Phoyunnanin E

Details

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Internal ID 8d73b8be-37bc-4bee-915b-3d2dcbb5ab08
Taxonomy Benzenoids > Phenanthrenes and derivatives > Hydrophenanthrenes
IUPAC Name 8-[(5-hydroxy-7-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-7-methoxy-9,10-dihydrophenanthrene-2,5-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H26O6/c1-34-21-13-18-4-3-17-12-20(7-10-22(17)28(18)25(32)14-21)36-30-24-8-5-16-11-19(31)6-9-23(16)29(24)26(33)15-27(30)35-2/h6-7,9-15,31-33H,3-5,8H2,1-2H3
InChI Key UNJANUINFLXLPN-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C30H26O6
Molecular Weight 482.50 g/mol
Exact Mass 482.17293854 g/mol
Topological Polar Surface Area (TPSA) 88.40 Ų
XlogP 6.20
Atomic LogP (AlogP) 6.14
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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886747-60-0
RefChem:173979
Phoyunnanin?E
orb1681003
HY-N9489
AKOS040762887
DA-66686
CS-0181895

2D Structure

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2D Structure of Phoyunnanin E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9660 96.60%
Caco-2 - 0.6856 68.56%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8068 80.68%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.8811 88.11%
OATP1B3 inhibitior + 0.9729 97.29%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9918 99.18%
P-glycoprotein inhibitior + 0.9113 91.13%
P-glycoprotein substrate - 0.8160 81.60%
CYP3A4 substrate + 0.6332 63.32%
CYP2C9 substrate - 0.6147 61.47%
CYP2D6 substrate + 0.5256 52.56%
CYP3A4 inhibition - 0.8034 80.34%
CYP2C9 inhibition + 0.5721 57.21%
CYP2C19 inhibition + 0.7080 70.80%
CYP2D6 inhibition - 0.7818 78.18%
CYP1A2 inhibition + 0.9583 95.83%
CYP2C8 inhibition + 0.8649 86.49%
CYP inhibitory promiscuity + 0.6155 61.55%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7920 79.20%
Carcinogenicity (trinary) Non-required 0.5256 52.56%
Eye corrosion - 0.9773 97.73%
Eye irritation - 0.8038 80.38%
Skin irritation - 0.5804 58.04%
Skin corrosion - 0.8887 88.87%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8940 89.40%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.8298 82.98%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.6394 63.94%
Acute Oral Toxicity (c) III 0.5762 57.62%
Estrogen receptor binding + 0.9331 93.31%
Androgen receptor binding + 0.8443 84.43%
Thyroid receptor binding + 0.7308 73.08%
Glucocorticoid receptor binding + 0.8342 83.42%
Aromatase binding + 0.6690 66.90%
PPAR gamma + 0.7752 77.52%
Honey bee toxicity - 0.8811 88.11%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6851 68.51%
Fish aquatic toxicity + 0.9226 92.26%

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 98.39% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 98.37% 98.35%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 97.95% 91.79%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.00% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.91% 95.56%
CHEMBL2056 P21728 Dopamine D1 receptor 94.24% 91.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.02% 96.09%
CHEMBL4208 P20618 Proteasome component C5 93.06% 90.00%
CHEMBL1951 P21397 Monoamine oxidase A 93.00% 91.49%
CHEMBL2535 P11166 Glucose transporter 90.84% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.76% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.22% 99.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.69% 95.89%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 88.39% 96.09%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 88.05% 82.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.00% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.66% 93.99%
CHEMBL2581 P07339 Cathepsin D 85.50% 98.95%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 85.44% 92.68%
CHEMBL267 P12931 Tyrosine-protein kinase SRC 84.69% 95.69%
CHEMBL1907 P15144 Aminopeptidase N 84.61% 93.31%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.45% 95.89%
CHEMBL261 P00915 Carbonic anhydrase I 83.91% 96.76%
CHEMBL5747 Q92793 CREB-binding protein 83.10% 95.12%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.76% 93.40%
CHEMBL3194 P02766 Transthyretin 82.54% 90.71%
CHEMBL205 P00918 Carbonic anhydrase II 82.51% 98.44%
CHEMBL1293289 P25440 Bromodomain-containing protein 2 81.88% 86.19%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.16% 91.07%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 80.88% 95.53%

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.
Coelogyne kouytcheensis

Cross-Links

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PubChem 11503968
LOTUS LTS0048900
wikiData Q105275996