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)
- GC63600Piperonyl alcoholCAS: 495-76-1纯度: >99.50%
Piperonyl alcohol 是一种苯并二恶英衍生物。它具有生物相容性,可作为引发剂用于化学合成。
- GC63604Sparfosic acidCAS: 51321-79-0
Sparfosic acid 是 DNA 抗代谢剂和天门冬氨酸氨甲酰转移酶 (aspartate transcarbamoyl transferase) 的有效抑制剂。Sparfosic acid 具有抗肿瘤活性。天冬氨酸氨甲酰转移酶催化第二步 de novo 嘧啶生物合成。
- GC63614TrichloroacetonitrileCAS: 545-06-2纯度: >99.00%
Trichloroacetonitrile 是饮用水中氯与背景有机物反应产生的一系列污染物之一。Trichloroacetonitrile 是芳基硼酸异丙醇羟基化为酚类化合物的有效活化剂。
- GC63625N-Palmitoyl-L-glutamineCAS: 58725-34-1纯度: >99.50% / >99.00%
N-Palmitoyl-L-glutamine是一种由棕榈酸与L-谷氨酰胺结合而成的生物活性脂酰胺,具有调节细胞功能和信号通路的潜力。
- GC63626ZINC05007751CAS: 591239-68-8纯度: >98.00%
ZINC05007751 is a potent NIMA-related kinase NEK6 inhibitor with an IC50 of 3.4 μM, shows antiproliferative activity against a panel of human cancer cell lines and displays a synergistic effect with Cisplatin and Paclitaxel in a BRCA2 mutated ovarian cancer cell line. DMSO is not recommended to dissolve platinum-based drugs, which can easily lead to drug inactivation.
- GC63629cis-2-Butene-1,4-diolCAS: 6117-80-2纯度: >96.00%
cis-2-Butene-1,4-diol 是一种用于合成抗病毒药物 oxetanocin A 的化合物。cis-2-Butene-1,4-diol 是研究异构化与氢化和氢解反应的探针。
- GC63633N7-Methyl-guanosine-5’-triphosphate-5’-adenosineCAS: 62828-63-1
N7-Methyl-guanosine-5’-triphosphate-5’-adenosine (m7GpppA) 是一种二核苷酸帽类似物,可用于体外 RNA 转录。
- GC63657N,N,N′,N′-Tetracyclohexyl-3-oxapentanediamideCAS: 74267-27-9纯度: >98.00%
A calcium ionophore
- GC63665BenzylacyclouridineCAS: 82857-69-0
Benzylacyclouridine (BAU) 是一种有效且特异性的尿苷磷酸化酶抑制剂,尿苷磷酸化酶是尿苷分解代谢中的第一种酶。Benzylacyclouridine 可以调节 5-氟尿嘧啶 (5-FU) 及其衍生物的细胞毒副作用。
- GC63677VPC-80051 racemateCAS: 877969-69-2
VPC-80051 is an potent inhibitor of hnRNP A1 splicing activity that targets hnRNP A1 RBD and reduces AR-V7 messenger levels in 22Rv1 CRPC cell line.
- GC63685(6R,7S)-Cefminox sodium heptahydrateCAS: 92636-39-0
(6R,7S)-Cefminox sodium heptahydrate 是 Cefminox sodium heptahydrate 的异构体。Cefminox sodium heptahydrate 是一种 β-内酰胺头孢菌素抗生素,具有广谱抗菌活性。
- GC63698Leucomalachite green-d5CAS: 947601-82-3
Leucomalachite green-d5 是 Leucomalachite green 的氘代物。Leucomalachite green 是一种三苯甲烷燃料,可用于检测血液。Leucomalachite green 是孔雀石绿的主要代谢物,是一种潜在的致癌物、致畸物和诱变剂。
- GC63712XL388-C2-amide-PEG9-NH2 hydrochloride纯度: >95.00%
XL388-C2-amide-PEG9-NH2 hydrochloride 是一种可用于合成 C26 连接的雷帕霉素类似物的中间体。
- GC63748SPOP-IN-6b dihydrochloride纯度: >99.50%
SPOP-IN-6b dihydrochloride 是一种有效的斑型 POZ 蛋白 (SPOP) 抑制剂,IC50 为 3.58 μM。
- GC63758cGAMP diammonium
cGAMP (Cyclic GMP-AMPP) diammonium 作为内源性第二信使发挥作用,并触发干扰素的产生以响应胞浆 DNA。cGAMP diammonium 激活干扰素基因刺激因子 (STING),激活导致产生 I 型干扰素和其他免疫介质的信号级联。
- GC63768Oxythiamine diphosphate ammonium纯度: >95.00%
Oxythiamin diphosphate ammonium 是一种有效的转酮酶 (TK) 抑制剂。
- GC63781(R)-BAY-899CAS: 2988191-40-6
(R)-BAY-899 是 BAY-899 的 R 型异构体。BAY-899 是一种口服有效和选择性的促黄体生成激素受体 (LH-R) 拮抗剂,对 hLH (人 LH) 和 rLH (大鼠 LH) 的 IC50 分别为 185 nM 和 46 nM。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC63600 | Piperonyl alcohol | 495-76-1 | >99.50% | |
Piperonyl alcohol 是一种苯并二恶英衍生物。它具有生物相容性,可作为引发剂用于化学合成。 | ||||
| GC63604 | Sparfosic acid | 51321-79-0 | - | |
Sparfosic acid 是 DNA 抗代谢剂和天门冬氨酸氨甲酰转移酶 (aspartate transcarbamoyl transferase) 的有效抑制剂。Sparfosic acid 具有抗肿瘤活性。天冬氨酸氨甲酰转移酶催化第二步 de novo 嘧啶生物合成。 | ||||
| GC63614 | Trichloroacetonitrile | 545-06-2 | >99.00% | |
Trichloroacetonitrile 是饮用水中氯与背景有机物反应产生的一系列污染物之一。Trichloroacetonitrile 是芳基硼酸异丙醇羟基化为酚类化合物的有效活化剂。 | ||||
| GC63618 | Antrafenine | 55300-29-3 | - | |
Antrafenine (Stakane) 是一种非麻醉性缓解疼痛试剂,在药理学和毒理学研究中表现出长时间的作用和良好的耐受性。 | ||||
| GC63625 | N-Palmitoyl-L-glutamine | 58725-34-1 | >99.50% / >99.00% | |
N-Palmitoyl-L-glutamine是一种由棕榈酸与L-谷氨酰胺结合而成的生物活性脂酰胺,具有调节细胞功能和信号通路的潜力。 | ||||
| GC63626 | ZINC05007751 | 591239-68-8 | >98.00% | |
ZINC05007751 is a potent NIMA-related kinase NEK6 inhibitor with an IC50 of 3.4 μM, shows antiproliferative activity against a panel of human cancer cell lines and displays a synergistic effect with Cisplatin and Paclitaxel in a BRCA2 mutated ovarian cancer cell line. DMSO is not recommended to dissolve platinum-based drugs, which can easily lead to drug inactivation. | ||||
| GC63629 | cis-2-Butene-1,4-diol | 6117-80-2 | >96.00% | |
cis-2-Butene-1,4-diol 是一种用于合成抗病毒药物 oxetanocin A 的化合物。cis-2-Butene-1,4-diol 是研究异构化与氢化和氢解反应的探针。 | ||||
| GC63633 | N7-Methyl-guanosine-5’-triphosphate-5’-adenosine | 62828-63-1 | - | |
N7-Methyl-guanosine-5’-triphosphate-5’-adenosine (m7GpppA) 是一种二核苷酸帽类似物,可用于体外 RNA 转录。 | ||||
| GC63637 | Esfenvalerate | 66230-04-4 | >99.50% | |
Esfenvalerate 是拟除虫菊酯杀虫剂 fenvalerate 的四个异构体之一。 | ||||
| GC63638 | Acetone-d6 | 666-52-4 | - | |
Acetone-d6 是 Acetone 的氘代物,可用作核磁共振波谱 (NMR) 的溶剂。 | ||||
| GC63640 | 7-Hydroxyflavone | 6665-86-7 | >97.00% | |
A flavonoid with diverse biological activities | ||||
| GC63657 | N,N,N′,N′-Tetracyclohexyl-3-oxapentanediamide | 74267-27-9 | >98.00% | |
A calcium ionophore | ||||
| GC63665 | Benzylacyclouridine | 82857-69-0 | - | |
Benzylacyclouridine (BAU) 是一种有效且特异性的尿苷磷酸化酶抑制剂,尿苷磷酸化酶是尿苷分解代谢中的第一种酶。Benzylacyclouridine 可以调节 5-氟尿嘧啶 (5-FU) 及其衍生物的细胞毒副作用。 | ||||
| GC63673 | ABT-384 | 868623-40-9 | - | |
ABT-384 是一种强效选择性的 11-β-羟基类固醇脱氢酶1型 (11β-HSD1) 抑制剂。ABT-384 对啮齿类、猴和人 11β-HSD1 具有很高的亲和力,Ki 值在 0.1-2.7 nM。ABT-384 阻断活性皮质醇的再生。ABT-384 可用于阿尔兹海默症的研究。 | ||||
| GC63677 | VPC-80051 racemate | 877969-69-2 | - | |
VPC-80051 is an potent inhibitor of hnRNP A1 splicing activity that targets hnRNP A1 RBD and reduces AR-V7 messenger levels in 22Rv1 CRPC cell line. | ||||
| GC63685 | (6R,7S)-Cefminox sodium heptahydrate | 92636-39-0 | - | |
(6R,7S)-Cefminox sodium heptahydrate 是 Cefminox sodium heptahydrate 的异构体。Cefminox sodium heptahydrate 是一种 β-内酰胺头孢菌素抗生素,具有广谱抗菌活性。 | ||||
| GC63697 | BSc3094 | 946857-84-7 | >98.00% | |
BSc3094 是一种 Tau aggregation 抑制剂。BSc3094 可用于阿尔茨海默病 (AD) 的研究。 | ||||
| GC63698 | Leucomalachite green-d5 | 947601-82-3 | - | |
Leucomalachite green-d5 是 Leucomalachite green 的氘代物。Leucomalachite green 是一种三苯甲烷燃料,可用于检测血液。Leucomalachite green 是孔雀石绿的主要代谢物,是一种潜在的致癌物、致畸物和诱变剂。 | ||||
| GC63712 | XL388-C2-amide-PEG9-NH2 hydrochloride | - | >95.00% | |
XL388-C2-amide-PEG9-NH2 hydrochloride 是一种可用于合成 C26 连接的雷帕霉素类似物的中间体。 | ||||
| GC63748 | SPOP-IN-6b dihydrochloride | - | >99.50% | |
SPOP-IN-6b dihydrochloride 是一种有效的斑型 POZ 蛋白 (SPOP) 抑制剂,IC50 为 3.58 μM。 | ||||
| GC63758 | cGAMP diammonium | - | - | |
cGAMP (Cyclic GMP-AMPP) diammonium 作为内源性第二信使发挥作用,并触发干扰素的产生以响应胞浆 DNA。cGAMP diammonium 激活干扰素基因刺激因子 (STING),激活导致产生 I 型干扰素和其他免疫介质的信号级联。 | ||||
| GC63760 | RS 09 TFA | - | >99.50% | |
RS 09 TFA 是一种 TLR4 激动剂。RS 09 TFA 在体外 RAW264.7 巨噬细胞中促进 NF-κB 核易位并诱导炎性细胞因子分泌。RS 09 TFA 作为体内佐剂。RS 09 TFA 在小鼠中与 X-15-KLH 一起给药时,可提高 X-15 特异性抗体的血清浓度。 | ||||
| GC63768 | Oxythiamine diphosphate ammonium | - | >95.00% | |
Oxythiamin diphosphate ammonium 是一种有效的转酮酶 (TK) 抑制剂。 | ||||
| GC63781 | (R)-BAY-899 | 2988191-40-6 | - | |
(R)-BAY-899 是 BAY-899 的 R 型异构体。BAY-899 是一种口服有效和选择性的促黄体生成激素受体 (LH-R) 拮抗剂,对 hLH (人 LH) 和 rLH (大鼠 LH) 的 IC50 分别为 185 nM 和 46 nM。 | ||||
