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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
184 Results for "
Rel
" in MedChemExpress (MCE) Product Catalog:
Products (184)
184 Results for "Rel" in MCE Product Catalog:
52
52 Publications Verification
Synonyms: DTT; Rel-(2R,3R)-1,4-Dimercapto-2,3-butanediol
8
8 Cited Publications
MALT1 inhibitor MI-2 is a MALT1 inhibitor (IC50=5.84 μM). MALT1 inhibitor MI-2 binds directly to MALT1, irreversibly suppresses protease function and is accompanied by NF-κB reporter activity suppression, c-REL nuclear localization inhibition, and NF-κB target gene downregulation. MALT1 inhibitor MI-2 shows nontoxic to animals .
4
4 Cited Publications
Art. -Nr.: HY-P73681
Reinheit: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: RelA; NF-Kappa-B Transcription Factor P65; Prev. NFKB3; P65 Iso5 Isoform Delta 10; Nuclear Factor Of Kappa Light Polypeptide Gene Enhancer In B-Cells 3; Alternative Protein RelA; P65; NF-Kappa-B P65delta3; V-Rel Avian Reticuloendotheliosis Viral Oncogene
Species:
Human
Source:
E. coli
2
2 Cited Publications
Synonyms: trans-ML-SI3
Target:
Forschungsgebiete:
(rel)-ML-SI3 is one of the active ingredients of ML-SI3 (HY-139426) (another component is (cis)-ML-SI3) that targets three isoforms of TRPML. (rel)-ML-SI3 is an inhibitor of TRPML1 and TRPML3 (IC50=3.1 μM/28.5 μM), and a potent activator of TRPML2 (EC50=3.3 μM) .
2
2 Cited Publications
IT-901 is an orally active and potent NF-κB subunit c-Rel inhibitor with an IC50 of 0.1 μM, 3 μM for NF-κB DNA binding and c-Rel DNA binding, respectively. IT-901, a bioactive naphthalenethiobarbiturate derivative, has the potential for human lymphoid tumors and ameliorate graft-versus-host disease (GVHD) .
1
1 Cited Publications
Synonyms: (Rel)-MC180295
MC180295 ((rel)-MC180295) is a potent and selective CDK9-Cyclin T1 inhibitor, with an IC50 of 5 nM, at least 22-fold more selective for CDK9 over other CDKs. MC180295 also inhibits GSK-3α and GSK-3β. MC180295 ((rel)-MC180295) has potent anti-tumor effect .
1
1 Cited Publications
Target:
Forschungsgebiete:
(rel)-AR234960 is a selective and competitive agonist of the G protein-coupled receptor MAS. (rel)-AR234960 binds to the MAS receptor to activate the downstream ERK1/2 signaling pathway, inducing the expression of connective tissue growth factor (CTGF) and its downstream collagen subtype genes (such as COL1A1, COL3A1). (rel)-AR234960 promotes collagen synthesis in cardiac fibroblasts through the MAS-ERK1/2-CTGF pathway and aggravates extracellular matrix remodeling. (rel)-AR234960's in vitro effect can be blocked by the MAS inverse agonist AR244555 and MEK1 inhibitor. (rel)-AR234960 regulates the expression of cardiac fibrosis-related genes and can be used in the study of heart failure .
1
1 Cited Publications
Synonyms: Rel-Cianidanol; Rel-Catechuic acid
Category:
Cardiovascular Disease Neurological Disease Theaceae Extract Infection Plant Phenols Polyphenols Camellia sinensis (L.) O. Ktze. Extract Disease Research Fields Inflammation/Immunology
Target:
1
1 Cited Publications
Art. -Nr.: HY-128838A
Reinheit: 98.18%
Target:
Forschungsgebiete:
(rel)-PROTAC ERRα Degrader-1 is a relative configuration of PROTAC ERRα Degrader-1. PROTAC ERRα Degrader-1 comprises a MDM2 ligand binding group, a linker and an estrogen-related receptor alpha (ERRa) binding group. PROTAC ERRα Degrader-1 is an estrogen-related receptor alpha (ERRa) degrader .
1
Category:
Plant Monophenols Metabolic Disease Agrostidoideae Extract Phenols Triticum aestivum L. Extract Disease Research Fields
Target:
Synonyms: Rel-eFT226
rel-Zotatifin is the racemic isomer of Zotatifin, acts as an eIF4A inhibitor with activity less than Zotatifin. Zotatifin (eFT226) is a potent, selective, and well-tolerated eIF4A inhibitor. Zotatifin promotes eIF4A binding to specific mRNA sequences with recognition motifs in the 5’-UTRs (IC50=2 nM) and interferes with the assembly of the eIF4F initiation complex .
Category:
Ketones, Aldehydes, Acids Metabolic Disease Endogenous metabolite Disease Research Fields Food Research
Target:
Art. -Nr.: HY-W710914A
CAS. Nr.: 219915-69-2
Target:
Forschungsgebiete:
rel-HDMP 28 hydrochloride (Compound 2g) is a methylphenidate analogue that binds selectively to SERT (Ki = 105 nM)[1].
Art. -Nr.: HY-482931C
CAS. Nr.: 1055345-76-0
Target:
Forschungsgebiete:
rel-(2R,3R)-2-Phenylpiperidin-3-amine dihydrochloride is a drug intermediate for synthesis of various active compounds.
Art. -Nr.: HY-101387
CAS. Nr.: 194918-76-8
Target:
Forschungsgebiete:
rel-ACPT-I is an agonist of group III mGluRs with diverse biological activities including neuroprotective, anticonvulsant, and anxiolytic-like effects .
Art. -Nr.: HY-17371A
CAS. Nr.: 63121-00-6
Target:
Forschungsgebiete:
(rel)-Oxaliplatin is a DNA synthesis inhibitor. (rel)-Oxaliplatin causes DNA crosslinking damage, prevents DNA replication and transcription and induces apoptosis. (rel)-Oxaliplatin can be used for cancer research .
Art. -Nr.: HY-17423S1
CAS. Nr.: 1217731-56-0
Art. -Nr.: HY-B0511S1
CAS. Nr.: 1217850-77-5
Synonyms: Rel-Vitamin B7-d4; Rel-Vitamin H-d4; Rel-D-Biotin-d4
Target:
Forschungsgebiete:
rel-Biotin-d4 is the deuterium labeled Biotin. Biotin is an enzyme co-factor present in minute amounts in every living cell.
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
