3,4,7-Trimethoxy-9,10-dihydrophenanthren-2-ol

Details

Top
Internal ID 0161741e-ea68-4649-84fb-9a663bedec51
Taxonomy Benzenoids > Phenanthrenes and derivatives > Hydrophenanthrenes
IUPAC Name 3,4,7-trimethoxy-9,10-dihydrophenanthren-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H18O4/c1-19-12-6-7-13-10(8-12)4-5-11-9-14(18)16(20-2)17(21-3)15(11)13/h6-9,18H,4-5H2,1-3H3
InChI Key QOROJTCHQYSUPK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H18O4
Molecular Weight 286.32 g/mol
Exact Mass 286.12050905 g/mol
Topological Polar Surface Area (TPSA) 47.90 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.18
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3,4,7-Trimethoxy-9,10-dihydrophenanthren-2-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9783 97.83%
Caco-2 + 0.9259 92.59%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7701 77.01%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior + 0.9197 91.97%
OATP1B3 inhibitior + 0.9664 96.64%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6157 61.57%
P-glycoprotein inhibitior - 0.9086 90.86%
P-glycoprotein substrate - 0.9401 94.01%
CYP3A4 substrate + 0.5273 52.73%
CYP2C9 substrate - 0.6180 61.80%
CYP2D6 substrate + 0.5879 58.79%
CYP3A4 inhibition - 0.7907 79.07%
CYP2C9 inhibition - 0.8186 81.86%
CYP2C19 inhibition + 0.5434 54.34%
CYP2D6 inhibition - 0.8958 89.58%
CYP1A2 inhibition + 0.9226 92.26%
CYP2C8 inhibition - 0.6362 63.62%
CYP inhibitory promiscuity - 0.5602 56.02%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8020 80.20%
Carcinogenicity (trinary) Non-required 0.5279 52.79%
Eye corrosion - 0.9797 97.97%
Eye irritation + 0.6578 65.78%
Skin irritation - 0.6525 65.25%
Skin corrosion - 0.9414 94.14%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7431 74.31%
Micronuclear - 0.6100 61.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8736 87.36%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7290 72.90%
Acute Oral Toxicity (c) III 0.5318 53.18%
Estrogen receptor binding + 0.8343 83.43%
Androgen receptor binding + 0.6292 62.92%
Thyroid receptor binding + 0.7262 72.62%
Glucocorticoid receptor binding + 0.7794 77.94%
Aromatase binding + 0.6792 67.92%
PPAR gamma + 0.5717 57.17%
Honey bee toxicity - 0.9533 95.33%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9207 92.07%

Targets

Top

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 98.64% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.63% 91.49%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 94.49% 91.79%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.94% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.13% 95.56%
CHEMBL4208 P20618 Proteasome component C5 90.97% 90.00%
CHEMBL2581 P07339 Cathepsin D 90.72% 98.95%
CHEMBL2056 P21728 Dopamine D1 receptor 90.40% 91.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.35% 99.15%
CHEMBL2535 P11166 Glucose transporter 85.69% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.37% 93.99%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.52% 93.40%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.88% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.82% 94.00%
CHEMBL1907 P15144 Aminopeptidase N 82.47% 93.31%
CHEMBL242 Q92731 Estrogen receptor beta 81.95% 98.35%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.93% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.51% 99.17%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.71% 96.67%

Plants that contains it

Top
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

Top
PubChem 44445441
NPASS NPC294884
LOTUS LTS0068713
wikiData Q105225076