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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T28824 | SNX0723 | SNX 0723,SNX- 0723 | HSP |
SNX0723 is a potent Hsp90 Inhibitor with anti-Plasmodium activity. SNX0723 shows high binding affinity for HsHsp90 and PfHsp90 with Kis of 4.4 and 47 nM, respectively. SNX0723 inhibits liver-stage P. berghei ANKA parasit... | |||
TP2118 | SNX-482 | SNX 482 | |
Potent and selective, voltage-dependent R-type CaV2.3 calcium channel blocker (IC50 = 30 nM). Antinociceptive; inhibits nociceptive C-fibre and Aδ-fibre-evoked neuronal responses. | |||
T6305 | SNX2112 | SNX-2112,PF 04928473,SNX 2112 | HSP |
SNX2112 (PF 04928473) is an orally active Hsp90 inhibitor, with a Kd of 16 nM. | |||
T68393 | SNX-7081 | ||
NX-7081 is a novel small molecule inhibitor of Hsp90, which blocks components of inflammation, including cytokine production, protein kinase activity, and angiogenic signaling. SNX-7081 showed strong binding affinity to ... | |||
T6341 | PF04929113 | PF-04929113,SNX-5422,PF 04929113 | HSP , HER |
PF04929113 (SNX-5422) is a synthetic, novel, small molecule Hsp90 Inhibitor. As an oral formulation that demonstrates strong efficacy and tolerability, PF04929113 is positioned as a breakthrough therapy with broad applic... | |||
T4342 | PF-04929113 Mesylate | PF-04929113 (Mesylate),SNX-5422 Mesylate | HSP , HER |
PF-04929113 Mesylate (SNX-5422 Mesylate), a prodrug of SNX-2112, is an orally available Hsp90 inhibitor (Kd: 41 nM) and also induces Her-2 degradation (IC50: 37 nM). | |||
T80443 | ω-Conotoxin MVIID | SNX-238 | Calcium Channel |
ω-Conotoxin MVIID (SNX-238) is a peptide from the Conus genus that inhibits the ω-Conotoxin-GVIA-sensitive, high-threshold calcium (Ca 2+) current in fish retinal ganglion cells [1]. | |||
T77613 | SNX7 | WAY-323879 | CDK |
SNX7 (WAY-323879) is an inhibitor of the cell cycle protein-dependent kinase inhibitor (CDKI) pathway. SNX7 can be utilized as a tool for investigating the aging process and other diseases associated with CDKI. | |||
T24811 | SNX2-1-108 | SNX-21108,SNX21108,SNX 21108 | |
SNX2-1-108 is a selective CDK8 and CDK19 inhibitor. | |||
TP1559L | Ziconotide Acetate (107452-89-1 free base) | Prialt,Ziconotide Acetate | Calcium Channel |
Ziconotide Acetate (107452-89-1 free base) (Prialt) is an analgesic agent and has been used to treat neuropathic and non-neuropathic pain. Ziconotide Acetate (107452-89-1 free base) acts by binding to N-type calcium chan... | |||
T81137 | SNX7886 | PROTACs | |
SNX7886 is a potent PROTAC (proteolysis-targeting chimera) that effectively degrades CDK8 and CDK19, achieving 90% degradation of CDK8 and 80% degradation of CDK19 in 293 cells [1]. | |||
T18018 | HS-27 | Others , HSP | |
HS-27 is a fluorescently-tethered inhibitor of Hsp90 with SNX-5422 tethered via a PEG linker to a fluorescein isothiocyanate or FITC. HS-27 can be used in see-and-treat paradigms. | |||
T75710 | Ziconotide TFA | ||
Ziconotide TFA (SNX-111 TFA), a peptide-based, potent, and selective N-type calcium channels antagonist, effectively reduces synaptic transmission and is utilized in chronic pain research [1]. |
Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPJ-00888 | ANXA7 Protein, Human, Recombinant | Human | E. coli |
Annexin A7 (ANXA7) is a member of the annexin family of calcium-dependent phospholipid binding proteins. Annexin A7 has a unique, highly hydrophobic N-terminal domain and a conserved C-terminal region. The C-terminal reg... | |||
TMPH-02127 | SNX16 Protein, Human, Recombinant (His) | Human | E. coli |
May be involved in several stages of intracellular trafficking. Plays a role in protein transport from early to late endosomes. Plays a role in protein transport to the lysosome. Promotes degradation of EGFR after EGF si... | |||
TMPH-02301 | VPS35 Protein, Human, Recombinant (His & Myc) | Human | E. coli |
Acts as component of the retromer cargo-selective complex (CSC). The CSC is believed to be the core functional component of retromer or respective retromer complex variants acting to prevent missorting of selected transm... |