20
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T14349 | Auristatin F | Microtubule Associated | |
Auristatin F is an effective inhibitor of microtubule and vascular damaging agent. Auristatin F can be used in antibody-drug conjugates. | |||
T6116L | Bleomycin hydrochloride | DNA/RNA Synthesis | |
Bleomycin hydrochloride is a potent antitumor antibiotic that functions as a DNA synthesis inhibitor and DNA damaging agent. | |||
T5780 | HYPOCRELLIN B | Apoptosis , Parasite , Antifungal | |
HYPOCRELLIN B are photosensitive pigments isolated from Hypocrella bambusae Sacc. Hypocrellin B causes DNA strand breakage, induces apoptosis in ovarian cancer cells, and inhibits proliferation of Staphylococcus by incre... | |||
T0146 | Tioconazole | UK-20349,Vagistat | Antibiotic , Antifection , Antifungal |
Tioconazole (Vagistat) is a synthetic imidazole derivative, inhibits cell wall synthesis by inhibiting the biosynthesis of ergosterol or other sterols, damaging the fungal cell membrane, altering its permeability, and pr... | |||
TMS2180 | Zeaxanthin | Anchovyxanthin,All-Trans-Zeaxanthin | Antioxidant , Endogenous Metabolite |
1. Lutein and Zeaxanthin (All-Trans-Zeaxanthin) in neural tissue may have biological effects that include antioxidation, anti-inflammation, and structural actions. 2. Lutein and Zeaxanthin may be protective against eye d... | |||
T2213 | Terconazole | Gyno-Terazol,Terazol 3,Terazol 7,Triaconazole,R42470 | Antifection , Antifungal |
Terconazole (Terazol 7) is a synthetic triazole derivative structurally related to fluconazole, antifungal Terconazole seems to disrupt cell wall synthesis by inhibiting biosynthesis of ergosterol or other sterols, damag... | |||
T77520 | AOH1996 | Apoptosis , DNA/RNA Synthesis | |
AOH1996 is an orally active ligand for the replicasome component PCNA (proliferating cell nuclear antigen), targeting the transcription-replication conflict (TRC).AOH1996 interferes with the interaction of PCNA with its ... | |||
T41245 | Trimethylamine N-oxide | Reactive Oxygen Species , NOD-like Receptor (NLR) , TGF-beta/Smad | |
Trimethylamine N-oxide (TMAO) is a colorless amine oxide produced from choline, betaine, and carnitine via intestinal microbial metabolism that accumulates in tissues of marine animals and prevents the protein-damaging e... | |||
T41163 | ZNL 02-096 | Pomalidomide-C3-adavosertib | Apoptosis , Wee1 |
ZNL 02-096 (Pomalidomide-C3-adavosertib) is a rapid and selective degrader of Wee1 (IC50=3.58 nM).ZNL 02-096 selectively degrades Wee1 at submolar concentrations without damaging PLK1, a secondary target of AZD 1775.ZNL ... | |||
T29263 | (S,S)-D211 | (S,S)-D-211,IQB dimer (S,S)-D211 | |
(S,S)-D211 is a DNA damaging payload. | |||
TN3623 | Cepharadione A | Others | |
Cepharadione A is a naturally occurring DNA damaging agent. | |||
T73719 | Azoxymethane | AOM | DNA |
Azoxymethane (AOM) is a DNA damaging agent that induces cancer and can be used in mouse models of colorectal cancer. | |||
T20788 | Empenthrin | MA-108,S2852,S 2852,MA108,S-2852,MA 108 | |
Empenthrin, a synthetic pyrethroid used in insecticides, is active against broad spectrum of flying insects including moths and other pests damaging textile. | |||
T24176 | (-)-Irofulven | MGI-114,NSC-683863,MGI 114,HMAF,MGI114,Irofulven | |
Irofulven is an agent of DNA-damaging and antitumor. It is used for the treatment of advanced solid tumors, including prostate, ovarian, and pancreatic cancers. | |||
T78166 | MEL24 | Others | |
MEL24, an Mdm2 E3 ligase inhibitor, diminishes cell viability and enhances sensitivity to DNA-damaging agents in a p53-dependent manner, suggesting its potential for in vitro antitumor research [1]. | |||
T37876 | Fengycin | ||
Fengycin, a cyclic lipopeptide, functions as an agricultural fungicide by exhibiting an anti-fungal infection effect through damaging the target's cell membrane[1]. | |||
T38414 | NSC 80467 | ||
NSC 80467, a selective DNA damaging agent, functions by inhibiting survivin. Specifically, it preferentially targets DNA synthesis, leading to the induction of two distinct markers of DNA damage, namely γH2AX and pKAP1. | |||
TN5072 | Strictosidine | Others | |
Strictosidine has DNA damaging activity in yeast RS 188N mutant, assessed as drug level required to produce 12 mm zone of inhibition. | |||
T16283 | Neocarzinostatin | 5-HT Receptor | |
Neocarzinostatin is an effective DNA-damaging, anti-tumor antibiotic. It recognizes double-stranded DNA bulge and induces DNA double strand breaks (DSBs). Neocarzinostatin leads to apoptosis. Neocarzinostatin has potenti... | |||
T36733 | HLI373 dihydrochloride | ||
HLI373 dihydrochloride is a potent Hdm2 inhibitor, efficiently restraining the ubiquitin ligase activity of Hdm2 and effectively prompting apoptosis in DNA-damaging agent-sensitive tumor cells[1]. Additionally, HLI373 di... |