T1058 |
Carboplatin
|
41575-94-4
|
99.72%
|
|
Carboplatin (JM-8) is a cisplatin derivative, a DNA synthesis inhibitor. Carboplatin binds to DNA, inhibits replication and transcription, and induces cell death...
|
T4517 |
L189
|
64232-83-3
|
99.72%
|
|
L189 is a human DNA ligase inhibitor, inhibits hLigI/III/IV (IC50: 5/9/5 μM).
|
T23820 |
BRD32048
|
433694-46-3
|
99.69%
|
|
BRD32048 is the ETV1 transcription factor oncoprotein inhibitor.
|
T0415 |
Guanidine hydrochloride
|
50-01-1
|
99.68%
|
|
Guanidine hydrochloride (Aminoformamidine Hydrochloride) is a strong organic base existing primarily as guanidium ions at physiological pH. It is found in the ur...
|
T9051 |
ZYN57939
|
1639357-93-9
|
99.68%
|
|
ZYN57939 (MTR-106) is RNA polymerase I inhibitor for treating RNA polymerase I- mediated diseases. ZYN57939 showed inhibitory activity with IC50 of 0.855 μM agai...
|
T15282 |
Filibuvir
|
877130-28-4
|
99.68%
|
|
Filibuvir (PF-00868554) is a selective and noncovalent inhibitor of HCV NS5B RNA-dependent RNA polymerase. Filibuvir inhibits genotype 1a and 1b replicons with E...
|
T0251 |
Gemcitabine
|
95058-81-4
|
99.67%
|
|
Gemcitabine (LY188011) is a synthetic cytosine nucleoside derivative and an inhibitor of DNA synthesis. Gemcitabine has antitumor and antimetabolic activities. G...
|
T14501 |
BAY-2402234
|
2225819-06-5
|
99.67%
|
|
BAY-2402234 is an inhibitor of dihydroorotate dehydrogenase (DHODH) for the treatment of myeloid malignancies.BAY 2402234 is a selective low-nanomolar inhibitor ...
|
T7174 |
Urolithin A
|
1143-70-0
|
99.66%
|
|
Urolithin A is a secondary metabolite of ellagic acid, a polyphenolic antioxidant, that has antiproliferative, anti-inflammatory, and anti-oxidant properties.
|
T1276 |
Danofloxacin mesylate
|
119478-55-6
|
99.66%
|
|
Danofloxacin mesylate (CP 76136-27) is a synthetic antibacterial agent of the fluoroquinolone class, acts principally by the inhibition of bacterial DNA-gyrase.
|
T8873 |
Bractoppin
|
2290527-07-8
|
99.65%
|
|
Bractoppin is a drug-like inhibitor of phosphopeptide recognition by the human BRCA1 tandem (t)BRCT domain (IC50 = 0.074 μM), which selectively inhibits substrat...
|
T72107 |
Werner syndrome RecQ helicase-IN-1
|
2869954-34-5
|
99.62%
|
|
Werner syndrome RecQ helicase-IN-1 is a potent Werne r syndrome RecQ DNA deconjugase (WRN) inhibitor that can be used to study cancers such as colon and stomach ...
|
T1272L |
Cytarabine hydrochloride
|
69-74-9
|
99.62%
|
|
Cytarabine hydrochloride (Ara-C hydrochloride) is a nucleoside analog that causes S phase cell cycle arrest and inhibits DNA polymerase. Cytarabine inhibits DNA ...
|
T2276 |
RI-1
|
415713-60-9
|
99.62%
|
|
RI-1 (RAD51 inhibitor 1) is a RAD51 inhibitor (IC50: 5-30 μM).
|
T67509 |
Cholesteryl Hemisuccinate
|
1510-21-0
|
99.61%
|
|
Cholesteryl Hemisuccinate (Cholesterol hydrogen succinate) is a highly soluble cholesterol analogue often used in polar solutions for its hepatoprotective, antic...
|
T1564 |
Cisplatin
|
15663-27-1
|
99.6%
|
|
Cisplatin (CDDP) is a DNA cross-linking agent. Cisplatin has antitumor activity and inhibits DNA synthesis by forming DNA adducts in cancer cells. Cisplatin also...
|
T40823 |
NCGC00029283
|
714240-31-0
|
99.6%
|
|
NCGC00029283 is a potent inhibitor of Werner syndrome helicase-nuclease (WRN), displaying inhibitory activity against WRN helicase with an IC 50 value of 2.3 μM....
|
T8800 |
NSAH
|
1099592-35-4
|
99.59%
|
|
NSAH (2-hydroxy-N'-[(E)-(2-hydroxynaphthalen-1-yl)methylidene]benzohydrazide) is a nonnucleoside inhibitor of human ribonucleotide reductase (hRR).with cell-free...
|
T1663 |
Deoxythymidine triphosphate
|
18423-43-3
|
99.59%
|
|
Deoxythymidine triphosphate (dTTP) is one of the four nucleoside triphosphates that are used in the in vivo synthesis of DNA.
|
T2601 |
Vidofludimus
|
717824-30-1
|
99.58%
|
|
Vidofludimus (SC12267) (4SC-101, SC12267) is a novel small molecule inhibitor of dihydroorotate dehydrogenase (DHODH).
|