Page last updated: 2024-12-08

notoginsenoside r1

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Description

notoginsenoside R1 : A ginsenoside found in Panax notoginseng that is dammarane which is substituted by hydroxy groups at the 3beta, 6alpha, 12beta and 20 pro-S positions, in which the hydroxy groups at positions 6 and 20 have been converted to the corresponding beta-D-xylopyranosyl-(1->2)-beta-D-glucopyranoside and beta-D-glucopyranoside respectively, and in which a double bond has been introduced at the 24-25 position. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

FloraRankFlora DefinitionFamilyFamily Definition
PanaxgenusAn araliaceous genus of plants that contains a number of pharmacologically active agents used as stimulants, sedatives, and tonics, especially in traditional medicine. Sometimes confused with Siberian ginseng (ELEUTHEROCOCCUS).[MeSH]AraliaceaeThe ginseng plant family of the order Apiales, subclass Rosidae, class Magnoliopsida. Leaves are generally alternate, large, and compound. Flowers are five-parted and arranged in compound flat-topped umbels. The fruit is a berry or (rarely) a drupe (a one-seeded fruit). It is well known for plant preparations used as adaptogens (immune support and anti-fatigue).[MeSH]
Panax notoginsengspeciesA plant species of the genus PANAX. It contains damarane-type tetracyclic TRITERPENES. The common names of Sanchi or Tienchi are also used for Panax pseudoginseng which is distinguished in containing oleanane-type pentacyclic triterpenoids.[MeSH]AraliaceaeThe ginseng plant family of the order Apiales, subclass Rosidae, class Magnoliopsida. Leaves are generally alternate, large, and compound. Flowers are five-parted and arranged in compound flat-topped umbels. The fruit is a berry or (rarely) a drupe (a one-seeded fruit). It is well known for plant preparations used as adaptogens (immune support and anti-fatigue).[MeSH]

Cross-References

ID SourceID
PubMed CID441934
CHEMBL ID507115
CHEBI ID77149
MeSH IDM0197347

Synonyms (36)

Synonym
(-)-pseudolaric acid b
z62692362z ,
hsdb 8111
o-acetylseudolaric acid c
unii-z62692362z
beta-d-glucopyranoside, (3beta,6alpha,12beta)-20-(beta-d-glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-o-beta-d-xylopyranosyl-
80418-24-2
C08961
notoginsenoside r1
notoginsenoside r 1
notoginsenoside-r1
CHEMBL507115 ,
chebi:77149 ,
S3785
AKOS025311471
CS-4167
(3beta,6alpha,12beta)-20-(beta-d-glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-o-beta-d-xylopyranosyl-beta-d-glucopyranoside
(20s)-ginsenoside r1
Q-100835
sanchinoside r1
.beta.-d-glucopyranoside, (3.beta.,6.alpha.,12.beta.)-20-(.beta.-d-glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-o-.beta.-d-xylopyranosyl-
notoginsenoside r1 (constituent of american ginseng, asian ginseng, and tienchi ginseng) [dsc]
sanqi glucoside r1
HY-N0615
mfcd00210535
notoginsenoside r1, analytical standard
notoginsenoside r1 (constituent of american ginseng, asian ginseng, and tienchi ginseng)
notoginsenoside r1, >=98% (hplc)
BS-17596
Q27105065
sanchinoside r1;sanqi glucoside r1
b-d-glucopyranoside,(3b,6a,12b)-20-(b-d-glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-o-b-d-xylopyranosyl-
CCG-270581
notoginsenosider1
AC-34698
DTXSID101036451

Research Excerpts

Overview

Notoginsenoside R1 (NGR1) is an effective saponin isolated from the roots of Panax notoginseng. It regulates various biological activities, including cardiovascular protection, neuro-protection, and anti-cancer effects.

ExcerptReferenceRelevance
"Notoginsenoside R1 is an effective saponin isolated from the roots of"( Notoginsenoside R1, An Active Compound from
Cao, S; Gong, X; Li, K; Shan, L; Wu, Y; Zhang, Q, 2022
)
2.89
"Notoginsenoside R1 (NGR1) is a primary bioactive natural compound that regulates various biological activities, including cardiovascular protection, neuro-protection, and anti-cancer effects."( Notoginsenoside R1 Promotes Migration, Adhesin, Spreading, and Osteogenic Differentiation of Human Adipose Tissue-Derived Mesenchymal Stromal Cells.
Jaspers, RT; Lan, H; Pathak, JL; Wang, H; Wei, N; Wu, G; Wu, L; Yan, Y; Zheng, Z, 2022
)
2.89
"Notoginsenoside R1 is a novel phytoestrogen with anti-inflammatory, antioxidant and anti-apoptosis properties."( Notoginsenoside R1 protects against hypobaric hypoxia-induced high-altitude pulmonary edema by inhibiting apoptosis via ERK1/2-P90rsk-BAD ignaling pathway.
He, Y; Huang, D; Jia, N; Li, S; Pei, C; Shen, Z; Shi, S; Wang, X; Wang, Y; Wang, Z; Wu, Y; Zhao, S, 2023
)
3.07
"Notoginsenoside R1 (NR1) is a compound isolated from the roots of Panax notoginseng; it has powerful ROS-scavenging activities."( Notoginsenoside R1 protects boar sperm during liquid storage at 17°C.
Feng, T; Hu, J; Liu, Q; Niu, T; Ren, F; Xiao, J; Xu, G; Yuan, Y, 2020
)
2.72
"Notoginsenoside R1 (NG-R1) is a neuroprotective drug that is commonly used to treat neurodegenerative and cerebrovascular diseases."( Anti-ischemia/reperfusion injury effects of notoginsenoside R1 on small molecule metabolism in rat brain after ischemic stroke as visualized by MALDI-MS imaging.
Pu, XP; Sun, GB; Sun, XB; Tian, F; Wang, L; Zhao, X; Zhu, T, 2020
)
1.54
"Notoginsenoside R1 (NGR1) is a proverbial active ingredient of the traditional Chinese medicine Panax notoginseng (PN) and possess undeniable roles in several cancers."( Notoginsenoside R1 counteracts mesenchymal stem cell-evoked oncogenesis and doxorubicin resistance in osteosarcoma cells by blocking IL-6 secretion-induced JAK2/STAT3 signaling.
Lu, L; Lu, M; Lu, X; Shi, Y; Tang, Y; Xie, K, 2021
)
2.79
"Notoginsenoside R1 (NGR1) is a predominant phytoestrogen extracted from Panax notoginseng that has recently been reported to play important roles in the treatment of cardiac dysfunction, diabetic kidney disease, and acute liver failure. "( Protective Effects of Notoginsenoside R1 via Regulation of the PI3K-Akt-mTOR/JNK Pathway in Neonatal Cerebral Hypoxic-Ischemic Brain Injury.
Chen, D; Li, Y; Shen, J; Tu, L; Wang, S; Wang, Y; Xiang, P, 2018
)
2.24
"Notoginsenoside R1 (NGR1) is a novel saponin that is derived from Panax notoginseng and has reported cardioprotective, neuroprotective and anti-inflammatory effects."( Notoginsenoside R1 inhibits vascular smooth muscle cell proliferation, migration and neointimal hyperplasia through PI3K/Akt signaling.
Fang, H; Feng, Y; Liu, R; Luo, Y; Rao, Y; Yang, S; Yu, J; Zhang, C, 2018
)
2.64
"Notoginsenoside R1 (NG-R1) is a major component of Panax notoginseng, which has been used clinically for the treatment of diabetic nephropathy for centuries in China. "( Notoginsenoside R1 protects oxygen and glucose deprivation-induced injury by upregulation of miR-21 in cardiomyocytes.
Cao, H; Hou, G; Liu, Z; Wang, H; Yang, B; Zhao, Y, 2019
)
3.4
"Notoginsenoside R1 (NGR1) is a neoteric phytoestrogen extracted from Panax notoginseng, and possesses comprehensive pharmacological functions in multitudinous ailments. "( Notoginsenoside R1 protects WI-38 cells against lipopolysaccharide-triggered injury via adjusting the miR-181a/TLR4 axis.
Li, Y; Qian, D; Shao, X; Sun, X, 2019
)
3.4
"Notoginsenoside R1 (NGR1) is a novel phytoestrogen that is isolated from Panax notoginseng. "( Suppression of NADPH oxidase- and mitochondrion-derived superoxide by Notoginsenoside R1 protects against cerebral ischemia-reperfusion injury through estrogen receptor-dependent activation of Akt/Nrf2 pathways.
Meng, X; Sun, G; Sun, X; Wang, M; Wang, X; Xu, H; Ye, J, 2014
)
2.08
"Notoginsenoside R1 (NGR1) is a novel saponin isolated from P."( Cardioprotective effects of Notoginsenoside R1 against ischemia/reperfusion injuries by regulating oxidative stress- and endoplasmic reticulum stress- related signaling pathways.
Ai, Q; Chen, R; Luo, Y; Sun, G; Sun, X; Wang, M; Xing, N; Yu, Y; Zhang, J, 2016
)
1.45
"Notoginsenoside R1 (NGR1) is a phytoestrogen that is isolated from Panax notoginseng It is used in China to treat many diseases, including hypoxic-ischemic encephalopathy (HIE), and it has been shown to target estrogen receptors. "( Notoginsenoside R1 Protects against Neonatal Cerebral Hypoxic-Ischemic Injury through Estrogen Receptor-Dependent Activation of Endoplasmic Reticulum Stress Pathways.
Chen, D; Li, Y; Tu, L; Wang, S; Wang, Y, 2016
)
3.32

Effects

ExcerptReferenceRelevance
"Notoginsenoside R1 (NGR1) has been involved in the modulation of antioxidative stress and anti-inflammatory response."( Notoginsenoside R1 alleviates spinal cord injury by inhibiting oxidative stress, neuronal apoptosis, and inflammation via activating the nuclear factor erythroid 2 related factor 2/heme oxygenase-1 signaling pathway.
Bao, Z; Chen, Y; Huang, Z; Luo, H; Zhou, M, 2022
)
2.89

Treatment

Notoginsenoside R1 treatment attenuates BBB permeability, cerebral infarction volume and neurological impairments in rats with acute cerebral ischemia.

ExcerptReferenceRelevance
"Notoginsenoside R1 treatment significantly reduced BBB leakage and cerebral infarction volume, weakened neurological deficits in post-stroke rats. "( Notoginsenoside R1 intervenes degradation and redistribution of tight junctions to ameliorate blood-brain barrier permeability by Caveolin-1/MMP2/9 pathway after acute ischemic stroke.
Han, Y; Li, P; Li, Y; Liu, B; Wang, S; Wang, Y; Yang, H; Zhao, Y, 2021
)
3.51
"Notoginsenoside R1 treatment attenuates BBB permeability, cerebral infarction volume and neurological impairments in rats with acute cerebral ischemia. "( Notoginsenoside R1 intervenes degradation and redistribution of tight junctions to ameliorate blood-brain barrier permeability by Caveolin-1/MMP2/9 pathway after acute ischemic stroke.
Han, Y; Li, P; Li, Y; Liu, B; Wang, S; Wang, Y; Yang, H; Zhao, Y, 2021
)
3.51

Pharmacokinetics

LC-MS/MS method was established to analyze five ingredients, notoginsenoside R1 (R1), ginsenosides Rg1 and Re (Re), in rats' plasma to describe the pharmacokinetic parameters of PNS.

ExcerptReferenceRelevance
" The concentrations of Rb1, Rg1 and R1 were measured by high performance liquid chromatography (HPLC), and statistic program DAS was applied to the calculation of pharmacokinetic parameters."( [In vivo distribution and pharmacokinetics of multiple effective components contained in Panax notoginseng saponins after intratympanic administration].
Chen, G; Hou, S; Mu, L; Nan, H; Zhang, X, 2011
)
0.37
" However, the pharmacokinetic parameters showed significant differences between the three components."( [In vivo distribution and pharmacokinetics of multiple effective components contained in Panax notoginseng saponins after intratympanic administration].
Chen, G; Hou, S; Mu, L; Nan, H; Zhang, X, 2011
)
0.37
" Pharmacokinetic parameters were estimated using non-compartmental methods."( In vivo distribution and pharmacokinetics of multiple active components from Danshen and Sanqi and their combination via inner ear administration.
Chen, G; Long, W; Mu, L; Wen, L; Yang, F; Zhang, SC, 2014
)
0.4
" The values of Cmax and AUC(0-t) after IT were significantly higher than IV."( In vivo distribution and pharmacokinetics of multiple active components from Danshen and Sanqi and their combination via inner ear administration.
Chen, G; Long, W; Mu, L; Wen, L; Yang, F; Zhang, SC, 2014
)
0.4
" Co-administration of Danshen and Sanqi could cause significant pharmacokinetic herb-herb interactions in guinea pigs."( In vivo distribution and pharmacokinetics of multiple active components from Danshen and Sanqi and their combination via inner ear administration.
Chen, G; Long, W; Mu, L; Wen, L; Yang, F; Zhang, SC, 2014
)
0.4
"To establish an HPLC-UV method for determining pharmacokinetic difference of notoginsenoside R1 between normal rats and ischemic rats."( [In vivo Pharmacokinetics of Notoginsenoside R1 in Ischemia Rats After Acute Myocardial Infarction].
Deng, ZJ; Guo, JW; Li, AR; Li, LM; Liu, RX; Qi, YQ; Ren, B, 2015
)
0.94
" The method was successfully applied to a pharmacokinetic study of Xuesaitong dispersible tablets in eight rats."( Simultaneous determination of notoginsenoside R1 and ginsenoside Re in rat plasma by ultra high performance liquid chromatography with tandem mass spectrometry and its application to a pharmacokinetic study.
Dai, G; Jiang, Z; Ju, W; Li, C; Liu, S; Zhang, Q; Zhu, L; Zong, Y, 2016
)
0.72
" The pharmacokinetic studies of FXT and PN were performed using the established method with the pharmacokinetic parameters being determined by non-compartmental analysis."( Effect of compatible herbs on the pharmacokinetics of effective components of Panax notoginseng in Fufang Xueshuantong Capsule.
Huang, JM; Li, MY; Ma, CH; Pang, HH; Tang, MK; Wang, Y,
)
0.13
" The analytical method was successfully applied to a pharmacokinetic study of the multi-components after oral administration of Sanjie Zhentong Capsule in rats."( Simultaneous determination of ten bioactive constituents of Sanjie Zhentong Capsule in rat plasma by ultra-high-performance liquid chromatography tandem mass spectrometry and its application to a pharmacokinetic study.
Hu, JH; Huang, W; Li, D; Li, J; Pan, Y; Wang, Y; Wang, ZZ; Xiao, W, 2017
)
0.46
"LC-MS/MS method was established to analyze five ingredients, notoginsenoside R1 (R1), ginsenoside Rg1 (Rg1), ginsenoside Rb1 (Rb1), ginsenoside Re (Re), and ginsenoside Rd (Rd), in rats' plasma to describe the pharmacokinetic parameters of PNS."( Pharmacokinetics of Panax notoginseng Saponins in Adhesive and Normal Preparation of Fufang Danshen.
Bai, J; Chen, XN; Du, SY; Li, DQ; Li, PY; Lu, Y; Tian, ZH; Wu, YL; Yu, GY; Zeng, YY; Zhao, MD, 2018
)
0.72
"The pharmacokinetic parameters were significantly different after oral administration three formulations."( Pharmacokinetics of Panax notoginseng Saponins in Adhesive and Normal Preparation of Fufang Danshen.
Bai, J; Chen, XN; Du, SY; Li, DQ; Li, PY; Lu, Y; Tian, ZH; Wu, YL; Yu, GY; Zeng, YY; Zhao, MD, 2018
)
0.48
" Furthermore, the method was successfully applied for pharmacokinetic study of these seven components in rat serum after oral administration of NDS."( Validated LC-MS/MS method for simultaneous quantification of seven components of Naodesheng in rat serum after oral administration and its application to a pharmacokinetic study.
Kang, J; Liang, S; Luo, L; Qi, Y; Zhao, W, 2019
)
0.51

Compound-Compound Interactions

ExcerptReferenceRelevance
" Overall, these findings suggest that SLI combined with XST (1X1S) has protective effects on co-culture of endothelial cells and pericytes after OGD/R."( Effects of salvianolate lyophilized injection combined with Xueshuantong injection in regulation of BBB function in a co-culture model of endothelial cells and pericytes.
Chai, LJ; Guo, H; Hu, LM; Jia, ZZ; Li, RL; Wang, JX; Wang, SX; Yuan, Q, 2021
)
0.62

Bioavailability

The method is simple, accurate and had high specificity and sensitivity. The relative bioavailability of notoginsenoside R1 is increased significantly in AMI group. The underlying mechanisms remain unknown.

ExcerptReferenceRelevance
" In our preliminary study, notoginsenoside R₁ was able significantly to improve the bioavailability of geniposide in beagle dogs, but the underlying mechanisms remain unknown."( The effects of notoginsenoside R₁ on the intestinal absorption of geniposide by the everted rat gut sac model.
Chula, S; Hang, L; Jianning, S; Shi, R; Yinying, B, 2012
)
0.38
"The method is simple, accurate and had high specificity and sensitivity, that could be applied in quantitative determination of notoginsenoside R1 and research of pharmacokinetics; the relative bioavailability of notoginsenoside R1 is increased significantly in AMI group,which indicates that notoginsenoside R1 has better effect in model rat."( [In vivo Pharmacokinetics of Notoginsenoside R1 in Ischemia Rats After Acute Myocardial Infarction].
Deng, ZJ; Guo, JW; Li, AR; Li, LM; Liu, RX; Qi, YQ; Ren, B, 2015
)
0.91
" The application is restricted by low bioavailability partly due to Panax notoginseng saponins (PNS) instability and low in vivo absorption."( Pharmacokinetics of Panax notoginseng Saponins in Adhesive and Normal Preparation of Fufang Danshen.
Bai, J; Chen, XN; Du, SY; Li, DQ; Li, PY; Lu, Y; Tian, ZH; Wu, YL; Yu, GY; Zeng, YY; Zhao, MD, 2018
)
0.48
"It was found that the modification with adhesive materials improved PNS bioavailability in Fufang Danshen formula."( Pharmacokinetics of Panax notoginseng Saponins in Adhesive and Normal Preparation of Fufang Danshen.
Bai, J; Chen, XN; Du, SY; Li, DQ; Li, PY; Lu, Y; Tian, ZH; Wu, YL; Yu, GY; Zeng, YY; Zhao, MD, 2018
)
0.48
"The chief objective of this research was to appraise liposomes embodying a bile salt, sodium glycocholate (SGC), as oral nanoscale drug delivery system to strengthen the bioavailability of a water-soluble and weakly penetrable pharmaceutical, notoginsenoside R1 (NGR1)."( Improved oral bioavailability of notoginsenoside R1 with sodium glycocholate-mediated liposomes: Preparation by supercritical fluid technology and evaluation in vitro and in vivo.
Fan, Q; Feng, N; Hou, X; Li, Z; Shao, Q; Zhang, K; Zhang, Y, 2018
)
0.94

Dosage Studied

ExcerptRelevanceReference
" When examining the proliferation of and ALP activity in the pre-osteoblasts, a bell-shaped dose-response pattern was observed when the cells were treated with various concentrations of NGR1, with a peak being observed at the concentration of 50 µg/ml."( Notoginsenoside R1 significantly promotes in vitro osteoblastogenesis.
Chen, J; Guo, J; Li, Y; Lin, Z; Liu, Y; Lv, H; Wu, G; Xu, G; Xu, T, 2016
)
1.88
" BLIN stimulated total anti-DHAV-1 antibody secretion in ducklings at the dosage of 4 mg per duckling, but did not stimulate IL-2 and IFN-γ secretion significantly."( Anti-DHAV-1 reproduction and immuno-regulatory effects of a flavonoid prescription on duck virus hepatitis.
Chen, Y; Hu, Y; Liu, J; Wang, D; Wang, Y; Wu, Y; Yang, J; Yao, F; Zeng, L, 2017
)
0.46
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (5)

RoleDescription
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
antioxidantA substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
neuroprotective agentAny compound that can be used for the treatment of neurodegenerative disorders.
apoptosis inducerAny substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms.
phytoestrogenAny compound produced by a plant that happens to have estrogenic activity.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (7)

ClassDescription
beta-D-glucosideAny D-glucoside in which the anomeric centre has beta-configuration.
12beta-hydroxy steroid
3beta-hydroxy steroidA 3-hydroxy steroid in which the 3-hydroxy substituent is in the beta-position.
disaccharide derivativeA carbohydrate derivative that is formally obtained from a disaccharide.
ginsenosideTriterpenoid saponins with a dammarane-like skeleton originally isolated from ginseng (Panax) species. Use of the term has been extended to include semi-synthetic derivatives.
tetracyclic triterpenoidAny triterpenoid consisting of a tetracyclic skeleton.
3beta-hydroxy-4,4-dimethylsteroidAny 3beta-hydroxy steroid which is substituted by two methyl groups at position 4.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Bioassays (3)

Assay IDTitleYearJournalArticle
AID337107Hepatoprotective activity against D-galactosamine/LPS-induced liver injury in ddY mouse assessed as inhibition of serum alanine transaminase level at 100 mg/kg, ip administered 1 hr before D-galactosamine/LPS challenge by Reitman-Frankel method2003Journal of natural products, Jul, Volume: 66, Issue:7
Structures of new dammarane-type Triterpene Saponins from the flower buds of Panax notoginseng and hepatoprotective effects of principal Ginseng Saponins.
AID337110Hepatoprotective activity against D-galactosamine/LPS-induced liver injury in ddY mouse assessed as inhibition of serum aspartate transaminase level at 100 mg/kg, ip administered 1 hr before D-galactosamine/LPS challenge by Reitman-Frankel method2003Journal of natural products, Jul, Volume: 66, Issue:7
Structures of new dammarane-type Triterpene Saponins from the flower buds of Panax notoginseng and hepatoprotective effects of principal Ginseng Saponins.
AID397814Induction of neurite outgrowth in human SK-N-SH cells at 100 uM after 5 days relative to control2002Journal of natural products, Sep, Volume: 65, Issue:9
Dammarane-type Saponins from Panax japonicus and their neurite outgrowth activity in SK-N-SH cells.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (169)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's5 (2.96)18.2507
2000's29 (17.16)29.6817
2010's86 (50.89)24.3611
2020's49 (28.99)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 23.53

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index23.53 (24.57)
Research Supply Index5.17 (2.92)
Research Growth Index5.37 (4.65)
Search Engine Demand Index26.67 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (23.53)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (0.57%)5.53%
Reviews6 (3.45%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other167 (95.98%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]