9-Methoxy-1,7-dimethylphenanthrene

Details

Top
Internal ID 28ab0fcd-4849-43be-9547-d5dfcce0c7b7
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name 9-methoxy-1,7-dimethylphenanthrene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O/c1-11-7-8-14-13-6-4-5-12(2)15(13)10-17(18-3)16(14)9-11/h4-10H,1-3H3
InChI Key ZEHUSAJBGJTSFV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H16O
Molecular Weight 236.31 g/mol
Exact Mass 236.120115130 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.62
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 9-Methoxy-1,7-dimethylphenanthrene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9018 90.18%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.5486 54.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9599 95.99%
OATP1B3 inhibitior + 0.9720 97.20%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8400 84.00%
P-glycoprotein inhibitior - 0.7903 79.03%
P-glycoprotein substrate - 0.8495 84.95%
CYP3A4 substrate - 0.5284 52.84%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate + 0.4608 46.08%
CYP3A4 inhibition - 0.8329 83.29%
CYP2C9 inhibition - 0.8991 89.91%
CYP2C19 inhibition - 0.7060 70.60%
CYP2D6 inhibition - 0.8887 88.87%
CYP1A2 inhibition + 0.9571 95.71%
CYP2C8 inhibition + 0.5793 57.93%
CYP inhibitory promiscuity - 0.5148 51.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7483 74.83%
Carcinogenicity (trinary) Non-required 0.4480 44.80%
Eye corrosion - 0.9366 93.66%
Eye irritation + 0.9438 94.38%
Skin irritation - 0.7836 78.36%
Skin corrosion - 0.9864 98.64%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6723 67.23%
Micronuclear - 0.6434 64.34%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.5388 53.88%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6867 68.67%
Acute Oral Toxicity (c) III 0.7711 77.11%
Estrogen receptor binding + 0.9551 95.51%
Androgen receptor binding + 0.6971 69.71%
Thyroid receptor binding + 0.7301 73.01%
Glucocorticoid receptor binding + 0.7710 77.10%
Aromatase binding + 0.8592 85.92%
PPAR gamma - 0.4935 49.35%
Honey bee toxicity - 0.9339 93.39%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.8300 83.00%
Fish aquatic toxicity + 0.9184 91.84%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.86% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.22% 91.11%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 91.65% 89.62%
CHEMBL1907 P15144 Aminopeptidase N 89.51% 93.31%
CHEMBL2535 P11166 Glucose transporter 87.32% 98.75%
CHEMBL2581 P07339 Cathepsin D 86.83% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.40% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.76% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.00% 96.09%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 84.42% 94.67%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 84.28% 100.00%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 82.62% 95.70%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 82.57% 96.47%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.24% 93.65%

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.
Neoboutonia mannii

Cross-Links

Top
PubChem 91163854
LOTUS LTS0109615
wikiData Q105373269