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]
Flora | Rank | Flora Definition | Family | Family Definition |
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Panax | genus | An 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] | Araliaceae | The 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 notoginseng | species | A 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] | Araliaceae | The 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] |
ID Source | ID |
---|---|
PubMed CID | 441934 |
CHEMBL ID | 507115 |
CHEBI ID | 77149 |
MeSH ID | M0197347 |
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 |
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.
Excerpt | Reference | Relevance |
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"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 |
Notoginsenoside R1 treatment attenuates BBB permeability, cerebral infarction volume and neurological impairments in rats with acute cerebral ischemia.
Excerpt | Reference | Relevance |
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"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 |
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.
Excerpt | Reference | Relevance |
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" 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 |
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.
Excerpt | Reference | Relevance |
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" 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 |
Excerpt | Relevance | Reference |
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" 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 |
Role | Description |
---|---|
plant metabolite | Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms. |
antioxidant | A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides. |
neuroprotective agent | Any compound that can be used for the treatment of neurodegenerative disorders. |
apoptosis inducer | Any substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms. |
phytoestrogen | Any 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] |
Class | Description |
---|---|
beta-D-glucoside | Any D-glucoside in which the anomeric centre has beta-configuration. |
12beta-hydroxy steroid | |
3beta-hydroxy steroid | A 3-hydroxy steroid in which the 3-hydroxy substituent is in the beta-position. |
disaccharide derivative | A carbohydrate derivative that is formally obtained from a disaccharide. |
ginsenoside | Triterpenoid 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 triterpenoid | Any triterpenoid consisting of a tetracyclic skeleton. |
3beta-hydroxy-4,4-dimethylsteroid | Any 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] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID337107 | Hepatoprotective 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 method | 2003 | Journal 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. |
AID337110 | Hepatoprotective 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 method | 2003 | Journal 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. |
AID397814 | Induction of neurite outgrowth in human SK-N-SH cells at 100 uM after 5 days relative to control | 2002 | Journal 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] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 5 (2.96) | 18.2507 |
2000's | 29 (17.16) | 29.6817 |
2010's | 86 (50.89) | 24.3611 |
2020's | 49 (28.99) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
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.
| This Compound (23.53) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 1 (0.57%) | 5.53% |
Reviews | 6 (3.45%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 167 (95.98%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |