Neoliquiritin

Details

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Internal ID 52f4003f-a104-473f-8de5-941732a0a8b7
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name (2S)-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one
SMILES (Canonical) C1C(OC2=C(C1=O)C=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O
SMILES (Isomeric) C1[C@H](OC2=C(C1=O)C=CC(=C2)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)C4=CC=C(C=C4)O
InChI InChI=1S/C21H22O9/c22-9-17-18(25)19(26)20(27)21(30-17)28-12-5-6-13-14(24)8-15(29-16(13)7-12)10-1-3-11(23)4-2-10/h1-7,15,17-23,25-27H,8-9H2/t15-,17+,18+,19-,20+,21+/m0/s1
InChI Key HJBUYKZTEBZNSH-ZRWXNEIDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O9
Molecular Weight 418.40 g/mol
Exact Mass 418.12638228 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.28
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

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5088-75-5
Liquiritigenin 7-beta-D-glucopyranoside
UNII-5X51Y867TK
5X51Y867TK
4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-2,3-dihydro-2-(4-hydroxyphenyl)-, (2S)-
CHEBI:191812
DTXSID501317518
(2S)-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one
HY-N2123
AKOS030530352
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Neoliquiritin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5116 51.16%
Caco-2 - 0.9314 93.14%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Mitochondria 0.6068 60.68%
OATP2B1 inhibitior - 0.5739 57.39%
OATP1B1 inhibitior + 0.8962 89.62%
OATP1B3 inhibitior + 0.9265 92.65%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6004 60.04%
P-glycoprotein inhibitior - 0.7250 72.50%
P-glycoprotein substrate - 0.8704 87.04%
CYP3A4 substrate + 0.6073 60.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8143 81.43%
CYP3A4 inhibition - 0.9193 91.93%
CYP2C9 inhibition - 0.9296 92.96%
CYP2C19 inhibition - 0.9289 92.89%
CYP2D6 inhibition - 0.9513 95.13%
CYP1A2 inhibition - 0.9084 90.84%
CYP2C8 inhibition + 0.4637 46.37%
CYP inhibitory promiscuity - 0.7728 77.28%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7144 71.44%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.9111 91.11%
Skin irritation - 0.8036 80.36%
Skin corrosion - 0.9691 96.91%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5683 56.83%
Micronuclear + 0.6533 65.33%
Hepatotoxicity - 0.8000 80.00%
skin sensitisation - 0.9122 91.22%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.4045 40.45%
Estrogen receptor binding + 0.6467 64.67%
Androgen receptor binding - 0.5157 51.57%
Thyroid receptor binding - 0.5302 53.02%
Glucocorticoid receptor binding - 0.4633 46.33%
Aromatase binding + 0.5282 52.82%
PPAR gamma + 0.7780 77.80%
Honey bee toxicity - 0.7350 73.50%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5950 59.50%
Fish aquatic toxicity + 0.8218 82.18%

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 99.28% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 97.53% 97.09%
CHEMBL2581 P07339 Cathepsin D 95.37% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.14% 96.09%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 93.00% 96.21%
CHEMBL4208 P20618 Proteasome component C5 89.47% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.27% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.05% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.92% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.23% 94.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.37% 86.92%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.64% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.59% 86.33%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.17% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.01% 99.15%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 85.38% 95.78%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 84.28% 85.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.79% 90.71%
CHEMBL2243 O00519 Anandamide amidohydrolase 80.82% 97.53%
CHEMBL242 Q92731 Estrogen receptor beta 80.49% 98.35%

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.
Glycyrrhiza glabra
Glycyrrhiza inflata
Glycyrrhiza uralensis
Glycyrrhiza uralensis
Mitracarpus hirtus

Cross-Links

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PubChem 51666248
NPASS NPC249374
LOTUS LTS0089772
wikiData Q27262993