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CAS 105650-12-2

:

chloropolysporin C

Description:
Chloropolysporin C, with the CAS number 105650-12-2, is a naturally occurring compound classified as a polyketide. It is produced by certain strains of bacteria, particularly those belonging to the genus Streptomyces. This compound exhibits a complex structure characterized by multiple functional groups, which contribute to its biological activity. Chloropolysporin C is known for its antimicrobial properties, making it of interest in pharmaceutical research, particularly in the development of new antibiotics. Its mechanism of action typically involves interference with bacterial cell wall synthesis or function, which can lead to cell lysis. Additionally, the compound may exhibit cytotoxic effects against various cancer cell lines, highlighting its potential in oncology. The stability and solubility of chloropolysporin C can vary depending on environmental conditions, which is an important consideration for its application in medicinal chemistry. Overall, chloropolysporin C represents a significant area of study due to its potential therapeutic benefits and the need for further research to fully understand its properties and applications.
Formula:C77H79Cl3N8O30
InChI:InChI=1/C77H79Cl3N8O30/c1-26-59(96)40(81)23-50(111-26)116-66-30-7-13-44(38(79)17-30)112-46-19-32-20-47(68(46)118-77-65(102)63(100)61(98)49(25-90)115-77)113-45-14-8-31(18-39(45)80)67(117-76-64(101)62(99)60(97)48(24-89)114-76)58(87-69(103)52(82-2)27-3-9-33(91)10-4-27)73(107)84-54(29-6-12-42(94)37(78)16-29)70(104)85-55(32)72(106)83-53-28-5-11-41(93)35(15-28)51-36(21-34(92)22-43(51)95)56(75(109)110)86-74(108)57(66)88-71(53)105/h3-22,26,40,48-50,52-67,76-77,82,89-102H,23-25,81H2,1-2H3,(H,83,106)(H,84,107)(H,85,104)(H,86,108)(H,87,103)(H,88,105)(H,109,110)
Synonyms:
  • 2-(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy-5,15-dichloro-22-(3-chloro-4-hydroxyphenyl)-32,35,37-trihydroxy-19-[[2-(4-hydroxyphenyl)-2-(methylamino)acetyl]amino]-20,23,26,42,44-pentaoxo-18,48-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-7,13-dioxa-21,24,27,41,43-pentazaoctacyclo[26.14.2.2^{3,6}.2^{14,17}.1^{8,12}.1^{29,33}.0^{10,25}.0^{34,39}]pentaconta-3,5,8(48),9,11,14,16,29(45),30,32,34(39),35,37,46,49-pentadecaene-40-carboxylic acid
  • Avoparcin alpha, 10,49-dichloro-2(sup D)-O-de(3-amino-2,3,6-trideoxy-alpha-L-ribo-hexopyranosyl)-59-O-de(6-deoxy-alpha-L-mannopyranosyl)-
  • Derhamnosylchloropolysporin B
  • chloropolysporin C
  • Chloropolysporin C
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  • Chloropolysporin C

    CAS:
    Chloropolysporin C exhibits significant activity against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and enterococci.
    Formula:C77H79Cl3N8O30
    Color and Shape:Solid
    Molecular weight:1702.85