Garciniaxanthone H

Details

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Internal ID d14b3022-975d-4edd-a184-de047dd64706
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 2,5,8-trihydroxy-1-methoxy-4-(2-methylbut-3-en-2-yl)xanthen-9-one
SMILES (Canonical) CC(C)(C=C)C1=CC(=C(C2=C1OC3=C(C=CC(=C3C2=O)O)O)OC)O
SMILES (Isomeric) CC(C)(C=C)C1=CC(=C(C2=C1OC3=C(C=CC(=C3C2=O)O)O)OC)O
InChI InChI=1S/C19H18O6/c1-5-19(2,3)9-8-12(22)17(24-4)14-15(23)13-10(20)6-7-11(21)18(13)25-16(9)14/h5-8,20-22H,1H2,2-4H3
InChI Key QRIMPNRPTNBDIP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O6
Molecular Weight 342.30 g/mol
Exact Mass 342.11033829 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.54
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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CHEBI:65949
2,5,8-trihydroxy-1-methoxy-4-(2-methylbut-3-en-2-yl)xanthen-9-one
2,5,8-trihydroxy-1-methoxy-4-(2-methylbut-3-en-2-yl)-9H-xanthen-9-one
RefChem:142658
184776-34-9
SCHEMBL8928225
Q27134450

2D Structure

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2D Structure of Garciniaxanthone H

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9774 97.74%
Caco-2 + 0.5998 59.98%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6866 68.66%
OATP2B1 inhibitior - 0.6999 69.99%
OATP1B1 inhibitior + 0.9137 91.37%
OATP1B3 inhibitior + 0.9721 97.21%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5876 58.76%
P-glycoprotein inhibitior - 0.5894 58.94%
P-glycoprotein substrate - 0.8927 89.27%
CYP3A4 substrate + 0.5224 52.24%
CYP2C9 substrate - 0.6228 62.28%
CYP2D6 substrate - 0.8460 84.60%
CYP3A4 inhibition + 0.7025 70.25%
CYP2C9 inhibition - 0.7557 75.57%
CYP2C19 inhibition + 0.7338 73.38%
CYP2D6 inhibition - 0.6977 69.77%
CYP1A2 inhibition + 0.7933 79.33%
CYP2C8 inhibition + 0.5098 50.98%
CYP inhibitory promiscuity + 0.6121 61.21%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5566 55.66%
Eye corrosion - 0.9838 98.38%
Eye irritation + 0.8143 81.43%
Skin irritation - 0.7557 75.57%
Skin corrosion - 0.9369 93.69%
Ames mutagenesis + 0.6636 66.36%
Human Ether-a-go-go-Related Gene inhibition - 0.4816 48.16%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation - 0.8041 80.41%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5063 50.63%
Acute Oral Toxicity (c) III 0.5884 58.84%
Estrogen receptor binding + 0.7521 75.21%
Androgen receptor binding + 0.6983 69.83%
Thyroid receptor binding + 0.6091 60.91%
Glucocorticoid receptor binding + 0.7953 79.53%
Aromatase binding + 0.8092 80.92%
PPAR gamma + 0.8149 81.49%
Honey bee toxicity - 0.8618 86.18%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9820 98.20%

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 98.78% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.92% 95.56%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 92.96% 80.78%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.38% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 91.34% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.11% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.38% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.64% 89.00%
CHEMBL2581 P07339 Cathepsin D 85.99% 98.95%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.36% 98.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.13% 89.34%
CHEMBL3194 P02766 Transthyretin 84.19% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.93% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.56% 99.23%

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 subelliptica
Garcinia xanthochymus

Cross-Links

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PubChem 10065952
NPASS NPC51968
LOTUS LTS0237429
wikiData Q27134450