This website is for informational and educational purposes only. Please do not self-medicate; contact a medical professional for advice before administration. This website is for informational and educational purposes only. Please do not self-medicate; contact a medical professional for advice before administration.

Ammonium Glycyrrhizate

PubChem CID: 62074

Connections displayed (default: 10).
Loading graph...

ℹ️ Click here to know more about the properties
Compound Synonyms Ammonium glycyrrhizate, AMMONIUM GLYCYRRHIZINATE, 53956-04-0, Glycamil, Monoammonium glycyrrhizinate, Glycyrram, Monoammonium glycyrrhizate, Ammoniated glycyrrhizin, 1407-03-0, Glycyrrhizic acid ammonium salt, Glycyrrhizic acid, ammonium salt, Glycyrrhizic acid, monoammonium salt, FEMA No. 2528, AMGZ, CCRIS 1897, Glycyrrhizinic acid, ammonium salt (1:1), NSC 2800, EINECS 258-887-7, UNII-3VRD35U26C, Glycyrrhizin, ammoniated, 3VRD35U26C, Ammonium Glycyrrhizinate (AMGZ), Glycyrrhizin, ammoniated (Glycyrrhiza spp.), Glycyron No.1 (TN), Ammonium glycyrrhizate (NF), MFCD00167400, Monoammonium glycyrrhizinate (JAN), AMMONIUM GLYCYRRHIZATE [II], NSC-2800, NSC-35348, alpha-D-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-D-glucopyranuronosyl-,, AMMONIUM GLYCYRRHIZATE [USP-RS], Monoammonium (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-D-glucopyranuronosyl-alpha-D-glucopyranosidu, AMMONIUM DIHYDROGEN GLYCYRRHIZINATE, MONOAMMONIUM GLYCYRRHIZINATE [JAN], AMMONIUM GLYCYRRHIZATE [EP MONOGRAPH], RDX013 COMPONENT AMMONIUM GLYCYRRHIZATE, (2S,3S,4S,5R,6R)-6-[(2S,3R,4S,5S,6S)-2-[[(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]-6-carboxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid, azane, RDX-013 COMPONENT AMMONIUM GLYCYRRHIZATE, GLYCYRRHIZIC ACID, AMMONIUM SALT [WHO-DD], .alpha.-D-Glucopyranosiduronic acid, (3.beta.,20.beta.)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-.beta.-D-glucopyranuronosyl-, monoammonium salt, alpha-D-Glucopyranosiduronic acid, (3-beta,20-beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-D-glucopyranuronosyl-, ammoniate, alpha-D-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-D-glucopyranuronosyl-, monoammonium salt, AMMONIUM GLYCYRRHIZATE (II), Glycyram, AMMONIUM GLYCYRRHIZATE (USP-RS), DTXSID2041204, .ALPHA.-D-GLUCOPYRANOSIDURONIC ACID, (3-.BETA.,20-.BETA.)-20-CARBOXY-11-OXO-30-NOROLEAN-12-EN-3-YL 2-O-.BETA.-D-GLUCOPYRANURONOSYL-, AMMONIATE, alpha-D-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-D-glucopyranuronosyl-, ammonium salt (1:1), GLYCYRRHIZIN AMMONIATED, AMMONIUM GLYCYRRHIZATE (EP MONOGRAPH), EINECS 268-402-0, NSC2800, AMGZ, Glycyram, Glycyron No.1, AmmoniumGlycyrrhizate, Glycyrrhizin ammoniacal, Glycyrrhizin monoammonium, SCHEMBL152097, Glycyrrhizin Acid Ammonium Salt, DTXCID0021204, CHEBI:81864, HY-N0184B, CS-M0783, AMMONIATED GLYCYRRHIZIN [FCC], AMMONIUM GLYCYRRHIZATE [INCI], s2376, s9143, GLYCYRRHIZIN, AMMONIATED [II], AKOS022168214, CCG-270522, CCG-270523, GLYCYRRHIZIN, AMMONIATED [FHFI], OG33320, GLYCYRRHIZIN, AMMONIATED ANHYDROUS, alpha-D-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norlean-12-en-3-yl-2-O-beta-D- -glucopyranuronosyl-, ammoniate, DA-61027, HY-76225, MONOAMMONIUM GLYCYRRHIZINATE [FCC], CS-0027757, C18610, D04987, AMMONIUM GLYCYRRHIZATE COMPONENT OF RDX013, 53956-04-0 1407-03-0(base), AMMONIUM GLYCYRRHIZATE COMPONENT OF RDX-013, Q27155631, Glycyrrhizic acid ammonium salt, analytical standard, for HPLC, Ammonium glycyrrhizate, European Pharmacopoeia (EP) Reference Standard, Ammonium glycyrrhizate, United States Pharmacopeia (USP) Reference Standard, Glycyrrhizate monoammonium, European Pharmacopoeia (EP) Reference Standard, Ammonium Glycyrrhizate, Pharmaceutical Secondary Standard, Certified Reference Material, (2S,3S,4S,5R,6R)-6-[(2S,3R,4S,5S,6S)-2-[[(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]-6-carboxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylicacid, azane, .ALPHA.-D-GLUCOPYRANOSIDURONIC ACID, (3-.BETA.,20.BETA.)-20-CARBOXY-11-OXO-30-NOROLEAN-12-EN-3-YL 2-O-.BETA.-D-GLUCOPYRANURONOSYL-, AMMONIATE, 258-887-7, alpha-D-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norlean-12-en-3-yl-2-O-beta-D--glucopyranuronosyl-, ammoniate
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 268.0
Hydrogen Bond Donor Count 9.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CC2C3CCCCC3CCC2C2CCC3CC(CC4CCCCC4CC4CCCCC4)CCC3C12
Np Classifier Class Oleanane triterpenoids
Deep Smiles O[C@@H][C@@H]O[C@@H]O[C@H]C=O)O))[C@H][C@@H][C@H]6O))O))O))))))[C@H]O[C@@H][C@H]6O))C=O)O))))O[C@H]CC[C@][C@H]C6C)C))CC[C@@][C@@H]6C=O)C=C[C@@]6C)CC[C@@][C@H]6C[C@]C)CC6))C=O)O)))))C)))))))))C)))))C.N
Heavy Atom Count 59.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level OC1CC2C3CCCCC3CCC2C2CCC3CC(OC4OCCCC4OC4CCCCO4)CCC3C12
Classyfire Subclass Terpene glycosides
Isotope Atom Count 0.0
Molecular Complexity 1730.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 19.0
Iupac Name (2S,3S,4S,5R,6R)-6-[(2S,3R,4S,5S,6S)-2-[[(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]-6-carboxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid, azane
Prediction Hob 0.0
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Gsk 4 400 Rule False
Molecular Formula C42H65NO16
Scaffold Graph Node Bond Level O=C1C=C2C3CCCCC3CCC2C2CCC3CC(OC4OCCCC4OC4CCCCO4)CCC3C12
Prediction Swissadme 0.0
Inchi Key ILRKKHJEINIICQ-OOFFSTKBSA-N
Fcsp3 0.8571428571428571
Rotatable Bond Count 7.0
Synonyms glycyrram
Functional Groups CC(=O)O, CC(C)=CC(C)=O, CO, CO[C@H](C)OC, N
Compound Name Ammonium Glycyrrhizate
Prediction Hob Swissadme 0.0
Exact Mass 839.43
Formal Charge 0.0
Monoisotopic Mass 839.43
Hydrogen Bond Acceptor Count 17.0
Molecular Weight 840.0
Covalent Unit Count 2.0
Total Atom Stereocenter Count 19.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 False
Esol -4.453532600000005
Inchi InChI=1S/C42H62O16.H3N/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), 1H3/t19-,21-,22-,23-,24-,25-,26-,27+,28-,29-,30+,31+,34-,35-,38+,39-,40-,41+,42+, /m0./s1
Smiles 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.N
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Triterpenoids

Back to Browse   Back to Home