77879-89-1 Usage
Uses
Used in Antibacterial Applications:
6H-Benzo(d)naphtho(1,2-b)pyran-6-one, 4-(6-deoxy-alpha-galactofuranosyl)-1-hydroxy-10,12-dimethoxy-8-methylis used as an antibacterial agent, particularly against S. aureus. It inhibits bacterial growth at a concentration of 32 μg/ml.
Used in Antifungal Applications:
6H-Benzo(d)naphtho(1,2-b)pyran-6-one, 4-(6-deoxy-alpha-galactofuranosy l)-1-hydroxy-10,12-dimethoxy-8-methylalso exhibits antifungal activity, making it a potential candidate for use in treating fungal infections.
Used in Antiviral Applications:
6H-Benzo(d)naphtho(1,2-b)pyran-6-one, 4-(6-deoxy-alpha-galactofuranosyl)-1-hydroxy-10,12-dimethoxy-8-methylhas antiviral properties, which can be utilized in the development of treatments for viral diseases.
Used in Antitumor Applications:
Although less active than its vinyl analogue (gilvocarcin V), 6H-Benzo(d)naphtho(1,2-b)pyran-6-one, 4-(6-deoxy-alpha-galactofuranosy l)-1-hydroxy-10,12-dimethoxy-8-methyl- still displays antitumor activity. It inhibits the growth of KB cells with an IC50 value of 0.52 μg/ml.
Used in DNA Interaction Applications:
6H-Benzo(d)naphtho(1,2-b)pyran-6-one, 4-(6-deoxy-alpha-galactofuranosyl)-1-hydroxy-10,12-dimethoxy-8-methylintercalates into bacteriophage PM2 DNA, suggesting its potential use in DNA-related applications.
Used in Pharmaceutical Industry:
Due to its diverse range of biological activities, 6H-Benzo(d)naphtho(1,2-b)pyran-6-one, 4-(6-deoxy-alpha-galactofuranosy l)-1-hydroxy-10,12-dimethoxy-8-methyl- can be used in the development of new drugs for various therapeutic applications in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 77879-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,7 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77879-89:
(7*7)+(6*7)+(5*8)+(4*7)+(3*9)+(2*8)+(1*9)=211
211 % 10 = 1
So 77879-89-1 is a valid CAS Registry Number.
InChI:InChI=1/C26H26O9/c1-10-7-14-18(16(8-10)32-3)13-9-17(33-4)20-15(27)6-5-12(19(20)24(13)35-26(14)31)25-23(30)22(29)21(28)11(2)34-25/h5-9,11,21-23,25,27-30H,1-4H3/t11-,21+,22+,23-,25-/m1/s1
77879-89-1Relevant academic research and scientific papers
Total synthesis of the gilvocarcins
Hosoya, Takamitsu,Takashiro, Eiji,Matsumoto, Takashi,Suzuki, Keisuke
, p. 1004 - 1015 (2007/10/02)
Convergent total syntheses of the aryl C-glycoside antibiotics gilvocarcin M (1a) and gilvocarcin V (1b) have been accomplished. Key steps include (1) contrasteric coupling of D-fucofuranosyl acetate 27 with iodophenol 26, which was achieved by employing
