Ornatipolide

Details

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Internal ID 8544849e-f158-4f43-9dc2-93a8ef6d251f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Diarylethers
IUPAC Name 4-hydroxy-2,10-dioxatricyclo[12.2.2.13,7]nonadeca-1(16),3,5,7(19),14,17-hexaene-11,12-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H14O5/c18-14-6-3-12-7-8-21-17(20)15(19)9-11-1-4-13(5-2-11)22-16(14)10-12/h1-6,10,18H,7-9H2
InChI Key MTLMXGMZDJWCOI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O5
Molecular Weight 298.29 g/mol
Exact Mass 298.08412354 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.40
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ornatipolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9632 96.32%
Caco-2 + 0.6303 63.03%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8928 89.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9490 94.90%
OATP1B3 inhibitior + 0.9301 93.01%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7532 75.32%
P-glycoprotein inhibitior - 0.8247 82.47%
P-glycoprotein substrate - 0.9476 94.76%
CYP3A4 substrate - 0.5759 57.59%
CYP2C9 substrate - 0.7838 78.38%
CYP2D6 substrate - 0.8105 81.05%
CYP3A4 inhibition - 0.9215 92.15%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition - 0.7451 74.51%
CYP2D6 inhibition - 0.9257 92.57%
CYP1A2 inhibition + 0.6464 64.64%
CYP2C8 inhibition - 0.8414 84.14%
CYP inhibitory promiscuity - 0.9603 96.03%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8561 85.61%
Carcinogenicity (trinary) Non-required 0.6051 60.51%
Eye corrosion - 0.9858 98.58%
Eye irritation + 0.7132 71.32%
Skin irritation - 0.7440 74.40%
Skin corrosion - 0.9732 97.32%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7258 72.58%
Micronuclear - 0.5867 58.67%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.7891 78.91%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5939 59.39%
Acute Oral Toxicity (c) III 0.6198 61.98%
Estrogen receptor binding + 0.7029 70.29%
Androgen receptor binding + 0.8272 82.72%
Thyroid receptor binding + 0.5449 54.49%
Glucocorticoid receptor binding + 0.7093 70.93%
Aromatase binding + 0.6266 62.66%
PPAR gamma + 0.7824 78.24%
Honey bee toxicity - 0.9078 90.78%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9440 94.40%

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 98.90% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.46% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.39% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 91.56% 93.40%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.30% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.19% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.46% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.47% 93.99%
CHEMBL4208 P20618 Proteasome component C5 81.36% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.29% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.82% 89.00%

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.
There are no matching plants.

Cross-Links

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PubChem 102120370
LOTUS LTS0210599
wikiData Q77374219