5,12-Dihydroxy-8-methoxy-5,9,13,14-tetramethyl-1-oxacyclotetradeca-3,6,9-trien-2-one

Details

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Internal ID 2732367b-9f69-4044-ad0e-962c7dc3ba04
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 5,12-dihydroxy-8-methoxy-5,9,13,14-tetramethyl-1-oxacyclotetradeca-3,6,9-trien-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H28O5/c1-12-6-7-15(19)13(2)14(3)23-17(20)9-11-18(4,21)10-8-16(12)22-5/h6,8-11,13-16,19,21H,7H2,1-5H3
InChI Key DTOLXYHWXCVHRL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H28O5
Molecular Weight 324.40 g/mol
Exact Mass 324.19367399 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.14
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,12-Dihydroxy-8-methoxy-5,9,13,14-tetramethyl-1-oxacyclotetradeca-3,6,9-trien-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9812 98.12%
Caco-2 + 0.7148 71.48%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5820 58.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8814 88.14%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5610 56.10%
P-glycoprotein inhibitior - 0.7775 77.75%
P-glycoprotein substrate - 0.7905 79.05%
CYP3A4 substrate + 0.6261 62.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8917 89.17%
CYP3A4 inhibition - 0.9163 91.63%
CYP2C9 inhibition - 0.9335 93.35%
CYP2C19 inhibition - 0.8795 87.95%
CYP2D6 inhibition - 0.9551 95.51%
CYP1A2 inhibition - 0.8261 82.61%
CYP2C8 inhibition - 0.8052 80.52%
CYP inhibitory promiscuity - 0.9345 93.45%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7796 77.96%
Carcinogenicity (trinary) Non-required 0.5162 51.62%
Eye corrosion - 0.9693 96.93%
Eye irritation - 0.9685 96.85%
Skin irritation - 0.5675 56.75%
Skin corrosion - 0.9463 94.63%
Ames mutagenesis - 0.5854 58.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3623 36.23%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.6773 67.73%
skin sensitisation - 0.6713 67.13%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.5761 57.61%
Acute Oral Toxicity (c) III 0.5068 50.68%
Estrogen receptor binding + 0.6541 65.41%
Androgen receptor binding - 0.5920 59.20%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7324 73.24%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.6163 61.63%
Honey bee toxicity - 0.8582 85.82%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.4007 40.07%

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 92.67% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.26% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.10% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.56% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.99% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 88.82% 91.49%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.68% 91.07%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.38% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.47% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 86.21% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.88% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.19% 100.00%
CHEMBL1871 P10275 Androgen Receptor 82.36% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.90% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.70% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.49% 97.09%
CHEMBL4530 P00488 Coagulation factor XIII 80.24% 96.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162934081
LOTUS LTS0251129
wikiData Q104988912