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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T7265 | HSP27 inhibitor J2 | J2 | HSP |
HSP27 inhibitor J2 (J2) (J2) is a HSP27 inhibitor, inhibits a production of HSP27 giant polymers, thereby having an effect of inhibiting a chaperone function of the HSP27 and reducing a cell protection function. | |||
T11476 | GSK-J2 | Others | |
GSK-J2, an isomer of GSK-J1, haven't any specific activity. GSK-J1 is a potent inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A. | |||
T73782 | Prostaglandin J2 | ||
Prostaglandin J2 (PGJ2), a derivative of Prostaglandin D2 (PGD2), serves as a potent agonist for PGD2 receptors (DP), exhibiting affinity constants (K i) of 0.9 nM and 6.6 nM for hDP and hCRTH2 receptors, respectively. I... | |||
T22473 | 15-deoxy-Δ-12,14-Prostaglandin J2 | Others | |
15-deoxy-Δ-12,14-Prostaglandin J2 is a PPARγ agonist. | |||
T68587 | Oxmetidine mesylate | ||
Oxmetidine mesylate is an antagonist to Histamine H2 Receptors | |||
T77644 | AJ2-30 | Others | |
AJ2-30 is an SLCl5A4 inhibitor that inhibits TLR9-mediated B cell activation and inhibits MDP transporter.AJ2-30 inhibits endogenous NOD signaling in human and mouse macrophages.AJ2-30 can be used for the study of inflam... | |||
T11701 | J22352 | Caspase | |
J22352, a PROTAC (proteolysis-targeting chimeras)-like and highly selective HDAC6 inhibitor with an IC50 value of 4.7 nM, enhances anticancer effects in glioblastoma by promoting HDAC6 degradation. It does so by inhibiti... | |||
T69572 | UAWJ248 | ||
UAWJ248 is a SARS-CoV-2 Protease inhibitor. UAWJ248 provides new directions for the development of Mpro inhibitors as SARS-CoV-2 antivirals. | |||
T80760 | XSJ2-46 | Influenza Virus | |
XSJ2-46, a 5'-amino NI analog, is an antiviral agent possessing anti-Zika virus properties and demonstrates reasonable inhibition of RNA-dependent RNA polymerases (RdRp), with an IC50 of 8.78 μM [1]. | |||
T83152 | AJ2-71 | ||
AJ2-71 is a SLC15A4 inhibitor that suppresses IFN-α production and obstructs SLC15A4-mediated MDP transport, making it suitable for research of inflammation [1]. | |||
T70690 | UAWJ246 | ||
UAWJ246 is a SARS-CoV-2 Protease inhibitor (IC50 = 45 nM). UAWJ246 provides new directions for the development of Mpro inhibitors as SARS-CoV-2 antivirals. | |||
T22881 | JNJ28871063 hydrochloride | JNJ 28871063 hydrochloride | Others |
ErbB receptor family inhibitor | |||
T80432 | δ-Buthitoxin-Hj2a | Sodium Channel | |
δ-Buthitoxin-Hj2a, a potent scorpion-venom peptide, acts as a NaV1.1 agonist with an EC50 value of 32 nM and is employed in Dravet syndrome (DS) research [1]. | |||
T79543 | J27644 | HDAC | |
J27644 is a potent HDAC (histone deacetylase) inhibitor that mitigates TGF-β (transforming growth factor beta)-induced pulmonary fibrosis [1]. | |||
T15277 | Fervenulin | Parasite | |
Fervenulin is isolated from a nematicidal actinomycete Streptomyces sp. CMU-MH021 with nematicidal activity. It also inhibits egg hatch and J2 mortality of M. incognita (MICs: 30 μg/mL and 120 μg/mL, respectively). | |||
TN3050 | 4'-Methoxyflavanone | Others | |
4'-Methoxyflavanone is a flavonoid isolated from natural Isaria fumosorosea KCH J2, which is used in the study of metabolic and cardiovascular diseases. | |||
TN5788 | Phyllostine | ||
Phyllostine appears to be their more immediate precursor, since PCMB-treated extracts of J2 converted Phyllostine but not isoepoxydon to these new metabolites. | |||
T22820 | GSK J5 HCl (1394854-51-3 free base) | GSK J5 HCl | Others |
GSK J5 HCl is the hydrochloride form of GSK J5. GSK J5 is an inactive isomer of GSK J4 and a cell-permeable ester derivative of inactive control GSK J2. | |||
T36180 | Azelaoyl PAF | ||
Oxidized low-density lipoprotein (oxLDL) particles contain low molecular weight species which promote the differentiation of monocytes via the nuclear receptor PPARγ. One of these substances was recently isolated and pur... | |||
T35551 | Gallocyanine | ||
Gallocyanine is a small molecule blue dye used to stain nuclei. It is known to inhibit Dickkopf-1 (Dkk1), an antagonist of the Wnt pathway. Gallocyanine can disrupt the interaction of Dkk1 with its receptor LRP5/6 (IC50 ... |