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DNA Alkylator/Crosslinker

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DNA Alkylator/Crosslinker

Chemical Structure Cat. No. Product Name CAS No.
SG2057 Chemical Structure
BCP46387 SG2057 260417-62-7
SG2057 is a pentyldioxy linked PBD dimer which binds sequence selectively in the minor groove of DNA forming DNA interstrand and intrastrand cross-linked adducts, and also mono-adducts depending on sequence.
SG3199 Chemical Structure
BCP46386 SG3199 1595275-71-0
SG3199 is a PBD dimer which binds in the minor groove of DNA, and forms covalent DNA interstrand cross-links in naked linear plasmid DNA. SG3199 is potently cytotoxic against a panel of human solid tumour and haematological cancer cell lines.
D-scyllo-Inositol, 1-azido-1-deoxy-2,3,4,5,6-pentakis-O-(phenylmethyl)- Chemical Structure
BCP34936 D-scyllo-Inositol, 1-azido-1-deoxy-2,3,4,5,6-pentakis-O-(phenylmethyl)- 868550-22-5
1-Amino-1-desoxy-scyllo-inosit Chemical Structure
BCP34937 1-Amino-1-desoxy-scyllo-inosit 16051-25-5
Sarcolysin hydrochloride Chemical Structure
BCP34935 Sarcolysin hydrochloride 1465-26-5
DL-Melphalan hydrochloride is a nitrogen mustard and alkylating agent that has been studied for use in multiple myeloma therapy.
Melphalan Hydrochloride Chemical Structure
BCP33593 Melphalan Hydrochloride 3223-07-2
Melphalan is an orally available phenylalanine derivative of nitrogen mustard with antineoplastic activity. Melphalan alkylates DNA at the N7 position of guanine and induces DNA inter-strand cross-linkages, resulting in the inhibition of DNA and RNA synthesis and cytotoxicity against both dividing and non-dividing tumor cells.
Treosulfa Chemical Structure
BCP31509 Treosulfa 299-75-2
Treosulfan is an alkylating agent with activity in ovarian cancer and other solid tumor types.
Cyano Temozolomide Chemical Structure
BCP22927 Cyano Temozolomide 287964-59-4
Temozolomide is an oral DNA alkylating agent used to treat some brain cancers.
Evofosfamide Chemical Structure
BCP06074 Evofosfamide 918633-87-1
Evofosfamide is a potent and selective hypoxia-activated phosphoramidate DNA cross-linking mustard; selectively potent under hypoxia and stable to liver microsomes; inhibits H246 cells and HT29 cells with IC50 of 0.1 uM and 0.2 uM respectively; active in an in vivo MIA PaCa-2 pancreatic cancer orthotopic xenograft model.
CEP-40125 Chemical Structure
BCP30791 CEP-40125 1456608-94-8
CEP-40125, also known as RXDX-107, is a DNA alkylating drug potentially for the treatment of advanced solid tumours.
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