7-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-1,2-dihydronaphthalene-2,3-dicarboxylic acid

Details

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Internal ID fc9eac95-45bd-4490-abe2-31c62978482d
Taxonomy Lignans, neolignans and related compounds > Aryltetralin lignans
IUPAC Name 7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-1,2-dihydronaphthalene-2,3-dicarboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H22O10/c1-29-12-7-10(8-13(30-2)18(12)23)15-16-9(5-11(21(25)26)17(15)22(27)28)6-14(31-3)19(24)20(16)32-4/h5-8,15,17,23-24H,1-4H3,(H,25,26)(H,27,28)
InChI Key MQRBOKLXGOXXGG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H22O10
Molecular Weight 446.40 g/mol
Exact Mass 446.12129689 g/mol
Topological Polar Surface Area (TPSA) 152.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-1,2-dihydronaphthalene-2,3-dicarboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 - 0.5881 58.81%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7955 79.55%
OATP2B1 inhibitior - 0.7158 71.58%
OATP1B1 inhibitior + 0.8618 86.18%
OATP1B3 inhibitior - 0.2329 23.29%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6120 61.20%
P-glycoprotein inhibitior - 0.5067 50.67%
P-glycoprotein substrate - 0.8572 85.72%
CYP3A4 substrate + 0.5447 54.47%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.8496 84.96%
CYP3A4 inhibition - 0.8548 85.48%
CYP2C9 inhibition + 0.5209 52.09%
CYP2C19 inhibition - 0.6103 61.03%
CYP2D6 inhibition - 0.8781 87.81%
CYP1A2 inhibition - 0.5229 52.29%
CYP2C8 inhibition + 0.5767 57.67%
CYP inhibitory promiscuity + 0.5557 55.57%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9017 90.17%
Carcinogenicity (trinary) Non-required 0.4328 43.28%
Eye corrosion - 0.9943 99.43%
Eye irritation - 0.5784 57.84%
Skin irritation - 0.7328 73.28%
Skin corrosion - 0.9725 97.25%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7292 72.92%
Micronuclear + 0.8300 83.00%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.8540 85.40%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8592 85.92%
Acute Oral Toxicity (c) II 0.4376 43.76%
Estrogen receptor binding + 0.7444 74.44%
Androgen receptor binding + 0.5924 59.24%
Thyroid receptor binding + 0.6282 62.82%
Glucocorticoid receptor binding + 0.7641 76.41%
Aromatase binding - 0.7668 76.68%
PPAR gamma + 0.6004 60.04%
Honey bee toxicity - 0.8266 82.66%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.9974 99.74%

Targets

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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%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.80% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.49% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.49% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.17% 96.00%
CHEMBL2535 P11166 Glucose transporter 86.05% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.94% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.75% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.16% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.97% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.05% 95.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.03% 92.62%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.92% 92.94%

Plants that contains it

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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

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PubChem 12444312
LOTUS LTS0138735
wikiData Q105170220