7-Methoxy-1-[(4-methoxyphenyl)methyl]-9,10-dihydrophenanthrene-2,4-diol

Details

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Internal ID 6fb43e22-1f69-48ba-8193-ca41f5569afe
Taxonomy Benzenoids > Phenanthrenes and derivatives > Hydrophenanthrenes
IUPAC Name 7-methoxy-1-[(4-methoxyphenyl)methyl]-9,10-dihydrophenanthrene-2,4-diol
SMILES (Canonical) COC1=CC=C(C=C1)CC2=C3CCC4=C(C3=C(C=C2O)O)C=CC(=C4)OC
SMILES (Isomeric) COC1=CC=C(C=C1)CC2=C3CCC4=C(C3=C(C=C2O)O)C=CC(=C4)OC
InChI InChI=1S/C23H22O4/c1-26-16-6-3-14(4-7-16)11-20-19-9-5-15-12-17(27-2)8-10-18(15)23(19)22(25)13-21(20)24/h3-4,6-8,10,12-13,24-25H,5,9,11H2,1-2H3
InChI Key MYHHFXMCMGRTKV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H22O4
Molecular Weight 362.40 g/mol
Exact Mass 362.15180918 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.47
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Methoxy-1-[(4-methoxyphenyl)methyl]-9,10-dihydrophenanthrene-2,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9579 95.79%
Caco-2 + 0.5405 54.05%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8664 86.64%
OATP2B1 inhibitior - 0.7147 71.47%
OATP1B1 inhibitior + 0.8527 85.27%
OATP1B3 inhibitior + 0.9356 93.56%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9507 95.07%
P-glycoprotein inhibitior + 0.7384 73.84%
P-glycoprotein substrate - 0.7523 75.23%
CYP3A4 substrate + 0.5628 56.28%
CYP2C9 substrate - 0.6180 61.80%
CYP2D6 substrate + 0.5879 58.79%
CYP3A4 inhibition - 0.6227 62.27%
CYP2C9 inhibition - 0.5684 56.84%
CYP2C19 inhibition + 0.7075 70.75%
CYP2D6 inhibition - 0.7097 70.97%
CYP1A2 inhibition + 0.9154 91.54%
CYP2C8 inhibition + 0.5643 56.43%
CYP inhibitory promiscuity + 0.7147 71.47%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7911 79.11%
Carcinogenicity (trinary) Non-required 0.7017 70.17%
Eye corrosion - 0.9817 98.17%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.7470 74.70%
Skin corrosion - 0.8585 85.85%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8698 86.98%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.8420 84.20%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.8368 83.68%
Acute Oral Toxicity (c) III 0.5853 58.53%
Estrogen receptor binding + 0.9449 94.49%
Androgen receptor binding + 0.8803 88.03%
Thyroid receptor binding + 0.7890 78.90%
Glucocorticoid receptor binding + 0.8341 83.41%
Aromatase binding + 0.5412 54.12%
PPAR gamma + 0.9142 91.42%
Honey bee toxicity - 0.8867 88.67%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9858 98.58%

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 99.32% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.52% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.91% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.30% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.76% 95.56%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 91.56% 91.79%
CHEMBL4208 P20618 Proteasome component C5 90.79% 90.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.76% 93.40%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.26% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.83% 93.99%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 88.67% 95.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.98% 99.17%
CHEMBL2535 P11166 Glucose transporter 87.64% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.54% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.67% 99.15%
CHEMBL226 P30542 Adenosine A1 receptor 84.36% 95.93%
CHEMBL4581 P52732 Kinesin-like protein 1 83.26% 93.18%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.25% 86.33%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 82.94% 95.70%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 82.54% 95.53%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.19% 92.68%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.05% 96.95%
CHEMBL3820 P35557 Hexokinase type IV 81.86% 91.96%
CHEMBL261 P00915 Carbonic anhydrase I 81.16% 96.76%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.74% 97.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.13% 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.
Pleione formosana

Cross-Links

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PubChem 162846909
LOTUS LTS0048925
wikiData Q105174895