69 Results for "

Go

" in MedChemExpress (MCE) Product Catalog:
Products (69)

69 Results for "Go" in MCE Product Catalog:

Cat. No.: HY-N1933
CAS No.: 485-91-6
Allocryptopine, a derivative of tetrahydropalmatine, is extracted from Macleaya cordata (Thunb.) Pers. Papaveraceae. Allocryptopine has antiarrhythmic effects and potently blocks human ether-a-go-go related gene (hERG) current .
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Cat. No.: HY-121495
CAS No.: 1951431-22-3
Purity:  98.77%
Target:  

Parasite

Research Areas:  

Infection

BKI-1369 is a bumped kinase inhibitor (BKI). BKI-1369 increases human Ether-a-go-go-related gene (hERG)-inhibitory activity with an IC50 of 1.52 μM. BKI-1369 reduces the parasite burden and diseases severity in the gnotobiotic pig model. BKI-1369 has been well characterized for potency, stability, metabolism, toxicity, pharmacokinetics and is potent against C. parvum in infected mice and calves .
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Cat. No.: HY-125820
CAS No.: 1639220-17-9
Purity:  99.47%
Research Areas:  

Neurological Disease

Sigma-1 receptor antagonist 3 (compound135) is a potent and selective Sigma-1 (σ1) receptor antagonist with a Ki of 1.14 nM. Sigma-1 receptor antagonist 3 inhibits Human Ether-a-go-go-Related Gene (hERG) with an IC50 of 1.54 μM. Sigma-1 receptor antagonist 3 has the potential for the neuropathic pain .
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Cat. No.: HY-W009641
CAS No.: 24463-15-8
Synonyms: PyM; 1-HMP
Research Areas:  

Others

1-Pyrenemethanol is an organic compound that can be used to prepare graphene films with excellent thermal conductivity, flexibility and mechanical properties. 1-Pyrenemethanol binds to graphene oxide sheets through hydrogen bonds and π-π interactions to form GO-PyM films, increasing the dispersion and stability of the material .
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Cat. No.: HY-P1925B
Target:  

Mucin

Research Areas:  

Cancer

L-GO-203 TFA is a potent MUC1-C oncoprotein inhibitor. L-GO-203 TFA is an anti-cancer peptide for targeting intracellular proteins .
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Cat. No.: HY-13867R
CAS No.: 133052-90-1
Synonyms: GF109203X (Standard); Go 6850 (Standard)
Research Areas:  

Metabolic Disease Cancer

Bisindolylmaleimide I (Standard) is the analytical standard of Bisindolylmaleimide I. This product is intended for research and analytical applications. Bisindolylmaleimide I (GF109203X) is a cell-permeable and reversible PKC inhibitor (IC50 of 20 nM, 17 nM, 16 nM, and 20 nM for PKCα, PKCβI, PKCβII, and PKCγ. Bisindolylmaleimide I is also a GSK-3 inhibitor .
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Cat. No.: HY-148610
CAS No.: 893739-96-3
Target:  

Others

Research Areas:  

Metabolic Disease

LDH-IN-2, a salicylic acid derivative, is an inhibitor of glycolate oxidase (GO). LDH-IN-2 decreases oxalate output in hyperoxaluric hepatocytes. LDH-IN-2 can be used for research of primary hyperoxaluria type 1 (PH1) .
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Cat. No.: HY-W009169
CAS No.: 2421-28-5
Synonyms: BTDA
Target:  

Drug Intermediate

Research Areas:  

Others

Benzophenonetetracarboxylic dianhydride is widely used in the synthesis of high-performance polyimides and other polymer materials. Benzophenonetetracarboxylic dianhydride reacts with various diamine compounds to form oligoimide chains. These oligimide chains can modify graphene oxide (Go) and enhance its properties .
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Cat. No.: HY-175504
CAS No.: 932544-59-7
Target:  

Dopamine Receptor PERK

Research Areas:  

Neurological Disease

MLS6357 is a D3 dopamine receptor (D3R)-selective positive allosteric modulator (PAM)-antagonist. MLS6357 exhibits antagonist activity in the D3R-mediated and the BRET-based β-arrestin recruitment assay with IC50s of 13 and 14 μM, and no activity for other DAR subtypes (D1R/D2R/D4R/D5R) (IC50 > 100 μM). MLS6357 is also an antagonist in the D3R-mediated Go-BRET assay with an IC50 of 17 μM. MLS6357 can be used for the study of neuropsychiatric disorders, including substance use disorder .
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Cat. No.: HY-13689R
CAS No.: 133053-19-7
Synonyms: Gö 6983 (Standard); Goe 6983 (Standard)
Target:  

PKC Reference Standards

Research Areas:  

Cancer

Go 6983 (Standard) is the analytical standard of Go 6983. This product is intended for research and analytical applications. Go 6983 is a pan-PKC inhibitor against for PKCα, PKCβ, PKCγ, PKCδ and PKCζ with IC50 of 7 nM, 7 nM, 6 nM, 10 nM and 60 nM, respectively.
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Cat. No.: HY-120914
CAS No.: 170950-29-5
Synonyms: Go-Y015
Target:  

TrxR Apoptosis

Research Areas:  

Cancer

TrxR1-IN-B19 (GO-Y015) (Compound B19) is a Curcumin (HY-N0005) derivative and colvalent TrxR1 inhibitor. TrxR1-IN-B19 inhibits TrxR1 enzyme activity to elevate oxidative stress, and then induce ROS-mediated ER Stress and mitochondrial dysfunction, subsequently resulting in cell cycle arrest and apoptosis .
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Cat. No.: HY-P1376
CAS No.: 143675-79-0
Research Areas:  

Endocrinology

G-Protein antagonist peptide is the substance P-related peptide that inhibits binding of G proteins to their receptors. G-Protein antagonist peptide competitively and reversibly inhibits M2 muscarinic receptor activation of Gi or Go and inhibits Gs activation by β-adrenoceptors.
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Cat. No.: HY-115875
CAS No.: 2776148-90-2
Target:  

Lactate Dehydrogenase

Research Areas:  

Metabolic Disease

LDHA-IN-5 is a novel, potent, dual GO/LDHA inhibitor for primary hyperoxaluria.
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Cat. No.: HY-B1482
CAS No.: 32672-69-8
Synonyms: TPS-23 benzenesulfonate
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Mesoridazine (TPS-23) benzenesulfonate, a metabolite of Thioridazine (HY-B0965A), acts as an orally active phenothiazine antipsychotic agent. Mesoridazine benzenesulfonate is a potent and rapid open-channel blocker of human ether-a-go-go related gene (hERG) channels and blocks hERG currents with an IC50 of 550 nM (at 0 mV) in human embryonic kidney 293 cells .Mesoridazine benzenesulfonate can be used for the research of schizophrenia, as well as certain other psychiatric disorders .
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Cat. No.: HY-17504D
CAS No.: 1242184-42-4
(3S,5R)-Rosuvastatin is the (3S,5R)-enantiomer of Rosuvastatin. Rosuvastatin is a competitive HMG-CoA reductase inhibitor with an IC50 of 11 nM . Rosuvastatin potently blocks human ether-a-go-go related gene (hERG) current with an IC50 of 195 nM . Rosuvastatin reduces the expression of the mature hERG and the interaction of heat shock protein 70 (Hsp70) with the hERG protein. Rosuvastatin is very effective in lowering low-density lipoprotein (LDL) cholesterol, triglycerides, and C-reactive protein levels .
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Cat. No.: HY-129995
CAS No.: 2143452-22-4
Purity:  99.06%
Target:  

TSH Receptor

Research Areas:  

Endocrinology

TSHR antagonist S37b is the less effective enantiomer of TSHR antagonist S37a (HY-129995A). TSHR antagonist S37b shows only a minor effect for thyrotropin receptor (TSHR) inhibition. TSHR antagonist S37b can be used for the research of thyroid function .
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Cat. No.: HY-W176012
CAS No.: 330977-65-6
Target:  

Others

Research Areas:  

Metabolic Disease

Glycolate oxidase-IN-1(compound 26), a salicylic acid derivative, is a glycolate oxidase (GO) inhibitor with an IC50 of 38.2 μM. Glycolate oxidase-IN-1 has the ability to reduce oxalate production in hyperoxalate hepatocytes and can be used in the study of primary hyperoxaluria type 1 (PH1) .
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Cat. No.: HY-117786
CAS No.: 153207-86-4
Target:  

PKC

Research Areas:  

Neurological Disease

Go 7874 is a protein kinase C (PKC) inhibitor. Go 7874 mediated neuroprotection against LPS/IFNg-induced neuronal cell death in an immune-mediated neurotoxicity model, not through PKC activity. In contrast, the neuroprotective mechanism of Go 7874 involves inhibition of inducible nitric oxide synthase (iNOS) gene expression, followed by reduced nitric oxide (NO) production .
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Cat. No.: HY-RS05600
Research Areas:  

Others

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

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Cat. No.: HY-RS05998
Research Areas:  

Others

HAO1 Human Pre-designed siRNA Set A contains three designed siRNAs for HAO1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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