Tomentodiplacone

Details

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Internal ID 3f42ea35-9ae3-49f8-b514-2d65d0e16735
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 6-prenylated flavans > 6-prenylated flavanones
IUPAC Name (2S)-5,7-dihydroxy-6-[(2E)-6-hydroxy-3,7-dimethylocta-2,7-dienyl]-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H30O7/c1-14(2)18(27)9-6-15(3)5-8-17-20(29)12-24-25(26(17)31)21(30)13-22(33-24)16-7-10-19(28)23(11-16)32-4/h5,7,10-12,18,22,27-29,31H,1,6,8-9,13H2,2-4H3/b15-5+/t18?,22-/m0/s1
InChI Key JDLZAZIAVULNSS-SGJLQWKXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H30O7
Molecular Weight 454.50 g/mol
Exact Mass 454.19915329 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.72
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 8

Synonyms

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CHEMBL459252

2D Structure

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2D Structure of Tomentodiplacone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9635 96.35%
Caco-2 - 0.7591 75.91%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.6219 62.19%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.8877 88.77%
OATP1B3 inhibitior + 0.8966 89.66%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8182 81.82%
P-glycoprotein inhibitior + 0.6509 65.09%
P-glycoprotein substrate - 0.6291 62.91%
CYP3A4 substrate + 0.6466 64.66%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7812 78.12%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.7414 74.14%
CYP2C19 inhibition - 0.5196 51.96%
CYP2D6 inhibition - 0.8072 80.72%
CYP1A2 inhibition + 0.6218 62.18%
CYP2C8 inhibition + 0.5623 56.23%
CYP inhibitory promiscuity - 0.5498 54.98%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7679 76.79%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.8431 84.31%
Skin irritation - 0.7441 74.41%
Skin corrosion - 0.9361 93.61%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5149 51.49%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8409 84.09%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.7877 78.77%
Acute Oral Toxicity (c) II 0.3655 36.55%
Estrogen receptor binding + 0.8287 82.87%
Androgen receptor binding + 0.6154 61.54%
Thyroid receptor binding + 0.6365 63.65%
Glucocorticoid receptor binding + 0.8286 82.86%
Aromatase binding + 0.5690 56.90%
PPAR gamma + 0.7984 79.84%
Honey bee toxicity - 0.7177 71.77%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9953 99.53%

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 99.75% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.89% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.82% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.58% 85.14%
CHEMBL2581 P07339 Cathepsin D 94.69% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.73% 95.56%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 92.06% 92.68%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.78% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.89% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.16% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 88.98% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.45% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.91% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.12% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.29% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.51% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.97% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.58% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.40% 92.62%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.01% 86.92%

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.
Paulownia tomentosa

Cross-Links

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PubChem 24861959
LOTUS LTS0023786
wikiData Q105125588