(4S)-4,9-dihydroxy-6-(hydroxymethyl)-8-methoxy-3,4-dihydro-2H-anthracen-1-one

Details

Top
Internal ID a073f780-28d0-4131-8301-bf9b3280296c
Taxonomy Benzenoids > Anthracenes
IUPAC Name (4S)-4,9-dihydroxy-6-(hydroxymethyl)-8-methoxy-3,4-dihydro-2H-anthracen-1-one
SMILES (Canonical) COC1=CC(=CC2=CC3=C(C(=O)CCC3O)C(=C21)O)CO
SMILES (Isomeric) COC1=CC(=CC2=CC3=C(C(=O)CC[C@@H]3O)C(=C21)O)CO
InChI InChI=1S/C16H16O5/c1-21-13-5-8(7-17)4-9-6-10-11(18)2-3-12(19)15(10)16(20)14(9)13/h4-6,11,17-18,20H,2-3,7H2,1H3/t11-/m0/s1
InChI Key BUZTYRAHGBWBIQ-NSHDSACASA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H16O5
Molecular Weight 288.29 g/mol
Exact Mass 288.09977361 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (4S)-4,9-dihydroxy-6-(hydroxymethyl)-8-methoxy-3,4-dihydro-2H-anthracen-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 - 0.6775 67.75%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8614 86.14%
OATP2B1 inhibitior - 0.5725 57.25%
OATP1B1 inhibitior + 0.8216 82.16%
OATP1B3 inhibitior + 0.9554 95.54%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8051 80.51%
P-glycoprotein inhibitior - 0.9070 90.70%
P-glycoprotein substrate - 0.7133 71.33%
CYP3A4 substrate + 0.5874 58.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7640 76.40%
CYP3A4 inhibition - 0.5901 59.01%
CYP2C9 inhibition - 0.6847 68.47%
CYP2C19 inhibition + 0.6938 69.38%
CYP2D6 inhibition - 0.8168 81.68%
CYP1A2 inhibition + 0.9463 94.63%
CYP2C8 inhibition + 0.4725 47.25%
CYP inhibitory promiscuity - 0.6072 60.72%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6684 66.84%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.7326 73.26%
Skin irritation - 0.7728 77.28%
Skin corrosion - 0.9614 96.14%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7082 70.82%
Micronuclear - 0.6382 63.82%
Hepatotoxicity - 0.5948 59.48%
skin sensitisation - 0.8986 89.86%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.8018 80.18%
Acute Oral Toxicity (c) III 0.7269 72.69%
Estrogen receptor binding + 0.7556 75.56%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5291 52.91%
Glucocorticoid receptor binding + 0.7576 75.76%
Aromatase binding - 0.6348 63.48%
PPAR gamma + 0.8357 83.57%
Honey bee toxicity - 0.8704 87.04%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6349 63.49%
Fish aquatic toxicity - 0.3653 36.53%

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 98.56% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.70% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.73% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.50% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.49% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.29% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.31% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.92% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.53% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.97% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.47% 92.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.23% 90.71%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.74% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.29% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.62% 93.99%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.13% 96.21%

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.
Eremurus chinensis

Cross-Links

Top
PubChem 10779698
LOTUS LTS0090285
wikiData Q104946417