(3S,4S)-6-hydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5,7-dimethoxy-3,4-dihydronaphthalene-2-carboxylic acid

Details

Top
Internal ID 07de4243-faad-4e46-8244-1532e16def4b
Taxonomy Lignans, neolignans and related compounds > Aryltetralin lignans
IUPAC Name (3S,4S)-6-hydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5,7-dimethoxy-3,4-dihydronaphthalene-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H24O9/c1-28-14-7-11(8-15(29-2)19(14)24)17-13(9-23)12(22(26)27)5-10-6-16(30-3)20(25)21(31-4)18(10)17/h5-8,13,17,23-25H,9H2,1-4H3,(H,26,27)/t13-,17-/m1/s1
InChI Key XCPQBTNKYMMDJL-CXAGYDPISA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C22H24O9
Molecular Weight 432.40 g/mol
Exact Mass 432.14203234 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.35
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3S,4S)-6-hydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5,7-dimethoxy-3,4-dihydronaphthalene-2-carboxylic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9839 98.39%
Caco-2 - 0.5261 52.61%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7959 79.59%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.8376 83.76%
OATP1B3 inhibitior + 0.8563 85.63%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7687 76.87%
P-glycoprotein inhibitior - 0.5860 58.60%
P-glycoprotein substrate - 0.8003 80.03%
CYP3A4 substrate + 0.5215 52.15%
CYP2C9 substrate - 0.7958 79.58%
CYP2D6 substrate - 0.8499 84.99%
CYP3A4 inhibition - 0.7800 78.00%
CYP2C9 inhibition + 0.6351 63.51%
CYP2C19 inhibition + 0.5743 57.43%
CYP2D6 inhibition - 0.8185 81.85%
CYP1A2 inhibition + 0.7147 71.47%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.8156 81.56%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9020 90.20%
Carcinogenicity (trinary) Non-required 0.6796 67.96%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.6785 67.85%
Skin irritation - 0.7839 78.39%
Skin corrosion - 0.9728 97.28%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6089 60.89%
Micronuclear + 0.6474 64.74%
Hepatotoxicity - 0.6341 63.41%
skin sensitisation - 0.8423 84.23%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8375 83.75%
Acute Oral Toxicity (c) III 0.5008 50.08%
Estrogen receptor binding + 0.7874 78.74%
Androgen receptor binding + 0.6856 68.56%
Thyroid receptor binding + 0.6975 69.75%
Glucocorticoid receptor binding + 0.8331 83.31%
Aromatase binding - 0.7410 74.10%
PPAR gamma + 0.5907 59.07%
Honey bee toxicity - 0.8698 86.98%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9911 99.11%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.84% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.89% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.68% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.09% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.08% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.65% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.63% 95.56%
CHEMBL2581 P07339 Cathepsin D 85.10% 98.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.20% 86.92%

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.
Ulmus thomasii

Cross-Links

Top
PubChem 92168874
LOTUS LTS0202865
wikiData Q105325320