9,10-Dihydro-2,3,5,6-tetramethoxyphenanthrene-1,4-dione

Details

Top
Internal ID db38e99f-46ec-4bb5-a1b8-06543bff0fe8
Taxonomy Phenylpropanoids and polyketides > Neoflavonoids > Dalbergiones
IUPAC Name 2,3,5,6-tetramethoxy-9,10-dihydrophenanthrene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H18O6/c1-21-11-8-6-9-5-7-10-13(12(9)16(11)22-2)15(20)18(24-4)17(23-3)14(10)19/h6,8H,5,7H2,1-4H3
InChI Key WFZYDHQWLRHFNX-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H18O6
Molecular Weight 330.30 g/mol
Exact Mass 330.11033829 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 9,10-Dihydro-2,3,5,6-tetramethoxyphenanthrene-1,4-dione

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.9319 93.19%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.8208 82.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9592 95.92%
OATP1B3 inhibitior + 0.9722 97.22%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6939 69.39%
P-glycoprotein inhibitior - 0.6814 68.14%
P-glycoprotein substrate - 0.8897 88.97%
CYP3A4 substrate + 0.5109 51.09%
CYP2C9 substrate - 0.8047 80.47%
CYP2D6 substrate - 0.7594 75.94%
CYP3A4 inhibition - 0.5732 57.32%
CYP2C9 inhibition - 0.5891 58.91%
CYP2C19 inhibition + 0.5223 52.23%
CYP2D6 inhibition - 0.9000 90.00%
CYP1A2 inhibition + 0.9094 90.94%
CYP2C8 inhibition - 0.8348 83.48%
CYP inhibitory promiscuity + 0.7278 72.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8935 89.35%
Carcinogenicity (trinary) Non-required 0.5725 57.25%
Eye corrosion - 0.9749 97.49%
Eye irritation + 0.5491 54.91%
Skin irritation - 0.7232 72.32%
Skin corrosion - 0.9659 96.59%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4236 42.36%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.7455 74.55%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5455 54.55%
Acute Oral Toxicity (c) III 0.4687 46.87%
Estrogen receptor binding + 0.8886 88.86%
Androgen receptor binding + 0.6276 62.76%
Thyroid receptor binding - 0.5514 55.14%
Glucocorticoid receptor binding + 0.8005 80.05%
Aromatase binding - 0.5888 58.88%
PPAR gamma + 0.5698 56.98%
Honey bee toxicity - 0.9401 94.01%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9843 98.43%

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 96.86% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.39% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.14% 93.99%
CHEMBL2535 P11166 Glucose transporter 87.89% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.79% 94.45%
CHEMBL2581 P07339 Cathepsin D 87.67% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.21% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.66% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.64% 91.11%
CHEMBL4208 P20618 Proteasome component C5 81.56% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.62% 99.23%

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.
Cannabis sativa

Cross-Links

Top
PubChem 129861810
LOTUS LTS0061346
wikiData Q105304270