603 56.03%
OATP1B1 inhibitior + 0.8733 87.33%
OATP1B3 inhibitior + 0.9258 92.58%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6865 68.65%
P-glycoprotein inhibitior - 0.7154 71.54%
P-glycoprotein substrate - 0.5285 52.85%
CYP3A4 substrate + 0.5698 56.98%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.8245 82.45%
CYP3A4 inhibition - 0.8205 82.05%
CYP2C9 inhibition - 0.9052 90.52%
CYP2C19 inhibition - 0.8965 89.65%
CYP2D6 inhibition - 0.9100 91.00%
CYP1A2 inhibition + 0.6485 64.85%
CYP2C8 inhibition + 0.6165 61.65%
CYP inhibitory promiscuity - 0.9433 94.33%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6958 69.58%
Eye corrosion - 0.9906 99.06%
Eye irritation + 0.6237 62.37%
Skin irritation - 0.7475 74.75%
Skin corrosion - 0.9319 93.19%
Ames mutagenesis + 0.7236 72.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6407 64.07%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8523 85.23%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8463 84.63%
Acute Oral Toxicity (c) III 0.6199 61.99%
Estrogen receptor binding + 0.8319 83.19%
Androgen receptor binding + 0.7295 72.95%
Thyroid receptor binding + 0.5835 58.35%
Glucocorticoid receptor binding + 0.8943 89.43%
Aromatase binding + 0.7602 76.02%
PPAR gamma + 0.9170 91.70%
Honey bee toxicity - 0.8254 82.54%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5249 52.49%
Fish aquatic toxicity + 0.9152 91.52%

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 99.49% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.33% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.72% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.75% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.49% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.96% 89.00%
CHEMBL2581 P07339 Cathepsin D 92.93% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.93% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 90.63% 94.73%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.96% 89.62%
CHEMBL3194 P02766 Transthyretin 87.38% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.75% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.17% 99.15%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 84.64% 98.21%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.32% 93.65%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 83.50% 80.78%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.73% 86.92%
CHEMBL2535 P11166 Glucose transporter 81.05% 98.75%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.81% 89.34%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.63% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.16% 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.
Cistanche salsa
Garcinia cowa
Garcinia nigrolineata
Garcinia oblongifolia
Piper wightii
Trifolium resupinatum

Cross-Links

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PubChem 11559542
NPASS NPC256925
ChEMBL CHEMBL565010
LOTUS LTS0073303
wikiData Q104400297