NOD-like Receptor (NLR)
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Nucleotide oligomerization domain (NOD)-like receptors (NLRs) are a specialized group of intracellular proteins that play a critical role in the regulation of the host innate immune response. NLRs act as scaffolding proteins that assemble signaling platforms that trigger nuclear factor-κB and mitogen-activated protein kinase signaling pathways and control the activation of inflammatory caspases. Importantly, mutations in several members of the NLR family have been linked to a variety of inflammatory diseases consistent with these molecules playing an important role in host-pathogen interactions and the inflammatory response. NLRs including Nod1 and Nod2 are thought to be kept in an inactive state by intra-molecular interactions.
The central role of the Nod-like receptor (NLR) protein family became increasingly appreciated in innate immune responses. NLRs are classified as part of the signal transduction ATPases with numerous domains (STAND) clade within the AAA+ ATPase family.
Products Related to NOD-like Receptor (NLR)(66)
- GC74298Oxidized low density lipoprotein (Human)
Oxidized low density lipoprotein (Human) (Human ox-LDL) is involved in atherogenesis.
- GC78965ACT001 hydrochlorideCAS: 1403357-80-1Purity: >98.00%
ACT001 (Dimethylaminomicheliolide; DMAMCL) hydrochloride is an orally active, blood-brain barrier-permeable anti-inflammatory and anti-tumor agent.
- GC79413NLRP3 modulator 7CAS: 2982797-42-0Purity: >99.00%
NLRP3 modulator 7 (Compound 17B) is a NLRP3 inflammasome modulator.
- GC79414NLRP3 modulator 7 TFAPurity: >98.00%
NLRP3 modulator 7 (Compound 17B) TFA is a NLRP3 inflammasome modulator.
- GC80890NEK7 degrader-3CAS: 3119435-52-5Purity: >98%
NEK7 degrader-3 is an orally active and brain-penetrant NEK7 molecular glue degrader with a DC 50 of 33.1 nM.
- GC80891NK7-902 diTFAPurity: >99.50%
NK7-902 diTFA is a selective and orally active CRBN-dependent NEK7 molecular glue degrader with K d values of 1.5 and 2.6 μM for hNEK7 and mNEK7.
- GC80922PROTAC HDAC6 degrader 7Purity: >98%
PROTAC HDAC6 degrader 7 is an orally active, highly efficient, and selective PROTAC degrader targeting histone deacetylase 6 ( HDAC6 ) ( IC 50 = 118 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 |
|---|---|---|---|---|
| GC73796 | CVN293 | 2815296-08-1 | >99.00% | |
CVN293 is a selective and brain permeable potassium ion (K+) channel KCNK13 inhibtor with IC50s of 41 nM and 28 nM for hKCNK13 and mKCNK13, respectively. | ||||
| GC73942 | NT-0249 free base | - | - | |
NT-0249 free base is an orally active NLRP3 inhibitor. | ||||
| GC74070 | INF 195 | 1211379-56-4 | >99.00% | |
INF 195 is an NLRP3 inhibitor. | ||||
| GC74298 | Oxidized low density lipoprotein (Human) | - | - | |
Oxidized low density lipoprotein (Human) (Human ox-LDL) is involved in atherogenesis. | ||||
| GC78965 | ACT001 hydrochloride | 1403357-80-1 | >98.00% | |
ACT001 (Dimethylaminomicheliolide; DMAMCL) hydrochloride is an orally active, blood-brain barrier-permeable anti-inflammatory and anti-tumor agent. | ||||
| GC79395 | NT-0527 | 2771019-10-2 | >99.50% | |
NT-0527 is a selective, orally active, and brain-permeable NLRP3 inflammasome inhibitor. | ||||
| GC79410 | (rac)-NDT-19795 | 2272918-42-8 | >99.00% | |
(rac)-NDT-19795 is the racemate of NDT-19795. | ||||
| GC79411 | TN-783 | - | >98% | |
TN-783 is an orally active, brain-penetrant NLRP3 ( IC 50 = 19.3 nM) inhibitor. | ||||
| GC79412 | IIIM-1270 | 4818-19-3 | >98.50% | |
IIIM-1270is a NLRP3 inflammasome inhibitor. | ||||
| GC79413 | NLRP3 modulator 7 | 2982797-42-0 | >99.00% | |
NLRP3 modulator 7 (Compound 17B) is a NLRP3 inflammasome modulator. | ||||
| GC79414 | NLRP3 modulator 7 TFA | - | >98.00% | |
NLRP3 modulator 7 (Compound 17B) TFA is a NLRP3 inflammasome modulator. | ||||
| GC80890 | NEK7 degrader-3 | 3119435-52-5 | >98% | |
NEK7 degrader-3 is an orally active and brain-penetrant NEK7 molecular glue degrader with a DC 50 of 33.1 nM. | ||||
| GC80891 | NK7-902 diTFA | - | >99.50% | |
NK7-902 diTFA is a selective and orally active CRBN-dependent NEK7 molecular glue degrader with K d values of 1.5 and 2.6 μM for hNEK7 and mNEK7. | ||||
| GC80922 | PROTAC HDAC6 degrader 7 | - | >98% | |
PROTAC HDAC6 degrader 7 is an orally active, highly efficient, and selective PROTAC degrader targeting histone deacetylase 6 ( HDAC6 ) ( IC 50 = 118 nM). | ||||
| GC81568 | M464 | - | >99.50% | |
M464, a non-steroidal anti-inflammatory compound, is a potent and orally active NLRP3 inflammasome inhibitor. | ||||
| 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. | ||||
| GN10172 | Ruscogenin | 472-11-7 | >98.00% | |
