184 Results for "

Rel

" in MedChemExpress (MCE) Product Catalog:
Products (184)

184 Results for "Rel" in MCE Product Catalog:

Cat. No.: HY-B0176AS
CAS No.: 1330180-66-9
rel-Sertraline-d3 (hydrochloride) is the deuterium labeled Sertraline hydrochloride. Sertraline hydrochloride is an antidepressant of the selective serotonin reuptake inhibitor (SSRI) class. Sertraline hydrochloride is researched for a number of diseases, such as major depressive disorder and obsessive .
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Cat. No.: HY-17371A
CAS No.: 63121-00-6
Research Areas:  

Cancer

(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 .
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Cat. No.: HY-17423S1
CAS No.: 1217731-56-0
rel-Abacavir-d4 is the deuterium labeled rel-Abacavir[1].
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Cat. No.: HY-RS11824
Research Areas:  

Others

Rel Mouse Pre-designed siRNA Set A contains three designed siRNAs for Rel gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-B0511S1
CAS No.: 1217850-77-5
Synonyms: Rel-Vitamin B7-d4; Rel-Vitamin H-d4; Rel-D-Biotin-d4
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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Cat. No.: HY-W045799
CAS No.: 1445951-33-6
Target:  

Drug Intermediate

Research Areas:  

Others

rel-2-(tert-Butoxycarbonyl)octahydrocyclopenta[c]pyrrole-3a-carboxylic acid is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-122359A
CAS No.: 31477-60-8
Synonyms: Rel-L-Centchroman; Ormeloxifene
rel-Levormeloxifene (rel-L-Centchroman) is the relative configuration of Levormeloxifene (HY-122359). rel-Levormeloxifene is a selective estrogen receptor modulator (SERM). rel-Levormeloxifene inhibits proliferation of leukemia cells with IC50 about 7 μM, arrests cell cycle at G0/G1 phase, and induces apoptosis. rel-Levormeloxifene induces differentation of myelogenesis leukemia, and enhances ROS production in K562 cells .
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Cat. No.: HY-14690B
CAS No.: 1227675-51-5
Synonyms: Rel-SCH 39166 hydrobromide
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

rel-Ecopipam (rel-SCH 39166) (Compound 6b) hydrobromide is a D1 receptor antagonist (Ki: 1.30 nM) .
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Cat. No.: HY-128837A
CAS No.: 2760669-71-2
(rel)-Nutlin carboxylic acid is the Nutlin 3-based MDM2 ligand. (rel)-Nutlin carboxylic acid can be connected to the ligand for protein by a linker to form PROTAC .
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Cat. No.: HY-178240
CAS No.: 102141-11-7
rel-(1S,2R)-Dihydro bupropion is a metabolite of bupropion. rel-(1S,2R)-Dihydro bupropion can promote endogenous IL-10 production and inhibit Th1 cytokines (IL-12 and TNF-α). rel-(1S,2R)-Dihydro bupropion can induce immune response transition from Th1 to Th2. rel-(1S,2R)-Dihydro bupropion can be used for research on inflammatory conditions .
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Cat. No.: HY-N2379
CAS No.: 131968-74-6
Research Areas:  

Others

Rel-(2R,3S)-3-Phenylisoserine methyl ester is a derivative of serine. Rel-(2R,3S)-3-Phenylisoserine methyl ester can be used as a side chain of Paclitaxel (HY-B0015) .
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Cat. No.: HY-18617
CAS No.: 371980-94-8
rel-SB-612111 hydrochloride is a novel and potent human opiate receptor-like orphan receptor (ORL-1) antagonist with a high affinity for hORL-1 (Ki=0.33 nM). rel-SB-612111 hydrochloride exhibits selectivity for μ-, κ- and δ-receptors with Ki values of 57.6 nM, 160.5 nM and 2109 nM, respecticely. rel-SB-612111 hydrochloride effectively antagonizes the pronociceptive action of Nociceptin (HY-P0183) in an acute pain model .
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Cat. No.: HY-113068R
CAS No.: 148-03-8
(rel)-β-Tocopherol (Standard) is the analytical standard of (rel)-β-Tocopherol. This product is intended for research and analytical applications. (rel)-β-Tocopherol is a relative configuration of β-Tocopherol.(±)-β-Tocopherol is a lipid-soluble form of vitamin E with antioxidant activity. β-Tocopherol can inhibit tyrosinase activity and melanin synthesis. β-Tocopherol also can prevent the inhibition of cell growth and of PKC activity caused by d-alpha-tocopherol .
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Cat. No.: HY-W364968
CAS No.: 1638768-80-5
Target:  

PROTAC Linkers

Research Areas:  

Cancer

rel-(1S,2R)-2-(((tert-butoxycarbonyl)amino)methyl)cyclopropane-1-carboxylic acid is a PROTAC linker that can be used in the synthesis of PROTACs.
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Cat. No.: HY-18295A
CAS No.: 533883-77-1
Synonyms: Rel-LY500307
Target:  

Estrogen Receptor/ERR

Research Areas:  

Neurological Disease

rel-Erteberel is rel isomer of Erteberel (HY-18295). Erteberel is a potent and selective estrogen receptor beta (ERβ) agonist with Ki and EC50 of 1.54 nM and 3.61 nM, respectively. Erteberel has anti-tumor activities .
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Cat. No.: HY-122495
CAS No.: 73625-62-4
Synonyms: Rel-LY 171555 dihydrochloride; Rel-LY 141865 dihydrochloride
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

rel-Quinpirole (rel-LY 171555) dihydrochloride, an ergot compound, is a selective dopamine (DA) D2 receptor agonist. rel-Quinpirole dihydrochloride can be used for research on neurological diseases .
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Cat. No.: HY-124874
CAS No.: 195966-93-9
Synonyms: (Rel)-Aspergillimide; (Rel)-VM55598
(rel)-Asperparaline A ((rel)-Aspergillimide), an anthelmintic metabolite, is isolated from okara that has been fermented with Aspergillus japonicas JV-23. (rel)-Asperparaline A is also a potent and selective antagonist of nAChR. (rel)-Asperparaline A exhibits paralytic activity in silk worms .
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Cat. No.: HY-144681A
CAS No.: 2241514-58-7
Synonyms: Rel-LY3372689
Target:  

OGA Tau Protein

Research Areas:  

Neurological Disease

rel-Ceperognastat (rel-LY3372689) (Compound Formula Ic) is a O-GlcNAcase (OGA) inhibitor that can be used to study the neurodegenerative diseases and disorders, such as Alzheimer's disease .
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Cat. No.: HY-151216S
CAS No.: 1217683-35-6
Synonyms: Rel-BRL29060-d4 hydrochloride; Rel-BRL29060A-d4
rel-Paroxetine-d4 (rel-BRL29060-d4) hydrochloride is an isotope-labeled rel-Paroxetine hydrochloride.
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Cat. No.: HY-18941B
CAS No.: 176027-90-0
Synonyms: (Rel)-LY354740; (Rel)-Eglumetad
Target:  

mGluR

Research Areas:  

Neurological Disease

(rel)-Eglumegad ((rel)-LY354740) is a relative configuration of Eglumegad (HY-18941). Eglumegad is a highly potent and selective group II (mGlu2/3) receptor agonist with EC50s of 5 and 24 nM for transfected human mGlu2 and mGlu3 receptors, respectively .
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