Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,279,233 papers from all fields of science
Search
Sign In
Create Free Account
U 77779
Known as:
U-77,779
, U-77779
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
Broader (1)
bizelesin
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2004
2004
V79 Chinese hamster lung cells resistant to the bis-alkylator bizelesin are multidrug-resistant
R. K. Butryn
,
Kathy S. Smith
,
+4 authors
B. Bhuyan
Cancer Chemotherapy and Pharmacology
2004
Corpus ID: 23425252
Bizelesin (U-77779) is a highly potent bis-alkylating antitumor agent that is effective against several tumor systems in vitro…
Expand
2001
2001
Novel seco cyclopropa[c]pyrrolo[3,2-e]indole bisalkylators bearing a 3,3'-arylenebisacryloyl group as a linker.
Y. Fukuda
,
S. Seto
,
H. Furuta
,
H. Ebisu
,
Y. Oomori
,
S. Terashima
Journal of Medicinal Chemistry
2001
Corpus ID: 24432577
We synthesized the novel seco cyclopropa[c]pyrrolo[3,2-e]indole (CPI) bisalkylators and evaluated their antitumor activity. Among…
Expand
1998
1998
The novel cyclopropapyrroloindole(CPI) bisalkylators bearing 3,3'-(1,4-phenylene)diacryloyl group as a linker.
Y. Fukuda
,
S. Seto
,
H. Furuta
,
H. Ebisu
,
Y. Oomori
,
S. Terashima
Bioorganic & Medicinal Chemistry Letters
1998
Corpus ID: 2946330
1997
1997
Effects of bizelesin (U-77,779), a bifunctional alkylating minor groove binder, on replication of genomic and simian virus 40 DNA in BSC-1 cells.
J. Woynarowski
,
T. Beerman
Biochimica et Biophysica Acta
1997
Corpus ID: 22684041
1995
1995
Effects of bizelesin (U-77779), a bifunctional alkylating minor groove agent, on genomic and simian virus 40 DNA.
J. Woynarowski
,
M. McHugh
,
L. Gawron
,
T. Beerman
Biochemistry
1995
Corpus ID: 19471059
Bizelesin is a bifunctional covalent minor groove binding agent which forms adducts with 3'-adenines on opposite DNA strands. DNA…
Expand
1993
1993
Nucleotide preferences for DNA interstrand cross-linking induced by the cyclopropylpyrroloindole analogue U-77,779.
Chong Soon Lee
,
Neil W. Gibson
Biochemistry
1993
Corpus ID: 41380795
Using a 21-base-pair duplex oligonucleotide containing a centrally located defined cross-linkable site, we have separated by gel…
Expand
1993
1993
In vitro evaluation of the novel chemotherapeutic agents U-73,975, U-77,779, and U-80,244 in gynecologic cancer cell lines.
Randall D. Hightower
,
B. Sevin
,
+4 authors
H. Averette
Cancer Investigation
1993
Corpus ID: 19636454
U-73,975 (U-73), U-77,779 (U-77), and U-80,244 (U-80) are analogs of the potent antitumor compound CC-1065. This class of drugs…
Expand
1992
1992
Resistance of CHO cells expressing P-glycoprotein to cyclopropylpyrroloindole (CPI) alkylating agents.
T. J. Zsido
,
T. Beerman
,
R. L. Meegan
,
J. Woynarowski
,
R. Baker
Biochemical Pharmacology
1992
Corpus ID: 12061827
1991
1991
DNA damage and differential cytotoxicity produced in human carcinoma cells by CC-1065 analogues, U-73,975 and U-77,779.
C. S. Lee
,
N. Gibson
Cancer Research
1991
Corpus ID: 34806438
U-73,975 (U-73) and U-77,779 (U-77), two analogues of the cyclopropylpyrroloindole antitumor antibiotic CC-1065, are promising…
Expand
1991
1991
DNA interstrand cross-linking, DNA sequence specificity, and induced conformational changes produced by a dimeric analog of (+)-CC-1065.
Z. Ding
,
L. Hurley
Anti-Cancer Drug Design
1991
Corpus ID: 2775703
U-77779 is a symmetrical dimer of the spirocyclopropyl alkylating subunit of (+)-CC-1065 in which the linker consists of two…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE