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Cytoskeleton & Motor Proteins

Products for  Cytoskeleton & Motor Proteins

  1. Cat.No. Nombre del producto Información
  2. GC41268 (E)-2-Hexadecenal Sphingosine-1-phosphate (S1P), a bioactive lipid involved in many signaling processes, is irreversibly degraded by the membrane-bound S1P lyase. (E)-2-Hexadecenal  Chemical Structure
  3. GC41701 (E)-2-Hexadecenal Alkyne (E)-2-Hexadecenal alkyne is an alkyne version of the sphingolipid degradation product (E)-2-hexadecenal that can be used as a click chemistry probe. (E)-2-Hexadecenal Alkyne  Chemical Structure
  4. GC41719 (R)-nitro-Blebbistatin (R)-nitro-Blebbistatin is a more stable form of (+)-blebbistatin, which is the inactive form of (-)-blebbistatin. (R)-nitro-Blebbistatin  Chemical Structure
  5. GC41557 (S)-3'-amino Blebbistatin (S)-3'-amino Blebbistatin is a more stable and less phototoxic form of (-)-blebbistatin, which is a selective cell-permeable inhibitor of non-muscle myosin II ATPases. (S)-3'-amino Blebbistatin  Chemical Structure
  6. GC41484 (S)-3'-hydroxy Blebbistatin (S)-3'-hydroxy Blebbistatin is a more stable and less phototoxic form of (-)-blebbistatin, which is a selective cell-permeable inhibitor of non-muscle myosin II ATPases. (S)-3'-hydroxy Blebbistatin  Chemical Structure
  7. GC52192 (S)-4'-nitro-Blebbistatin (S)-4'-nitro-Blebbistatin es un inhibidor de miosina II no citotÓxico, fotoestable, fluorescente y especÍfico, utilizado en el estudio del papel especÍfico de la miosina II en estudios fisiolÓgicos, de desarrollo y biolÓgicos celulares. (S)-4'-nitro-Blebbistatin  Chemical Structure
  8. GC41739 (S)-nitro-Blebbistatin (S)-nitro-Blebbistatin is a more stable form of (-)-blebbistatin, which is a selective cell-permeable inhibitor of non-muscle myosin II ATPases. (S)-nitro-Blebbistatin  Chemical Structure
  9. GC49736 10-acetyl Docetaxel 10-acetyl Docetaxel (10-Acetyl docetaxel) es un anÁlogo de Docetaxel, con actividad anticancerÍgena. Docetaxel es un inhibidor del desensamblaje de microtÚbulos, con actividad antimitÓtica. 10-acetyl Docetaxel  Chemical Structure
  10. GC41110 16-epi Latrunculin B 16-epi Latrunculin B, first isolated from the Red Sea sponge N. 16-epi Latrunculin B  Chemical Structure
  11. GC48423 19-O-Acetylchaetoglobosin A La 19-O-acetilquetoglobosina A, un alcaloide del citocalasano, es un metabolito fÚngico aislado originalmente de C. globosum que tiene actividades inhibidoras de la polimerizaciÓn de actina y citotÓxicas. La 19-O-acetilquetoglobosina A es citotÓxica para las células de cÁncer de cuello uterino HeLa. 19-O-Acetylchaetoglobosin A  Chemical Structure
  12. GC52029 2-Aminoflubendazole El 2-aminoflubendazol es el metabolito de los bencimidazoles. 2-Aminoflubendazole  Chemical Structure
  13. GC49244 4-oxo Isotretinoin An active metabolite of isotretinoin 4-oxo Isotretinoin  Chemical Structure
  14. GC48721 6-O-Demethyl Griseofulvin A metabolite of griseofulvin 6-O-Demethyl Griseofulvin  Chemical Structure
  15. GC40844 9-(2,2-Dicyanovinyl)julolidine La 9-(2,2-Dicianovinil)julolidina (9-(2,2-Dicianovinil)julolidina), un rotor molecular y un tinte fluorescente Único, se une a la tubulina y la actina y aumenta drÁsticamente la intensidad de su fluorescencia tras la polimerizaciÓn. 9-(2,2-Dicyanovinyl)julolidine  Chemical Structure
  16. GC25025 Abraxane Abraxane (Nab-Paclitaxel), a novel solvent-free taxane with the binding ratio of Paclitaxel to human serum albumin of 1:9, is an anti-microtubule drug that promotes microtubule aggregation in tubulin dimer and inhibits microtubule depolymerization to stabilize the microtubule system. Abraxane  Chemical Structure
  17. GC18274 Amiprofos-methyl El amiprofos-metilo (BAY-NTN 6867) es un herbicida de amida fosfórica. Amiprofos-methyl  Chemical Structure
  18. GC25075 Ansamitocin p-3 (Maytansinol isobutyrate, NSC292222) Ansamitocin p-3 (Maytansinol isobutyrate, NSC292222, Antibiotic C 15003P3) is a potent inhibitor of tubulin polymerization with IC50 of 3.4 μM. Ansamitocin p-3 (Maytansinol isobutyrate, NSC292222)  Chemical Structure
  19. GC42933 Binucleine 2 Binucleine 2 is an isoform-specific and ATP-competitive inhibitor of Drosophila Aurora B kinase (Ki = 0.36 μM), a kinase involved in cell division. Binucleine 2  Chemical Structure
  20. GC18408 BML-278 BML-278 is an activator of sirtuin 1 (SIRT1) that has an EC150 value (effective concentration able to increase the enzyme by 150%) of 1 uM. BML-278  Chemical Structure
  21. GC46946 BPC 157 (acetate) A pentadecapeptide with diverse biological activities BPC 157 (acetate)  Chemical Structure
  22. GC45395 Cabazitaxel-d9 Cabazitaxel-d9 es cabazitaxel marcado con deuterio. Cabazitaxel es un derivado semisintético del taxoide natural 10-desacetilbacatina III con potencial actividad antineoplÁsica. Cabazitaxel-d9  Chemical Structure
  23. GC43135 Cambendazol Cambendazol es uno de los agentes mÁs efectivos para la terapia de estrongiloidiasis humana y . Cambendazol  Chemical Structure
  24. GC40890 CAY10701 CAY10701 is a 7-deazahypoxanthine analog that prevents microtubule formation, blocking the proliferation of HeLa and MCF-7 cells (GI50s = 22 and 38 nM, respectively). CAY10701  Chemical Structure
  25. GC52367 Citrullinated Vimentin (G146R) (R144 + R146) (139-159)-biotin Peptide A biotinylated and citrullinated mutant vimentin peptide Citrullinated Vimentin (G146R) (R144 + R146) (139-159)-biotin Peptide  Chemical Structure
  26. GC52370 Citrullinated Vimentin (R144) (139-159)-biotin Peptide A biotinylated and citrullinated vimentin peptide Citrullinated Vimentin (R144) (139-159)-biotin Peptide  Chemical Structure
  27. GC40664 Colcemid Colcemid es una inhibición de citoesqueleto, cuando las células de mamíferos y los ovocitos inducen la detención mitótica o la detención meiótica respectivamente durante la fase de ruptura de la vesícula. Colcemid  Chemical Structure
  28. GC47117 Colchicine-d6 La colchicina-d6 es la colchicina marcada con deuterio. La colchicina es un inhibidor de la tubulina y un agente disruptor de los microtÚbulos. La colchicina inhibe la polimerizaciÓn de microtÚbulos con una IC50 de 3 nM. La colchicina también es un antagonista competitivo de los receptores de glicina α3 (GlyR). Colchicine-d6  Chemical Structure
  29. GC49913 Davunetide (acetate) A neuroprotective ADNP-derived peptide Davunetide (acetate)  Chemical Structure
  30. GC43469 Diminutol Diminutol is a cell-permeable purine derivative that inhibits the NADP-dependent oxidoreductase, NQO1 (Ki = 1.72 μM), to destabilize microtubules and disrupt mitosis. Diminutol  Chemical Structure
  31. GC48968 Docetaxel (hydrate)

    An analog of taxol with antitumor properties

    Docetaxel (hydrate)  Chemical Structure
  32. GC47250 Docetaxel-d9 Docetaxel-d9 (RP-56976-d9) es el docetaxel etiquetado con deuterio. Docetaxel (RP-56976) es un inhibidor de la despolimerizaciÓn de microtÚbulos, con una IC50 de 0,2 μM. Docetaxel atenÚa los efectos de la expresiÓn de los genes bcl-2 y bcl-xL. Docetaxel detiene el ciclo celular en G2/M y conduce a la apoptosis celular. El docetaxel tiene actividad anticancerÍgena. Docetaxel-d9  Chemical Structure
  33. GC49124 EN219 EN219 es un ligando covalente sintético moderadamente selectivo frente a una cisteÍna N-terminal (C8) de RNF114 con una IC50 de 470 nM. EN219 inhibe la autoubiquitinaciÓn mediada por RNF114 y la ubiquitinaciÓn de p21. EN219  Chemical Structure
  34. GC48720 Griseofulvic Acid A metabolite of griseofulvin Griseofulvic Acid  Chemical Structure
  35. GC48688 Griseofulvin-d3 An internal standard for the quantification of griseofulvin Griseofulvin-d3  Chemical Structure
  36. GC40048 MPS1/TTK Inhibitor MPS1/TTK inhibitor is an inhibitor of monopolar spindle 1 (MPS1/TTK; IC50 = 5.8 nM), a kinase involved in mitotic spindle checkpoint signaling that is overexpressed in certain cancerous tumors. MPS1/TTK Inhibitor  Chemical Structure
  37. GC41564 MPT0B014 An inhibitor of tubulin polymerization MPT0B014  Chemical Structure
  38. GC18445 N-Deacetylcolchicine An inhibitor of microtubule polymerization N-Deacetylcolchicine  Chemical Structure
  39. GC49404 Paclitaxel C A taxoid and an inhibitor of microtubule depolymerization Paclitaxel C  Chemical Structure
  40. GC45944 para-amino-Blebbistatin

    Una forma más estable y menos fototóxica de (-)-blebbistatina con una mayor solubilidad en agua.

    para-amino-Blebbistatin  Chemical Structure
  41. GC44618 Phalloidin-AMCA Conjugate Phalloidin-AMCA conjugate is a blue fluorophore that specifically labels filamentous actin (F-actin). Phalloidin-AMCA Conjugate  Chemical Structure
  42. GC44620 Phalloidin-Tetramethylrhodamine Conjugate Phalloidin-retramethylrhodamine conjugate is an orange fluorescent probe (ex/em = 546/575 nm) that selectively binds to F-actin. Phalloidin-Tetramethylrhodamine Conjugate  Chemical Structure
  43. GC48394 Phomopsinamine An inhibitor of microtubule polymerization Phomopsinamine  Chemical Structure
  44. GC49077 Podophyllotoxin-d6 An internal standard for the quantification of podophyllotoxin and picropodophyllotoxin Podophyllotoxin-d6  Chemical Structure
  45. GC44800 Quininib A CysLT1 and CysLT2 receptor antagonist Quininib  Chemical Structure
  46. GC45688 STX140 An estrogen sulfamate STX140  Chemical Structure
  47. GC48119 Suprafenacine An inhibitor of tubulin polymerization with anticancer activity Suprafenacine  Chemical Structure
  48. GC44976 Swinholide A Swinholide A es el policétido marino que se une a la actina y dimeriza la actina con una Kd de ~ 50 nM. Swinholide A  Chemical Structure
  49. GC45750 Thymosin β4 (human, mouse, rat, porcine, bovine) (acetate) An actin-sequestering peptide Thymosin β4 (human, mouse, rat, porcine, bovine) (acetate)  Chemical Structure
  50. GC18763 TN-16 TN-16 es un potente inhibidor de la polimerizaciÓn de microtÚbulos con IC50 de 0,4-1,7 μM. TN-16  Chemical Structure
  51. GC52364 Vimentin (139-159)-biotin Peptide A biotinylated vimentin peptide Vimentin (139-159)-biotin Peptide  Chemical Structure
  52. GC52371 Vimentin (G146R) (139-159)-biotin Peptide A biotinylated mutant vimentin peptide Vimentin (G146R) (139-159)-biotin Peptide  Chemical Structure
  53. GC45595 Vulpinic Acid El Ácido vulpÍnico, un metabolito del liquen, disminuye la producciÓn de ROS inducida por H2O2, el estrés oxidativo y los daÑos relacionados con el estrés oxidativo en las células endoteliales de la vena umbilical humana (HUVEC). Vulpinic Acid  Chemical Structure
  54. GC18578 YK-3-237 YK-3-237, un activador de SIRT1, se dirige al mutante p53. YK-3-237 inhibe la proliferaciÓn de células de cÁncer de mama triple negativas. YK-3-237  Chemical Structure

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