Immunology/Inflammation
Immunology/Inflammation(免疫及炎症)
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.
- 5-Lipoxygenase(11)
- Papain(1)
- PGDS(1)
- PGE synthase(24)
- SIKs(12)
- IκB/IKK(67)
- AP-1(6)
- KEAP1-Nrf2(65)
- NOD1(1)
- TLR(140)
- NF-κB(241)
- Interleukin Related(171)
- 15-lipoxygenase(2)
- Others(63)
- Aryl Hydrocarbon Receptor(36)
- CD73(14)
- Complement System(58)
- Galectin(12)
- IFNAR(25)
- NO Synthase(77)
- NOD-like Receptor (NLR)(51)
- STING(110)
- Reactive Oxygen Species(465)
- Apoptosis(802)
- FKBP(20)
- eNOS(5)
- iNOS(29)
- nNOS(20)
- Glutathione(57)
- Adaptive Immunity(222)
- Allergy(130)
- Arthritis(34)
- Autoimmunity(190)
- Gastric Disease(101)
- Immunosuppressants(39)
- Immunotherapeutics(5)
- Innate Immunity(593)
- Pulmonary Diseases(119)
- Reactive Nitrogen Species(55)
- Reactive Sulfur Species(28)
- Specialized Pro-Resolving Mediators(50)
- Cyclic GMP-AMP Synthase(2)
- BCL6(3)
- CD20(3)
- CD22
- CD28(1)
- FAP(7)
- PSMA(7)
- Nuclear Factor of activated T Cells (NFAT)(1)
- Glycoprotein VI(1)
- Tim3(2)
- Hapten(1)
- Nectin-4(2)
Immunology/Inflammation 相关产品(4245)
- GC31693AdelmidrolCAS: 1675-66-7纯度: >98.00%
Adelmidrol is an analogue of palmitoylethanolamide (PEA) with anti-inflammatory activities.
- GC31696cGAMP (Cyclic AMP-GMP)CAS: 849214-04-6
cGAMP (Cyclic AMP-GMP)是一种环状二核苷酸,是哺乳动物细胞内的第二信使,是在细胞受到威胁时“即时”合成的。
- GC31709Succinobucol (AGI-1067)CAS: 216167-82-7纯度: >99.50% / >98.00%
A probucol derivative with diverse biological activities
- GC31732Tapinarof (WBI 1001)CAS: 79338-84-4纯度: >99.50%
Tapinarof (GSK2894512, Benvitimod, WBI 1001, DHPS, DMVT 505) is a natural agonist of aryl hydrocarbon receptor (AhR) and induces nuclear translocation of AhR in immortalized keratinocytes (HaCaT) with EC50 of 0.16 nM. Tapinarof induces cellular apoptosis in CD4+ T cells in a dosedependent manner with IC50 of 5.2 μM.
- GC31783Methyl 3,4-dihydroxybenzoate (Protocatechuic acid methyl ester)CAS: 2150-43-8纯度: >98.00%
Methyl protocatechuate (Methyl 3,4-dihydroxybenzoate, 3,4-Dihydroxybenzoic acid methyl ester, Protocatechuic Acid Methyl Ester) is also known as Protocatechuic Acid Methyl Ester. Protocatechuic Acid, a dihydroxybenzoic acid, is a major metabolite of antioxidant polyphenols found in green tea with antioxidant and anti-inflammatory effects.
- GC31791Veledimex (INXN-1001)CAS: 1093130-72-3纯度: >98.00%
Veledimex (INXN-1001) (INXN-1001) 是昆虫蜕皮激素蜕皮激素的合成类似物,是专有基因治疗启动子系统的口服活性激活剂配体。
- GC31792PF-4878691 (3M-852A)CAS: 532959-63-0纯度: >98.50%
PF-4878691 (3M-852A) (3M-852A) 是一种有效的、具有口服活性的选择性 Toll 样受体 7 (TLR7) 激动剂,模拟其抗病毒和炎症活性。
- GC31794Methyl vanillateCAS: 3943-74-6纯度: >99.00%
Methyl Vanillate, one of the ingredients in Hovenia dulcis Thunb, activates the Wnt/β-catenin pathway and induces osteoblast differentiation in vitro.
- GC31798WAY-204688 (SIM-688)CAS: 796854-35-8
WAY-204688 (SIM-688) 是一种雌激素受体 (ER-α) 选择性、口服活性的 NF-κB 转录活性抑制剂,IC50 为 122±30 nM 作用于 NF-κB-荧光素酶κB-luc) 在 HAECT-1 细胞中。
- GC31799IFN alpha-IFNAR-IN-1 (IFN-alpha and IFNAR interaction inhibitor)CAS: 844882-93-5
IFN α-IFNAR-IN-1(IFN-α 和 IFNAR 相互作用抑制剂)是一种非肽类、低分子量的 IFN-α 相互作用抑制剂;和 IFNAR;抑制 MVA 诱导的 IFN-α; BM-pDCs 的反应 (IC50=2-8 uM)。
- GC31817Ginsenoside Rk3CAS: 364779-15-7纯度: >98.50% / >98.00%
Ginsenoside Rk3是从人参或三七中提取的稀有皂苷成分,具有多种生物学功能,可抑制抑制 TNF-α诱导的NF-κB转录活性(IC 50 =14.24±1.30μM)。
- GC31875CL656 (c-[2'FdAMP(S)-2'FdIMP(S)])CAS: 1951464-79-1
CL656 (c-[2'FdAMP(S)-2'FdIMP(S)]) 是干扰素基因 (STING) 刺激物的激活剂。
- GC31892Decursin ((+)-Decursin)CAS: 5928-25-6纯度: >98.00%
A phytochemical with diverse biological activities
- GC31928C3a 70-77 (Complement 3a (70-77))CAS: 63555-63-5
C3a 70-77 (Complement 3a (70-77)) 是一种对应于 C3a 的 COOH 末端的八肽,具有 C3a 的特异性和 1% 至 2% 的生物活性。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC31693 | Adelmidrol | 1675-66-7 | >98.00% | |
Adelmidrol is an analogue of palmitoylethanolamide (PEA) with anti-inflammatory activities. | ||||
| GC31696 | cGAMP (Cyclic AMP-GMP) | 849214-04-6 | - | |
cGAMP (Cyclic AMP-GMP)是一种环状二核苷酸,是哺乳动物细胞内的第二信使,是在细胞受到威胁时“即时”合成的。 | ||||
| GC31706 | Ginsenoside Rg5 | 186763-78-0 | >98.00% | |
A ginsenoside with diverse biological activities | ||||
| GC31709 | Succinobucol (AGI-1067) | 216167-82-7 | >99.50% / >98.00% | |
A probucol derivative with diverse biological activities | ||||
| GC31717 | Ginkgetin | 481-46-9 | >98.00% / >98.50% | |
Ginkgetin一种从银杏叶中提取的双黄酮类天然化合物,能够抑制Wnt信号通路(IC₅₀=5.92μM)。 | ||||
| GC31729 | CU-CPT-9b (TLR8-specific antagonist 1) | 2162962-69-6 | >98.00% | |
A TLR8 antagonist | ||||
| GC31732 | Tapinarof (WBI 1001) | 79338-84-4 | >99.50% | |
Tapinarof (GSK2894512, Benvitimod, WBI 1001, DHPS, DMVT 505) is a natural agonist of aryl hydrocarbon receptor (AhR) and induces nuclear translocation of AhR in immortalized keratinocytes (HaCaT) with EC50 of 0.16 nM. Tapinarof induces cellular apoptosis in CD4+ T cells in a dosedependent manner with IC50 of 5.2 μM. | ||||
| GC31733 | NIK SMI1 | 1660114-31-7 | >99.50% | |
NIK SMI1 is a highly potent and selective NF-κB-inducing kinase (NIK) inhibitor with Ki of 0.23 nM for NIK-catalyzed hydrolysis of ATP to ADP. | ||||
| GC31745 | CU-CPT-9a | 2165340-32-7 | >99.50% | |
A TLR8 antagonist | ||||
| GC31776 | MD2-IN-1 | 111797-22-9 | >99.50% | |
MD2-IN-1 is an inhibitor of Myeloid differentiation protein 2 (MD2) with a KD value of 189?μM. | ||||
| GC31783 | Methyl 3,4-dihydroxybenzoate (Protocatechuic acid methyl ester) | 2150-43-8 | >98.00% | |
Methyl protocatechuate (Methyl 3,4-dihydroxybenzoate, 3,4-Dihydroxybenzoic acid methyl ester, Protocatechuic Acid Methyl Ester) is also known as Protocatechuic Acid Methyl Ester. Protocatechuic Acid, a dihydroxybenzoic acid, is a major metabolite of antioxidant polyphenols found in green tea with antioxidant and anti-inflammatory effects. | ||||
| GC31791 | Veledimex (INXN-1001) | 1093130-72-3 | >98.00% | |
Veledimex (INXN-1001) (INXN-1001) 是昆虫蜕皮激素蜕皮激素的合成类似物,是专有基因治疗启动子系统的口服活性激活剂配体。 | ||||
| GC31792 | PF-4878691 (3M-852A) | 532959-63-0 | >98.50% | |
PF-4878691 (3M-852A) (3M-852A) 是一种有效的、具有口服活性的选择性 Toll 样受体 7 (TLR7) 激动剂,模拟其抗病毒和炎症活性。 | ||||
| GC31794 | Methyl vanillate | 3943-74-6 | >99.00% | |
Methyl Vanillate, one of the ingredients in Hovenia dulcis Thunb, activates the Wnt/β-catenin pathway and induces osteoblast differentiation in vitro. | ||||
| GC31798 | WAY-204688 (SIM-688) | 796854-35-8 | - | |
WAY-204688 (SIM-688) 是一种雌激素受体 (ER-α) 选择性、口服活性的 NF-κB 转录活性抑制剂,IC50 为 122±30 nM 作用于 NF-κB-荧光素酶κB-luc) 在 HAECT-1 细胞中。 | ||||
| GC31799 | IFN alpha-IFNAR-IN-1 (IFN-alpha and IFNAR interaction inhibitor) | 844882-93-5 | - | |
IFN α-IFNAR-IN-1(IFN-α 和 IFNAR 相互作用抑制剂)是一种非肽类、低分子量的 IFN-α 相互作用抑制剂;和 IFNAR;抑制 MVA 诱导的 IFN-α; BM-pDCs 的反应 (IC50=2-8 uM)。 | ||||
| GC31804 | RP-54745 | 135330-08-4 | >99.50% | |
RP54745是一种潜在的治风湿化合物,能够抑制噬细胞刺激和的白介素-1(interleukin-1)的产生。 | ||||
| GC31809 | Yangonin | 500-62-9 | >98.00% | |
A kavalactone with affinity for the CB 1 receptor | ||||
| GC31817 | Ginsenoside Rk3 | 364779-15-7 | >98.50% / >98.00% | |
Ginsenoside Rk3是从人参或三七中提取的稀有皂苷成分,具有多种生物学功能,可抑制抑制 TNF-α诱导的NF-κB转录活性(IC 50 =14.24±1.30μM)。 | ||||
| GC31875 | CL656 (c-[2'FdAMP(S)-2'FdIMP(S)]) | 1951464-79-1 | - | |
CL656 (c-[2'FdAMP(S)-2'FdIMP(S)]) 是干扰素基因 (STING) 刺激物的激活剂。 | ||||
| GC31886 | Chelidonic acid | 99-32-1 | - | |
A pyran with diverse biological activities | ||||
| GC31892 | Decursin ((+)-Decursin) | 5928-25-6 | >98.00% | |
A phytochemical with diverse biological activities | ||||
| GC31914 | CD73-IN-1 | 2132396-40-6 | >98.50% | |
An inhibitor of CD73 | ||||
| GC31928 | C3a 70-77 (Complement 3a (70-77)) | 63555-63-5 | - | |
C3a 70-77 (Complement 3a (70-77)) 是一种对应于 C3a 的 COOH 末端的八肽,具有 C3a 的特异性和 1% 至 2% 的生物活性。 | ||||
