6545-99-9 Usage
Description
Phebalosin is a naturally occurring isoprenylated coumarin that exhibits a range of biological activities, including anti-tumor, antibacterial, insecticidal, analgesic, and anti-inflammatory properties. It is derived from various plant sources and has garnered significant interest due to its potential therapeutic applications.
Uses
Used in Pharmaceutical Industry:
Phebalosin is used as an anti-tumor agent for its ability to inhibit tumor growth and progression. It targets multiple oncological signaling pathways, making it a promising candidate for cancer treatment.
Used in Agricultural Industry:
Phebalosin is used as an insecticidal agent for its effectiveness in controlling and managing insect populations, thereby reducing crop damage and improving agricultural productivity.
Used in Medical Industry:
Phebalosin is used as an analgesic for its pain-relieving properties, providing relief from various types of pain and discomfort.
Used in Anti-Inflammatory Applications:
Phebalosin is used as an anti-inflammatory agent for its ability to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Antibacterial Applications:
Phebalosin is used as an antibacterial agent for its effectiveness in inhibiting bacterial growth, making it a potential candidate for the development of new antibiotics to combat drug-resistant bacteria.
Check Digit Verification of cas no
The CAS Registry Mumber 6545-99-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6545-99:
(6*6)+(5*5)+(4*4)+(3*5)+(2*9)+(1*9)=119
119 % 10 = 9
So 6545-99-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O4/c1-8(2)13-15(19-13)12-10(17-3)6-4-9-5-7-11(16)18-14(9)12/h4-7,13,15H,1H2,2-3H3/t13-,15-/m1/s1
6545-99-9Relevant articles and documents
A route to the structure proposed for puetuberosanol and approaches to the natural products marshrin and phebalosin
Gillmore, Adam,Lauret, Christelle,Roberts, Stanley M.
, p. 4363 - 4375 (2007/10/03)
Synthesis of the structure claimed for puetuberosanol 1 (using the Juliá-Colonna oxidation in a key step) showed that the natural product was a different material. The isomeric epoxy alcohols 16-18 can be discounted from the alternatives. An analogue 19 of marshrin 2 was prepared but the synthesis of the natural product was thwarted by failure of a Juliá-Colonna oxidation in the key step. The epoxy ketone 29 was prepared by Darzens condensation and was converted into (±)-phebalosin 3.
