3,6-bis(5-chloro-2-piperidyl)-2,5-piperazinedione

RN = 64474-15-3
RR = 41109-80-2 (di-HCl(3S-(3alpha(2S*,5R*),6alpha(2S*,5R*)))-isomer)
RR = 41871-93-6 ((3S-(3alpha(2S*,5R*),6alpha(2S*,5R*)))-isomer)
SY = 593A
SY = NSC-135758
SY = piperazinedione
SY = 3,6-bis(5-chloro-2-piperidyl)-2,5-piperazinedione, dihydrochloride, (3S-(3alpha(2S*,5R*),6alpha(2S*,5R*)))-isomer
SY = 3,6-bis(5-chloro-2-piperidyl)-2,5-piperazinedione, (3S-(3alpha(2S*,5R*),6alpha(2S*,5R*)))-isomer
HM = *Piperazines
SO = Can Treat Rep 62(7):1101;1978
SO = Cancer 40(4):1386;1977
SO = Cancer Chemother Rep 57(1):21;1973
SO = Cancer Res 35(11):5996;1975
SO = Cancer Treat Rep 1979;63(8):1367
SO = Cancer Treat Rep 63(6):939;1979
SO = Cancer Treatment Rep 60(9):1397-25;1976
SO = Cancer Treatment Rep 61(9):1617-1731;1977
SO = Int J Radiat Oncol Biol Phys 1979;5(9):1709
SO = J Chromatogr 152(1):280;1978
SO = J Nat Cancer Inst 57(6):1305;1976
SO = Lancet I(8115):514;1979
PA = Antibiotics, Antineoplastic
FR = 28
NO = isolated from Streptomyces griseoluteus fermentation broth; RN given refers to cpd without isomeric designation; structure
DA = 19730101
MR = 20000802
UI = C003905

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