2-(7-Hydroxy-4-methoxyphenanthren-2-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID 48f47c59-c0b0-43ea-9e9a-e46d0c57a754
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 2-(7-hydroxy-4-methoxyphenanthren-2-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) COC1=C2C(=CC(=C1)OC3C(C(C(C(O3)CO)O)O)O)C=CC4=C2C=CC(=C4)O
SMILES (Isomeric) COC1=C2C(=CC(=C1)OC3C(C(C(C(O3)CO)O)O)O)C=CC4=C2C=CC(=C4)O
InChI InChI=1S/C21H22O8/c1-27-15-8-13(28-21-20(26)19(25)18(24)16(9-22)29-21)7-11-3-2-10-6-12(23)4-5-14(10)17(11)15/h2-8,16,18-26H,9H2,1H3
InChI Key WMZBYVNQADXHMK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O8
Molecular Weight 402.40 g/mol
Exact Mass 402.13146766 g/mol
Topological Polar Surface Area (TPSA) 129.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 0.89
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(7-Hydroxy-4-methoxyphenanthren-2-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6352 63.52%
Caco-2 - 0.8898 88.98%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.4980 49.80%
OATP2B1 inhibitior - 0.7105 71.05%
OATP1B1 inhibitior + 0.9072 90.72%
OATP1B3 inhibitior + 0.9760 97.60%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7317 73.17%
P-glycoprotein inhibitior - 0.7896 78.96%
P-glycoprotein substrate - 0.6706 67.06%
CYP3A4 substrate + 0.5483 54.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7747 77.47%
CYP3A4 inhibition - 0.9043 90.43%
CYP2C9 inhibition - 0.9220 92.20%
CYP2C19 inhibition - 0.8567 85.67%
CYP2D6 inhibition - 0.9072 90.72%
CYP1A2 inhibition - 0.8165 81.65%
CYP2C8 inhibition + 0.6655 66.55%
CYP inhibitory promiscuity - 0.7449 74.49%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6128 61.28%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.9297 92.97%
Skin irritation - 0.8292 82.92%
Skin corrosion - 0.9656 96.56%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6988 69.88%
Micronuclear + 0.5659 56.59%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.9221 92.21%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.7801 78.01%
Acute Oral Toxicity (c) III 0.7324 73.24%
Estrogen receptor binding + 0.5988 59.88%
Androgen receptor binding + 0.5761 57.61%
Thyroid receptor binding + 0.6427 64.27%
Glucocorticoid receptor binding + 0.6856 68.56%
Aromatase binding + 0.6759 67.59%
PPAR gamma + 0.7336 73.36%
Honey bee toxicity - 0.8240 82.40%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5449 54.49%
Fish aquatic toxicity - 0.4591 45.91%

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 98.78% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.33% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.76% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 91.80% 89.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.65% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.28% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.96% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.61% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.48% 92.94%
CHEMBL220 P22303 Acetylcholinesterase 84.28% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.99% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.11% 89.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.01% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.67% 92.62%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.41% 86.92%
CHEMBL242 Q92731 Estrogen receptor beta 82.20% 98.35%
CHEMBL3401 O75469 Pregnane X receptor 80.82% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.66% 95.56%
CHEMBL4208 P20618 Proteasome component C5 80.57% 90.00%

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.
Bletilla striata

Cross-Links

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PubChem 162931423
LOTUS LTS0011406
wikiData Q105308927