Kinsenoside structure
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Common Name | Kinsenoside | ||
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CAS Number | 151870-74-5 | Molecular Weight | 264.229 | |
Density | 1.6±0.1 g/cm3 | Boiling Point | 570.2±50.0 °C at 760 mmHg | |
Molecular Formula | C10H16O8 | Melting Point | N/A | |
MSDS | N/A | Flash Point | 226.2±23.6 °C |
Use of KinsenosideKinsenoside is a main active component isolated from plants of the genus Anoectochilus, and exhibits many biological activities and pharmacological effects[1]. Kinsenoside rescues the nucleus pulposus cells (NPCs) viability under oxidative stress and protects against apoptosis, senescence and mitochondrial dysfunction in a Nrf2-dependent way[2]. |
Name | Kinsenoside |
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Synonym | More Synonyms |
Description | Kinsenoside is a main active component isolated from plants of the genus Anoectochilus, and exhibits many biological activities and pharmacological effects[1]. Kinsenoside rescues the nucleus pulposus cells (NPCs) viability under oxidative stress and protects against apoptosis, senescence and mitochondrial dysfunction in a Nrf2-dependent way[2]. |
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Related Catalog | |
References |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 570.2±50.0 °C at 760 mmHg |
Molecular Formula | C10H16O8 |
Molecular Weight | 264.229 |
Flash Point | 226.2±23.6 °C |
Exact Mass | 264.084503 |
PSA | 125.68000 |
LogP | -3.83 |
Vapour Pressure | 0.0±3.6 mmHg at 25°C |
Index of Refraction | 1.584 |
Storage condition | 2-8℃ |
~98% Kinsenoside CAS#:151870-74-5 |
Literature: Suzuki, Katsuhiko; Suzuki, Nobuyuki; Yamaura, Masanori; Yoshizawa, Toyokichi Journal of Carbohydrate Chemistry, 2005 , vol. 24, # 1 p. 73 - 84 |
~% Kinsenoside CAS#:151870-74-5 |
Literature: Suzuki, Katsuhiko; Suzuki, Nobuyuki; Yamaura, Masanori; Yoshizawa, Toyokichi Journal of Carbohydrate Chemistry, 2005 , vol. 24, # 1 p. 73 - 84 |
Precursor 1 | |
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DownStream 0 |
2(3H)-Furanone, 4-(β-D-glucopyranosyloxy)dihydro-, (4R)- |
goodyeroside |
(4R)-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-one |
(3R)-5-Oxotetrahydro-3-furanyl β-D-glucopyranoside |