131724-59-9 Usage
Chemical Origin
21-oxoisopteropodine is found in plants of the genus Annona, notably in Annona muricata (soursop or graviola).
Chemical Class
It belongs to the class of alkaloids, characterized by organic compounds with one or more basic nitrogen atoms.
Pharmacological Interests
21-oxoisopteropodine has potential antitumor and anticancer effects, making it a subject of interest for pharmaceutical research.
Mechanism of Action
It may exhibit cytotoxic properties, which enables it to inhibit the growth and proliferation of cancer cells.
Additional Properties
Besides its anticancer potential, 21-oxoisopteropodine also demonstrates anti-inflammatory and antioxidant activities, suggesting broader therapeutic applications.
Research Status
Ongoing studies are dedicated to understanding its complete range of pharmacological effects and potential therapeutic applications in detail.
Check Digit Verification of cas no
The CAS Registry Mumber 131724-59-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,7,2 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 131724-59:
(8*1)+(7*3)+(6*1)+(5*7)+(4*2)+(3*4)+(2*5)+(1*9)=109
109 % 10 = 9
So 131724-59-9 is a valid CAS Registry Number.
InChI:InChI=1/C21H22N2O5/c1-11-17-12(13(10-28-11)19(25)27-2)9-16-21(7-8-23(16)18(17)24)14-5-3-4-6-15(14)22-20(21)26/h3-6,10-12,16-17H,7-9H2,1-2H3,(H,22,26)/t11-,12+,16-,17-,21-/m1/s1
131724-59-9Relevant articles and documents
New methods for the synthesis of oxindole alkaloids. Total syntheses of isopteropodine and pteropodine
Martin, Stephen F.,Mortimore, Michael
, p. 4557 - 4560 (2007/10/02)
The 2-oxindole alkaloids isopteropodine (11) and pteropodine (12) were conveniently synthesised from the known pentacycle (9) via a new and general protocol for oxidation and rearrangement of carboline lactams into 3,3-disubstituted-2-oxindoles.