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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T39185 | Pp60 (v-SRC) Autophosphorylation Site, Phosphorylated | pp60 (v-SRC) Autophosphorylation Site, Phosphorylated | |
pp60 (v-SRC) Autophosphorylation Site, Phosphorylated is a phosphorylated peptide derived from an EGFR substrate. It serves as a valuable tool for quantifying phosphorylated substrates in screening EGFR Kinase inhibitors... | |||
T13342L | WIN site inhibitor 1 TFA (2407457-36-5 free base) | WIN site inhibitor 1 TFA | Others |
WIN site inhibitor 1 TFA is a WIN site of chromatin-associated WD repeat-containing protein 5 (WDR5) inhibitor (Kd: 0.1 nM). | |||
T76381 | H1-7 (histone H1 phosphorylation site), PKA Substrate | ||
H1-7 (histone H1 phosphorylation site), a synthetic polypeptide serving as a PKA substrate, demonstrates utility in PKA substrate applications [1] [2]. | |||
T13342 | WDR5-IN-4 | WIN site inhibitor 1 | Others |
WIN site inhibitor 1 is a WIN site of chromatin-associated WD repeat-containing protein 5 (WDR5) inhibitor (Kd: 0.1 nM), with anti-cancer activity. | |||
T83756 | S1H TFA | Site 1-binding Helix | |
S1H, a synthetic peptide mimetic of human growth hormone amino acids 36-51, acts as an antagonist to the growth hormone receptor. It forms an α-helical structure in solution and inhibits STAT5 phosphorylation triggered b... | |||
T8868 | 4BP-TQS | AChR | |
4BP-TQS is an allosteric agonist of α7 nAChRs. | |||
T11351 | Galanthamine N-Oxide | AChE | |
Galanthamine N-Oxide, an alkaloid extracted from Zephyranthes concolor bulbs, effectively inhibits acetylcholinesterase (AChE) from electric eel with an EC50 of 26.2 μM. It acts as a significant inhibitor of substrate ac... | |||
T8230 | PNU112455A hydrochloride | PNU 112455A | CDK |
PNU112455A hydrochloride is an ATP site competetive inhibitor of CDK2 and CDK5,binds to the ATP site of CDK2 and CDK5 with Kms of 3.6 and 3.2 μM, respectively. | |||
T8533 | ML318 | Others , Antibiotic | |
ML318 is a biaryl nitrile PvdQ acylase inhibitor (IC50 of 20 nM for binding in the acyl-binding site). ML318 inhibits P. aeruginosa (PAO1) with IC50 of 19 μM. ML318 prevents pyoverdine production and limits the growth of... | |||
T60072 | ZL0590 | Epigenetic Reader Domain | |
ZL0590 is an effective and selective inhibitor of BD1-BRD4 (IC50 = 90 nM) with anti-inflammatory activities. | |||
T8336 | OGG1-IN-08 | OGG1-IN-O8 | Others |
OGG1-IN-08 (OGG1-IN-O8) is an inhibitor of 8-oxoguanine DNA glycosylase 1 (OGG1;IC50 : 0.35 μM) | |||
T9627 | PHD-1-IN-1 | HIF/HIF Prolyl-Hydroxylase | |
PHD-1-IN-1 is a potent inhibitor of hypoxia-inducible factor prolylhydroxylase domain-1 (PHD-1) enzyme(IC50 = 0.034 μM). | |||
T15012 | Crolibulin | EPC2407 | Microtubule Associated |
Crolibulin (EPC2407) is an inhibitor of small molecule tubulin polymerization. | |||
T10066 | 2',5'-Dideoxyadenosine | Adenylyl cyclase , Adrenergic Receptor , AChR | |
2',5'-Dideoxyadenosine is a potent and non-competitive adenylyl cyclase inhibitor via binding the P-site (IC50: 3 μM). | |||
T41302 | Itaconate-alkyne | ITalk | Others |
Itaconate-alkyne (ITalk) is a bioorthogonal probe for quantitative and site-specific chemoproteomic profiling of itaconate in inflammatory macrophages and enables biochemical evaluation and proteomic analysis of its dire... | |||
T38862 | Nandrolone acetate | 19-Nortestosterone 17β-acetate | Others |
Nandrolone acetate (19-Nortestosterone 17β-acetate) is a competitive inhibitor of isomerase with the Ki of 7 μM for Δ5-3-ketosteroid isomerase of Pseudomonas testosreroni. | |||
T1901 | (E/Z)-TG003 | TG003 | BCL , CDK |
(E/Z)-TG003 is a potent and ATP-competitive Cdc2-like kinase (Clk) inhibitor. | |||
T1909 | L-701324 | L701324 | NMDAR , iGluR |
L-701324 is an NMDA receptor with high affinity and selectivity for the glycine site, used as an orally active and long-acting anticonvulsant. | |||
T22517 | 5,7-Dichlorokynurenic acid | 5,7-dichlorokynurenic acid sodium,5,7-DCKA | NMDAR |
5,7-Dichlorokynurenic acid (5,7-dichlorokynurenic acid sodium) is an NMDA receptor antagonist. | |||
T21065 | Artemisitene | Others | |
Artemisitene is the oxidized form of Artemisinin and is an antimalarial agent. Artemisinin precursors are the important basic substances for biosynthesis of Artemisinin, including Artemisinin B, Artemisitene, Artemisini... |