U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Approval Year

Substance Class Structurally Diverse
Created
by admin
on Mon Mar 31 23:13:32 GMT 2025
Edited
by admin
on Mon Mar 31 23:13:32 GMT 2025
Source Materials Class ORGANISM
Source Materials Type PLANT
Source Materials Parent
Part rhizome; root; stolon
Record UNII
42B5YD8F0K
Record Status Validated (UNII)
Record Version
  • Download
Related Record Type
Name Type Language
GLYCYRRHIZA URALENSIS
Preferred Name English
GLYCYRRHIZA URALENSIS ROOT
WHO-DD  
Common Name English
GANCAO (GLYCYRRHIZA URALENSIS)
Common Name English
LOLOZ WITH CAVIBLOC
Brand Name English
Glycyrrhiza uralensis root [WHO-DD]
Common Name English
LIQUORICE ROOT (GLYCYRRHIZA URALENSIS)
Common Name English
GLYCYRRHIZAE RADIX ET RHIZOMA (GLYCYRRHIZA URALENSIS)
CHP  
Common Name English
PHY-906 COMPONENT GLYCYRRHIZA URALENSIS ROOT
Common Name English
URAL LICORICE ROOT
Common Name English
GLYCYRRHIZAE RADIX ET RHIZOMA (GLYCYRRHIZA URALENSIS) [CHP]
Common Name English
WU LA GAN CAO ROOT
Common Name English
GLYCYRRHIZA URALENSIS ROOT WITH RHIZOME
WHO-DD  
Common Name English
Glycyrrhiza uralensis root with rhizome [WHO-DD]
Common Name English
CHINESE HERBAL FORMULATION PHY906 COMPONENT GLYCYRRHIZA URALENSIS ROOT
Common Name English
GLYCYRRHIZA (GLYCYRRHIZA URALENSIS) [JP]
Common Name English
YIV-906 COMPONENT GLYCYRRHIZA URALENSIS ROOT
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C79664
Created by admin on Mon Mar 31 23:13:32 GMT 2025 , Edited by admin on Mon Mar 31 23:13:32 GMT 2025
DSLD 3014 (Number of products:192)
Created by admin on Mon Mar 31 23:13:32 GMT 2025 , Edited by admin on Mon Mar 31 23:13:32 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C80296
Created by admin on Mon Mar 31 23:13:32 GMT 2025 , Edited by admin on Mon Mar 31 23:13:32 GMT 2025
PRIMARY
EVMPD
SUB130189
Created by admin on Mon Mar 31 23:13:32 GMT 2025 , Edited by admin on Mon Mar 31 23:13:32 GMT 2025
PRIMARY
RXCUI
1342493
Created by admin on Mon Mar 31 23:13:32 GMT 2025 , Edited by admin on Mon Mar 31 23:13:32 GMT 2025
PRIMARY RxNorm
FDA UNII
42B5YD8F0K
Created by admin on Mon Mar 31 23:13:32 GMT 2025 , Edited by admin on Mon Mar 31 23:13:32 GMT 2025
PRIMARY
DAILYMED
42B5YD8F0K
Created by admin on Mon Mar 31 23:13:32 GMT 2025 , Edited by admin on Mon Mar 31 23:13:32 GMT 2025
PRIMARY
EVMPD
SUB33295
Created by admin on Mon Mar 31 23:13:32 GMT 2025 , Edited by admin on Mon Mar 31 23:13:32 GMT 2025
PRIMARY
SMS_ID
100000128526
Created by admin on Mon Mar 31 23:13:32 GMT 2025 , Edited by admin on Mon Mar 31 23:13:32 GMT 2025
PRIMARY
Related Record Type Details
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
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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.
CONSTITUENT ALWAYS PRESENT -> PARENT
Anti-H1N1 (IC50 in uM) activity of compound was shown to be 42.7 uM. 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.
CONSTITUENT ALWAYS PRESENT -> PARENT
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.
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
Anti-H1N1 (IC50 in uM) activity of compound was shown to be 49.1 uM. Anti-HIV (IC50 in uM) activity of compound was shown to be 29.5 uM. 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.
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
Anti-H1N1 (IC50 in uM) activity of compound was shown to be 39.6 uM. 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.
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
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.
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
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.
ACTIVE CONSTITUENT ALWAYS PRESENT -> PARENT
The compound showed strong ferric reducing activities and effectively scavenged DPPH, ABTS+, and singlet oxygen radicals.
CONSTITUENT ALWAYS PRESENT -> PARENT
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.
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
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.
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
SUB_CONCEPT->SUBSTANCE
CONSTITUENT ALWAYS PRESENT -> PARENT
Structure elucidation of compound.
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
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.
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
Structure elucidation of compound.
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT
Anti-H1N1 (IC50 in uM) activity of compound was shown to be 48.0 uM. 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.
CONSTITUENT ALWAYS PRESENT -> PARENT
CONSTITUENT ALWAYS PRESENT -> PARENT