Nigrolineaxanthone V

Details

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Internal ID 80eb8f64-190b-4fdd-a5d2-1cdd77fe8816
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 7,12-dihydroxy-9-methoxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one
SMILES (Canonical) CC(=CCC1=C(C=C(C2=C1OC3=C(C2=O)C=C4C=CC(OC4=C3O)(C)C)O)OC)C
SMILES (Isomeric) CC(=CCC1=C(C=C(C2=C1OC3=C(C2=O)C=C4C=CC(OC4=C3O)(C)C)O)OC)C
InChI InChI=1S/C24H24O6/c1-12(2)6-7-14-17(28-5)11-16(25)18-19(26)15-10-13-8-9-24(3,4)30-21(13)20(27)23(15)29-22(14)18/h6,8-11,25,27H,7H2,1-5H3
InChI Key OCYZJBDJUYIHMM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H24O6
Molecular Weight 408.40 g/mol
Exact Mass 408.15728848 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.06
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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864516-31-4
7,12-dihydroxy-9-methoxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one
2H,6H-Pyrano[3,2-b]xanthene-6-one, 7,12-dihydroxy-9-methoxy-2,2-dimethyl-10-(3-methyl-2-butenyl)- ; 7,12-Dihydroxy-9-methoxy-2,2-dimethyl-10-(3-methyl-2-buten-1-yl)-2H,6H-pyrano[3,2-b]xanthene-6-one
AKOS032961778

2D Structure

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2D Structure of Nigrolineaxanthone V

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9859 98.59%
Caco-2 + 0.5368 53.68%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6413 64.13%
OATP2B1 inhibitior - 0.7083 70.83%
OATP1B1 inhibitior + 0.8536 85.36%
OATP1B3 inhibitior + 0.8737 87.37%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9451 94.51%
P-glycoprotein inhibitior + 0.8113 81.13%
P-glycoprotein substrate + 0.5909 59.09%
CYP3A4 substrate + 0.6473 64.73%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.8082 80.82%
CYP2C9 inhibition + 0.6131 61.31%
CYP2C19 inhibition + 0.8525 85.25%
CYP2D6 inhibition - 0.6505 65.05%
CYP1A2 inhibition + 0.5713 57.13%
CYP2C8 inhibition + 0.6100 61.00%
CYP inhibitory promiscuity + 0.7707 77.07%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6042 60.42%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.5113 51.13%
Skin irritation - 0.7392 73.92%
Skin corrosion - 0.9527 95.27%
Ames mutagenesis + 0.6336 63.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5704 57.04%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.5426 54.26%
skin sensitisation - 0.7371 73.71%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6419 64.19%
Acute Oral Toxicity (c) III 0.7390 73.90%
Estrogen receptor binding + 0.8690 86.90%
Androgen receptor binding + 0.5756 57.56%
Thyroid receptor binding + 0.6644 66.44%
Glucocorticoid receptor binding + 0.9177 91.77%
Aromatase binding + 0.7242 72.42%
PPAR gamma + 0.9220 92.20%
Honey bee toxicity - 0.7054 70.54%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9821 98.21%

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 99.79% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.55% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.91% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 94.80% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.76% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 93.56% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.33% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.38% 93.99%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 90.26% 85.30%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.35% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.10% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.24% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.19% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.26% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 84.86% 94.73%
CHEMBL3194 P02766 Transthyretin 82.10% 90.71%
CHEMBL1255126 O15151 Protein Mdm4 82.00% 90.20%
CHEMBL4208 P20618 Proteasome component C5 81.68% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.48% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.15% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.44% 99.23%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.20% 89.34%

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 11553272
NPASS NPC242414
LOTUS LTS0221315
wikiData Q104400295