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dc.creator US National Cancer Institute
dc.date 2004-12-12T18:00:44Z
dc.date 2004-12-12T18:00:44Z
dc.date 2003-02-01
dc.date 2004-12-12T18:00:44Z
dc.date.accessioned 2022-05-24T19:19:02Z
dc.date.available 2022-05-24T19:19:02Z
dc.identifier NSC3088
dc.identifier http://www.dspace.cam.ac.uk/handle/1810/4536
dc.identifier.uri http://localhost:8080/xmlui/handle/CUHPOERS/122206
dc.format 7402 bytes
dc.format 7066 bytes
dc.format chemical/x-cml
dc.format chemical/x-cml
dc.language en_GB
dc.publisher Unilever Center for Molecular Informatics, Cambridge University
dc.title NSC3088
dc.title .gamma.-(p-bis(2-chloroethyl)aminophenyl)butyric acid
dc.title .gamma.-[p-bis(2-chloroethyl)aminophenyl]butyric acid
dc.title .gamma.-[p-Di(2-chloroethyl)aminophenyl]butyric acid
dc.title p-(N, N-Di-2-chloroethyl)aminophenyl butyric acid
dc.title p-N, N-Di-(.beta.-chloroethyl)aminophenyl butyric acid
dc.title Ambochlorin
dc.title Amboclorin
dc.title Benzenebutanoic acid, 4-[bis(2-chloroethyl)amino]- (9CI)
dc.title Butyric acid, 4-(p-bis(2-chloroethyl)aminophenyl)-
dc.title Butyric acid, 4-(p-[bis(2-chloroethyl)amino]phenyl)-
dc.title Butyric acid, 4-[p-[bis(2-chloroethyl)amino]phenyl]- (8CI)
dc.title Cb l348
dc.title Chlorambucil
dc.title Chloraminophen
dc.title Chloraminophene
dc.title Chlorbutin
dc.title Chlorbutine
dc.title Chloroambucil
dc.title Chlorobutin
dc.title Chlorobutine
dc.title CB 1348
dc.title Ecloril
dc.title Elcoril
dc.title Leukeran
dc.title Leukersan
dc.title Leukoran
dc.title Linfolizin
dc.title Linfolysin
dc.title N,N-Di-2-chloroethyl-.gamma.-p-aminophenylbutyric acid
dc.title NCI-C03485
dc.title NSC 3088
dc.title Phenylbutyric acid nitrogen mustard
dc.title WLN: QV3R DN2G2G
dc.title 4-[p-[Bis(2-chloroethyl)amino]phenyl]butyric acid
dc.title 4-[p-Bis(.beta.-chloroethyl)aminophenyl]butyric acid
dc.title 4-[Bis(2-chloroethyl)amino]benzenebutanoic acid
dc.title 4-[Bis(2-chloroethyl)amino]phenylbutyric acid
dc.title 4[p-Bis(.beta.-chloroethyl)aminophenyl]butyric acid
dc.type Chemical Structures


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