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Home > Encyclopedia > Antibiotic CC 1065

Antibiotic CC 1065

Antibiotic CC 1065 structure

Antibiotic CC 1065 

structure
  • CAS No:

    69866-21-3

  • Formula:

    C37H33N7O8

  • Chemical Name:

    Antibiotic CC 1065

  • Synonyms:

    Benzo[1,2-b:4,3-b′]dipyrrole-3(2H)-carboxamide,7-[[1,6-dihydro-4-hydroxy-5-methoxy-7-[[(7bR,8aS)-4,5,8,8a-tetrahydro-7-methyl-4-oxocyclopropa[c]pyrrolo[3,2-e]indol-2(1H)-yl]carbonyl]benzo[1,2-b:4,3-b′]dipyrrol-3(2H)-yl]carbonyl]-1,6-dihydro-4-hydroxy-5-methoxy-;Benzo[1,2-b:4,3-b′]dipyrrole-3(2H)-carboxamide,7-[[1,6-dihydro-4-hydroxy-5-methoxy-7-[(4,5,8,8a-tetrahydro-7-methyl-4-oxocyclopropa[c]benzo[1,2-b:4,3-b′]dipyrrol-2(1H)-yl)carbonyl]benzo[1,2-b:4,3-b′]dipyrrol-3(2H)-yl]carbonyl]-1,6-dihydro-4-hydroxy-5-methoxy-,(7bR)-;Benzo[1,2-b:4,3-b′]dipyrrole-3(2H)-carboxamide,7-[[1,6-dihydro-4-hydroxy-5-methoxy-7-[(4,5,8,8a-tetrahydro-7-methyl-4-oxocyclopropa[c]pyrrolo[3,2-e]indol-2(1H)-yl)carbonyl]benzo[1,2-b:4,3-b′]dipyrrol-3(2H)-yl]carbonyl]-1,6-dihydro-4-hydroxy-5-methoxy-,(7bR,8aS)-;Cyclopropa[c]benzo[1,2-b:4,3-b′]dipyrrole,benzo[1,2-b:4,3-b′]dipyrrole-3(2H)-carboxamide deriv.;7-[[1,6-Dihydro-4-hydroxy-5-methoxy-7-[[(7bR,8aS)-4,5,8,8a-tetrahydro-7-methyl-4-oxocyclopropa[c]pyrrolo[3,2-e]indol-2(1H)-yl]carbonyl]benzo[1,2-b:4,3-b′]dipyrrol-3(2H)-yl]carbonyl]-1,6-dihydro-4-hydroxy-5-methoxybenzo[1,2-b:4,3-b′]dipyrrole-3(2H)-carboxamide;Antibiotic CC 1065;NSC 298223;Rachelmycin;CC 1065;(+)-CC 1065;CC 1065,(+)-;MCMC 10279;127232-81-9;76011-17-1;76567-22-1

Antibiotic CC 1065 Basic Attributes

703.70000

703.70

617542|298223

Characteristics

210.31000

4.62030

1.75g/cm3

1.878

Drug Information

Chemical substances, produced by microorganisms, inhibiting or preventing the proliferation of neoplasms. (See all compounds classified as Antibiotics, Antineoplastic.)|A class of drugs that differs from other alkylating agents used clinically in that they are monofunctional and thus unable to cross-link cellular macromolecules. Among their common properties are a requirement for metabolic activation to intermediates with antitumor efficacy and the presence in their chemical structures of N-methyl groups, that after metabolism, can covalently modify cellular DNA. The precise mechanisms by which each of these drugs acts to kill tumor cells are not completely understood. (From AMA, Drug Evaluations Annual, 1994, p2026) (See all compounds classified as Antineoplastic Agents, Alkylating.)

Benzo(1,2-b:4,3-b')dipyrrole-3(2H)-carboxamide, 7-((1,6-dihydro-4-hydroxy-5-methoxy-7-((4,5,8,8a-tetrahydro-7-methyl-4-oxocyclopropa(c)pyrrolo(3,2-e)indol-2(1H)-yl)carbonyl)benzo(1,2-b:4,3-b')dipyrrol-3(2H)-yl)carbonyl)-1,6-dihydro-4-hydroxy-5-methox

Computed Properties

Molecular Weight:703.7
XLogP3:2.4
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:4
Exact Mass:703.23906104
Monoisotopic Mass:703.23906104
Topological Polar Surface Area:210
Heavy Atom Count:52
Complexity:1610
Undefined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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