1,7,8-Trimethoxy-2,3-(methylenebisoxy)xanthone

Details

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Internal ID eb95b512-e22b-413b-862a-861495a2213f
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 8,9,11-trimethoxy-[1,3]dioxolo[4,5-b]xanthen-10-one
SMILES (Canonical) COC1=C(C2=C(C=C1)OC3=CC4=C(C(=C3C2=O)OC)OCO4)OC
SMILES (Isomeric) COC1=C(C2=C(C=C1)OC3=CC4=C(C(=C3C2=O)OC)OCO4)OC
InChI InChI=1S/C17H14O7/c1-19-9-5-4-8-12(15(9)20-2)14(18)13-10(24-8)6-11-16(17(13)21-3)23-7-22-11/h4-6H,7H2,1-3H3
InChI Key SKKVGEYOXAYAOP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O7
Molecular Weight 330.29 g/mol
Exact Mass 330.07395278 g/mol
Topological Polar Surface Area (TPSA) 72.40 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.70
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,7,8-Trimethoxy-2,3-(methylenebisoxy)xanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9829 98.29%
Caco-2 + 0.8951 89.51%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6778 67.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9707 97.07%
OATP1B3 inhibitior + 0.9614 96.14%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5945 59.45%
P-glycoprotein inhibitior + 0.6958 69.58%
P-glycoprotein substrate - 0.9016 90.16%
CYP3A4 substrate - 0.5378 53.78%
CYP2C9 substrate - 0.8423 84.23%
CYP2D6 substrate - 0.8020 80.20%
CYP3A4 inhibition + 0.8421 84.21%
CYP2C9 inhibition + 0.6582 65.82%
CYP2C19 inhibition + 0.9214 92.14%
CYP2D6 inhibition + 0.6287 62.87%
CYP1A2 inhibition + 0.7137 71.37%
CYP2C8 inhibition - 0.7408 74.08%
CYP inhibitory promiscuity + 0.8853 88.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4717 47.17%
Eye corrosion - 0.9748 97.48%
Eye irritation - 0.5356 53.56%
Skin irritation - 0.7829 78.29%
Skin corrosion - 0.9746 97.46%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8512 85.12%
Micronuclear + 0.7574 75.74%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.7199 71.99%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.7331 73.31%
Acute Oral Toxicity (c) III 0.4531 45.31%
Estrogen receptor binding + 0.9038 90.38%
Androgen receptor binding + 0.6723 67.23%
Thyroid receptor binding + 0.5920 59.20%
Glucocorticoid receptor binding + 0.8833 88.33%
Aromatase binding + 0.8563 85.63%
PPAR gamma + 0.7899 78.99%
Honey bee toxicity - 0.8289 82.89%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9330 93.30%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.05% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.60% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.34% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.73% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.14% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.92% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.63% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.73% 89.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.68% 94.80%
CHEMBL2581 P07339 Cathepsin D 87.35% 98.95%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 85.73% 82.67%
CHEMBL2535 P11166 Glucose transporter 85.52% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.77% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.44% 92.62%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 83.07% 85.00%
CHEMBL4208 P20618 Proteasome component C5 81.71% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.10% 96.09%

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.
Bredemeyera brevifolia
Jagera pseudorhus
Linum catharticum
Myristica gigantea
Nothofagus pumilio

Cross-Links

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PubChem 10065197
NPASS NPC248684
LOTUS LTS0048949
wikiData Q105254882