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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
TP1268 | CEF19, Epstein-Barr Virus latent NA-3A (458-466) | CEF19,Epstein-Barr Virus latent NA-3A 458-466 | |
CEF19, Epstein-Barr Virus latent NA-3A (458-466) is a single peptide epitope, YPLHEQHGM, representing residues 458-466 of the type 1 Epstein-Barr Virus (EBV) nuclear antigen 3A protein (B95.8 strain). | |||
T0850 | Primaquine diphosphate | Primaquine phosphate,Primaquine bisphosphate | Antibiotic , Parasite |
Primaquine diphosphate is the phosphate salt form of primaquine, a synthetic, 8-aminoquinoline derivative with antimalarial properties. Although its mechanism of action is unclear, primaquine bind to and alter the proper... | |||
T32668 | Leucomalachite green | NSC36379,NSC 36379,NSC-36379 | Others |
Leucomalachite green (NSC-36379) is used in detecting latent bloodstains and in the forensic field because of convenience and cost/time-effectiveness. | |||
T10603 | BRD-6929 | HIV Protease , HDAC | |
BRD-6929 is a selective, brain-penetrant HDAC1 and HDAC2 inhibitor (IC50: 1 and 8 nM). BRD-6929 (Cpd-60) shows high-affinity to HDAC1 and HDAC2 (Kis: 0.2 and 1.5 nM) [2]. BRD-6929 potentiates the efficacy of gnidimacrin... | |||
T5S2017 | Ingenol | (-)-Ingenol | PKC |
1. Ingenol ((-)-Ingenol) mebutate is an effective treatment for actinic keratosis. 2. Formulating novel derivatives from Ingenol esters may be an innovative approach to develop new lead compounds to reactivate latent HIV... | |||
T3926 | Echinatin | Retrochalcone | Free radical scavengers |
Echinatin (Retrochalcone) disturb the mitochondrial energy transfer reactions and membrane permeability, at a low concentration cause deterioration of respiratory control and oxidative phosphorylation of isolated rat liv... | |||
T27611 | Ingenol 3-Hexanoate | ||
Ingenol 3-Hexanoate is a novel potent reactivator of latent HIV-1. | |||
T28818 | SMAPP1 | ||
SMAPP1 is an activator of protein phosphatase 1 (PP1). SMAPP1 induces PP1 activity in vitro and activates latent HIV-1 provirus in cultured and primary T cells. | |||
T61310 | HIV-1 inhibitor-37 | ||
HIV-1 inhibitor-37 (Compound 83) is a highly powerful HIV-1 inhibitor. It exhibits significant potential for use as an innovative latent HIV-1 reactivating agent [1]. | |||
T27988 | MDG486 | BAF IN A01,A01,MDG-486,MDG 486,BAF-IN-A01 | |
MDG486, an inhibitor of BAF, works by activating latent HIV-1. | |||
T40191 | 17-GMB-APA-GA | ||
17-GMB-APA-GA, a potent HSP90 inhibitor, is an ADC cytotoxin commonly employed for studying latent T. gondii infection. | |||
T24132 | HDAC3-IN-T326 | HDAC3 inhibitor-T326,T326,HDAC3 IN T326,HDAC3 inhibitor T326,HDAC3INT326 | |
HDAC3-IN-T326 is a potent and selective HDAC3 inhibitor that acts by increasing NF-κB acetylation and activating HIV gene expression in latent HIV-infected cells. | |||
T81931 | Linavonkibart | ||
Linavonkibart (SRK 181) is a fully human antibody with high affinity for latent TGFβ1, selectively binding and inhibiting its activation. This compound is significant in the context of cancer [1]. | |||
T68502 | Dibrospidium Free Base | ||
Dibrospidium Free Base is a dispirotripiperazine derivative and alkylating agent with potential antineoplastic and anti-inflammatory activities. The duration of DNA synthesis inhibition in tumor cells was found to correl... | |||
T77067 | Livmoniplimab | ||
Livmoniplimab (ABBV-151; ARGX-115), a potent humanized monoclonal antibody targeting LRRC32 (GARP)/TGFβ1, inhibits LRRC32-mediated activation of latent TGFβ1. This compound shows promise for cancer research [1]. | |||
T69009 | Gnidimacrin | ||
Gnidimacrin activated HIV-1 replication and killed persistently-infected cells at picomolar concentrations. In addition to its potential to purge HIV-1 from latently infected cells, gnidimacrin potently inhibited a panel... | |||
TN3914 | Echinatine | ATPase , IL Receptor , TNF | |
Echinatin exerts a protective effect against ischemia/reperfusion (I/R)-induced myocardial injury on hearts, this effect may be attributed to the antioxidant and anti-inflammatory activities of this compound. Echinatin c... | |||
T73986 | ONX-0914 TFA | ||
ONX-0914 (PR-957) TFA is a selective, noncompetitive, irreversible inhibitor targeting the chymotrypsin-like subunit (LMP7) of the immunoproteasome, effectively blocking cytokine production and mitigating the progression... |