(R) -ginsenoside Rh1
20(R)Ginsenoside Rh1
CAS: 80952-71-2
Molecular Formula: C36H62O9
(R) -ginsenoside Rh1 - Names and Identifiers
(R) -ginsenoside Rh1 - Physico-chemical Properties
| Molecular Formula | C36H62O9 |
| Molar Mass | 638.88 |
| Density | 1.23±0.1 g/cm3 (20 ºC 760 Torr) |
| Melting Point | 154-158°C |
| Boling Point | 755.1±60.0 °C(Predicted) |
| Specific Rotation(α) | (c, 0.23 in MeOH)+28.4 |
| Solubility | Soluble in water, methanol, ethanol, insoluble in petroleum ether, ether, benzene. |
| Appearance | White powder |
| pKa | 12.91±0.70(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| MDL | MFCD22200424 |
| Physical and Chemical Properties | White powder, soluble in methanol, ethanol, DMSO and other organic solvents, derived from ginseng. |
(R) -ginsenoside Rh1 - Reference
| Reference Show more | 1. Hong Zhang, Jia-Ming Jiang, Dan Zheng, Ming Yuan, Zhi-Ying Wang, Hong-Mei Zhang, Chang-Wu Zheng, Lian-Bo Xiao, Hong-Xi Xu,A multidimensional analytical approach based on time-decoupled online comprehensive two-dimensional liquid chromatography coupled wit 2. Hong Zhang, Jia-Ming Jiang, Dan Zheng, Ming Yuan, Zhi-Ying Wang, Hong-Mei Zhang, Chang-Wu Zheng, Lian-Bo Xiao, Hong-Xi Xu,A multidimensional analytical approach based on time-decoupled online comprehensive two-dimensional liquid chromatography coupled wit 3. Hong Zhang, Jia-Ming Jiang, Dan Zheng, Ming Yuan, Zhi-Ying Wang, Hong-Mei Zhang, Chang-Wu Zheng, Lian-Bo Xiao, Hong-Xi Xu,A multidimensional analytical approach based on time-decoupled online comprehensive two-dimensional liquid chromatography coupled wit 4. Joo, Kyung-Mi, et al. "Pharmacokinetic study of ginsenoside Re with pure ginsenoside Re and ginseng berry extracts in mouse using ultra performance liquid chromatography/mass spectrometric method." Journal of pharmaceutical and biomedical analysis 51.1 (20 5. [IF=5.34] Shan-Shan Zhou et al."Stronger anti-obesity effect of white ginseng over red ginseng and the potential mechanisms involving chemically structural/compositional specificity to gut microbiota."Phytomedicine. 2020 Aug;74:152761 6. [IF=3.935] Hong-Mei Zhang et al."Holistic quality evaluation of commercial white and red ginseng using a UPLC-QTOF-MS/MS-based metabolomics approach."J Pharmaceut Biomed. 2012 Mar;62:258 7. [IF=3.935] Hong Zhang et al."A multidimensional analytical approach based on time-decoupled online comprehensive two-dimensional liquid chromatography coupled with ion mobility quadrupole time-of-flight mass spectrometry for the analysis of ginsenosides from white a 8. [IF=3.935] Shan-Shan Zhou et al."Synchronous characterization of carbohydrates and ginsenosides yields deeper insights into the processing chemistry of ginseng."J Pharmaceut Biomed. 2017 Oct;145:59 9. [IF=6.06] Zhenzhuo Li et al."Ginsenosides repair UVB-induced skin barrier damage in BALB/c hairless mice and HaCaT keratinocytes."J Ginseng Res. 2021 May;: 10. [IF=5.396] Hui Wang et al."Ginsenoside extract from ginseng extends lifespan and health span in Caenorhabditis elegans."Food Funct. 2021 Aug;12(15):6793-6808 11. [IF=4.142] Wang Chenxi et al."Rapid discovery of potential ADR compounds from injection of total saponins from Panax notoginseng using data-independent acquisition untargeted metabolomics."Analytical And Bioanalytical Chemistry. 2021 Oct 26 12. [IF=3.935] Ruimei Lin et al."Global identification and determination of the major constituents in Kai-Xin-San by ultra-performance liquid chromatography-quadrupole-Orbitrap mass spectrometry and gas chromatography-mass spectrometry."J Pharmaceut Biomed. 2021 Nov;206 |
(R) -ginsenoside Rh1 - Reference Information
| biological activity | (20R)-Ginsenoside Rh1 is the R-isomer of Ginsenoside Rh1, it can be isolated from Panax ginsen and can inhibit the conversion of fibrinogen to fibrin induced by thrombin. |
| Use | for content determination/identification/pharmacological experiments. Pharmacological effects: fluid, Fumai solid off and other effects. (20R)-ginsenoside Rh1 is an isomer of (20s)-ginsenoside Rh1 and has anti-inflammatory and anti-cancer effects. |
Last Update：2024-04-09 21:21:28
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View History
(R) -ginsenoside Rh1
2-[5-(3-FLUORO-BENZYLIDENE)-4-OXO-2-THIOXO-THIAZOLIDIN-3-YL]-PROPIONIC ACID
118045-31-1
Cyclobutanecarboxylic acid, 1-(aminomethyl)-3-propyl-, ethyl ester
5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-7-methyl-(9CI)
(+)-PICFELTARRAENIN IA
2-氨基-4-氯-6-氧代-1,6-二氢嘧啶-5-甲腈
Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-hydroxy-, (S)- (9CI)
γ-(2-Hydroxy-phenyl)-buttersaeure-aethylester
Trichoplein keratin filament-binding protein
2-[5-(3-FLUORO-BENZYLIDENE)-4-OXO-2-THIOXO-THIAZOLIDIN-3-YL]-PROPIONIC ACID
118045-31-1
Cyclobutanecarboxylic acid, 1-(aminomethyl)-3-propyl-, ethyl ester
5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-7-methyl-(9CI)
(+)-PICFELTARRAENIN IA
2-氨基-4-氯-6-氧代-1,6-二氢嘧啶-5-甲腈
Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-hydroxy-, (S)- (9CI)
γ-(2-Hydroxy-phenyl)-buttersaeure-aethylester
Trichoplein keratin filament-binding protein