About: CC-1065 CBI analogs: an example of enhancement of DNA alkylation efficiency through introduction of stabilizing electrostatic interactions

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About: CC-1065 CBI analogs: an example of enhancement of DNA alkylation efficiency through introduction of stabilizing electrostatic interactions Goto Sponge NotDistinct Permalink

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scientific article published on 01 June 1995

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 1995 (uk) im Juni 1995 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunu de 1995 (ast) scientific article published on 01 June 1995 (en)
publication date	wds:Q71797735-ED8E7009-40C8-437E-B3C6-F020D4EED6EF
publication date	1995-06-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q71797735-7784D289-4A49-4377-9B86-DF13DB45F673
language of work or name	English
cites work	wds:Q71797735-4A9A83E0-7ED3-4FCE-8868-810ABAAC2AB9 wds:Q71797735-C1E8B3F0-28ED-4570-A815-EAAD8D031489 wds:Q71797735-E064E6B2-EFDD-4DE5-838F-2AB850695A54 wds:Q71797735-E6B6E0EF-3348-4106-BB88-3A8F03A364AF wds:Q71797735-E82F55F2-7123-4A03-A369-49BE837ED20C wds:Q71797735-FCAB94F4-A353-45CD-A1A9-57124B240659
cites work	Duocarmycin SA, a new antitumor antibiotic from Streptomyces sp Structures of duocarmycins, novel antitumor antibiotics produced by Streptomyces sp. DC89-A1, a new antitumor antibiotic from Streptomyces Duocarmycin A, a new antitumor antibiotic from Streptomyces. Pyrindamycins A and B, new antitumor antibiotics Duocarmycins, new antitumor antibiotics produced by Streptomyces; producing organisms and improved production
author name string	wds:Q71797735-0649C573-CD82-473A-9A5B-C52170A618B8 wds:Q71797735-4872CFA0-6BD6-44B6-99B1-8DE6103C53A1 wds:Q71797735-66E3BD78-986D-47B1-A2C9-EF6741FEBCAE wds:Q71797735-9F596045-E6EF-461B-BCAE-5D8870FBDD4C
author name string	D L Boger D S Johnson N Han W Yun
rdfs:label	CC-1065 CBI analogs: an example of enhancement of DNA alkylation efficiency through introduction of stabilizing electrostatic interactions (en) CC-1065 CBI analogs: an example of enhancement of DNA alkylation efficiency through introduction of stabilizing electrostatic interactions (nl)
skos:prefLabel	CC-1065 CBI analogs: an example of enhancement of DNA alkylation efficiency through introduction of stabilizing electrostatic interactions (en) CC-1065 CBI analogs: an example of enhancement of DNA alkylation efficiency through introduction of stabilizing electrostatic interactions (nl)
name	CC-1065 CBI analogs: an example of enhancement of DNA alkylation efficiency through introduction of stabilizing electrostatic interactions (en) CC-1065 CBI analogs: an example of enhancement of DNA alkylation efficiency through introduction of stabilizing electrostatic interactions (nl)
title	wds:Q71797735-EAF2A9BF-44CD-484F-AC3F-AB24DB6B9DC9
title	CC-1065 CBI analogs: an example of enhancement of DNA alkylation efficiency through introduction of stabilizing electrostatic interactions (en)
page(s)	wds:Q71797735-4A6D6F6B-2F36-40C8-B60F-EB83D1654B49
page(s)	611-621
instance of	wds:Q71797735-BBED3214-BEDC-4634-A356-EDE4A9B32FDD
instance of	scholarly article
PubMed ID	wds:Q71797735-3B18709F-C2B2-40BB-9D5F-D338D1895EF0
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7582940
PubMed ID	7582940
published in	wds:Q71797735-7BB29077-3E92-4039-8CA3-F59F5EADD8AD
published in	Bioorganic & Medicinal Chemistry
issue	wds:Q71797735-EA12E9F4-887A-4C83-A3E7-2426AEC49E1E
volume	wds:Q71797735-2BF59C39-4950-40DA-8FCA-061165856E0A
issue	6
volume	3
DOI	wds:Q71797735-3600E31E-6C80-497D-B12F-362F0DD269C5
DOI	http://dx.doi.org/10.1016/0968-0896(95)00048-L
DOI	10.1016/0968-0896(95)00048-L
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71797735
is cites work of	A unique class of duocarmycin and CC-1065 analogues subject to reductive activation Asymmetric synthesis of 1,2,9,9a-tetrahydrocyclopropa[c]benzo[e]indol-4-one (CBI). Establishment of substituent effects in the DNA binding subunit of CBI analogues of the duocarmycins and CC-1065. CC-1065/duocarmycin and bleomycin A2 hybrid agents: lack of enhancement of DNA alkylation by attachment to noncomplementary DNA binding subunits Synthesis and Evaluation of Duocarmycin and CC-1065 Analogues Incorporating the 1,2,9,9a-Tetrahydrocyclopropa[c]benz[e]-3-azaindol-4-one (CBA) Alkylation Subunit Synthesis and characterization of a cyclobutane duocarmycin derivative incorporating the 1,2,10,11-tetrahydro-9H-cyclobuta[c]benzo[e]indol-4-one (CbBI) alkylation subunit Studies on duocarmycin SA and its derivatives
is cites work of	wds:Q73133485-B0B29AE2-5099-4208-8A7E-44BA095A8D43 wds:Q34813734-8C3EC54C-93DA-4342-B08E-AA76D317CEDA wds:Q36846628-92EE940A-C25E-4FD9-B59F-6843756F7428 wds:Q34187473-54CEC06D-4D9C-40B6-B033-F8C0D2C8AC69 wds:Q44539072-EE950969-9BC5-4929-AACE-14FFE9165829 wds:Q73253772-62898C58-B6BE-4592-9057-52508B04648A wds:Q44646404-FBC54707-4A22-46A6-90AE-40CB2C7F585A

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