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Other Signal Transduction

Signal Transduction

Cellular responses are triggered by proteins, drugs, or pathogens binding to specific receptors. Receptor mediated signaling is a cascade of enzymatic reactions that amplifies the signal. The agonists and antagonists modulating receptor functionality are essential tools for research and medical practice. read more

Products for  Other Signal Transduction

  1. Numéro de catégorie Nom du produit Informations
  2. GC52141 2-Chloro-N-methyl-N-(4-nitrophenyl)acetamide 2-Chloro-N-methyl-N-(4-nitrophenyl)acetamide  Chemical Structure
  3. GC52129 3-Amino-5-hydroxybenzoic Acid 3-Amino-5-hydroxybenzoic Acid  Chemical Structure
  4. GC49494 4-Aminobenzylphosphonic Acid An alkaline phosphatase inhibitor 4-Aminobenzylphosphonic Acid  Chemical Structure
  5. GC49110 AICA Ribonucleotide An AMPK activator AICA Ribonucleotide  Chemical Structure
  6. GC52361 AMARA Peptide (trifluoroacetate salt) A peptide substrate for AMPK AMARA Peptide (trifluoroacetate salt)  Chemical Structure
  7. GC49403 Benzarone Benzarone (Fragivix) est un puissant inhibiteur du transporteur 1 de l'acide urique humain (hURAT1), avec une IC50 de 2,8 μM dans l'ovocyte. Benzarone  Chemical Structure
  8. GC49300 BIM-46187 (hydrochloride) An inhibitor of heterotrimeric G-protein signaling BIM-46187 (hydrochloride)  Chemical Structure
  9. GC49079 C82 An Mtb CdnP inhibitor C82  Chemical Structure
  10. GC49332 Calcineurin Substrate (trifluoroacetate salt) A synthetic peptide substrate Calcineurin Substrate (trifluoroacetate salt)  Chemical Structure
  11. GC49433 Capsiate Capsiate, en tant qu'analogue de capsaÏcine extrait d'un cultivar non piquant de poivron rouge CH-19, est un agoniste actif par voie orale du TRPV1 . Capsiate  Chemical Structure
  12. GC48992 CGP 77675 (hydrate) An inhibitor of Src family kinases CGP 77675 (hydrate)  Chemical Structure
  13. GC49392 CHIR98024 CHIR98024 (composé L) est un inhibiteur de la glycogène synthase kinase 3 (GSK3) avec une CE50 de 0,2566 μM. CHIR98024  Chemical Structure
  14. GC49334 Chroman 1 (hydrochloride hydrate) A ROCK2 inhibitor Chroman 1 (hydrochloride hydrate)  Chemical Structure
  15. GC49556 Cl-Necrostatin-1 A RIPK1 inhibitor Cl-Necrostatin-1  Chemical Structure
  16. GC13855 Eeyarestatin I Eeyarestatin I, un puissant inhibiteur de la dégradation des protéines associées au réticulum endoplasmique (ERAD), est un puissant inhibiteur de la translocation des protéines. Eeyarestatin I cible le processus de désubiquitination associé À p97 (PAD) et inhibe la désubiquitination dépendante d'atx3. L'Eeyarestatine I induit la mort cellulaire via la protéine pro-apoptotique NOXA et a des effets anticancéreux. Eeyarestatin I  Chemical Structure
  17. GC52002 Emavusertib L'emavusertib (CA-4948) est un puissant inhibiteur d'IRAK4/FLT3 avec une activité anti-tumorale. Emavusertib  Chemical Structure
  18. GC52336 ENPP1 Inhibitor 43 An ENPP1 inhibitor ENPP1 Inhibitor 43  Chemical Structure
  19. GC52277 ENPP3 Inhibitor An ENPP3 inhibitor ENPP3 Inhibitor  Chemical Structure
  20. GC52362 ENPP3 Inhibitor 4g An ENPP1 and ENPP3 inhibitor ENPP3 Inhibitor 4g  Chemical Structure
  21. GC52322 ENPP3 Inhibitor 4t An ENPP3 inhibitor ENPP3 Inhibitor 4t  Chemical Structure
  22. GC49074 Forphenicine A bacterial metabolite and an inhibitor of alkaline phosphatase Forphenicine  Chemical Structure
  23. GC25450 GATA4-NKX2-5-IN-1

    GATA4-NKX2-5-IN-1 (3i-1000) is a small-molecule compound inhibiting GATA4 and NKX2-5 transcriptional synergy with IC50 of 3 uM

    GATA4-NKX2-5-IN-1  Chemical Structure
  24. GC49284 GSK-A1 GSK-A1 est un inhibiteur sélectif de la phosphatidylinositol 4-kinase PI4KA (PI4KIIIα) de type III avec un pIC50 de 8,5 À 9,8. GSK-A1  Chemical Structure
  25. GC52328 KYL (trifluoroacetate salt) An EphA4 inhibitor KYL (trifluoroacetate salt)  Chemical Structure
  26. GC17779 Levetiracetam Le lévétiracétam, un agent antiépileptique, se lie À la protéine de la vésicule synaptique SV2A. Levetiracetam  Chemical Structure
  27. GC49269 Myr-ZIP A PKMζ inhibitor Myr-ZIP  Chemical Structure
  28. GC49090 Nilvadipine-d4 An internal standard for the quantification of nilvadipine Nilvadipine-d4  Chemical Structure
  29. GC52151 PKCθ Inhibitor (hydrochloride) PKCθ Inhibitor (hydrochloride)  Chemical Structure
  30. GC49265 PKI (14-22) amide (myristoylated) (trifluoroacetate salt) A PKA inhibitor PKI (14-22) amide (myristoylated) (trifluoroacetate salt)  Chemical Structure
  31. GC49221 QLT0267 An ILK inhibitor QLT0267  Chemical Structure
  32. GC52115 S-99 An inhibitor of ASK1 S-99  Chemical Structure
  33. GC49692 Tofacitinib-d3 (citrate) An internal standard for the quantification of tofacitinib Tofacitinib-d3 (citrate)  Chemical Structure
  34. GC49150 Tpl2 Kinase Inhibitor (hydrochloride) A Tpl2 inhibitor Tpl2 Kinase Inhibitor (hydrochloride)  Chemical Structure
  35. GC52274 Y-33075 (hydrochloride) An inhibitor of ROCK2 Y-33075 (hydrochloride)  Chemical Structure

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