Dodoviscin B

Details

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Internal ID ecccd208-14c0-4a52-811f-595535b150c6
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 3-prenylated flavones
IUPAC Name 5,7-dihydroxy-2-[4-hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)-5-(3-methylbut-2-enyl)phenyl]-3,6-dimethoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H30O8/c1-13(2)7-8-15-9-17(10-16(22(15)30)11-18(28)14(3)4)25-27(34-6)24(32)21-20(35-25)12-19(29)26(33-5)23(21)31/h7,9-10,12,18,28-31H,3,8,11H2,1-2,4-6H3
InChI Key FNHZTQPLQXIFKH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H30O8
Molecular Weight 482.50 g/mol
Exact Mass 482.19406791 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 8

Synonyms

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CHEMBL2037149

2D Structure

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2D Structure of Dodoviscin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9874 98.74%
Caco-2 - 0.6056 60.56%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5746 57.46%
OATP2B1 inhibitior - 0.5663 56.63%
OATP1B1 inhibitior + 0.8854 88.54%
OATP1B3 inhibitior + 0.8847 88.47%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8667 86.67%
P-glycoprotein inhibitior + 0.7347 73.47%
P-glycoprotein substrate - 0.6214 62.14%
CYP3A4 substrate + 0.6129 61.29%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.7986 79.86%
CYP3A4 inhibition - 0.6261 62.61%
CYP2C9 inhibition + 0.5251 52.51%
CYP2C19 inhibition + 0.7543 75.43%
CYP2D6 inhibition - 0.6310 63.10%
CYP1A2 inhibition + 0.5632 56.32%
CYP2C8 inhibition + 0.6359 63.59%
CYP inhibitory promiscuity + 0.6650 66.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7555 75.55%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.7853 78.53%
Skin irritation - 0.7744 77.44%
Skin corrosion - 0.9373 93.73%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6999 69.99%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5276 52.76%
skin sensitisation - 0.7866 78.66%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7874 78.74%
Acute Oral Toxicity (c) III 0.5344 53.44%
Estrogen receptor binding + 0.8730 87.30%
Androgen receptor binding + 0.6416 64.16%
Thyroid receptor binding + 0.6166 61.66%
Glucocorticoid receptor binding + 0.8265 82.65%
Aromatase binding + 0.6692 66.92%
PPAR gamma + 0.7845 78.45%
Honey bee toxicity - 0.6898 68.98%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9890 98.90%

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 99.74% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.79% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.67% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.58% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 93.99% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.31% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.67% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.00% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.84% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.38% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 86.11% 91.49%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 84.37% 80.96%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.04% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.64% 99.15%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.57% 96.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.49% 89.34%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.74% 92.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.03% 95.50%

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.
Dodonaea viscosa

Cross-Links

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PubChem 57409963
LOTUS LTS0104231
wikiData Q104998304