25406-64-8 Usage
Description
Morroniside, also known as Dendrobium extract, is a natural compound derived from the Dendrobium nobile orchid. It is characterized by its ability to enhance microvascular functional integrity and improve vascular elements of the neurovascular unit. Morroniside has been recognized for its potential in the treatment of cerebral ischemia and other related conditions.
Uses
Used in Pharmaceutical Industry:
Morroniside is used as a pharmaceutical agent for improving microvascular functional integrity and vascular elements of the neurovascular unit. This application is particularly relevant in the treatment of cerebral ischemia, where it can help enhance blood flow and reduce the risk of stroke-related complications.
In the treatment of cerebral ischemia, Morroniside is used as a therapeutic agent to:
1. Enhance microvascular functional integrity, which is crucial for maintaining proper blood flow and oxygen supply to the brain.
2. Improve vascular elements of the neurovascular unit, which is essential for the overall health and function of the brain.
Morroniside's role in the pharmaceutical industry is significant, as it offers a natural and potentially effective treatment option for patients suffering from cerebral ischemia and related conditions. Further research and development in this area may lead to the discovery of additional applications and benefits of Morroniside in various medical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 25406-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,0 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25406-64:
(7*2)+(6*5)+(5*4)+(4*0)+(3*6)+(2*6)+(1*4)=98
98 % 10 = 8
So 25406-64-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H26O11/c1-6-11-7(3-10(19)26-6)8(15(23)24-2)5-25-16(11)28-17-14(22)13(21)12(20)9(4-18)27-17/h5-7,9-14,16-22H,3-4H2,1-2H3/t6-,7+,9+,10+,11+,12+,13-,14+,16-,17-/m0/s1
25406-64-8Relevant articles and documents
INTERMEDIACY OF 6-HYDROXYLOGANIN IN THE RING CLEAVAGE COURSE OF LOGANIN TO SECOLOGANIN
Inoue, Kenichiro,Tanahashi, Takao,Inouye, Hiroyuki,Kuwajima, Hiroshi,Takaishi, Kiyokazu
, p. 2971 - 2980 (2007/10/02)
A possible biosynthetic pathway from loganin to secologanin through ring cleavage of 6-hydroxyloganin was ruled out in feeding experiments in which Eustoma russellianum, Swertia japonica, Lonicera morrowii and Adina pilulifera were each presented with three C-6 and C-7 stereoisomers of hydroxy -loganin as well as - and -loganin.In an associated experiment, the reduction of the aldehyde group of secologanin leading to sweroside was shown to proceed by hydride ion attack from the si face.Key Word Index - Biosynthesis; ring cleavage; loganin; 6,7-stereoisomer of 6-hydroxyloganin; secologanin; stereochemical course of the reduction; deuterium labelling.