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.
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Immunology/Inflammation 相关产品(4245)
- GC60622BAY 2416964CAS: 2242464-44-2纯度: >99.50% / >98.00%
BAY 2416964是一种强效且具有口服活性的芳烃受体(AhR)抑制剂,IC 50 值为341nM。
- GC60636Benzyl butyl phthalateCAS: 85-68-7纯度: >97.00%
Benzylbutylphthalate是邻苯二甲酸酯(PAEs)的一员,通过上调Zeb1的表达,可引起血管瘤(HA)细胞的迁移和侵袭。Benzylbutylphthalate激活乳腺癌细胞中的芳香烃受体(AhR),刺激SPHK1/S1P/S1PR3信号传导,促进转移性乳腺癌干细胞(BCSCs)的形成。
- GC60668Calcimycin hemimagnesiumCAS: 72124-77-7
Calcimycin(A-23187)hemimagnesium是一种抗生素和独特的二价阳离子离子载体(divalentcationionophore),如钙离子和镁离子。Calcimycinhemimagnesium通过增加细胞内钙浓度诱导Ca2+依赖性细胞死亡。Calcimycinhemimagnesium抑制革兰氏阳性细菌和一些真菌的生长,还抑制ATP酶的活性并解耦哺乳动物细胞的氧化磷酸化(OXPHOS),诱导细胞凋亡(apoptosis)。
- GC60674Catalase from Aspergillus niger(≥100000U/g)CAS: 9001-05-2纯度: BA-101000U/g
Catalase是重要的抗氧化酶,在清除ROS。在维持氧化还原状态的平衡方面发挥着重要作用。Catalase与肿瘤的发生,发展关系密切。有潜力用于肿瘤的预防研究。
- GC60693Chitoheptaose heptahydrochlorideCAS: 127171-89-5
Chitoheptaoseheptahydrochloride是一种具有抗氧化,抗炎,抗凋亡和心脏保护作用的壳聚糖寡糖。Chitoheptaoseheptahydrochloride显着增强了小麦幼苗的生长和光合作用参数。
- GC60694Chitohexaose hexahydrochlorideCAS: 127171-88-4
Chitohexaosehexahydrochloride是具有抗炎作用的壳聚糖低聚糖。Chitohexaosehexahydrochloride与TLR4的活性位点结合并抑制LPS诱导的炎症。
- GC60708Cinchonine hydrochlorideCAS: 5949-11-1
Cinchoninehydrochloride((8R,9S)-Cinchoninehydrochloride)是金鸡纳树皮中的天然化合物。Cinchoninehydrochloride可激活内质网应激诱导的人肝癌细胞凋亡。
- GC60824Ethylene dimethanesulfonateCAS: 4672-49-5纯度: >98.00%
Ethylenedimethanesulfonate是一种温和的烷基化乙二醇非挥发性甲烷磺酸二酯。Ethylenedimethanesulfonate对LC具有选择性的促凋亡作用。
- GC60826Etoposide phosphateCAS: 117091-64-2纯度: >96.00%
Etoposidephosphate(BMY-40481)是一种有效的抗癌(anti-cancer)化疗试剂和一种选择性拓扑异构酶II(topoisomeraseII)抑制剂,可以防止DNA链的重新连接。Etoposidephosphate是依托泊苷的磷酸酯前药,被认为与Etoposide活性相当。Etoposidephosphate诱导细胞周期阻滞、凋亡(apoptosis)和自噬(autophagy)。
- GC60836FenobucarbCAS: 3766-81-2纯度: >99.50%
Fenobucarb是一种广泛使用的氨基甲酸酯杀虫剂。Fenobucarb通过炎症、氧化应激、变性和凋亡等途径诱导斑马鱼发育神经毒性。Fenobucarb可能对动物心脑血管系统有危害。
- GC60897Hesperidin methylchalconeCAS: 24292-52-2纯度: >95.00%
Hesperidin methylchalcone is the Citrus original products with powerful antioxidant activity.
- GC60914Hydrocortisone hemisuccinateCAS: 2203-97-6纯度: >98.00%
Hydrocortisone hemisuccinate (A-hydrocort, Hydrocortisone 21-hemisuccinate), a physiological glucocorticoid with anti-inflammatory properties, is an inhibitor of proinflammatory cytokine with IC50 of 6.7 μM and 21.4 μM for Interleukin-6 (IL-6) and IL-3, respectively.
- GC60927IFN alpha-IFNAR-IN-1 hydrochlorideCAS: 2070014-98-9纯度: >99.50%
An inhibitor of the IFN-α-IFNAR protein-protein interaction
- GC60949IsolongifoleneCAS: 1135-66-6纯度: >98.00%
Isolongifolene((-)-Isolongifolene)是一种从Murrayakoenigii中分离的三环倍半萜烯。Isolongifolene通过调节P13K/AKT/GSK-3β信号通路来减轻鱼藤酮诱导的氧化应激,线粒体功能障碍和细胞凋亡。Isolongifolene具有抗氧化,抗炎,抗癌和神经保护的特性。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC60622 | BAY 2416964 | 2242464-44-2 | >99.50% / >98.00% | |
BAY 2416964是一种强效且具有口服活性的芳烃受体(AhR)抑制剂,IC 50 值为341nM。 | ||||
| GC60624 | BAY-985 | 2409479-29-2 | >99.50% | |
A dual inhibitor of TBK1 and IKKε | ||||
| GC60628 | BD750 | 892686-59-8 | >99.50% | |
BD750 is an immunosuppressant and a dual inhibitor of JAK3 and STAT5 that inhibits IL-2-induced JAK3/STAT5-dependent T cell proliferation with IC50 of 1.5 μM and 1.1 μM for mouse and human T-cell proliferation, respectively. | ||||
| GC60636 | Benzyl butyl phthalate | 85-68-7 | >97.00% | |
Benzylbutylphthalate是邻苯二甲酸酯(PAEs)的一员,通过上调Zeb1的表达,可引起血管瘤(HA)细胞的迁移和侵袭。Benzylbutylphthalate激活乳腺癌细胞中的芳香烃受体(AhR),刺激SPHK1/S1P/S1PR3信号传导,促进转移性乳腺癌干细胞(BCSCs)的形成。 | ||||
| GC60668 | Calcimycin hemimagnesium | 72124-77-7 | - | |
Calcimycin(A-23187)hemimagnesium是一种抗生素和独特的二价阳离子离子载体(divalentcationionophore),如钙离子和镁离子。Calcimycinhemimagnesium通过增加细胞内钙浓度诱导Ca2+依赖性细胞死亡。Calcimycinhemimagnesium抑制革兰氏阳性细菌和一些真菌的生长,还抑制ATP酶的活性并解耦哺乳动物细胞的氧化磷酸化(OXPHOS),诱导细胞凋亡(apoptosis)。 | ||||
| GC60674 | Catalase from Aspergillus niger(≥100000U/g) | 9001-05-2 | BA-101000U/g | |
Catalase是重要的抗氧化酶,在清除ROS。在维持氧化还原状态的平衡方面发挥着重要作用。Catalase与肿瘤的发生,发展关系密切。有潜力用于肿瘤的预防研究。 | ||||
| GC60693 | Chitoheptaose heptahydrochloride | 127171-89-5 | - | |
Chitoheptaoseheptahydrochloride是一种具有抗氧化,抗炎,抗凋亡和心脏保护作用的壳聚糖寡糖。Chitoheptaoseheptahydrochloride显着增强了小麦幼苗的生长和光合作用参数。 | ||||
| GC60694 | Chitohexaose hexahydrochloride | 127171-88-4 | - | |
Chitohexaosehexahydrochloride是具有抗炎作用的壳聚糖低聚糖。Chitohexaosehexahydrochloride与TLR4的活性位点结合并抑制LPS诱导的炎症。 | ||||
| GC60700 | Chloroquine D5 | 1854126-41-2 | - | |
An internal standard for the quantification of chloroquine | ||||
| GC60708 | Cinchonine hydrochloride | 5949-11-1 | - | |
Cinchoninehydrochloride((8R,9S)-Cinchoninehydrochloride)是金鸡纳树皮中的天然化合物。Cinchoninehydrochloride可激活内质网应激诱导的人肝癌细胞凋亡。 | ||||
| GC60725 | Cortisone | 53-06-5 | >99.00% | |
Cortisone(17-Hydroxy-11-dehydrocorticosterone)是一种用于研究感染或过敏的激素药物。 | ||||
| GC60782 | Disitertide TFA | - | >96.00% | |
Disitertide TFA是转化生长因子β1(TGF-β1)受体I型的特异性抑制剂。 | ||||
| GC60824 | Ethylene dimethanesulfonate | 4672-49-5 | >98.00% | |
Ethylenedimethanesulfonate是一种温和的烷基化乙二醇非挥发性甲烷磺酸二酯。Ethylenedimethanesulfonate对LC具有选择性的促凋亡作用。 | ||||
| GC60826 | Etoposide phosphate | 117091-64-2 | >96.00% | |
Etoposidephosphate(BMY-40481)是一种有效的抗癌(anti-cancer)化疗试剂和一种选择性拓扑异构酶II(topoisomeraseII)抑制剂,可以防止DNA链的重新连接。Etoposidephosphate是依托泊苷的磷酸酯前药,被认为与Etoposide活性相当。Etoposidephosphate诱导细胞周期阻滞、凋亡(apoptosis)和自噬(autophagy)。 | ||||
| GC60836 | Fenobucarb | 3766-81-2 | >99.50% | |
Fenobucarb是一种广泛使用的氨基甲酸酯杀虫剂。Fenobucarb通过炎症、氧化应激、变性和凋亡等途径诱导斑马鱼发育神经毒性。Fenobucarb可能对动物心脑血管系统有危害。 | ||||
| GC60845 | Flavokawain A | 3420-72-2 | >99.50% | |
A chalcone with diverse biological activities | ||||
| GC60860 | FSL-1 TFA | - | >98.00% | |
FSL-1, a bacterial-derived toll-like receptor 2/6 (TLR2/6) agonist, enhances resistance to experimental HSV-2 infection. | ||||
| GC60875 | GKT136901 | 955272-06-7 | >99.00% | |
A dual inhibitor of NOX1 and NOX4 | ||||
| GC60882 | Glyphosate | 1071-83-6 | ≥99.00% | |
An herbicide | ||||
| GC60887 | GSK717 | 1595278-21-9 | >99.50% / >99.00% | |
GSK717是一种有效的、选择性的NOD2(核苷酸结合寡聚结构域2)抑制剂。GSK717抑制壁酰二肽(MDP)诱导的NOD2介导的信号转导,抑制MDP刺激的HEK293/hNOD2细胞分泌IL-8中的IC50为400nM。 | ||||
| GC60897 | Hesperidin methylchalcone | 24292-52-2 | >95.00% | |
Hesperidin methylchalcone is the Citrus original products with powerful antioxidant activity. | ||||
| GC60914 | Hydrocortisone hemisuccinate | 2203-97-6 | >98.00% | |
Hydrocortisone hemisuccinate (A-hydrocort, Hydrocortisone 21-hemisuccinate), a physiological glucocorticoid with anti-inflammatory properties, is an inhibitor of proinflammatory cytokine with IC50 of 6.7 μM and 21.4 μM for Interleukin-6 (IL-6) and IL-3, respectively. | ||||
| GC60927 | IFN alpha-IFNAR-IN-1 hydrochloride | 2070014-98-9 | >99.50% | |
An inhibitor of the IFN-α-IFNAR protein-protein interaction | ||||
| GC60949 | Isolongifolene | 1135-66-6 | >98.00% | |
Isolongifolene((-)-Isolongifolene)是一种从Murrayakoenigii中分离的三环倍半萜烯。Isolongifolene通过调节P13K/AKT/GSK-3β信号通路来减轻鱼藤酮诱导的氧化应激,线粒体功能障碍和细胞凋亡。Isolongifolene具有抗氧化,抗炎,抗癌和神经保护的特性。 | ||||
