754 Results for "

regulator

" in MedChemExpress (MCE) Product Catalog:
Products (754)

754 Results for "regulator" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-P9966
CAS No.: 1353485-38-7
Synonyms: MGA271

Target:  

CD276/B7-H3

Research Areas:  

Cancer

Enoblituzumab (MGA271) is a humanized IgG1κ monoclonal antibody recognizing human B7-H3 protein, a member of the B7 family of immune regulators .
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1 Cited Publications
Cat. No.: HY-145603A
CAS No.: 2374124-48-6
Purity:  98.07%
Synonyms: (R)-VX-121
Target:  

CFTR

Research Areas:  

Inflammation/Immunology

(R)-Vanzacaftor ((R)-VX-121) is a Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) modulator with max activity of 30-60% and EC50 <1 μM in enteroid cells. (R)-Vanzacaftor can be used for the research of cystic fibrosis .
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1 Cited Publications
Cat. No.: HY-126015
CAS No.: 2748196-63-4
Purity:  ≥97.0%
Target:  

Acyltransferase

Research Areas:  

Metabolic Disease

P053 is a potent, non-competitive and selective ceramide synthase 1 (CerS1) inhibitor wirh an IC50 of 0.5 μM. P053 acts as an endogenous inhibitor of mitochondrial fatty acid oxidation in muscle. Whole-body adiposity regulator .
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1 Cited Publications
Cat. No.: HY-B0400B
CAS No.: 50-70-4
Synonyms: Sorbito, for cell culture; D-Glucitol, for cell culture
D-Sorbitol (D-Glucitol), for cell culture is a six-carbon sugar alcohol that can be used as a sugar substitute. D-Sorbitol, for cell culture serves as an osmotic regulator, cryoprotectant and carbon source in various plant and microbial cell culture media .
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1 Cited Publications
Cat. No.: HY-18219
CAS No.: 878419-78-4
Walrycin B, an analogue of toxoflavin, is a potent SARS-CoV-2 3CL pro inhibitor with an IC50 of 0.26 μM. Walrycin B is a WalR response regulator inhibitor. Walrycin B has potent activity of inhibiting bacteria growth .
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1 Cited Publications
Cat. No.: HY-148788
CAS No.: 2417955-18-9
Purity:  99.83%
Synonyms: GBT-601; GBT-021601
Target:  

Hemoglobin

Research Areas:  

Others

Osivelotor is an orally effective small molecule. Osivelotor is an allosteric regulator of deoxyhemoglobin S (HbS). Osivelotor increases the affinity of HbS to oxygen, inhibits HbS polymerization, and thus prevents erythrocyte sickling in the blood. Osivelotor can be used for research of sickle cell disease (SCD) .
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1 Cited Publications
Cat. No.: HY-B2062
CAS No.: 1861-32-1
Synonyms: Dimethyl tetrachloroterephthalate
Chlorthal-dimethyl (Dimethyl tetrachloroterephthalate) is a plant growth regulator. Chlorthal-dimethyl affects cell division and differentiation, interfering with the normal development of vascular tissue. Chlorthal-dimethyl causes localized swelling of tomato hypocotyls and disrupts normal mitosis in germinating millet seedlings .
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1 Cited Publications
Cat. No.: HY-W005355
CAS No.: 2013-26-5
Sodium 2-oxobutanoate is an organic compound commonly used as a food additive and industrial raw material. It can be used as an acidity regulator, leavening agent and preservative, and is often used in the fields of bread, baked goods and canning. In addition, the compound is used in the production of certain industrial products, such as in plastics, textiles and dyes.
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1 Cited Publications
Cat. No.: HY-126394
CAS No.: 2204245-48-5
Purity:  99.09%
Synonyms: VX-659
Target:  

CFTR

Research Areas:  

Endocrinology

Bamocaftor (VX-659) is a cystic fibrosis transmembrane conductance regulator (CFTR) corrector designed to restore F508del-CFTR protein function. Bamocaftor can be used combine with Tezacaftor (HY-15448) and Ivacaftor (HY-13017) in cystic fibrosis research .
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1 Cited Publications
Cat. No.: HY-129099
CAS No.: 31750-48-8
N-Desmethyltamoxifen is the major metabolite of tamoxifen in humans. N-Desmethyltamoxifen, a poor antiestrogen, is a ten-fold more potent protein kinase C (PKC) inhibitor than Tamoxifen. N-Desmethyltamoxifen is also a potent regulator of ceramide metabolism in human AML cells, limiting ceramide glycosylation, hydrolysis, and sphingosine phosphorylation .
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1 Cited Publications
Cat. No.: HY-129099A
CAS No.: 15917-65-4
Purity:  99.93%
N-Desmethyltamoxifen hydrochloride is the major metabolite of tamoxifen in humans. N-Desmethyltamoxifen, a poor antiestrogen, is a ten-fold more potent protein kinase C (PKC) inhibitor than Tamoxifen. N-Desmethyltamoxifen hydrochloride is also a potent regulator of ceramide metabolism in human AML cells, limiting ceramide glycosylation, hydrolysis, and sphingosine phosphorylation .
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1 Cited Publications
Cat. No.: HY-126437A
CAS No.: 26124-78-7
Poly-L-lysine hydrochloride is a nonspecific attachment factor for cells useful in promoting cell adhesion to solid substrates by enhancing electrostatic interaction between negatively charged ions of the cell membrane and the culture surface. Poly-L-lysine hydrochloride is a strong-attraction regulator that promotes liquid-liquid phase separation (LLPS) at low concentrations but suppresses LLPS at high concentrations. Antibacterial cationic peptide. .
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1 Cited Publications
Cat. No.: HY-148853
CAS No.: 2727872-68-4
Purity:  99.80%
Target:  

HuR

Research Areas:  

Others

SRI-42127 is a HuR translocation inhibitor. HuR is an RNA regulator that binds to AREs, and HuR translocations promote the production of inflammatory cytokines in glial cells. However, SRI-42127 can destroy mRNA stability and inhibit gene promoter activation. SRI-42127 also inhibits microglial cell activation and attenuates recruitment/chemotaxis of neutrophils and monocytes .
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1 Cited Publications
Cat. No.: HY-P80030
Synonyms: BCL2L, BCLX, BCL2L1, Bcl-2-like protein 1, Bcl2-L-1, Apoptosis regulator Bcl-X

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP, FC, IF-Tissue

Reactivity:  

Human

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1 Cited Publications
Cat. No.: HY-14803
CAS No.: 609799-22-6
Purity:  99.68%
Synonyms: BMS-214778; VEC-162
Target:  

Melatonin Receptor

Research Areas:  

Neurological Disease Endocrinology

Tasimelteon (BMS-214778) is an orally active and selective dual melatonin receptor agonist (DMRA). Tasimelteon has 2.1-4.4 times greater affinity for the MT2 receptor than for the MT1 receptor. Tasimelteon is a circadian regulator and has the potential for Non-24-Hour Sleep-Wake Disorder (Non-24) .
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1 Cited Publications
Cat. No.: HY-N13022
CAS No.: 1415-93-6
Humic acid is an important component of organic matter in soil and water, and serves as a plant regulator. Humic acid has multiple reactive activities such as surface adsorption, ion exchange, and complexation. Humic acid can enhance pyrene degradation by Mycobacterium NJS-1. Humic acid can inhibit the activity of superoxide dismutase and scavenge hydroxyl radicals. Humic acid is also toxic to CEM cells .
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1 Cited Publications
Cat. No.: HY-122611A
CAS No.: 1353749-74-2
Purity:  99.97%
Research Areas:  

Cancer

CSRM617 hydrochloride is a selective small-molecule inhibitor of the transcription factor ONECUT2 (OC2, a master regulator of androgen receptor) with a Kd of 7.43 uM in SPR assays, binding to OC2-HOX domain directly. CSRM617 hydrochloride induces apoptosis by appearance of cleaved Caspase-3 and PARP. CSRM617 hydrochloride is well tolerated in the prostate cancer mouse model
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1 Cited Publications
Cat. No.: HY-126833A
CAS No.: 187100-75-0
Purity:  95.50%
Myristoyl coenzyme A lithium is lithium-labeled myristoylated coenzyme A (CoA). Myristoylation is an essential process in viruses and is generally controlled by N-myristoyltransferase (NMT). And NMT is more active in colon epithelial tumors than in normal cells. Reduced Ccoenzyme A (CoA) is known to be a key regulator of NMT activity, whereas oxidized CoA does not allow NMT to promote myristoylation. Myristoyl coenzyme A blocks the demyristoylation process and has potential anticancer and antiviral mechanisms .
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1 Cited Publications
Cat. No.: HY-P2878
CAS No.: 9025-82-5
Synonyms: PDE
Research Areas:  

Neurological Disease Cancer

Phosphodiesterase I (PDE) is an enzyme that can catalyze the hydrolysis of the 3' ring phosphate bond of cyclic nucleotides, and is often used in biochemical research. Phosphodiesterase I acts as an important regulator of signal transduction mediated by the second messenger molecules cAMP and cGMP. According to their specificity to cyclic nucleotides, they can also be divided into different types, such as PDE1-PDE11, which also have certain potential in various diseases .
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1 Cited Publications
Cat. No.: HY-P80563
Synonyms: BAK1; BAK; BCL2L7; CDN1; Bcl-2 homologous antagonist/killer; Apoptosis regulator BAK; Bcl-2-like protein 7; Bcl2-L-7

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP, FC

Reactivity:  

Human, Mouse

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