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)
- GC60962Kauran-16,17-diolCAS: 16836-31-0
Kauran-16,17-diol(ent-Kauran-16β,17-diol)是一个天然的二萜化合物,具有抗肿瘤诱导凋亡的活性。其抑制LPS诱导的RAW264.7细胞产生NO的IC50值为17μM。
- GC60969KRAS inhibitor-9CAS: 300809-71-6纯度: >99.50%
KRASinhibitor-9是有效的KRAS抑制剂(Kd=92μM),阻止GTP-KRAS的形成和KRAS下游激活。KRASinhibitor-9以中等的结合亲和力与KRASG12D,KRASG12C和KRASQ61H蛋白结合。KRASinhibitor-9导致G2/M细胞周期停滞并诱导凋亡(apoptosis)。KRASinhibitor-9选择性抑制具有KRAS突变的NSCLC细胞的增殖,但不抑制正常肺细胞的增殖。KRASinhibitor-9
- GC60997Lixisenatide acetateCAS: 1997361-87-1纯度: >98.50%
Lixisenatideacetate是胰高血糖素样肽1受体(GLP-1R)的激动剂,可用于2型糖尿病的研究。
- GC61015Luteolin 5-O-glucosideCAS: 20344-46-1纯度: >98.00%
Luteolin5-O-glucoside来自Cirsiummaackii,具有抗炎活性。Luteolin5-O-glucoside抑制LPS诱导的NO生成和t-BHP诱导的ROS生成。Luteolin5-O-glucoside作用于巨噬细胞,还抑制iNOS和COX-2表达。
- GC61021Malachite green oxalateCAS: 2437-29-8纯度: >98.00%
Malachite green (Aniline green, Basic green 4, Diamond green B, Victoria green B) is a synthetic dyestuff and antimicrobial with potential carcinogenicity.
- GC61041Mepazine hydrochlorideCAS: 2975-36-2纯度: >98.00%
Mepazinehydrochloride(Pecazinehydrochloride)是一种有效的选择性MALT1蛋白酶抑制剂。Mepazinehydrochloride抑制全长GSTMALT1和GSTMALT1325-760段的IC50分别为0.83和0.42μM。Mepazinehydrochloride通过增强细胞凋亡(apoptosis)来影响ABC-DLBCL细胞的生存能力。
- GC61043Mesalamine impurity PCAS: 887256-40-8
MesalamineimpurityP是Mesalamine的杂质。5-Aminosalicylicacid(Mesalamine)是一种特异性的 PPARγ 激动剂,还抑制p21-激活激酶1(PAK1)和 NF-κB。
- GC61047Methotrexate disodiumCAS: 7413-34-5纯度: >98.00%
Methotrexate sodium, an inhibitor of tetrahydrofolate dehydrogenase, is an antineoplastic antimetabolite with immunosuppressant properties.
- GC61183Physalin BCAS: 23133-56-4
PhysalinB是Capegooseberry中主要的甾体活性成分之一,通过调节p53依赖的凋亡途径,诱导乳腺癌细胞周期阻滞和诱导凋亡(apoptosis)。PhysalinB抑制人结肠癌细胞泛素-蛋白酶体通路并诱导不完全自噬反应。
- GC61184Physalin FCAS: 57423-71-9
PhysalinF是一种具有强烈抗炎和免疫调节作用的分泌型甾体。PhysalinF诱导人外周血单个核细胞凋亡,降低人T淋巴细胞1型病毒(HTLV-1)感染后的自发增殖和细胞因子的产生。
- GC61224PyrazoloacridineCAS: 99009-20-8纯度: >98.00%
Pyrazoloacridine(NSC366140)具有抗癌活性,抑制拓扑异构酶1和2的活性(topoisomerases1and2)。Pyrazoloacridine(NSC366140)对K562髓系白血病细胞中的IC50值为1.25μM(24h)。
- GC61227Quercetin D5CAS: 263711-78-0纯度: >99.00%
Quercetin D5是天然产物槲皮素(Quercetin)的氘代同位素内标,其化学结构通常在槲皮素的A环上由5个D原子取代了原有的5个H原子。
- GC61229Quinacrine dihydrochlorideCAS: 69-05-6纯度: >99.00%
Quinacrine 2HCl(Quinacrine dihydrochloride) is a lipophilic cationic drug with multiple actions that is commonly used as an anti-protozoal agent. Quinacrine is an effective phospholipase A2 inhibitor.
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC60958 | JC-171 | 2112809-98-8 | >99.50% | |
JC-171是选择性的NLRP3炎症小体抑制剂,抑制LPS/ATP诱导的巨噬细胞释放IL-1β的IC50值为8.45μM。 | ||||
| GC60962 | Kauran-16,17-diol | 16836-31-0 | - | |
Kauran-16,17-diol(ent-Kauran-16β,17-diol)是一个天然的二萜化合物,具有抗肿瘤诱导凋亡的活性。其抑制LPS诱导的RAW264.7细胞产生NO的IC50值为17μM。 | ||||
| GC60969 | KRAS inhibitor-9 | 300809-71-6 | >99.50% | |
KRASinhibitor-9是有效的KRAS抑制剂(Kd=92μM),阻止GTP-KRAS的形成和KRAS下游激活。KRASinhibitor-9以中等的结合亲和力与KRASG12D,KRASG12C和KRASQ61H蛋白结合。KRASinhibitor-9导致G2/M细胞周期停滞并诱导凋亡(apoptosis)。KRASinhibitor-9选择性抑制具有KRAS突变的NSCLC细胞的增殖,但不抑制正常肺细胞的增殖。KRASinhibitor-9 | ||||
| GC60997 | Lixisenatide acetate | 1997361-87-1 | >98.50% | |
Lixisenatideacetate是胰高血糖素样肽1受体(GLP-1R)的激动剂,可用于2型糖尿病的研究。 | ||||
| GC61002 | Lomibuvir | 1026785-55-6 | >99.50% | |
An HCV polymerase inhibitor | ||||
| GC61015 | Luteolin 5-O-glucoside | 20344-46-1 | >98.00% | |
Luteolin5-O-glucoside来自Cirsiummaackii,具有抗炎活性。Luteolin5-O-glucoside抑制LPS诱导的NO生成和t-BHP诱导的ROS生成。Luteolin5-O-glucoside作用于巨噬细胞,还抑制iNOS和COX-2表达。 | ||||
| GC61021 | Malachite green oxalate | 2437-29-8 | >98.00% | |
Malachite green (Aniline green, Basic green 4, Diamond green B, Victoria green B) is a synthetic dyestuff and antimicrobial with potential carcinogenicity. | ||||
| GC61041 | Mepazine hydrochloride | 2975-36-2 | >98.00% | |
Mepazinehydrochloride(Pecazinehydrochloride)是一种有效的选择性MALT1蛋白酶抑制剂。Mepazinehydrochloride抑制全长GSTMALT1和GSTMALT1325-760段的IC50分别为0.83和0.42μM。Mepazinehydrochloride通过增强细胞凋亡(apoptosis)来影响ABC-DLBCL细胞的生存能力。 | ||||
| GC61043 | Mesalamine impurity P | 887256-40-8 | - | |
MesalamineimpurityP是Mesalamine的杂质。5-Aminosalicylicacid(Mesalamine)是一种特异性的 PPARγ 激动剂,还抑制p21-激活激酶1(PAK1)和 NF-κB。 | ||||
| GC61047 | Methotrexate disodium | 7413-34-5 | >98.00% | |
Methotrexate sodium, an inhibitor of tetrahydrofolate dehydrogenase, is an antineoplastic antimetabolite with immunosuppressant properties. | ||||
| GC61071 | MK-0608 | 443642-29-3 | >99.00% | |
MK-0608是一种有效的HCV复制抑制剂,在亚基因组复制子测定中,EC50为0.3μM(EC90=1.3μM)。 | ||||
| GC61079 | Monensin | 17090-79-8 | >98.00% | |
莫能菌素(蛋白质转运抑制剂)是一种离子载体,可破坏高尔基体,抑制细胞内蛋白质转运。 | ||||
| GC61092 | MSA-2 | 129425-81-6 | >98.50% | |
MSA-2是一种口服非核苷酸干扰素基因刺激因子(STING)激动剂,对人的STING亚型WT和HAQ的EC 50 分别为8.3和24μM。 | ||||
| GC61093 | MSAB | 173436-66-3 | >99.50% / >99.00% | |
MSAB(methyl 3-{[(4-methylphenyl)sulfonyl]amino}benzoate)是一种选择性Wnt/β-catenin信号抑制剂,与β-catenin结合并促进其降解,其EC 50 为0.583μM。 | ||||
| GC61096 | MSN-125 | 1592908-16-1 | >98.50% | |
MSN-125是一种Bax和Bak寡聚化的抑制剂,其IC 50 为4μM。 | ||||
| GC61141 | NSC 15364 | 4550-72-5 | >98.00% | |
NSC15364是一种VDAC1寡聚化和细胞凋亡(apoptosis)抑制剂。 | ||||
| GC61142 | NSC745885 | 4219-52-7 | >98.00% | |
NSC745885是一种有效的抗肿瘤(anti-tumor)试剂,对多种癌细胞株有选择性毒性,但对正常细胞没有毒性。NSC745885是一种有效的EZH2的下调因子通过蛋白酶体降解途径。NSC745885为晚期膀胱癌和口腔鳞癌的研究提供了可能性。 | ||||
| GC61179 | Phenazine methylsulfate | 299-11-6 | >98.00% | |
A free radical generator | ||||
| GC61183 | Physalin B | 23133-56-4 | - | |
PhysalinB是Capegooseberry中主要的甾体活性成分之一,通过调节p53依赖的凋亡途径,诱导乳腺癌细胞周期阻滞和诱导凋亡(apoptosis)。PhysalinB抑制人结肠癌细胞泛素-蛋白酶体通路并诱导不完全自噬反应。 | ||||
| GC61184 | Physalin F | 57423-71-9 | - | |
PhysalinF是一种具有强烈抗炎和免疫调节作用的分泌型甾体。PhysalinF诱导人外周血单个核细胞凋亡,降低人T淋巴细胞1型病毒(HTLV-1)感染后的自发增殖和细胞因子的产生。 | ||||
| GC61203 | Ponicidin | 52617-37-5 | >99.50% | |
Ponicidin(RubescensineB)是源于冬凌草的二萜,具有免疫调节、抗炎、抗病毒和抗癌作用。Ponicidin(RubescensineB)可诱导胃癌细胞凋亡(apoptosis),降低JAK2和STAT3的磷酸化水平,单对其蛋白水平无作用。 | ||||
| GC61224 | Pyrazoloacridine | 99009-20-8 | >98.00% | |
Pyrazoloacridine(NSC366140)具有抗癌活性,抑制拓扑异构酶1和2的活性(topoisomerases1and2)。Pyrazoloacridine(NSC366140)对K562髓系白血病细胞中的IC50值为1.25μM(24h)。 | ||||
| GC61227 | Quercetin D5 | 263711-78-0 | >99.00% | |
Quercetin D5是天然产物槲皮素(Quercetin)的氘代同位素内标,其化学结构通常在槲皮素的A环上由5个D原子取代了原有的5个H原子。 | ||||
| GC61229 | Quinacrine dihydrochloride | 69-05-6 | >99.00% | |
Quinacrine 2HCl(Quinacrine dihydrochloride) is a lipophilic cationic drug with multiple actions that is commonly used as an anti-protozoal agent. Quinacrine is an effective phospholipase A2 inhibitor. | ||||
