Garciduol B

Details

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Internal ID 52fd9539-c5a7-484a-a5b0-b784defb9d26
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 2-[2,4-dihydroxy-3-(3-hydroxybenzoyl)-6-methoxyphenyl]-1,4,5-trihydroxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H18O10/c1-36-18-10-16(30)20(22(32)11-4-2-5-12(28)8-11)25(35)19(18)14-9-17(31)27-21(24(14)34)23(33)13-6-3-7-15(29)26(13)37-27/h2-10,28-31,34-35H,1H3
InChI Key XKZFGJPNYONQOM-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C27H18O10
Molecular Weight 502.40 g/mol
Exact Mass 502.08999677 g/mol
Topological Polar Surface Area (TPSA) 174.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.09
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

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CHEBI:192465
DTXSID601124239
2-[2,4-Dihydroxy-3-(3-hydroxybenzoyl)-6-methoxyphenyl]-1,4,5-trihydroxy-9H-xanthen-9-one
2-[2,4-dihydroxy-3-(3-hydroxybenzoyl)-6-methoxyphenyl]-1,4,5-trihydroxyxanthen-9-one
176257-86-6

2D Structure

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2D Structure of Garciduol B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9240 92.40%
Caco-2 - 0.8725 87.25%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6469 64.69%
OATP2B1 inhibitior + 0.5822 58.22%
OATP1B1 inhibitior + 0.8760 87.60%
OATP1B3 inhibitior + 0.9695 96.95%
MATE1 inhibitior - 0.5600 56.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7534 75.34%
P-glycoprotein inhibitior + 0.7327 73.27%
P-glycoprotein substrate + 0.5431 54.31%
CYP3A4 substrate + 0.6599 65.99%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8299 82.99%
CYP3A4 inhibition - 0.5146 51.46%
CYP2C9 inhibition + 0.7405 74.05%
CYP2C19 inhibition + 0.6274 62.74%
CYP2D6 inhibition - 0.7756 77.56%
CYP1A2 inhibition + 0.8682 86.82%
CYP2C8 inhibition + 0.8776 87.76%
CYP inhibitory promiscuity + 0.6844 68.44%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6329 63.29%
Eye corrosion - 0.9830 98.30%
Eye irritation - 0.6904 69.04%
Skin irritation - 0.6361 63.61%
Skin corrosion - 0.9134 91.34%
Ames mutagenesis + 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5179 51.79%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.5351 53.51%
skin sensitisation - 0.9378 93.78%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6992 69.92%
Acute Oral Toxicity (c) III 0.7084 70.84%
Estrogen receptor binding + 0.8849 88.49%
Androgen receptor binding + 0.7098 70.98%
Thyroid receptor binding - 0.5534 55.34%
Glucocorticoid receptor binding + 0.7178 71.78%
Aromatase binding - 0.5606 56.06%
PPAR gamma + 0.7856 78.56%
Honey bee toxicity - 0.8593 85.93%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5549 55.49%
Fish aquatic toxicity + 0.8768 87.68%

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 97.68% 91.11%
CHEMBL2535 P11166 Glucose transporter 96.91% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.37% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.28% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.59% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.02% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.84% 93.99%
CHEMBL3194 P02766 Transthyretin 93.63% 90.71%
CHEMBL1907 P15144 Aminopeptidase N 93.52% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.56% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.90% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.79% 99.23%
CHEMBL1255126 O15151 Protein Mdm4 89.24% 90.20%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.07% 95.50%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 87.16% 96.00%
CHEMBL4208 P20618 Proteasome component C5 86.06% 90.00%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 85.67% 98.21%
CHEMBL3401 O75469 Pregnane X receptor 83.47% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.04% 92.62%
CHEMBL340 P08684 Cytochrome P450 3A4 81.95% 91.19%

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 dulcis

Cross-Links

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PubChem 101689964
LOTUS LTS0043240
wikiData Q105329794