47 Results for "

SCD1

" in MedChemExpress (MCE) Product Catalog:
Products (47)

47 Results for "SCD1" in MCE Product Catalog:

Cat. No.: HY-N8144
CAS No.: 95262-48-9
Niga-ichigoside F1, an orally active ursane triterpenoid, has antihyperlipidemic and antioxidant activities. Niga-ichigoside F1 can prevent high-fat diet (HFD)-induced hepatic steatosis [1].
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Cat. No.: HY-124751
CAS No.: 2225824-53-1
Purity:  99.06%
Research Areas:  

Neurological Disease

YTX-465 is a stearoyl-CoA desaturase (Ole1/SCD) inhibitor. YTX-465 inhibits Ole1 and SCD1 with IC50s of 0.039 μM and 30.4 μM, respectively. YTX-465 can be used in the research of Parkinson’s disease and other synucleinopathies [1].
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Cat. No.: HY-34603
CAS No.: 25016-20-0
Research Areas:  

Others

1-Methyl-1H-pyrazole-3-carboxylic acid is a pyrazole carboxylic acid compound. 1-Methyl-1H-pyrazole-3-carboxylic acid can be used to prepare lanthanide complexes for applications in OLEDs and bioimaging. 1-Methyl-1H-pyrazole-3-carboxylic acid is applicable to the synthesis of Compound 91 (an inhibitor of SCD1 and SCD5) [1] .
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Cat. No.: HY-150125
CAS No.: 1111078-63-7
Research Areas:  

Inflammation/Immunology

SCD1-IN-1 is a SCD1 inhibitor (IC50: 5.8 nM). SCD1-IN-1 can be used in the research of dermatologic condition [1].
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Cat. No.: HY-N6807R
CAS No.: 487-11-6
Elemicin is an orally active alkenylbenzene widely distributed in many herbs and spices. Elemicin inhibits Stearoyl-CoA Desaturase 1 (SCD1) by metabolic activation. Elemicin has anti-influenza activities, antimicrobial, antioxidant, and antiviral activities. Elemicin and its reactive metabolite of 1′-Hydroxyelemicin can induce hepatotoxicity [1] .
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Cat. No.: HY-50709R
CAS No.: 1032229-33-6
Research Areas:  

Cancer

A939572 (Standard) is the analytical standard of A939572. This product is intended for research and analytical applications. A939572 is a potent, and orally bioavailable stearoyl-CoA desaturase1 (SCD1) inhibitor with IC50 values of <4 nM and 37 nM for mSCD1 and hSCD1, respectively.
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Cat. No.: HY-170570
CAS No.: 3053859-57-4
PFM046 is the antagonist for liver X receptor (LXR), that inhibits the activation of LXRα and LXRβ with IC50 of 2.04 μM and 1.58 μM. PFM046 inhibits the expression of SCD1 and FASN, upregulates the expression of ABCA1, and exhibits antitumor efficacy in mouse models [1].
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Cat. No.: HY-E70265
CAS No.: 799812-87-6
18:0 Coenzyme A (triammonium) is a preferred substrate of stearoyl-CoA desaturases (SCDs) .
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Cat. No.: HY-P991667

Target:  

Inhibitory Antibodies

Research Areas:  

Cardiovascular Disease

NKTT 120 is a humanized monoclonal antibody against the iNKT cells. NKTT 120 is promising for research of sickle cell disease (SCD) .
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Cat. No.: HY-N7521
CAS No.: 37064-31-6
Synonyms: Procyanidine C2
Procyanidin C2 (Procyanidine C2) is a lipid metabolism regulator and antioxidant with free radical scavenging activity. Procyanidin C2 down-regulates ACC, SREBP-1c, FAS, SCD-1 and PPARγ. Procyanidin C2 increases the level of phosphorylated AMPKα and inhibits the level of phosphorylated mTOR. Procyanidin C2 reduces lipid accumulation, alleviates oxidative stress, enhances fatty acid oxidation and improves mitochondrial function. Procyanidin C2 can be used in the research of non-alcoholic fatty liver disease [1].
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Cat. No.: HY-111315
CAS No.: 840489-44-3
Research Areas:  

Metabolic Disease

XEN103 is a SCD1 inhibitor, with IC50s of 14 nM and 12 nM for mSCD1 and SCD1 in HepG2 cell. XEN103 can be used for research of obesity and type 2 diabetes. XEN103 also induces sebaceous gland atrophy in mice [1] .
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Cat. No.: HY-12756AR
CAS No.: 1345675-25-3
E6446 (dihydrochloride) (Standard) is the analytical standard of E6446 (dihydrochloride). This product is intended for research and analytical applications. E6446 dihydrochloride is a potent and orally acitve TLR7 and TLR9 antagonist, used in the research of deleterious inflammatory responses. E6446 dihydrochloride is also a potent SCD1 inhibitor (KD: 4.61 μM), significantly inhibiting adipogenic differentiation and hepatic lipogenesis through SCD1-ATF3 signaling. E6446 dihydrochloride also improves liver pathology in high-fat diet (HFD)-fed mice and may be useful in the study of non-alcoholic fatty liver disease (NAFLD) [1] .
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Cat. No.: HY-P81418
Synonyms: SCD1; FADS5; SCDOS; MSTP008

Host:  

Rabbit

Application:  

IHC-P

Reactivity:  

Human

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Cat. No.: HY-P81418A
Synonyms: SCD1; FADS5; SCDOS; MSTP008

Host:  

Rabbit

Application:  

IHC-P

Reactivity:  

Human

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Cat. No.: HY-RS12495

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

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Cat. No.: HY-P702428
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: SCD; Stearoyl-CoA Desaturase Opposite Strand; Prev. SCDOS; HSCD1; FADS5; Predicted Protein Of HQ0998; SCD1; Delta-9-Desaturase; Fatty Acid Desaturase; Delta-9 Desaturase; Acyl-CoA Desaturase; MSTP008; Stearoyl-CoA Desaturase (Delta-9-Desaturase); Stearoyl
Species:  
Human
Source:  
E. coli Cell-free
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Cat. No.: HY-189199
CAS No.: 3093981-26-8
SARS-CoV-2-IN-124 is an antiviral compound. SARS-CoV-2-IN-124 directly binds to NCOA1 and promotes its lysosome-dependent degradation. SARS-CoV-2-IN-124 downregulates the expression of lipogenic enzymes FASN and SCD1. SARS-CoV-2-IN-124 inhibits SARS-CoV-2 replication in multiple cell lines. SARS-CoV-2-IN-124 can be used for research related to SARS-CoV-2 infection [1].
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Cat. No.: HY-100249R
CAS No.: 1072803-08-7
XEN723 (Standard) is the analytical standard of XEN723 (HY-100249). This product is intended for research and analytical applications. XEN723 is a novel and potent thiazolylimidazolidinone inhibitor of Stearoyl-CoA Desaturase (SCD1) with IC50s of 45 and 524 nM in mouse and HepG2 cell, respectively.
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Cat. No.: HY-RS12494

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

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Cat. No.: HY-118117
CAS No.: 204386-76-5
Synonyms: S0373
Research Areas:  

Endocrinology

Rovatirelin is an orally active thyrotropin-releasing hormone (TRH) analog. Rovatirelin binds to the human TRH receptor with a Ki value of 702 nM. Rovatirelin can be used to study spinocerebellar degeneration (SCD) .
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