1-(2-Hydroxy-3,4,7-trimethoxy-9,10-dihydrophenanthren-1-yl)-3,4,7-trimethoxy-9,10-dihydrophenanthren-2-ol

Details

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Internal ID 9cb1125a-740d-4e83-8564-1ceefec0fe6e
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name 1-(2-hydroxy-3,4,7-trimethoxy-9,10-dihydrophenanthren-1-yl)-3,4,7-trimethoxy-9,10-dihydrophenanthren-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H34O8/c1-37-19-9-13-21-17(15-19)7-11-23-25(21)31(39-3)33(41-5)29(35)27(23)28-24-12-8-18-16-20(38-2)10-14-22(18)26(24)32(40-4)34(42-6)30(28)36/h9-10,13-16,35-36H,7-8,11-12H2,1-6H3
InChI Key DHZIKJUILFCXKY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C34H34O8
Molecular Weight 570.60 g/mol
Exact Mass 570.22536804 g/mol
Topological Polar Surface Area (TPSA) 95.80 Ų
XlogP 6.50
Atomic LogP (AlogP) 6.35
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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SCHEMBL23203388

2D Structure

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2D Structure of 1-(2-Hydroxy-3,4,7-trimethoxy-9,10-dihydrophenanthren-1-yl)-3,4,7-trimethoxy-9,10-dihydrophenanthren-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9732 97.32%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8459 84.59%
OATP2B1 inhibitior - 0.7271 72.71%
OATP1B1 inhibitior + 0.8788 87.88%
OATP1B3 inhibitior + 0.9291 92.91%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9544 95.44%
P-glycoprotein inhibitior + 0.9037 90.37%
P-glycoprotein substrate - 0.9294 92.94%
CYP3A4 substrate + 0.5529 55.29%
CYP2C9 substrate - 0.6180 61.80%
CYP2D6 substrate + 0.5879 58.79%
CYP3A4 inhibition - 0.7819 78.19%
CYP2C9 inhibition + 0.5191 51.91%
CYP2C19 inhibition + 0.6065 60.65%
CYP2D6 inhibition - 0.8682 86.82%
CYP1A2 inhibition + 0.8887 88.87%
CYP2C8 inhibition + 0.5453 54.53%
CYP inhibitory promiscuity + 0.6573 65.73%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8020 80.20%
Carcinogenicity (trinary) Non-required 0.5105 51.05%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.7801 78.01%
Skin irritation - 0.7026 70.26%
Skin corrosion - 0.9278 92.78%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8804 88.04%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.9012 90.12%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.7776 77.76%
Acute Oral Toxicity (c) III 0.5622 56.22%
Estrogen receptor binding + 0.8752 87.52%
Androgen receptor binding + 0.7699 76.99%
Thyroid receptor binding + 0.7529 75.29%
Glucocorticoid receptor binding + 0.8409 84.09%
Aromatase binding + 0.7266 72.66%
PPAR gamma + 0.7005 70.05%
Honey bee toxicity - 0.9481 94.81%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9440 94.40%

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 98.88% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.87% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.61% 96.09%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 93.28% 91.79%
CHEMBL2581 P07339 Cathepsin D 92.45% 98.95%
CHEMBL4208 P20618 Proteasome component C5 92.41% 90.00%
CHEMBL2056 P21728 Dopamine D1 receptor 92.14% 91.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.97% 95.56%
CHEMBL2535 P11166 Glucose transporter 87.61% 98.75%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.73% 96.12%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.09% 99.15%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.70% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.39% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.19% 94.00%
CHEMBL1907 P15144 Aminopeptidase N 84.17% 93.31%
CHEMBL242 Q92731 Estrogen receptor beta 82.71% 98.35%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.34% 93.40%
CHEMBL4581 P52732 Kinesin-like protein 1 81.87% 93.18%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.73% 99.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.45% 95.89%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.10% 96.67%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.93% 93.99%

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.
Dendrobium nobile

Cross-Links

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PubChem 24762427
NPASS NPC262297
LOTUS LTS0086243
wikiData Q104981059