3,6,8-Trihydroxy-2-methoxy-1-[(1,3,3-trimethyl-7-oxabicyclo[2.2.1]heptan-2-yl)methyl]xanthen-9-one

Details

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Internal ID 466ba318-9bd0-4a92-8e45-ecd6566f18cc
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 3,6,8-trihydroxy-2-methoxy-1-[(1,3,3-trimethyl-7-oxabicyclo[2.2.1]heptan-2-yl)methyl]xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H26O7/c1-23(2)17(24(3)6-5-18(23)31-24)9-12-19-16(10-14(27)22(12)29-4)30-15-8-11(25)7-13(26)20(15)21(19)28/h7-8,10,17-18,25-27H,5-6,9H2,1-4H3
InChI Key RCBJTBFVHREOHR-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C24H26O7
Molecular Weight 426.50 g/mol
Exact Mass 426.16785316 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.21
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,6,8-Trihydroxy-2-methoxy-1-[(1,3,3-trimethyl-7-oxabicyclo[2.2.1]heptan-2-yl)methyl]xanthen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9321 93.21%
Caco-2 + 0.5506 55.06%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7844 78.44%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.8726 87.26%
OATP1B3 inhibitior + 0.9203 92.03%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.4644 46.44%
P-glycoprotein inhibitior + 0.6358 63.58%
P-glycoprotein substrate - 0.6545 65.45%
CYP3A4 substrate + 0.6719 67.19%
CYP2C9 substrate - 0.5773 57.73%
CYP2D6 substrate - 0.8165 81.65%
CYP3A4 inhibition - 0.7193 71.93%
CYP2C9 inhibition - 0.7966 79.66%
CYP2C19 inhibition - 0.7674 76.74%
CYP2D6 inhibition - 0.8169 81.69%
CYP1A2 inhibition - 0.5895 58.95%
CYP2C8 inhibition + 0.7196 71.96%
CYP inhibitory promiscuity - 0.6396 63.96%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6206 62.06%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.7625 76.25%
Skin irritation - 0.7481 74.81%
Skin corrosion - 0.9374 93.74%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5177 51.77%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.5203 52.03%
skin sensitisation - 0.8912 89.12%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.8314 83.14%
Acute Oral Toxicity (c) III 0.3892 38.92%
Estrogen receptor binding + 0.9053 90.53%
Androgen receptor binding + 0.6753 67.53%
Thyroid receptor binding + 0.6801 68.01%
Glucocorticoid receptor binding + 0.9044 90.44%
Aromatase binding + 0.8085 80.85%
PPAR gamma + 0.8654 86.54%
Honey bee toxicity - 0.7521 75.21%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9811 98.11%

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 99.71% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.94% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.60% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.98% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 90.45% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.61% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.36% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.97% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.35% 97.09%
CHEMBL233 P35372 Mu opioid receptor 87.36% 97.93%
CHEMBL2581 P07339 Cathepsin D 87.04% 98.95%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.85% 96.12%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.67% 92.62%
CHEMBL3194 P02766 Transthyretin 84.69% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.92% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.57% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.44% 99.15%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.42% 96.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.44% 92.94%
CHEMBL4208 P20618 Proteasome component C5 82.40% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.99% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.35% 97.14%
CHEMBL340 P08684 Cytochrome P450 3A4 80.79% 91.19%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.58% 99.17%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.14% 91.07%

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 parvifolia

Cross-Links

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PubChem 85346827
LOTUS LTS0075195
wikiData Q105233491