1,3-Dihydroxy-7-(7-hydroxy-3,7-dimethylocta-2,5-dienoxy)xanthen-9-one

Details

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Internal ID 101e90e7-ed42-4f1f-b91b-6c7b53bacffc
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3-dihydroxy-7-(7-hydroxy-3,7-dimethylocta-2,5-dienoxy)xanthen-9-one
SMILES (Canonical) CC(=CCOC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)CC=CC(C)(C)O
SMILES (Isomeric) CC(=CCOC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)CC=CC(C)(C)O
InChI InChI=1S/C23H24O6/c1-14(5-4-9-23(2,3)27)8-10-28-16-6-7-19-17(13-16)22(26)21-18(25)11-15(24)12-20(21)29-19/h4,6-9,11-13,24-25,27H,5,10H2,1-3H3
InChI Key CWGFICUYZGEREO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O6
Molecular Weight 396.40 g/mol
Exact Mass 396.15728848 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.40
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,3-Dihydroxy-7-(7-hydroxy-3,7-dimethylocta-2,5-dienoxy)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 + 0.9679 96.79%
Caco-2 - 0.6039 60.39%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7186 71.86%
OATP2B1 inhibitior - 0.7108 71.08%
OATP1B1 inhibitior + 0.8294 82.94%
OATP1B3 inhibitior + 0.9203 92.03%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9162 91.62%
P-glycoprotein inhibitior + 0.6554 65.54%
P-glycoprotein substrate - 0.6881 68.81%
CYP3A4 substrate + 0.6533 65.33%
CYP2C9 substrate - 0.5959 59.59%
CYP2D6 substrate - 0.8238 82.38%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition + 0.6688 66.88%
CYP2C19 inhibition + 0.7524 75.24%
CYP2D6 inhibition - 0.7062 70.62%
CYP1A2 inhibition + 0.8472 84.72%
CYP2C8 inhibition + 0.7273 72.73%
CYP inhibitory promiscuity + 0.8139 81.39%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6609 66.09%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.8446 84.46%
Skin irritation - 0.7699 76.99%
Skin corrosion - 0.9585 95.85%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7632 76.32%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.7418 74.18%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7330 73.30%
Acute Oral Toxicity (c) III 0.6922 69.22%
Estrogen receptor binding + 0.9309 93.09%
Androgen receptor binding + 0.8127 81.27%
Thyroid receptor binding + 0.7437 74.37%
Glucocorticoid receptor binding + 0.8322 83.22%
Aromatase binding + 0.8438 84.38%
PPAR gamma + 0.8919 89.19%
Honey bee toxicity - 0.8041 80.41%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9965 99.65%

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 98.92% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.82% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 97.18% 94.73%
CHEMBL1929 P47989 Xanthine dehydrogenase 95.93% 96.12%
CHEMBL240 Q12809 HERG 95.92% 89.76%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.84% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.40% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.35% 98.95%
CHEMBL2039 P27338 Monoamine oxidase B 95.23% 92.51%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.87% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.50% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.43% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 88.18% 94.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.88% 99.15%
CHEMBL2535 P11166 Glucose transporter 87.69% 98.75%
CHEMBL4208 P20618 Proteasome component C5 86.86% 90.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.06% 93.65%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.05% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.01% 93.99%
CHEMBL4531 P17931 Galectin-3 81.78% 96.90%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.01% 92.94%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.28% 80.78%

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.
Cratoxylum cochinchinense

Cross-Links

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PubChem 162846414
LOTUS LTS0185800
wikiData Q104971245