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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
TD0081 | EDANS | EDANS acid [5-((2-Aminoethyl)amino)naphthalene-1-sulfonic acid],1,5-EDANS,EDANS acid [5-((2-Aminoethyl)amino)napht | Others |
EDANS (EDANS acid [5-((2-Aminoethyl)amino)naphthalene-1-sulfonic acid]) is a novel and quenched fluorogenic substrate for assaying retroviral protease by resonance energy transfer (RET). | |||
T11495L | GSK 4027 | Others | |
GSK 4027 is a PCAF/GCN5 bromodomain chemical probe. In a time-resolved fluorescence resonance energy transfer (TR-FRET) assay, it has a pIC50 of 7.4±0.11 for PCAF. | |||
T81839 | MCA succinimidyl ester | ||
MCA succinimidyl ester, a derivative of MCA, selectively reacts with amines and serves as a peptide substrate for fluorescence resonance energy transfer (FRET) [1]. | |||
T81669 | NKG2D-IN-2 | ||
NKG2D-IN-2 (compound 47) is an inhibitor of the natural killer group 2D receptor (NKG2D), demonstrating half-maximal inhibitory concentrations (IC50s) of 0.1 µM for NKG2D/MICA and 0.2 µM for ULBP6 in time-resolved fluore... | |||
T78434 | Mca-(endo-1a-Dap(Dnp))-TNF-Alpha (-5 to +6) amide (human) TFA | ||
Mca-(endo-1α-Dap(Dnp))-TNF-α(-5 to +6) amide (human) TFA is a peptide that functions as a fluorescence resonance energy transfer (FRET)-based substrate, with its activity determined by the change in fluorescence intensit... | |||
T78697 | Keap1-Nrf2-IN-15 | ||
Keap1-Nrf2-IN-15 (Compound 24a) is a potent inhibitor of the Keap1-Nrf2 protein-protein interaction, displaying IC50 values of 77 nM in a fluorescence polarization (FP) assay and 2.5 nM in a time-resolved fluorescence re... | |||
T81838 | Mca-(endo-1a-Dap(Dnp))-TNF-Alpha (-5 to +6) amide (human) | ||
Mca-(endo-1a-Dap(Dnp))-TNF-Alpha (-5 to +6) amide (human) is a peptide utilized as a fluorescence resonance energy transfer (FRET) based substrate for proteolytic activity assays, wherein the cleavage-induced change in f... | |||
T78689 | HAChE-IN-1 | ||
hAChE-IN-1 (Compound 24) is a potent inhibitor of human acetylcholinesterase (hAChE), exhibiting an inhibition concentration half-maximum (IC50) of 1.09 μM. Additionally, it inhibits tau-oligomerization with an effective... | |||
T37040 | DiIC1(5) | DiIC1(5) | |
DiIC1(5) is a signal-off fluorescent probe for the detection of mitochondrial membrane potential disruption. It accumulates in mitochondria and its fluorescence intensity decreases when the mitochondrial membrane potenti... | |||
T81836 | Mca-SEVNLDAEFK(Dnp)-NH2 | ||
Mca-SEVNLDAEFK(Dnp)-NH2 is a fluorogenic substrate featuring a 7-methoxycoumarin moiety whose fluorescence is quenched by the adjacent 2,4-dinitrophenyl group through resonance energy transfer. This compound serves as a ... | |||
T78389 | Coelenteramine 400a | Bisdeoxycoelenterazine,Coelenterazine 400a | |
Coelenteramine 400a (Coelenterazine 400a), a Coelenterazine derivative, serves as a substrate for Renilla luciferase (RLuc), facilitating the emission of blue light at 395 nm [1] [2]. This compound alters the bioluminesc... | |||
T41171 | BODIPY FL VH032 | ||
BODIPY FL VH032 is a high-affinity VHL fluorescent probe (Kd= 3.01 nM) with application in time-resolved fluorescence resonance energy-transfer (TR-FRET) assays for high-throughput identification and characterization of ... | |||
T80846 | WAAG-3R | ||
WAAG-3R is a bioactive peptide utilized in an ADAMTS-4 (Aggrecanase-1) assay, where aggrecanases, a subset of the ADAMTS (A disintegrin and metalloprotease with thrombospondin motifs) family, target aggrecan, a key struc... | |||
T83957 | CELT-211 | ||
CELT-211 is a potent, selective fluorescent ligand for the h5HT2B serotonin receptor, demonstrating full selectivity over h5HT2A and h5HT2C receptors with a Ki value of 56.3 nM in radioligand binding assays for h5HT2B re... | |||
T83956 | CELT-133 | ||
CELT-133 is a selective fluorescent antagonist for the hα1A adrenergic receptor, demonstrating complete selectivity towards α1A over α2A receptors, with a Ki of 5 nM and 15% displacement at 1 μM in radioligand binding as... | |||
T83676 | Tianeptine Metabolite MC5 sodium | ||
Tianeptine metabolite MC5, an active derivative of the atypical antidepressant tianeptine produced through β-oxidation, exhibits selective G protein activation in bioluminescence resonance energy transfer (BRET) assays. ... | |||
T83664 | Europium W1024 ITC | Eu-W1024 ITC,Europium W1024 Isothiocyanate | |
Europium W1024 isothiocyanate (ITC) is a lanthanide-based fluorophore characterized by its long emission lifetime and significant Stokes shift, featuring excitation and emission maxima at 340 and 613 nm, respectively. Th... | |||
T83952 | CoraFluor 1, amine reactive | ||
CoraFluor 1, an amine-reactive terbium-based compound, serves as a potent donor in time-resolved Förster resonance energy transfer (TR-FRET) assays, including applications in target engagement and ternary complex assessm... | |||
T83959 | CELT-426 | ||
CELT-426 is a potent, partially selective fluorescent antagonist of the human D2 dopamine receptor, exhibiting Ki values of 89.3 nM, 194.8 nM, and 263.6 nM for D2, D3, and D4 dopamine receptors, respectively, in radiolig... |