Inicio >> Signaling Pathways >> Immunology/Inflammation

Immunology/Inflammation

The immune and inflammation-related pathway including the Toll-like receptors pathway, the B cell receptor signaling pathway, the T cell receptor signaling pathway, etc.

Toll-like receptors (TLRs) play a central role in host cell recognition and responses to microbial pathogens. TLR4 initially recruits TIRAP and MyD88. MyD88 then recruits IRAKs, TRAF6, and the TAK1 complex, leading to early-stage activation of NF-κB and MAP kinases [1]. TLR4 is endocytosed and delivered to intracellular vesicles and forms a complex with TRAM and TRIF, which then recruits TRAF3 and the protein kinases TBK1 and IKKi. TBK1 and IKKi catalyze the phosphorylation of IRF3, leading to the expression of type I IFN [2].

BCR signaling is initiated through ligation of mIg under conditions that induce phosphorylation of the ITAMs in CD79, leading to the activation of Syk. Once Syk is activated, the BCR signal is transmitted via a series of proteins associated with the adaptor protein B-cell linker (Blnk, SLP-65). Blnk binds CD79a via non-ITAM tyrosines and is phosphorylated by Syk. Phospho-Blnk acts as a scaffold for the assembly of the other components, including Bruton’s tyrosine kinase (Btk), Vav 1, and phospholipase C-gamma 2 (PLCγ2) [3]. Following the assembly of the BCR-signalosome, GRB2 binds and activates the Ras-guanine exchange factor SOS, which in turn activates the small GTPase RAS. The original RAS signal is transmitted and amplified through the mitogen-activated protein kinase (MAPK) pathway, which including the serine/threonine-specific protein kinase RAF followed by MEK and extracellular signal related kinases ERK 1 and 2 [4]. After stimulation of BCR, CD19 is phosphorylated by Lyn. Phosphorylated CD19 activates PI3K by binding to the p85 subunit of PI3K and produce phosphatidylinositol-3,4,5-trisphosphate (PIP3) from PIP2, and PIP3 transmits signals downstream [5].

Central process of T cells responding to specific antigens is the binding of the T-cell receptor (TCR) to specific peptides bound to the major histocompatibility complex which expressed on antigen-presenting cells (APCs). Once TCR connected with its ligand, the ζ-chain–associated protein kinase 70 molecules (Zap-70) are recruited to the TCR-CD3 site and activated, resulting in an initiation of several signaling cascades. Once stimulation, Zap-70 forms complexes with several molecules including SLP-76; and a sequential protein kinase cascade is initiated, consisting of MAP kinase kinase kinase (MAP3K), MAP kinase kinase (MAPKK), and MAP kinase (MAPK) [6]. Two MAPK kinases, MKK4 and MKK7, have been reported to be the primary activators of JNK. MKK3, MKK4, and MKK6 are activators of P38 MAP kinase [7]. MAP kinase pathways are major pathways induced by TCR stimulation, and they play a key role in T-cell responses.

Phosphoinositide 3-kinase (PI3K) binds to the cytosolic domain of CD28, leading to conversion of PIP2 to PIP3, activation of PKB (Akt) and phosphoinositide-dependent kinase 1 (PDK1), and subsequent signaling transduction [8].

 

References

[1] Kawai T, Akira S. The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors[J]. Nature immunology, 2010, 11(5): 373-384.

[2] Kawai T, Akira S. Toll-like receptors and their crosstalk with other innate receptors in infection and immunity[J]. Immunity, 2011, 34(5): 637-650.

[3] Packard T A, Cambier J C. B lymphocyte antigen receptor signaling: initiation, amplification, and regulation[J]. F1000Prime Rep, 2013, 5(40.10): 12703.

[4] Zhong Y, Byrd J C, Dubovsky J A. The B-cell receptor pathway: a critical component of healthy and malignant immune biology[C]//Seminars in hematology. WB Saunders, 2014, 51(3): 206-218.

[5] Baba Y, Matsumoto M, Kurosaki T. Calcium signaling in B cells: regulation of cytosolic Ca 2+ increase and its sensor molecules, STIM1 and STIM2[J]. Molecular immunology, 2014, 62(2): 339-343.

[6] Adachi K, Davis M M. T-cell receptor ligation induces distinct signaling pathways in naive vs. antigen-experienced T cells[J]. Proceedings of the National Academy of Sciences, 2011, 108(4): 1549-1554.

[7] Rincón M, Flavell R A, Davis R A. The Jnk and P38 MAP kinase signaling pathways in T cell–mediated immune responses[J]. Free Radical Biology and Medicine, 2000, 28(9): 1328-1337.

[8] Bashour K T, Gondarenko A, Chen H, et al. CD28 and CD3 have complementary roles in T-cell traction forces[J]. Proceedings of the National Academy of Sciences, 2014, 111(6): 2241-2246.

Targets for  Immunology/Inflammation

Products for  Immunology/Inflammation

  1. Cat.No. Nombre del producto Información
  2. GC35412 Asperulosidic Acid El Ácido asperulosÍdico (ASPA), un glucÓsido iridoide bioactivo, se extrae de las hierbas de Hedyotis diffusa Willd. Asperulosidic Acid  Chemical Structure
  3. GC42860 Aspochalasin D Aspochalasin D is a co-metabolite originally isolated from A. Aspochalasin D  Chemical Structure
  4. GC46886 Aspyrone A fungal metabolite with diverse biological activities Aspyrone  Chemical Structure
  5. GC31350 Astaxanthin La astaxantina, el carotenoide dietético rojo, es un antioxidante potente y eficaz por vÍa oral. Astaxanthin  Chemical Structure
  6. GC68702 Astegolimab

    Astegolimab (MSTT 1041A; RG 6149) es un anticuerpo monoclonal humano IgG2 que puede bloquear la señalización de IL-33 al dirigirse al receptor ST2 de IL-33. Astegolimab tiene potencial para su uso en la investigación de enfermedad pulmonar obstructiva crónica (EPOC).

    Astegolimab  Chemical Structure
  7. GC41640 Asterriquinol D dimethyl ether El asterriquinol D dimetil éter es un metabolito fÚngico que puede inhibir las lÍneas celulares NS-1 del mieloma de ratÓn con una IC50 de 28 μg/mL. Asterriquinol D dimethyl ether  Chemical Structure
  8. GN10415 Astilbin

    Taxifolin 3-O-rhamnoside

    Astilbin  Chemical Structure
  9. GC42863 Asukamycin

    AM1042, Asukamycin A

    Asukamycin is polyketide isolated from the S. Asukamycin  Chemical Structure
  10. GC32457 Asymmetric dimethylarginine

    ADMA, Asymmetric dimethylarginine

    La dimetilarginina asimétrica es un inhibidor endÓgeno de la Óxido nÍtrico sintasa (NOS) y funciona como marcador de disfunciÓn endotelial en varios estados patolÓgicos. Asymmetric dimethylarginine  Chemical Structure
  11. GC46091 Aszonapyrone A La aszonapirona A es un metabolito producido por Aspergillus zonatus. Aszonapyrone A  Chemical Structure
  12. GC39554 AT2 receptor agonist C21

    Compound 21

    El agonista del receptor AT2 C21 es un agonista selectivo del receptor AT2 de la angiotensina II similar a un fÁrmaco con valores de Ki de 0,4 nM y >10 μM para el receptor AT2 y el receptor AT1, respectivamente. AT2 receptor agonist C21  Chemical Structure
  13. GC62334 AT791 AT791 es un inhibidor de TLR7 y TLR9 potente y biodisponible por vÍa oral. AT791  Chemical Structure
  14. GC46887 Atazanavir-d6 An internal standard for the quantification of atazanavir Atazanavir-d6  Chemical Structure
  15. GC12537 ATB-337

    ACS 15,S-Diclofenac

    ATB-337 es una molécula hÍbrida de un donante de H2S y el AINE diclofenaco. ATB-337  Chemical Structure
  16. GC16245 ATB-343 hybrid molecule of an H2S donor and the NSAID indomethacin ATB-343  Chemical Structure
  17. GC46892 ATRA-BA Hybrid A prodrug form of all-trans retinoic acid and butyric acid ATRA-BA Hybrid  Chemical Structure
  18. GN10627 Atractylenolide I Atractylenolide I  Chemical Structure
  19. GC48925 Aureonitol A fungal metabolite Aureonitol  Chemical Structure
  20. GC41490 Aureusimine B

    Phevalin

    Aureusimine B, also known as phevalin, is a natural pyrazinone produced by certain fungi and by Staphylococcus spp., including S. Aureusimine B  Chemical Structure
  21. GC46895 Aurintricarboxylic Acid (ammonium salt)

    ATA

    A protein synthesis inhibitor with diverse biological activities Aurintricarboxylic Acid (ammonium salt)  Chemical Structure
  22. GC40005 Aurodox

    1-methyl-Mocimycin

    Aurodox is a polyketide antibiotic originally isolated from S.

    Aurodox  Chemical Structure
  23. GC49646 Aurothioglucose (hydrate)

    Gold Thioglucose

    A TrxR inhibitor Aurothioglucose (hydrate)  Chemical Structure
  24. GC42877 AUY954 AUY954 is an orally bioavailable and selective agonist of the sphingosine-1-phosphate receptor 1 (S1P1; EC50 = 1.2 nM for stimulating GTPγS binding to S1P1 in CHO cells). AUY954  Chemical Structure
  25. GC32486 AVE-3085 AVE-3085 es un potente potenciador de la sintasa de óxido nítrico endotelial, utilizado para el tratamiento de enfermedades cardiovasculares. AVE-3085  Chemical Structure
  26. GC42880 Avenanthramide-C methyl ester Avenanthramide-C methyl ester is an inhibitor of NF-κB activation that acts by blocking the phosphorylation of IKK and IκB (IC50 ~ 40 μM). Avenanthramide-C methyl ester  Chemical Structure
  27. GC45388 Averantin

    (–)-Averantin

    La averantina es el metabolito menor del hongo Cercospora arachidicola. Averantin  Chemical Structure
  28. GC42881 Avermectin B1a aglycone Avermectin B1a aglycone is an aglycone form of the anthelmintic and insecticide avermectin B1a. Avermectin B1a aglycone  Chemical Structure
  29. GC42882 Avermectin B1a monosaccharide Avermectin B1a monosaccharide is a macrolide anthelmintic and monosaccharide form of avermectin B1a. Avermectin B1a monosaccharide  Chemical Structure
  30. GC45984 Avilamycin A An antibiotic Avilamycin A  Chemical Structure
  31. GC48511 Avrainvillamide

    CJ-17,665

    La avrainvillamida ((+)-Avrainvillamida) es un alcaloide natural con efectos antiproliferativos, se une a la chaperona nuclear nucleofosmina, una proteÍna oncogénica propuesta que se sobreexpresa en muchos tumores humanos diferentes. Avrainvillamide  Chemical Structure
  32. GC42885 AX 048 The group IVA phospholipase A2 (PLA2), known as calcium-dependent cytosolic PLA2 (cPLA2), selectively releases arachidonic acid from membrane phospholipids, playing a central role in initiating the synthesis of prostaglandins and leukotrienes. AX 048  Chemical Structure
  33. GC35440 AX-024 AX-024 es un inhibidor primero en su clase disponible por vÍa oral de la interacciÓn TCR-Nck que inhibe selectivamente la activaciÓn de células T desencadenada por TCR con un IC50 ~ 1 nM. AX-024  Chemical Structure
  34. GC19046 AX-024 hydrochloride El clorhidrato de AX-024 es un inhibidor primero en su clase disponible por vÍa oral de la interacciÓn TCR-Nck que inhibe selectivamente la activaciÓn de células T desencadenada por TCR con un IC50 ~1 nM. AX-024 hydrochloride  Chemical Structure
  35. GC65283 AXC-715 trihydrochloride

    T785 trihydrochloride

    El trihidrocloruro de AXC-715 (T785) es un agonista dual de TLR7/TLR8, extraÍdo de la patente WO2020168017 A1. AXC-715 trihydrochloride  Chemical Structure
  36. GC64938 AZD-7648 AZD-7648 es un potente inhibidor selectivo de DNA-PK activo por vÍa oral con una IC50 de 0,6 nM. AZD-7648 induce apoptosis y muestra actividad antitumoral. AZD-7648  Chemical Structure
  37. GC10135 AZD3264 AZD3264 es un inhibidor selectivo de IkB-quinasa IKK2. AZD3264  Chemical Structure
  38. GC62488 AZD8848 AZD8848 es un agonista antifÁrmaco selectivo del receptor 7 tipo toll (TLR7) desarrollado para la investigaciÓn del asma y la rinitis alérgica. AZD8848  Chemical Structure
  39. GC49057 Azelastine-13C-d3 (hydrochloride) An internal standard for the quantification of azelastine Azelastine-13C-d3 (hydrochloride)  Chemical Structure
  40. GC42891 azido-FTY720 Azido-FTY720 es un anÁlogo fotoactivable de FTY720. azido-FTY720  Chemical Structure
  41. GC46903 Azithromycin-d3 La azitromicina-d3 (CP 62993-d3) es la azitromicina marcada con deuterio. Azithromycin-d3  Chemical Structure
  42. GC46904 Azoxystrobin

    ICI-A 5504

    La azoxistrobina es un fungicida de β-metoxiacrilato de amplio espectro. Azoxystrobin  Chemical Structure
  43. GC60616 AZT triphosphate

    3'-Azido-3'-deoxythymidine-5'-triphosphate

    El trifosfato de AZT (3'-azido-3'-desoxitimidina-5'-trifosfato) es un metabolito trifosfato activo de la zidovudina (AZT). AZT triphosphate  Chemical Structure
  44. GC60617 AZT triphosphate TEA

    3'-Azido-3'-deoxythymidine-5'-triphosphate TEA

    AZT trifosfato TEA (3'-azido-3'-desoxitimidina-5'-trifosfato TEA) es un metabolito trifosfato activo de zidovudina (AZT). AZT triphosphate TEA  Chemical Structure
  45. GC45795 Aztreonam-d6

    SQ 26,776-d6

    An internal standard for the quantification of aztreonam Aztreonam-d6  Chemical Structure
  46. GC39280 B022 B022 es un inhibidor potente y selectivo de la cinasa inductora de NF-κB (NIK) (Ki de 4,2 nM; IC50 = 15,1 nM). B022  Chemical Structure
  47. GC18580 B355252 B355252, una molécula pequeña de fenoxi tiofeno sulfonamida, es un potente agonista del receptor de NGF. B355252  Chemical Structure
  48. GC42895 Bacillosporin C Bacillosporin C is an oxaphenalenone dimer originally isolated from T. Bacillosporin C  Chemical Structure
  49. GC49793 Bacitracin A (technical grade)

    NSC 45737

    A polypeptide antibiotic Bacitracin A (technical grade)  Chemical Structure
  50. GC46905 Bacitracin Complex A mixture of bacitracin polypeptides in complex with copper Bacitracin Complex  Chemical Structure
  51. GC45938 Bacopaside X

    Bacopaside VII, Jujubogenin isomer of Bacopasaponin C

    El bacopasido X se encuentra en Bacopa monnieri y muestra una afinidad de uniÓn hacia el receptor D1. Bacopaside X  Chemical Structure
  52. GC49302 Bactenecin (bovine) (trifluoroacetate salt)

    H-Arg-Leu-Cys-Arg-Ile-Val-Val-Ile-Arg-Val-Cys-Arg-OH, RLCRIVVIRVCR-OH

    A cationic peptide Bactenecin (bovine) (trifluoroacetate salt)  Chemical Structure
  53. GN10018 Baicalin

    Baicalein 7-glucuronide

    Un flavonoide con diversas actividades biológicas.

    Baicalin  Chemical Structure
  54. GC52344 Bak BH3 (72-87) (human) (trifluoroacetate salt) A Bak-derived peptide Bak BH3 (72-87) (human) (trifluoroacetate salt)  Chemical Structure
  55. GC18126 Balsalazide La balsalazida podrÍa suprimir la carcinogénesis asociada a la colitis mediante la modulaciÓn de la vÍa IL-6/STAT3. Balsalazide  Chemical Structure
  56. GC35466 Balsalazide sodium hydrate El hidrato de sodio de balsalazida podrÍa suprimir la carcinogénesis asociada a la colitis a través de la modulaciÓn de la vÍa IL-6/STAT3. Balsalazide sodium hydrate  Chemical Structure
  57. GC17574 BAPTA BAPTA es un quelante selectivo del calcio. BAPTA  Chemical Structure
  58. GC18313 BAR501 Impurity BAR501 impurity is an impurity found in the preparation of BAR501 that acts as an agonist of the G protein-coupled bile acid-activated receptor (GP-BAR1). BAR501 Impurity  Chemical Structure
  59. GC66331 Basiliximab

    CHI 621

    Basiliximab (CHI 621) es un anticuerpo anti-receptor de interleucina-2 monoclonal murino/humano IgG1 recombinante quimérico. Basiliximab se puede utilizar para la investigaciÓn del trasplante renal. Basiliximab  Chemical Structure
  60. GC52476 Bax Inhibitor Peptide V5 (trifluoroacetate salt)

    BIP V5, VPMLK

    A Bax inhibitor Bax Inhibitor Peptide V5 (trifluoroacetate salt)  Chemical Structure
  61. GC10345 Bay 11-7085 BAY 11-7085 (BAY 11-7083) es un inhibidor de la activaciÓn de NF-κB y la fosforilaciÓn de IκBα; estabiliza el IκBα con una IC50 de 10 μM. Bay 11-7085  Chemical Structure
  62. GC13035 Bay 11-7821

    BAY 11-7082

    Un inhibidor selectivo e irreversible de NF-κB.

    Bay 11-7821  Chemical Structure
  63. GC42897 BAY 61-3606 (hydrochloride) BAY 61-3606 is a cell-permeable, reversible inhibitor of spleen tyrosine kinase (Syk; Ki = 7.5 nM; IC50 = 10 nM). BAY 61-3606 (hydrochloride)  Chemical Structure
  64. GC35474 Bay 65-1942 free base La base libre Bay 65-1942 es un inhibidor de IKKβ selectivo y competitivo con ATP. Bay 65-1942 free base  Chemical Structure
  65. GC16303 Bay 65-1942 HCl salt Bay 65-1942 HCl salt  Chemical Structure
  66. GC35475 Bay 65-1942 R form La forma R de Bay 65-1942 es la forma R menos activa de Bay 65-1942. Bay 65-1942 R form  Chemical Structure
  67. GC60624 BAY-985 BAY-985 es un inhibidor dual de TBK1 e IKKε altamente potente, oralmente activo y selectivo competitivo con ATP con IC50 de 2/30 y 2 nM para TBK1 (ATP bajo/alto) e IKKε, respectivamente. Eficacia antitumoral. BAY-985  Chemical Structure
  68. GC12232 BAY-X 1005

    BAY X 1005; DG-031

    BAY-X 1005 (BAY X 1005; DG-031) es un inhibidor de la proteÍna activadora de la 5-lipoxigenasa (FLAP) selectivo y activo por vÍa oral. BAY-X 1005  Chemical Structure
  69. GC18487 BC-1215 BC-1215 es un inhibidor de la proteÍna 3 de la caja F (Fbxo3). BC-1215  Chemical Structure
  70. GC41583 BCN-E-BCN BCN-E-BCN is a strained cycloalkyne probe for detecting proteins that have been sulfenylated, the first intermediate step in protein oxidation. BCN-E-BCN  Chemical Structure
  71. GC35481 BCX 1470 BCX 1470 inhibe la actividad esterolÍtica del factor D (IC50=96 nM) y C1s (IC50=1,6 nM), 3,4 y 200 veces mejor, respectivamente, que la de la tripsina. BCX 1470  Chemical Structure
  72. GC35482 BCX 1470 methanesulfonate El metanosulfonato BCX 1470 inhibe la actividad esterolÍtica del factor D (IC50=96 nM) y C1s (IC50=1,6 nM), 3,4 y 200 veces mejor, respectivamente, que la de la tripsina. BCX 1470 methanesulfonate  Chemical Structure
  73. GC46908 BE-24566B

    L-755,805

    A fungal metabolite BE-24566B  Chemical Structure
  74. GC46910 Beauvericin A A cyclodepsipeptide with diverse biological activities Beauvericin A  Chemical Structure
  75. GC49038 Benanomicin A A microbial metabolite with antifungal, fungicidal, and antiviral activities Benanomicin A  Chemical Structure
  76. GC52468 Benanomicin B

    Antibiotic BU 3608C, Pradimicin C

    A microbial metabolite with antifungal, fungicidal, and antiviral activities Benanomicin B  Chemical Structure
  77. GC49040 Benanomicin B (formate) A microbial metabolite with antifungal, fungicidal, and antiviral activities Benanomicin B (formate)  Chemical Structure
  78. GC49042 Benastatin A A bacterial metabolite with diverse biological activities Benastatin A  Chemical Structure
  79. GC49043 Benastatin B A bacterial metabolite with diverse biological activities Benastatin B  Chemical Structure
  80. GC49044 Benastatin C A bacterial metabolite with diverse biological activities Benastatin C  Chemical Structure
  81. GC64354 Bendamustine La bendamustina (SDX-105 base libre), un anÁlogo de purina, es un agente de entrecruzamiento del ADN. La bendamustina activa la respuesta al estrés por daÑo del ADN y la apoptosis. La bendamustina tiene potentes propiedades alquilantes, anticancerÍgenas y antimetabolitos. Bendamustine  Chemical Structure
  82. GC34046 Bendazol Bendazol es un fÁrmaco hipotensor que también puede aumentar la actividad de la NO sintasa en los glomérulos renales y tÚbulos colectores. Bendazol  Chemical Structure
  83. GC15949 Benfotiamine

    Benzoylthiamine monophosphate

    A lipid-soluble form of vitamin B1 Benfotiamine  Chemical Structure
  84. GC49836 Benoxaprofen

    LRCL 3794, NSC 299582

    El benoxaprofeno (LRCL 3794) es un compuesto antiinflamatorio y antipirético potente y de acciÓn prolongada. Benoxaprofen  Chemical Structure
  85. GC39346 Benralizumab

    MEDI-563; BIW-8405

    Benralizumab (MEDI-563) es un anticuerpo monoclonal citolÍtico dirigido por el receptor de la interleucina-5 α (IL-5Rα) que induce la depleciÓn directa, rÁpida y casi completa de los eosinÓfilos a través de una citotoxicidad mediada por células dependiente de anticuerpos mejorada. Benralizumab  Chemical Structure
  86. GC35494 Benzoyloxypaeoniflorin La benzoiloxipaeoniflorina, aislada de la raÍz de Paeonia suffruticosa, es un inhibidor de la tirosinasa contra la tirosinasa del hongo con IC50 de 0,453 mM. Benzoyloxypaeoniflorin  Chemical Structure
  87. GC15058 Benzydamine HCl El clorhidrato de bencidamina es un fÁrmaco antiinflamatorio no esteroideo de acciÓn local con propiedades analgésicas y anestésicas locales; se une selectivamente a la prostaglandina sintetasa y tiene una notable actividad antibacteriana in vitro. Benzydamine HCl  Chemical Structure
  88. GC60636 Benzyl butyl phthalate El ftalato de bencilo butilo, un miembro de los ésteres de Ácido ftÁlico (PAE), puede desencadenar la migraciÓn e invasiÓn de células de hemangioma (HA) a través de la regulaciÓn positiva de Zeb1. El ftalato de butilo de bencilo activa el receptor de hidrocarburo de arilo (AhR) en las células de cÁncer de mama para estimular la seÑalizaciÓn de SPHK1/S1P/S1PR3 y mejora la formaciÓn de células madre de cÁncer de mama iniciadoras de metÁstasis (BCSC). Benzyl butyl phthalate  Chemical Structure
  89. GN10443 Berbamine Berbamine  Chemical Structure
  90. GN10358 Berbamine hydrochloride Berbamine hydrochloride  Chemical Structure
  91. GN10221 Berberine

    La berberina (Amarillo Natural 18) es un alcaloide aislado de la medicina herbal china Huanglian, como antibiótico. La berberina (Amarillo Natural 18) induce la generación de especies reactivas de oxígeno (ROS) e inhibe la topoisomerasa del ADN.

    Berberine  Chemical Structure
  92. GC35497 Berberine chloride hydrate El cloruro de berberina hidratado (Natural Yellow 18 cloruro hidrato) es un alcaloide que actÚa como antibiÓtico. El hidrato de cloruro de berberina induce la generaciÓn de especies reactivas de oxÍgeno (ROS) e inhibe la topoisomerasa del ADN. Propiedades antineoplÁsicas. Berberine chloride hydrate  Chemical Structure
  93. GN10208 Berberine hydrochloride

    BBR, Umbellatine, NSC 163088, NSC 646666

    Berberine hydrochloride is an isoquinoline alkaloid derived from the Ranunculaceae medicinal plant Coptis chinensis. It has various pharmacological activities such as anti-tumor, anti-inflammatory, and hypoglycemic activities.

    Berberine hydrochloride  Chemical Structure
  94. GN10523 Berberine Sulfate Berberine Sulfate  Chemical Structure
  95. GC49387 Berberine-d6 (chloride)

    BBR-d6, Umbellatine-d6

    An internal standard for the quantification of berberine Berberine-d6 (chloride)  Chemical Structure
  96. GC46098 Berkeleylactone E A macrolide antibiotic Berkeleylactone E  Chemical Structure
  97. GC42925 Berteroin

    5-Methylthiopentyl isothiocyanate

    BerteroÍna, un anÁlogo de sulforafano de origen natural, entre otros, un agente antimetastÁsico. Berteroin  Chemical Structure
  98. GC46922 Betamethasone 21-phosphate (sodium salt hydrate) A synthetic glucocorticoid Betamethasone 21-phosphate (sodium salt hydrate)  Chemical Structure
  99. GC52329 Betamethasone-d5

    β-Methasone-d5, SCH 4831-d5

    An internal standard for the quantification of betamethasone Betamethasone-d5  Chemical Structure
  100. GC10480 Betulinic acid

    Lupatic Acid, NSC 113090

    A plant triterpenoid similar to bile acids Betulinic acid  Chemical Structure
  101. GC48504 Betulinic Aldehyde oxime

    Betulin 28-oxime

    A derivative of betulin Betulinic Aldehyde oxime  Chemical Structure

Artículos 601 al 700 de 2909 totales

por página
  1. 5
  2. 6
  3. 7
  4. 8
  5. 9

Fijar Dirección Descendente