Immunology/Inflammation
Read More about this categoryShow Less
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.
Research Areas
- 5-Lipoxygenase(17)
- Apoptosis(914)
- Cyclic GMP-AMP Synthase(7)
- TLR(139)
- Papain(1)
- PGDS(1)
- PGE synthase(26)
- SIKs(13)
- IκB/IKK(72)
- AP-1(15)
- KEAP1-Nrf2(65)
- NOD1(1)
- NF-κB(336)
- Interleukin Related(364)
- 15-lipoxygenase(2)
- Others(10)
- Aryl Hydrocarbon Receptor(43)
- CD73(18)
- Complement System(83)
- Galectin(14)
- IFNAR(72)
- NO Synthase(108)
- NOD-like Receptor (NLR)(77)
- STING(125)
- Reactive Oxygen Species(557)
- FKBP(17)
- eNOS(4)
- iNOS(29)
- nNOS(20)
- Glutathione(54)
- Adaptive Immunity(210)
- Allergy(118)
- Arthritis(34)
- Autoimmunity(181)
- Gastric Disease(95)
- Immunosuppressants(38)
- Immunotherapeutics(4)
- Innate Immunity(566)
- Pulmonary Diseases(110)
- Reactive Nitrogen Species(50)
- Specialized Pro-Resolving Mediators(49)
- Reactive Sulfur Species(28)
- BCL6(9)
- CD20(15)
- CD22(2)
- CD28(10)
- PSMA(17)
- FAP(27)
- Nuclear Factor of activated T Cells (NFAT)(4)
- Glycoprotein VI(2)
- Tim3(6)
- Hapten(1)
- Nectin-4(3)
- DOCK(4)
- MHC(15)
- Transmembrane Glycoprotein(56)
- TREM receptor(14)
- Inflammation or Immune System Disease(2)
- Musculoskeletal and Skin Disease(1)
- Fc Receptor (FcR)(16)
- IKZF Family(5)
- C-type Lectin-like Receptors (CTLRs)(13)
- Asialoglycoprotein Receptor (ASGPR)(3)
- Human leukocyte immunoglobulin (Ig)-like receptors (LILR)(2)
- RIG-I-like receptor (RLR)(1)
- VAP-1(1)
Products Related to Immunology/Inflammation(4985)
- GC72511L-Cystathionine dihydrochlorideCAS: 61125-50-6Purity: >99.50%
L-Cystathionine dihydrochloride es un tioéter no proteico y es un aminoácido clave asociado con el estado metabólico de los aminoácidos que contienen azufre.
- GC72573Sodium 2-oxopropanoate-13CCAS: 124052-04-6Purity: >98.50%
Sodium 2-oxopropanoate-13C es el deuterio marcado como ácido 5-hidroxiindo3-acético.
- GC725742-Oxopropanoate-13C5 sodiumCAS: 89196-78-1
2-Oxopropanoate-13C5 sodium es el 13C marcado 2-oxopropanode sodio.
- GC72575L-Glutamic acid monosodium (hydrate)CAS: 6106-04-3Purity: >98.00%
L-Glutamic acid monosodium (hydrate) es un aditivo nutricional y agente saborizante.
- GC72610Cartap hydrochlorideCAS: 15263-52-2Purity: >90.00%
Cartap hydrochloride, un insecticide de organonitrogen, puede causar una marcada e irreversible contracdependiente de Ca2+ tanto en ratones aislados como en conejos.
- GC72791Delmitide acetateCAS: 501019-16-5Purity: >98.00%
Delmitide acetate es un décapéptido oral activo del isómero d con potente actividad antiinflam.
- GC72792CyclopentenylcytosineCAS: 90597-22-1Purity: >99.00%
Cyclopentenylcytosine (CPC) es un análogo de nucleósique que reduce los niveles de citidina trifosfato (CTP) y desoxicitidina trifosfato (dCTP) en las células leucémicas al inhibide la CTP sintetasa.
- GC72803Aspidin BBCAS: 584-28-1Purity: >98.00%
Aspidin BB es un derivado del floroglucin, que puede ser aislado de la parte aérea de Dryopteris championii.
- GC72817BAI1 hydrochlorideCAS: 329349-20-4Purity: >99.00%
BAI1 hydrochloride es un inhibidor alostérico BAX de factor de apoptosis selectivo.
- GC72851BelapectinCAS: 1980787-47-0Purity: >99.00%
Belapectin (GR-MD-02) es un inhibidor de Galectin-3 (Gal-3).
- GC72852Helenalin acetateCAS: 10180-86-6Purity: >98.00%
Helenalin acetate, un inhibidor natural de NF-κB, es un potente inhibidor de C/EBPβ.
- GC72858Avenanthramide ACAS: 108605-70-5Purity: >99.00%
Avenanthramide A es una ptoalexina, que se puede encontrar en Avena (Avena sativa L.).
- GC72864PZ703b hydrochloridePurity: >99.00%
PZ703b hydrochloride es un degrabcl-xl PROTAC que induce apoptosis e inhila la proliferación de células cancerosas.
- GC72875Justicidin ACAS: 25001-57-4Purity: >99.00%
Justicidin A es un producto natural que puede ser aislado de Justicia procumbens.
- GC72878UCD38B hydrochlorideCAS: 1115177-19-9Purity: >99.00%
UCD38B hydrochloride es un inhibiinhibidel uPA competitivo enzimcon un valor de IC50 de 7 μM.
- GC72892Oblimersen sodiumPurity: >98.00%
Oblimersen sodium es un inhibibcl-2 que se dirige al ARN BCL-2.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC72511 | L-Cystathionine dihydrochloride | 61125-50-6 | >99.50% | |
L-Cystathionine dihydrochloride es un tioéter no proteico y es un aminoácido clave asociado con el estado metabólico de los aminoácidos que contienen azufre. | ||||
| GC72573 | Sodium 2-oxopropanoate-13C | 124052-04-6 | >98.50% | |
Sodium 2-oxopropanoate-13C es el deuterio marcado como ácido 5-hidroxiindo3-acético. | ||||
| GC72574 | 2-Oxopropanoate-13C5 sodium | 89196-78-1 | - | |
2-Oxopropanoate-13C5 sodium es el 13C marcado 2-oxopropanode sodio. | ||||
| GC72575 | L-Glutamic acid monosodium (hydrate) | 6106-04-3 | >98.00% | |
L-Glutamic acid monosodium (hydrate) es un aditivo nutricional y agente saborizante. | ||||
| GC72610 | Cartap hydrochloride | 15263-52-2 | >90.00% | |
Cartap hydrochloride, un insecticide de organonitrogen, puede causar una marcada e irreversible contracdependiente de Ca2+ tanto en ratones aislados como en conejos. | ||||
| GC72755 | Tempol-d17,15N | 90429-66-6 | - | |
Tempol-d17,15N es el deuterio llamado Tempol. | ||||
| GC72757 | SPC 839 | 219773-55-4 | >99.00% | |
SPC 839 (compuesto 10) es un inhibidor activo oral de la activación transcripcional mediada por AP-1 y NF-kB con IC50 de 0,008 μM. | ||||
| GC72791 | Delmitide acetate | 501019-16-5 | >98.00% | |
Delmitide acetate es un décapéptido oral activo del isómero d con potente actividad antiinflam. | ||||
| GC72792 | Cyclopentenylcytosine | 90597-22-1 | >99.00% | |
Cyclopentenylcytosine (CPC) es un análogo de nucleósique que reduce los niveles de citidina trifosfato (CTP) y desoxicitidina trifosfato (dCTP) en las células leucémicas al inhibide la CTP sintetasa. | ||||
| GC72803 | Aspidin BB | 584-28-1 | >98.00% | |
Aspidin BB es un derivado del floroglucin, que puede ser aislado de la parte aérea de Dryopteris championii. | ||||
| GC72817 | BAI1 hydrochloride | 329349-20-4 | >99.00% | |
BAI1 hydrochloride es un inhibidor alostérico BAX de factor de apoptosis selectivo. | ||||
| GC72824 | KX2-361 | 897016-26-1 | >99.00% | |
KX2-361 (KX-02) es un inhibide la polimeride de src-quinasa y tubulina. | ||||
| GC72826 | CB7993113 | 819827-50-4 | >98.00% | |
CB7993113 es un potente antagonista de la AHR, con una IC50 de 0,33 μM. | ||||
| GC72835 | NSC260594 | 906718-66-9 | >96.00% | |
NSC260594 induce Apoptosis. | ||||
| GC72851 | Belapectin | 1980787-47-0 | >99.00% | |
Belapectin (GR-MD-02) es un inhibidor de Galectin-3 (Gal-3). | ||||
| GC72852 | Helenalin acetate | 10180-86-6 | >98.00% | |
Helenalin acetate, un inhibidor natural de NF-κB, es un potente inhibidor de C/EBPβ. | ||||
| GC72858 | Avenanthramide A | 108605-70-5 | >99.00% | |
Avenanthramide A es una ptoalexina, que se puede encontrar en Avena (Avena sativa L.). | ||||
| GC72862 | Erasin | 2256056-21-8 | >95.00% | |
Erasin es un potente inhibidor de STAT3 con IC50s de 9,7 y 24 μM contra STAT3 y STAT1, respectivamente. | ||||
| GC72864 | PZ703b hydrochloride | - | >99.00% | |
PZ703b hydrochloride es un degrabcl-xl PROTAC que induce apoptosis e inhila la proliferación de células cancerosas. | ||||
| GC72868 | AZA197 | 1249398-09-1 | >98.00% | |
AZA197 es un inhibiselectivo de moléculas pequeñas de Cdc42. | ||||
| GC72875 | Justicidin A | 25001-57-4 | >99.00% | |
Justicidin A es un producto natural que puede ser aislado de Justicia procumbens. | ||||
| GC72878 | UCD38B hydrochloride | 1115177-19-9 | >99.00% | |
UCD38B hydrochloride es un inhibiinhibidel uPA competitivo enzimcon un valor de IC50 de 7 μM. | ||||
| GC72888 | CPS-11 | 145945-21-7 | >99.00% | |
CPS-11 (N-(droxymetl) talidomide) un análogo de talidomi, es un potente agente anticanceroso. | ||||
| GC72892 | Oblimersen sodium | - | >98.00% | |
Oblimersen sodium es un inhibibcl-2 que se dirige al ARN BCL-2. | ||||
