Philonotisflavone

Details

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Internal ID e4c4a0c4-271c-495d-ad7e-1c5a518cc30f
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones
IUPAC Name 8-[6-(5,7-dihydroxy-4-oxochromen-2-yl)-2,3-dihydroxyphenyl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H18O12/c31-12-6-17(35)26-20(38)10-23(41-24(26)7-12)13-2-4-15(33)29(40)25(13)28-19(37)8-18(36)27-21(39)9-22(42-30(27)28)11-1-3-14(32)16(34)5-11/h1-10,31-37,40H
InChI Key MJRDPDQSEGRCID-UHFFFAOYSA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C30H18O12
Molecular Weight 570.50 g/mol
Exact Mass 570.07982601 g/mol
Topological Polar Surface Area (TPSA) 214.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.55
H-Bond Acceptor 12
H-Bond Donor 8
Rotatable Bonds 3

Synonyms

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8-[6-(5,7-dihydroxy-4-oxochromen-2-yl)-2,3-dihydroxyphenyl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one
8-(6-(5,7-dihydroxy-4-oxochromen-2-yl)-2,3-dihydroxyphenyl)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one
RefChem:173164
124615-12-9
NSC683134
SCHEMBL27198446
SCHEMBL29664228
NSC-683134
NCI60_029788

2D Structure

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2D Structure of Philonotisflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8150 81.50%
Caco-2 - 0.8840 88.40%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6193 61.93%
OATP2B1 inhibitior + 0.5824 58.24%
OATP1B1 inhibitior + 0.7993 79.93%
OATP1B3 inhibitior + 0.9836 98.36%
MATE1 inhibitior + 0.6600 66.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7424 74.24%
P-glycoprotein inhibitior - 0.4950 49.50%
P-glycoprotein substrate - 0.5885 58.85%
CYP3A4 substrate + 0.6185 61.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8553 85.53%
CYP3A4 inhibition + 0.5291 52.91%
CYP2C9 inhibition + 0.5136 51.36%
CYP2C19 inhibition - 0.8558 85.58%
CYP2D6 inhibition - 0.9431 94.31%
CYP1A2 inhibition + 0.7008 70.08%
CYP2C8 inhibition + 0.8799 87.99%
CYP inhibitory promiscuity - 0.7149 71.49%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7279 72.79%
Eye corrosion - 0.9922 99.22%
Eye irritation - 0.6837 68.37%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9174 91.74%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7323 73.23%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.8223 82.23%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7923 79.23%
Acute Oral Toxicity (c) II 0.6981 69.81%
Estrogen receptor binding + 0.8939 89.39%
Androgen receptor binding + 0.9247 92.47%
Thyroid receptor binding + 0.6027 60.27%
Glucocorticoid receptor binding + 0.7554 75.54%
Aromatase binding + 0.5481 54.81%
PPAR gamma + 0.8381 83.81%
Honey bee toxicity - 0.7589 75.89%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9201 92.01%

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
CHEMBL1951 P21397 Monoamine oxidase A 99.54% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.26% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 97.37% 98.35%
CHEMBL3194 P02766 Transthyretin 97.37% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.69% 89.00%
CHEMBL2581 P07339 Cathepsin D 96.66% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.66% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.11% 94.00%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 90.07% 95.64%
CHEMBL308 P06493 Cyclin-dependent kinase 1 89.29% 91.73%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 89.01% 96.21%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.45% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.98% 95.56%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 86.69% 85.11%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 86.18% 98.11%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.19% 96.12%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.95% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 84.86% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.68% 86.33%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 82.98% 83.10%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.67% 97.28%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 82.38% 89.23%
CHEMBL3038469 P24941 CDK2/Cyclin A 82.28% 91.38%
CHEMBL4530 P00488 Coagulation factor XIII 80.21% 96.00%

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.
Anacolia webbii
Aulacomnium androgynum
Bartramia ithyphylla
Bartramia laevisphaera
Bartramia mossmaniana
Bartramia potosica
Bartramia stricta
Mnium hornum
Rhizogonium distichum

Cross-Links

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PubChem 5469098
NPASS NPC80821
LOTUS LTS0021548
wikiData Q104403579