39723-40-5 Usage
General Description
ALATERNIN is a chemical compound belonging to the class of alkaloids, specifically from the diterpenoid family. It is primarily found in the leaves of the plant Aconitum kusnezoffii, also known as Kusnezoff monkshood. ALATERNIN has been identified as a potent cardiotoxic and neurotoxic agent, causing negative effects on the cardiovascular and nervous systems. Its chemical structure and properties make it highly poisonous and potentially lethal if ingested or absorbed. Due to its toxicity, ALATERNIN is often used in scientific research for its pharmacological properties and potential medical applications, but extreme caution must be taken when handling and working with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 39723-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,2 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39723-40:
(7*3)+(6*9)+(5*7)+(4*2)+(3*3)+(2*4)+(1*0)=135
135 % 10 = 5
So 39723-40-5 is a valid CAS Registry Number.
39723-40-5Relevant articles and documents
STRUKTUR UND SYNTHESE VON FLAVONOL-TRIOSIDEN AUS RHAMNUS-ARTEN
Riess-Mauer, Ingrid,Wagner, Hildebert
, p. 1269 - 1278 (2007/10/02)
By synthesis and (13)C-NMR spectroscopic investigations of rhamnocitrin-, rhamnazin- and rhamnetin-3-O-4)-O-α-L-rhamnopyranosyl-(1->6)>-β-D-galactopyranosides and of rhamnocitrin-3-O-3)-O-α-L-rhamnopyranosyl-(1->6)-β-D-galactopyranoside (rhamnocitrin-3-O-β-rhamninoside) it was proved that all naturally occuring flavonol-triosides, so far isolated from different Rhamnus species, contain the sugar-moiety rhamninose.Thus it was shown that catharticin (rhamnocitrin-3-O-β-rhamninoside) is identical withalaternin and xanthorhamnin A (rhamnetin-3-O-β-rhamninoside) with xanthorhamnin B, whereas xanthohamnin C is rhamnazin-3-O-β-rhamninoside.From Rhamnus saxatilis JACQ., ssp. saxat. a new flavonol-acetyl-trioside was isolated and the structure by MS and (13)C-NMR spectroscopic means elucidated to be the rhamnetin-3-O-3)-O-(4-O-acetyl-)-α-L-rhamnopyranosyl-(1->6)>-β-D-galactopyranoside.
