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Details

Stereochemistry ABSOLUTE
Molecular Formula C42H62O16
Molecular Weight 822.9321
Optical Activity UNSPECIFIED
Defined Stereocenters 19 / 19
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLYCYRRHIZIN

SMILES

[H][C@@]7(O[C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@]1([H])O[C@H]2CC[C@@]3(C)[C@@]([H])(CC[C@]4(C)[C@]3([H])C(=O)C=C5[C@]6([H])C[C@](C)(CC[C@]6(C)CC[C@@]45C)C(O)=O)C2(C)C)C(O)=O)O[C@@H]([C@@H](O)[C@H](O)[C@H]7O)C(O)=O

InChI

InChIKey=LPLVUJXQOOQHMX-QWBHMCJMSA-N
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)/t19-,21-,22-,23-,24-,25-,26-,27+,28-,29-,30+,31+,34-,35-,38+,39-,40-,41+,42+/m0/s1

HIDE SMILES / InChI
Molecular Formula C42H62O16
Molecular Weight 822.9321
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 19 / 19
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:00:04 UTC 2023
Edited
by admin
on Fri Dec 15 16:00:04 UTC 2023
Record UNII
6FO62043WK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLYCYRRHIZIN
HSDB   II   JAN  
Common Name English
Glycyrrhizic acid [WHO-DD]
Common Name English
GLYCYRRHIZIC ACID (GLYCYRRHIZIN) (CONSTITUENT OF LICORICE) [DSC]
Common Name English
GLYCYRRHIZIC ACID [USP-RS]
Common Name English
GLYCYRRHIZIN [JAN]
Common Name English
GLYCYRRHIZIC ACID [MART.]
Common Name English
GLYCYRRHIZIC ACID [MI]
Common Name English
GLYCYRRHIZIC ACID
INCI   MART.   MI   USP-RS   WHO-DD  
INCI  
Official Name English
GLYCYRRHIZIN [II]
Common Name English
GLYCYRRHIZINIC ACID
Common Name English
GLYCYRRHIZIC ACID [INCI]
Common Name English
GLYCYRRHIZATE
Common Name English
POTENLINI
Common Name English
GLYCYRRHIZINATE
Common Name English
NSC-167409
Code English
18.BETA.-GLYCYRRHIZIC ACID
Common Name English
.BETA.-GLYCYRRHIZIN
Common Name English
(3.BETA.,20.BETA.)-20-CARBOXY-11-OXO-30-NOROLEAN-12-EN-3-YL 2-O-.BETA.-D-GLUCOPYRANURONOSYL-.ALPHA.-D-GLUCOPYRANOSIDURONIC ACID
Common Name English
NSC-234419
Code English
GLYCYRRHIZIN [HSDB]
Common Name English
GLYCYRON
Common Name English
Classification Tree Code System Code
DSLD 3011 (Number of products:14)
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
WHO-ATC A05BA08
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
WHO-VATC QA05BA08
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
Code System Code Type Description
SMS_ID
100000078200
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
RXCUI
26143
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY RxNorm
EU FOOD ADDITIVES
GLYCYRRHIZIN
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
RXCUI
1370586
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
ALTERNATIVE
EVMPD
SUB14004MIG
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
DAILYMED
6FO62043WK
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
ECHA (EC/EINECS)
215-785-7
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
FDA UNII
6FO62043WK
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
EPA CompTox
DTXSID8047006
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
NSC
167409
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
RXCUI
1359426
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
ALTERNATIVE
CHEBI
29807
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
WIKIPEDIA
GLYCYRRHIZIN
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
HSDB
496
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
DRUG CENTRAL
1325
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
RS_ITEM_NUM
1295888
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
CAS
1405-86-3
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
DRUG BANK
DB13751
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
ChEMBL
CHEMBL441687
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
NSC
234419
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
MERCK INDEX
m5811
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY Merck Index
NCI_THESAURUS
C1117
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
PUBCHEM
14982
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
MESH
D019695
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
CHEBI
15939
Created by admin on Fri Dec 15 16:00:04 UTC 2023 , Edited by admin on Fri Dec 15 16:00:04 UTC 2023
PRIMARY
Related Record Type Details
GLYCYRRHIZA URALENSIS ROOT
PARENT -> CONSTITUENT ALWAYS PRESENT
GLYCYRRHIZA GLABRA (LICORICE) ROOT POWDER
PARENT -> CONSTITUENT ALWAYS PRESENT
GLYCYRRHIZA INFLATA ROOT
PARENT -> CONSTITUENT ALWAYS PRESENT
2.49% of dry weight of contents.
Structure of MAGNESIUM GLYCYRRHIZINATE
SALT/SOLVATE -> PARENT
Structure of TRISODIUM GLYCYRRHIZATE
SALT/SOLVATE -> PARENT
Structure of AMMONIUM GLYCYRRHIZATE
SALT/SOLVATE -> PARENT
Structure of MONOSODIUM GLYCYRRHIZINATE
SALT/SOLVATE -> PARENT
GLYCYRRHIZA INFLATA ROOT EXTRACT
PARENT -> CONSTITUENT ALWAYS PRESENT
Structure of ISOGLYCYRRHIZINIC ACID
DERIVATIVE -> PARENT
Structure of TRIPOTASSIUM GLYCYRRHIZINATE
SALT/SOLVATE -> PARENT
Structure of AMMONIUM GLYCYRRHIZINATE TRIHYDRATE
SALT/SOLVATE -> PARENT
GLYCYRRHIZA URALENSIS ROOT
PARENT -> CONSTITUENT ALWAYS PRESENT
3.27% of dry weight of contents.
Structure of GLYCYRRHIZINATE DIPOTASSIUM
SALT/SOLVATE -> PARENT
LICORICE ROOT EXTRACT
PARENT -> CONSTITUENT ALWAYS PRESENT
Structure of AMMONIUM GLYCYRRHIZATE PENTAHYDRATE
SALT/SOLVATE -> PARENT
LICORICE
PARENT -> ACTIVE CONSTITUENT ALWAYS PRESENT
USP
GLYCYRRHIZA URALENSIS ROOT
PARENT -> CONSTITUENT ALWAYS PRESENT
The compound did not show significant cytotoxicity against uninfected MDCK cells at 100 uM, but showed inhibitory activity against the H1N1 virus at 100 uM. The compound was also evaluated for anti-HIV activity.
GLYCYRRHIZA URALENSIS (LICORICE) ROOT EXTRACT
PARENT -> CONSTITUENT ALWAYS PRESENT
GLYCYRRHIZA LEPIDOTA ROOT
PARENT -> CONSTITUENT ALWAYS PRESENT
Related Record Type Details
Structure of ENOXOLONE
ACTIVE MOIETY
NIH
NCATS
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