1,6-Bis(4-hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol

Details

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Internal ID e0b28aba-4ae1-4ed6-8460-48b181a644aa
Taxonomy Benzenoids > Phenanthrenes and derivatives > Hydrophenanthrenes
IUPAC Name 1,6-bis[(4-hydroxyphenyl)methyl]-4-methoxy-9,10-dihydrophenanthrene-2,7-diol
SMILES (Canonical) COC1=C2C(=C(C(=C1)O)CC3=CC=C(C=C3)O)CCC4=CC(=C(C=C42)CC5=CC=C(C=C5)O)O
SMILES (Isomeric) COC1=C2C(=C(C(=C1)O)CC3=CC=C(C=C3)O)CCC4=CC(=C(C=C42)CC5=CC=C(C=C5)O)O
InChI InChI=1S/C29H26O5/c1-34-28-16-27(33)25(13-18-4-9-22(31)10-5-18)23-11-6-19-15-26(32)20(14-24(19)29(23)28)12-17-2-7-21(30)8-3-17/h2-5,7-10,14-16,30-33H,6,11-13H2,1H3
InChI Key ZDIPZSHKEZTSRZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H26O5
Molecular Weight 454.50 g/mol
Exact Mass 454.17802393 g/mol
Topological Polar Surface Area (TPSA) 90.20 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.46
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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1,6-Bis(4-hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol

2D Structure

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2D Structure of 1,6-Bis(4-hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9818 98.18%
Caco-2 - 0.7923 79.23%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.9034 90.34%
OATP2B1 inhibitior - 0.7142 71.42%
OATP1B1 inhibitior + 0.8198 81.98%
OATP1B3 inhibitior + 0.9571 95.71%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9358 93.58%
P-glycoprotein inhibitior + 0.9180 91.80%
P-glycoprotein substrate - 0.5660 56.60%
CYP3A4 substrate + 0.5974 59.74%
CYP2C9 substrate - 0.6180 61.80%
CYP2D6 substrate + 0.5879 58.79%
CYP3A4 inhibition - 0.6891 68.91%
CYP2C9 inhibition + 0.5650 56.50%
CYP2C19 inhibition + 0.8178 81.78%
CYP2D6 inhibition - 0.8128 81.28%
CYP1A2 inhibition + 0.9482 94.82%
CYP2C8 inhibition + 0.8531 85.31%
CYP inhibitory promiscuity + 0.6401 64.01%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7332 73.32%
Carcinogenicity (trinary) Non-required 0.5921 59.21%
Eye corrosion - 0.9835 98.35%
Eye irritation - 0.6953 69.53%
Skin irritation - 0.6940 69.40%
Skin corrosion - 0.9055 90.55%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9188 91.88%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8743 87.43%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6473 64.73%
Acute Oral Toxicity (c) III 0.5891 58.91%
Estrogen receptor binding + 0.9020 90.20%
Androgen receptor binding + 0.8281 82.81%
Thyroid receptor binding + 0.6306 63.06%
Glucocorticoid receptor binding + 0.7432 74.32%
Aromatase binding + 0.5535 55.35%
PPAR gamma + 0.7490 74.90%
Honey bee toxicity - 0.8266 82.66%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.5851 58.51%
Fish aquatic toxicity + 0.9856 98.56%

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 98.34% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.63% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.87% 98.95%
CHEMBL2535 P11166 Glucose transporter 95.46% 98.75%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 94.48% 91.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.96% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 93.38% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.21% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.57% 95.89%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 91.42% 95.17%
CHEMBL242 Q92731 Estrogen receptor beta 89.67% 98.35%
CHEMBL4208 P20618 Proteasome component C5 88.98% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.71% 94.00%
CHEMBL261 P00915 Carbonic anhydrase I 88.53% 96.76%
CHEMBL5747 Q92793 CREB-binding protein 88.31% 95.12%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 88.29% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.03% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.48% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.20% 94.45%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.23% 91.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.01% 93.99%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 82.58% 95.78%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.39% 92.62%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.37% 96.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.73% 95.50%
CHEMBL5896 O75164 Lysine-specific demethylase 4A 80.48% 99.09%
CHEMBL1255126 O15151 Protein Mdm4 80.47% 90.20%

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.
Bletilla formosana
Bletilla striata
Syzygium aromaticum

Cross-Links

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PubChem 14630663
NPASS NPC165273
LOTUS LTS0032806
wikiData Q105372263