Immunology/Inflammation
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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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Products Related to Immunology/Inflammation(4435)
- GC81596SHMT2-IN-1Purity: >99.50%
SHMT2-IN-1 is a potent serine hydroxymethyltransferase 2 ( SHMT2 ) inhibitor with an IC 50 of 1.21 μM and a K D of 10.6 μM.
- GC81597Momilactone BCAS: 51415-08-8Purity: >99.00%
Momilactone B is an inhibitor of α-amylase and α-glucosidase, with an IC 50 of 146.85 μg/mL against Aspergillus oryzae α-amylase and an IC 50 of 612.03 μg/mL against Saccharomyces cerevisiae α-glucosidase.
- GC816012-HydroxymelatoninCAS: 229018-17-1Purity: >98.00%
2-Hydroxymelatonin is a major hydroxylated metabolite of Melatonin.
- GC81602Glucosamine sulfate potassium chlorideCAS: 1296149-08-0Purity: >98.00%
Glucosamine sulfate potassium chloride is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement.
- GC816034’-PhosphopantetheineCAS: 2226-71-3Purity: >97.50%
4’-Phosphopantetheine is an orally active coenzyme A (CoA) precursor.
- GC81606DX-8951 Hydroxy-acid sodiumPurity: >98.50%
DX-8951 Hydroxy-acid sodium is a prodrug of phosphoramide.
- GC81611Nrf2-IN-4 hydrobromidePurity: >99.00%
Nrf2-IN-4 (Compound PhcY) hydrobromide is a Nrf2 inhibitor.
- GC81616Flumethrin-d 5Purity: >98%
Flumethrin -d 5 (FCR 2769-d 5 ) is the deuterium labeled Flumethrin.
- GC816264-Methoxyestradiol-d 5Purity: >98%
4-Methoxyestradiol -d 5 is the deuterium labeled 4-Methoxyestradiol.
- GC81631WollastoniteCAS: 13983-17-0Purity: >98.00%
Wollastonite is a white, chain-structured pyroxene silicate mineral with biocompatibility, biodegradability, osteogenicity and antibacterial properties.
- GC816326-Carboxy-H2DCFDACAS: 247044-02-6Purity: >95.00%
6-Carboxy-H2DCFDA (6-Carboxy-2',7'-dichlorodihydrofluorescein) is a non-fluorescent, cell-permeable intracellular ROS indicator.
- GC816342-Acetamidophenol-d 3CAS: 122258-87-1Purity: >99.00%
2-Acetamidophenol -d 3 (Orthocetamol-d 3 ) is the deuterium labeled 2-Acetamidophenol.
- GC81638PROTAC GPX4 degrader-5CAS: 3119292-91-7Purity: >95.00%
PROTAC GPX4 degrader-5 (compound N15) is an efficient and highly selective PROTAC GPX4 degrader ( DC 50 = 28 nM).
- GC81669ATP- 13 C 10 , 15 N 5 ,d 14 (dilithium)Purity: >98%
ATP- 13 C 10, 15 N 5,d 14 ( Adenosine 5'-triphosphate- 13 C 10, 15 N 5,d 14 ) dilithium is the 13 C-, 15 N- and deuterium labeled ATP dilithium.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC81596 | SHMT2-IN-1 | - | >99.50% | |
SHMT2-IN-1 is a potent serine hydroxymethyltransferase 2 ( SHMT2 ) inhibitor with an IC 50 of 1.21 μM and a K D of 10.6 μM. | ||||
| GC81597 | Momilactone B | 51415-08-8 | >99.00% | |
Momilactone B is an inhibitor of α-amylase and α-glucosidase, with an IC 50 of 146.85 μg/mL against Aspergillus oryzae α-amylase and an IC 50 of 612.03 μg/mL against Saccharomyces cerevisiae α-glucosidase. | ||||
| GC81601 | 2-Hydroxymelatonin | 229018-17-1 | >98.00% | |
2-Hydroxymelatonin is a major hydroxylated metabolite of Melatonin. | ||||
| GC81602 | Glucosamine sulfate potassium chloride | 1296149-08-0 | >98.00% | |
Glucosamine sulfate potassium chloride is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement. | ||||
| GC81603 | 4’-Phosphopantetheine | 2226-71-3 | >97.50% | |
4’-Phosphopantetheine is an orally active coenzyme A (CoA) precursor. | ||||
| GC81605 | PGK1-IN-1 | 3093312-81-0 | >99.50% | |
PGK1-IN-1 (Compound 6e) is a potent and selective PGK1 inhibitor ( IC 50 : 33 nM). | ||||
| GC81606 | DX-8951 Hydroxy-acid sodium | - | >98.50% | |
DX-8951 Hydroxy-acid sodium is a prodrug of phosphoramide. | ||||
| GC81609 | YHV98-4 | 132858-26-5 | >98.00% | |
YHV98-4 is a selective, blood-brain barrier-permeable Hv1 inhibitor with an IC 50 of 0.7 μM. | ||||
| GC81610 | SK-129 | 1919889-97-6 | >98% | |
SK-129 is a blood-brain barrier-permeable inhibitor of α-synuclein ( αS ) oligomers with a K d of 221 nM. | ||||
| GC81611 | Nrf2-IN-4 hydrobromide | - | >99.00% | |
Nrf2-IN-4 (Compound PhcY) hydrobromide is a Nrf2 inhibitor. | ||||
| GC81612 | Y1693 | 2812381-74-9 | >99.50% | |
Y1693 is an orally active RANKL inhibitor with a K d of 5.03 μM for hRANKL. | ||||
| GC81616 | Flumethrin-d 5 | - | >98% | |
Flumethrin -d 5 (FCR 2769-d 5 ) is the deuterium labeled Flumethrin. | ||||
| GC81618 | Urolithin A- 13 C 6 | - | >99.50% | |
Urolithin A - 13 C 6 is the 13 C-labeled Urolithin A. | ||||
| GC81626 | 4-Methoxyestradiol-d 5 | - | >98% | |
4-Methoxyestradiol -d 5 is the deuterium labeled 4-Methoxyestradiol. | ||||
| GC81631 | Wollastonite | 13983-17-0 | >98.00% | |
Wollastonite is a white, chain-structured pyroxene silicate mineral with biocompatibility, biodegradability, osteogenicity and antibacterial properties. | ||||
| GC81632 | 6-Carboxy-H2DCFDA | 247044-02-6 | >95.00% | |
6-Carboxy-H2DCFDA (6-Carboxy-2',7'-dichlorodihydrofluorescein) is a non-fluorescent, cell-permeable intracellular ROS indicator. | ||||
| GC81634 | 2-Acetamidophenol-d 3 | 122258-87-1 | >99.00% | |
2-Acetamidophenol -d 3 (Orthocetamol-d 3 ) is the deuterium labeled 2-Acetamidophenol. | ||||
| GC81638 | PROTAC GPX4 degrader-5 | 3119292-91-7 | >95.00% | |
PROTAC GPX4 degrader-5 (compound N15) is an efficient and highly selective PROTAC GPX4 degrader ( DC 50 = 28 nM). | ||||
| GC81639 | SH-26 | - | >98% | |
SH-26 is a PHD1 PROTAC degrader with DC 50 s of 1.06 μM, 4.16 μM and 4.91 μM in MDA-MB-231, HepG2 and HEK-293T cells, respectively. | ||||
| GC81669 | ATP- 13 C 10 , 15 N 5 ,d 14 (dilithium) | - | >98% | |
ATP- 13 C 10, 15 N 5,d 14 ( Adenosine 5'-triphosphate- 13 C 10, 15 N 5,d 14 ) dilithium is the 13 C-, 15 N- and deuterium labeled ATP dilithium. | ||||
| GC81674 | MKI-3 | 3084702-28-0 | >98% | |
MKI-3 is a selective microtubule-associated serine/threonine kinase-like ( MASTL ) inhibitor with an IC 50 of 5.72 nM and a K d of 1.89 nM. | ||||
| GC81678 | ML278 | 1604821-43-3 | >97.50% | |
ML278 is a scavenger receptor-BI ( SR-BI ) inhibitor with an IC 50 of 0.93 nM in mice. | ||||
| GC81679 | PLT012 | - | >98.50% | |
PLT012 is a humanized IgG4 antibody targeting CD36. | ||||
| GC81683 | AM9053 | 157469-21-1 | >98.00% | |
AM9053 is a selective, effective and slowly reversible inhibitor of N-acyl ethanolamine acid amidease ( NAAA ) ( IC 50 = 30 nM). | ||||
