Gaboxanthone

Details

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Internal ID 4de7b317-c6da-47d8-a626-3b108ca06ee2
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 5,10-dihydroxy-8,9-dimethoxy-2,2-dimethyl-12-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one
SMILES (Canonical) CC(=CCC1=C2C(=C(C3=C1OC4=C(C(=C(C=C4C3=O)OC)OC)O)O)C=CC(O2)(C)C)C
SMILES (Isomeric) CC(=CCC1=C2C(=C(C3=C1OC4=C(C(=C(C=C4C3=O)OC)OC)O)O)C=CC(O2)(C)C)C
InChI InChI=1S/C25H26O7/c1-12(2)7-8-14-21-13(9-10-25(3,4)32-21)18(26)17-19(27)15-11-16(29-5)24(30-6)20(28)23(15)31-22(14)17/h7,9-11,26,28H,8H2,1-6H3
InChI Key CAEVETBYJYICTB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C25H26O7
Molecular Weight 438.50 g/mol
Exact Mass 438.16785316 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.07
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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5,10-dihydroxy-8,9-dimethoxy-2,2-dimethyl-12-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one

2D Structure

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2D Structure of Gaboxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 + 0.5434 54.34%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6742 67.42%
OATP2B1 inhibitior - 0.7131 71.31%
OATP1B1 inhibitior + 0.8338 83.38%
OATP1B3 inhibitior + 0.8881 88.81%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9180 91.80%
P-glycoprotein inhibitior + 0.7990 79.90%
P-glycoprotein substrate + 0.5320 53.20%
CYP3A4 substrate + 0.6397 63.97%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.7828 78.28%
CYP2C9 inhibition + 0.5721 57.21%
CYP2C19 inhibition + 0.8909 89.09%
CYP2D6 inhibition - 0.6215 62.15%
CYP1A2 inhibition + 0.5116 51.16%
CYP2C8 inhibition + 0.6118 61.18%
CYP inhibitory promiscuity + 0.7987 79.87%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6148 61.48%
Eye corrosion - 0.9892 98.92%
Eye irritation + 0.5720 57.20%
Skin irritation - 0.7388 73.88%
Skin corrosion - 0.9508 95.08%
Ames mutagenesis + 0.5982 59.82%
Human Ether-a-go-go-Related Gene inhibition - 0.5681 56.81%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.7503 75.03%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8010 80.10%
Acute Oral Toxicity (c) III 0.7498 74.98%
Estrogen receptor binding + 0.8451 84.51%
Androgen receptor binding + 0.6181 61.81%
Thyroid receptor binding + 0.6660 66.60%
Glucocorticoid receptor binding + 0.8778 87.78%
Aromatase binding + 0.7456 74.56%
PPAR gamma + 0.8609 86.09%
Honey bee toxicity - 0.6970 69.70%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9817 98.17%

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 99.76% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.09% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.90% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.20% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.12% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.26% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.11% 99.17%
CHEMBL2581 P07339 Cathepsin D 89.57% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 89.34% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.15% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.64% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 86.40% 94.73%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.38% 89.62%
CHEMBL1255126 O15151 Protein Mdm4 84.30% 90.20%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.97% 92.62%
CHEMBL2413 P32246 C-C chemokine receptor type 1 82.42% 89.50%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.01% 85.30%
CHEMBL2535 P11166 Glucose transporter 80.61% 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.
Symphonia globulifera

Cross-Links

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PubChem 11704807
LOTUS LTS0218783
wikiData Q104951103