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(4623)
- GC804104'-Acetoxy resveratrolCAS: 411233-11-9Purity: >99.50%
4'-Acetoxy resveratrol is a Resveratrol derivative.
- GC80411Leonuriside ACAS: 121748-12-7Purity: >99.50%
Leonuriside A is a phenolic compound that can be isolated from Leonurus japonicus.
- GC80412(E)-Sinapoyl glucoseCAS: 78185-48-5Purity: >99.50%
(E)-Sinapoyl glucose is an inflammatory pathway inhibitor.
- GC80415(S)-Flurbiprofen-d 3Purity: >98%
(S)-Flurbiprofen-d3 (Esflurbiprofen-d3) is the deuterium labeled (S)-Flurbiprofen.
- GC80416Omaveloxolone-d 3Purity: >98%
Omaveloxolone -d 3 (RTA 408-d 3 ) is the deuterated-labeled Omaveloxolone.
- GC80469ω-Hexatoxin-Hv1a TFAPurity: >97.00%
ω-Hexatoxin-Hv1a (ω-ACTX-Hv1; ω-Atracotoxin-HV1) TFA is an orally active insecticidal neurotoxin containing an inhibitor cystine knot motif and a selective calcium channel inhibitor.
- GC804763-Hydroxykynurenine- 13 C 2 , 15 N hydrochloridePurity: >98.50%
3-Hydroxykynurenine - 13 C 2, 15 N (3-Hydroxy-DL-kynurenine- 13 C 2, 15 N) hydrochloride is the 13 C and 15 N labeled 3-Hydroxykynurenine hydrochloride [1] . 3-Hydroxykynurenine, a metabolite of tryptophan, is a potential endogenous neurotoxin whose increased levels have been described in several neurodegenerative disorders.
- GC80477Sodium butyrate-d 3CAS: 347840-05-5Purity: >99.50%
Sodium butyrate -d 3 (Butanoic acid-d 3 sodium) is the deuterium labeled Sodium butyrate.
- GC80509Nervonic acid-d 18Purity: >98%
Nervonic acid -d 18 (Selacholeic acid-d 18 ) is the deuterium labeled Nervonic acid.
- GC80846Myristic acid- 13 C 2CAS: 287111-20-0Purity: >98%
Myristic acid - 13 C 2 is the 13 C-labeled Myristic acid.
- GC80853(4R,5S)-YX-02-030CAS: 3049077-01-9Purity: >99.50%
(4R,5S)-YX-02-030 is an isomer of YX-02-030.
- GC80863(R)-BalcinrenoneCAS: 1850385-65-7Purity: >99.50%
(R)-Balcinrenone ((R)-AZD9977) is an isomer of Balcinrenone.
- GC80873Tovophyllin ACAS: 40738-44-1Purity: >98%
Tovophyllin A is an orally active xanthonoid compound.
- GC80877LD-110 triTFAPurity: >99.50%
LD-110 triTFA is a highly efficient and effective LSD1 PROTAC degrader ( DC 50 = 0.44 μM).
- GC80879JWZ-8-103 hydrochloridePurity: >99.50%
JWZ-8-103 hydrochloride is an orally active analog of PRLX-93936 and a molecular glue targeting TRIM21.
- GC80881PROTAC DAPK1 Degrader-1CAS: 3063030-38-3Purity: >96.50%
PROTAC DAPK1 Degrader-1 is a death-associated protein kinase 1 (DAPK1) degrader with a DC 50 of 119.6 nM.
- GC80883Thalidomide-O-amide-C5-NH2 hydrochlorideCAS: 2716130-28-6Purity: >95.50%
Thalidomide-O-amide-C5-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology [1] [2] .
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC80408 | Meloxicam- 13 C 6 | - | >98.00% | |
Meloxicam -13C6 is 13 C 6 -labeled Meloxicam. | ||||
| GC80409 | Deltoin | 19662-71-6 | >98% | |
Deltoin is a Coumarine derivative. | ||||
| GC80410 | 4'-Acetoxy resveratrol | 411233-11-9 | >99.50% | |
4'-Acetoxy resveratrol is a Resveratrol derivative. | ||||
| GC80411 | Leonuriside A | 121748-12-7 | >99.50% | |
Leonuriside A is a phenolic compound that can be isolated from Leonurus japonicus. | ||||
| GC80412 | (E)-Sinapoyl glucose | 78185-48-5 | >99.50% | |
(E)-Sinapoyl glucose is an inflammatory pathway inhibitor. | ||||
| GC80415 | (S)-Flurbiprofen-d 3 | - | >98% | |
(S)-Flurbiprofen-d3 (Esflurbiprofen-d3) is the deuterium labeled (S)-Flurbiprofen. | ||||
| GC80416 | Omaveloxolone-d 3 | - | >98% | |
Omaveloxolone -d 3 (RTA 408-d 3 ) is the deuterated-labeled Omaveloxolone. | ||||
| GC80469 | ω-Hexatoxin-Hv1a TFA | - | >97.00% | |
ω-Hexatoxin-Hv1a (ω-ACTX-Hv1; ω-Atracotoxin-HV1) TFA is an orally active insecticidal neurotoxin containing an inhibitor cystine knot motif and a selective calcium channel inhibitor. | ||||
| GC80476 | 3-Hydroxykynurenine- 13 C 2 , 15 N hydrochloride | - | >98.50% | |
3-Hydroxykynurenine - 13 C 2, 15 N (3-Hydroxy-DL-kynurenine- 13 C 2, 15 N) hydrochloride is the 13 C and 15 N labeled 3-Hydroxykynurenine hydrochloride [1] . 3-Hydroxykynurenine, a metabolite of tryptophan, is a potential endogenous neurotoxin whose increased levels have been described in several neurodegenerative disorders. | ||||
| GC80477 | Sodium butyrate-d 3 | 347840-05-5 | >99.50% | |
Sodium butyrate -d 3 (Butanoic acid-d 3 sodium) is the deuterium labeled Sodium butyrate. | ||||
| GC80509 | Nervonic acid-d 18 | - | >98% | |
Nervonic acid -d 18 (Selacholeic acid-d 18 ) is the deuterium labeled Nervonic acid. | ||||
| GC80846 | Myristic acid- 13 C 2 | 287111-20-0 | >98% | |
Myristic acid - 13 C 2 is the 13 C-labeled Myristic acid. | ||||
| GC80853 | (4R,5S)-YX-02-030 | 3049077-01-9 | >99.50% | |
(4R,5S)-YX-02-030 is an isomer of YX-02-030. | ||||
| GC80863 | (R)-Balcinrenone | 1850385-65-7 | >99.50% | |
(R)-Balcinrenone ((R)-AZD9977) is an isomer of Balcinrenone. | ||||
| GC80868 | Antcin K | 741268-13-3 | >98% | |
Antcin K is a selective inhibitor targeting the PI3K/Akt, NF-κB, MEK1/2-ERK, p38 and AP-1 pathways. | ||||
| GC80869 | Calebin A | 336784-82-8 | >98.00% | |
Calebin A is a PI3K/Akt/mTOR, MAPK, and NF-κB inhibitor with oral effectiveness. | ||||
| GC80873 | Tovophyllin A | 40738-44-1 | >98% | |
Tovophyllin A is an orally active xanthonoid compound. | ||||
| GC80876 | G9D-4 TFA | - | >99.00% | |
G9D-4 TFA is a G9a PROTAC degrader. | ||||
| GC80877 | LD-110 triTFA | - | >99.50% | |
LD-110 triTFA is a highly efficient and effective LSD1 PROTAC degrader ( DC 50 = 0.44 μM). | ||||
| GC80879 | JWZ-8-103 hydrochloride | - | >99.50% | |
JWZ-8-103 hydrochloride is an orally active analog of PRLX-93936 and a molecular glue targeting TRIM21. | ||||
| GC80880 | dCASP1-55 | - | >98% | |
dCASP1-55 is a cereblon-dependent caspase-1 ( CASP1 ) PROTAC degrader. | ||||
| GC80881 | PROTAC DAPK1 Degrader-1 | 3063030-38-3 | >96.50% | |
PROTAC DAPK1 Degrader-1 is a death-associated protein kinase 1 (DAPK1) degrader with a DC 50 of 119.6 nM. | ||||
| GC80882 | ZLY025 | 3070379-34-6 | >99.00% | |
ZLY025 is a potent and orally active CCNK molecular glue degrader with an DC 50 of 42.7 nM. | ||||
| GC80883 | Thalidomide-O-amide-C5-NH2 hydrochloride | 2716130-28-6 | >95.50% | |
Thalidomide-O-amide-C5-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology [1] [2] . | ||||
