Glycyrrhizin-6 inverted exclamation marka inverted exclamation marka-methylester

Details

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Internal ID d10b2e21-2683-4e97-8dc9-198e7f76ddc9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,11S,12aR,14aR,14bS)-11-carboxy-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]-3,4-dihydroxy-5-[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methoxycarbonyloxan-2-yl]oxyoxane-2-carboxylic acid
SMILES (Canonical) CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)OC)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)OC)O)O)O)C)(C)C(=O)O
InChI InChI=1S/C43H64O16/c1-38(2)22-9-12-43(7)32(21(44)17-19-20-18-40(4,37(53)54)14-13-39(20,3)15-16-42(19,43)6)41(22,5)11-10-23(38)56-36-31(27(48)26(47)29(57-36)33(50)51)59-35-28(49)24(45)25(46)30(58-35)34(52)55-8/h17,20,22-32,35-36,45-49H,9-16,18H2,1-8H3,(H,50,51)(H,53,54)/t20-,22-,23-,24-,25-,26-,27-,28+,29-,30-,31+,32+,35-,36+,39+,40-,41-,42+,43+/m0/s1
InChI Key JENBECQUKVEUTQ-ILVQQCHOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C43H64O16
Molecular Weight 837.00 g/mol
Exact Mass 836.41943595 g/mol
Topological Polar Surface Area (TPSA) 256.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 2.33
H-Bond Acceptor 14
H-Bond Donor 7
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Glycyrrhizin-6 inverted exclamation marka inverted exclamation marka-methylester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8721 87.21%
Caco-2 - 0.8780 87.80%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8056 80.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.4214 42.14%
OATP1B3 inhibitior - 0.2207 22.07%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.5929 59.29%
BSEP inhibitior + 0.6259 62.59%
P-glycoprotein inhibitior + 0.7656 76.56%
P-glycoprotein substrate - 0.6640 66.40%
CYP3A4 substrate + 0.7366 73.66%
CYP2C9 substrate - 0.7915 79.15%
CYP2D6 substrate - 0.8989 89.89%
CYP3A4 inhibition - 0.8410 84.10%
CYP2C9 inhibition - 0.8618 86.18%
CYP2C19 inhibition - 0.8904 89.04%
CYP2D6 inhibition - 0.9363 93.63%
CYP1A2 inhibition - 0.8318 83.18%
CYP2C8 inhibition + 0.7257 72.57%
CYP inhibitory promiscuity - 0.9607 96.07%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5998 59.98%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.9082 90.82%
Skin irritation - 0.5826 58.26%
Skin corrosion - 0.9281 92.81%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4523 45.23%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.6283 62.83%
skin sensitisation - 0.8232 82.32%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.6006 60.06%
Acute Oral Toxicity (c) IV 0.5139 51.39%
Estrogen receptor binding + 0.7874 78.74%
Androgen receptor binding + 0.7368 73.68%
Thyroid receptor binding - 0.7549 75.49%
Glucocorticoid receptor binding + 0.7459 74.59%
Aromatase binding + 0.6661 66.61%
PPAR gamma + 0.7881 78.81%
Honey bee toxicity - 0.6574 65.74%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9781 97.81%

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 99.19% 94.78%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.32% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.61% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 94.31% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.00% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.00% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.90% 95.89%
CHEMBL3714130 P46095 G-protein coupled receptor 6 87.95% 97.36%
CHEMBL1951 P21397 Monoamine oxidase A 86.74% 91.49%
CHEMBL2581 P07339 Cathepsin D 85.98% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.11% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.73% 91.07%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.10% 94.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.73% 93.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.52% 92.62%
CHEMBL340 P08684 Cytochrome P450 3A4 81.74% 91.19%

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 uralensis
Mitracarpus hirtus

Cross-Links

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PubChem 46226470
NPASS NPC262199