19427-82-8 Usage
General Description
Selindin is a chemical compound classified as a phenanthroindolizidine alkaloid, which is a type of plant-derived organic compound with nitrogen atoms in the heterocyclic ring. It is found in certain species of plants such as Delphinium, Aconitum, and Anisodus, and is known for its potent toxic and psychoactive effects on the central nervous system. Selindin acts as a sodium channel blocker, leading to muscle paralysis, cardiac arrhythmias, and neurotoxicity. It is also a highly lipophilic compound, allowing it to easily cross the blood-brain barrier and exert its effects on the central nervous system. Due to its toxic properties, selindin is considered a poisonous substance and should be handled with caution.
Check Digit Verification of cas no
The CAS Registry Mumber 19427-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,2 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19427-82:
(7*1)+(6*9)+(5*4)+(4*2)+(3*7)+(2*8)+(1*2)=128
128 % 10 = 8
So 19427-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H20O5/c1-5-11(2)18(21)22-15-10-13-14(24-19(15,3)4)8-6-12-7-9-16(20)23-17(12)13/h5-9,15H,10H2,1-4H3/b11-5-/t15-/m1/s1
19427-82-8Relevant articles and documents
The absolute configuration of angular 3′-acyloxypyranocoumarins by vibrational circular dichroism exciton chirality
Buenda-Trujillo, Abigail I.,Torrres-Valencia, J. Martn,Joseph-Nathan, Pedro,Burgueo-Tapia, Eleuterio
, p. 1418 - 1423 (2015/02/02)
A complex mixture of lomatin C-3′ esters and (-)-O-angeloyllomatin 1 was isolated from the seeds of Prionosciadium thapsoides. Since a literature search revealed that some lomatin C-3′ monoesters have positive specific rotations, while others had negative values, the absolute configuration of all of the molecules was determined to be (R) by exciton chirality in the infrared region, and by chemical correlation. A single crystal X-ray study of acetyllomatin 3, using the Flack and Hooft parameters, independently confirmed this absolute configuration.