Glycyrrhizinate(3-)

Details

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Internal ID c7b92669-4d66-4cae-bc15-1899d2447442
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name (2S,3S,4S,5R,6R)-6-[(2S,3R,4S,5S,6S)-2-[[(3S,4aR,6aR,6bS,8aS,11S,12aR,14aR,14bS)-11-carboxylato-4,4,6a,6b,8a,11,14b-heptamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl]oxy]-6-carboxylato-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate
SMILES (Canonical) CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)C(=O)[O-])O)O)OC5C(C(C(C(O5)C(=O)[O-])O)O)O)C)C(=O)C=C6C3(CCC7(C6CC(CC7)(C)C(=O)[O-])C)C)C)C
SMILES (Isomeric) C[C@]12CC[C@](C[C@H]1C3=CC(=O)[C@@H]4[C@]5(CC[C@@H](C([C@@H]5CC[C@]4([C@@]3(CC2)C)C)(C)C)O[C@@H]6[C@@H]([C@H]([C@@H]([C@H](O6)C(=O)[O-])O)O)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)C(=O)[O-])O)O)O)C)(C)C(=O)[O-]
InChI InChI=1S/C42H62O16/c1-37(2)21-8-11-42(7)31(20(43)16-18-19-17-39(4,36(53)54)13-12-38(19,3)14-15-41(18,42)6)40(21,5)10-9-22(37)55-35-30(26(47)25(46)29(57-35)33(51)52)58-34-27(48)23(44)24(45)28(56-34)32(49)50/h16,19,21-31,34-35,44-48H,8-15,17H2,1-7H3,(H,49,50)(H,51,52)(H,53,54)/p-3/t19-,21-,22-,23-,24-,25-,26-,27+,28-,29-,30+,31+,34-,35-,38+,39-,40-,41+,42+/m0/s1
InChI Key LPLVUJXQOOQHMX-QWBHMCJMSA-K
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C42H59O16-3
Molecular Weight 819.90 g/mol
Exact Mass 819.38031079 g/mol
Topological Polar Surface Area (TPSA) 276.00 Ų
XlogP 5.70
Atomic LogP (AlogP) -1.76
H-Bond Acceptor 16
H-Bond Donor 5
Rotatable Bonds 7

Synonyms

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CHEBI:29807
LS-190360
Q27104090
(3beta,20beta)-20-Carboxy-11-oxo-30-norolean-12-en-3-yl-2-O-beta-D-glucuronosyl-beta-D-glucosiduronic acid

2D Structure

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2D Structure of Glycyrrhizinate(3-)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7183 71.83%
Caco-2 - 0.8793 87.93%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7919 79.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.4313 43.13%
OATP1B3 inhibitior + 0.8159 81.59%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior + 0.6059 60.59%
P-glycoprotein inhibitior + 0.7608 76.08%
P-glycoprotein substrate - 0.7295 72.95%
CYP3A4 substrate + 0.7366 73.66%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate - 0.8886 88.86%
CYP3A4 inhibition - 0.8342 83.42%
CYP2C9 inhibition - 0.8879 88.79%
CYP2C19 inhibition - 0.9258 92.58%
CYP2D6 inhibition - 0.9363 93.63%
CYP1A2 inhibition - 0.8311 83.11%
CYP2C8 inhibition + 0.6561 65.61%
CYP inhibitory promiscuity - 0.9675 96.75%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5645 56.45%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9082 90.82%
Skin irritation - 0.5626 56.26%
Skin corrosion - 0.9181 91.81%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4544 45.44%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.5678 56.78%
skin sensitisation - 0.8055 80.55%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5106 51.06%
Acute Oral Toxicity (c) IV 0.4850 48.50%
Estrogen receptor binding + 0.7736 77.36%
Androgen receptor binding + 0.7324 73.24%
Thyroid receptor binding - 0.8319 83.19%
Glucocorticoid receptor binding + 0.7152 71.52%
Aromatase binding + 0.6753 67.53%
PPAR gamma + 0.7700 77.00%
Honey bee toxicity - 0.7144 71.44%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5250 52.50%
Fish aquatic toxicity + 0.9851 98.51%

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
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 98.87% 94.78%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.89% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.09% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.84% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.67% 95.56%
CHEMBL3714130 P46095 G-protein coupled receptor 6 92.66% 97.36%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.08% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.75% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.37% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.36% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.42% 97.09%
CHEMBL5255 O00206 Toll-like receptor 4 82.93% 92.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.40% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.15% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.08% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.05% 95.71%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.60% 97.14%

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

Cross-Links

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PubChem 5460305
NPASS NPC278983