35287-69-5 Usage
General Description
Secalonic Acid D is a compound isolated from the fungus Penicillium oxalicum, and it belongs to the class of fungal secondary metabolites known as secalonic acids. SECALONIC ACID D FROM PENICILLIUM*OXALICUM has been found to possess various pharmacological properties, including anti-inflammatory, antimicrobial, and antitumor activities. It has also been investigated for its potential as an anti-cancer agent. Secalonic Acid D has the ability to inhibit the growth of cancer cells and induce apoptosis, making it a promising candidate for further research and development in the field of oncology. Additionally, its anti-inflammatory and antimicrobial properties suggest potential applications in treating inflammation-related disorders and infections.
Check Digit Verification of cas no
The CAS Registry Mumber 35287-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,8 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35287-69:
(7*3)+(6*5)+(5*2)+(4*8)+(3*7)+(2*6)+(1*9)=135
135 % 10 = 5
So 35287-69-5 is a valid CAS Registry Number.
InChI:InChI=1/C32H30O14/c1-11-9-15(33)21-25(37)19-17(45-31(21,27(11)39)29(41)43-3)7-5-13(23(19)35)14-6-8-18-20(24(14)36)26(38)22-16(34)10-12(2)28(40)32(22,46-18)30(42)44-4/h5-8,11-12,27-28,35-40H,9-10H2,1-4H3
35287-69-5Relevant articles and documents
Total syntheses of secalonic acids A and D
Qin, Tian,Porco Jr., John A.
, p. 3107 - 3110 (2014)
Total syntheses of the dimeric tetrahydroxanthone natural products secalonic acids A and D are described. Key steps involve kinetic resolution of the tetrahydroxanthone core structure using homobenzotetramisole catalysis and late-stage copper(I)-mediated homodimerization of complex aryl stannane monomers. It takes two: Concise syntheses of the natural products secalonic acids A and D using copper(I)-mediated dimerization of complex aryl stannane monomers to construct the requisite 2,2′-biphenol linkage are reported. Highly efficient kinetic resolution of the monomeric tetrahydroxanthone core structures was achieved using homobenzotetramisole catalysis. DMA=N,N-dimethyl acetamide, MOM=methoxymethyl.
