293 Results for "

mixed

" in MedChemExpress (MCE) Product Catalog:
Products (293)

293 Results for "mixed" in MCE Product Catalog:

25
25 Cited Publications
Art. -Nr.: HY-112292
CAS. Nr.: 579515-63-2
Reinheit:  99.33%
Forschungsgebiete:  

Others

GW806742X, an ATP mimetic and a potent MLKL (Mixed Lineage Kinase Domain-Like protein) inhibitor, binds the MLKL pseudokinase domain with a Kd of 9.3 μM. GW806742X has activity against VEGFR2 (IC50=2 nM). GW806742X retards MLKL membrane translocation and inhibits necroptosis .
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25
25 Cited Publications
Art. -Nr.: HY-112292A
CAS. Nr.: 2930350-95-9
Reinheit:  98.77%
Forschungsgebiete:  

Cancer

GW806742X hydrochloride, an ATP mimetic and a potent MLKL (Mixed Lineage Kinase Domain-Like protein) inhibitor, binds the MLKL pseudokinase domain with a Kd of 9.3 μM. GW806742X hydrochloride has activity against VEGFR2 (IC50=2 nM). GW806742X hydrochloride retards MLKL membrane translocation and inhibits necroptosis .
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17
17 Cited Publications
Art. -Nr.: HY-103454B
CAS. Nr.: 2863676-89-3
Reinheit:  99.28%
Forschungsgebiete:  

Endocrinology Cancer

MPP hydrochloride is a potent and selective ER (estrogen receptor) modulator. MPP hydrochloride induces significant apoptosis in the endometrial cancer and oLE cell lines. MPP hydrochloride reverses the the positive effects of beta-estradiol. MPP hydrochloride has mixed agonist/antagonist action on murine uterine ERalpha in vivo .
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17
17 Cited Publications
Art. -Nr.: HY-103454
CAS. Nr.: 911295-24-4
Reinheit:  99.54%
Forschungsgebiete:  

Endocrinology Cancer

MPP dihydrochloride is a potent and selective ER (estrogen receptor) modulator. MPP dihydrochloride induces significant apoptosis in the endometrial cancer and oLE cell lines. MPP dihydrochloride reverses the positive effects of beta-estradiol. MPP dihydrochloride has mixed agonist/antagonist action on murine uterine ERalpha in vivo .
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11
11 Cited Publications
Art. -Nr.: HY-B1777
CAS. Nr.: 71-44-3
Synonyms: NSC 268508; Neuridine
Spermine is a natural antioxidant and anti-inflammatory agent. Spermine is known to inhibit some bacterial cultures, especially strains of Staphylococcus aureus. Spermine can reversibly inhibits DNA synthetic response, mixed lymphocyte response and the induction of cytolytic lymphocyte response in primary cultures of murine spleen cells. Spermine is a polyamine nitric oxide donor that can provide nitric oxide to platelets and inhibit platelet activation to a certain extent concentration-dependently. Spermine occurs in mammalian tissues, plants, bacteria, ribosomes and bacteriophage. Spermine inhibits primary human embryo lung fibroblasts in vitro .
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11
11 Cited Publications
Art. -Nr.: HY-B1777A
CAS. Nr.: 306-67-2
Spermine tetrahydrochloride is a polyamine nitric oxide donor that can provide nitric oxide to platelets and inhibit platelet activation to a certain extent concentration-dependently. Spermine tetrahydrochloride occurs in mammalian tissues, plants, bacteria, ribosomes and bacteriophage. Spermine tetrahydrochloride inhibits primary human embryo lung fibroblasts in vitro. Spermine is a natural antioxidant and anti-inflammatory agent. Spermine is known to inhibit some bacterial cultures, especially strains of Staphylococcus aureus. Spermine induces neurotoxicity in the striarum dose-dependently. Spermine can reversibly inhibits DNA synthetic response, mixed lymphocyte response and the induction of cytolytic lymphocyte response in primary cultures of murine spleen cells .
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9
9 Cited Publications
Art. -Nr.: HY-115670
CAS. Nr.: 866924-39-2
Reinheit:  99.30%
Target:  

MMP

Forschungsgebiete:  

Inflammation/Immunology Cancer

GW280264X is the mixed ADAM10/TACE (ADAM17) metalloproteinases inhibitor. GW280264X potently blocks TACE (ADAM17) and ADAM10 with IC50s of 8.0 nM and 11.5 nM, respectively . ADAM10 and 17 modulate the immunogenicity of glioblastoma-initiating cells .
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8
8 Cited Publications
Art. -Nr.: HY-100691
CAS. Nr.: 132819-92-2
Reinheit:  99.48%
Forschungsgebiete:  

Inflammation/Immunology

NOD-IN-1 is a potent mixed inhibitor of nucleotide-binding oligomerization domain (NOD)-like receptors, NOD1 and NOD2, with IC50 of 5.74 μM and 6.45 μM, respectively.
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8
8 Cited Publications
Art. -Nr.: HY-14532
CAS. Nr.: 444805-28-1
Reinheit:  99.46%
Synonyms: CMX001; HDP-CDV
Target:  

CMV HSV Orthopoxvirus

Forschungsgebiete:  

Infection

Brincidofovir (CMX001), the lipid-conjugated prodrug of Cidofovir (HY-17438), is an orally available, long-acting antiviral. Brincidofovir shows activity against a broad spectrum of DNA viruses including cytomegalovirus (CMV), adenovirus (ADV), varicella zoster virus, herpes simplex virus, polyomaviruses, papillomaviruses, poxviruses, and mixed double-stranded DNA virus infections. Brincidofovir, an oral antiviral in late stage development, has proven effective against orthopoxviruses in vitro and in vivo .
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7
7 Cited Publications
Art. -Nr.: HY-12599
CAS. Nr.: 1229582-33-5
Reinheit:  99.34%
Forschungsgebiete:  

Neurological Disease Cancer

URMC-099 is an orally bioavailable and potent mixed lineage kinase type 3 (MLK3) (IC50=14 nM) inhibitor with with excellent blood-brain barrier penetration properties.
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6
6 Cited Publications
Art. -Nr.: HY-15940
CAS. Nr.: 72088-94-9
Synonyms: 5(6)-FAM; 5-(and-6)-Carboxyfluorescein mixed isomers
5(6)-Carboxyfluorescein (5(6)-FAM) is an amine-reactive pH-sensitive green fluorescent probe. 5(6)-Carboxyfluorescein (5(6)-FAM) can be used to label proteins, peptides and nucleotides. 5(6)-Carboxyfluorescein can be used for the detection of tumour areas in vivo .
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6
6 Cited Publications
Art. -Nr.: HY-N0319
CAS. Nr.: 115841-09-3
Salvianolic acid C is a noncompetitive Cytochrome P4502C8 (CYP2C8) inhibitor and a moderate mixed inhibitor of Cytochrome P45022J2 (CYP2J2), with Kis of 4.82 μM and 5.75 μM for CYP2C8 and CYP2J2, respectively.
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6
6 Cited Publications
Art. -Nr.: HY-100034
CAS. Nr.: 383907-43-5
Reinheit:  99.29%
Synonyms: DA-3003-1
Forschungsgebiete:  

Cancer

NSC 663284 (DA-3003-1) is a potent, cell-permeable, and irreversible Cdc25 dual specificity phosphatase inhibitor, has an IC50 for Cdc25B2 of 0.21 μM. NSC 663284 exhibits mixed competitive kinetics against Cdc25A, Cdc25B(2), and Cdc25C with Ki values of 29, 95, and 89 nM, respectively . NSC 663284 inhibits NSD2 (IC50 of 170 nM) through a direct interaction with the catalytic SET domain (Kd of 370 nM) .
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5
5 Cited Publications
Art. -Nr.: HY-B0569
CAS. Nr.: 55-97-0
Target:  

nAChR Apoptosis

Hexamethonium Bromide is a non-selective ganglionic nicotinic-receptor antagonist (nAChR) antagonist, with mixed competitive and noncompetitive activity. Hexamethonium Bromide has anti-hypertensive activity. Hexamethonium Bromide attenuates sympathetic activity and blood pressure in spontaneously hypertensive animal models .
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4
4 Cited Publications
Art. -Nr.: HY-15937
CAS. Nr.: 117548-22-8
Synonyms: 5(6)-Carboxyfluorescein N-hydroxysuccinimide ester; 5(6)-Carboxyfluorescein succinimidyl ester mixed isomers
5(6)-FAM SE is a green fluorescent dye widely used for protein labeling.
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3
3 Cited Publications
Art. -Nr.: HY-101524
CAS. Nr.: 2093393-05-4
Reinheit:  99.04%
Target:  

Mixed Lineage Kinase

Forschungsgebiete:  

Cancer

TC13172 is a mixed lineage kinase domain-like protein (MLKL) inhibitor with an EC50 value of 2 nM for HT-29 cells .
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3
3 Cited Publications
Art. -Nr.: HY-P702574
Reinheit:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: MLKL; FLJ34389; mixed Lineage Kinase Domain Like Pseudokinase; HMLKL; mixed Lineage Kinase Domain-Like Protein; mixed Lineage Kinase Domain-Like
Species:  
Human
Source:  
E. coli
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3
3 Cited Publications
Art. -Nr.: HY-KE7055

RNase R is a magnesium ion-dependent 3'-5' exoribonuclease that can increase the abundance of circular RNA by degrading linear RNA in mixed RNA, thereby enriching circular RNA.

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3
3 Cited Publications
Art. -Nr.: HY-19347
CAS. Nr.: 890190-22-4
Synonyms: WD-Repeat Protein 5-0103
Target:  

WDR5

Forschungsgebiete:  

Neurological Disease Cancer

WDR5-0103 (WD-Repeat Protein 5-0103) is a potent and selective WD repeat-containing protein 5 (WDR5) antagonist with a Kd of 450 nM. WDR5-0103 competitively binds to the peptide-binding pocket of WDR5, blocking the interaction between WDR5 and mixed-lineage leukemia (MLL) protein and inhibiting the methyltransferase activity of MLL. WDR5-0103 is mainly used in the research of cancer and neurodegenerative diseases .
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3
3 Cited Publications
Art. -Nr.: HY-14183
CAS. Nr.: 748810-28-8
Reinheit:  99.33%
Synonyms: RSD1235 hydrochloride
Target:  

Potassium Channel

Forschungsgebiete:  

Cardiovascular Disease

Vernakalant hydrochloride is a mixed voltage- and frequency-dependent Na + and atria-preferred K + channel blocker. IC50 for block by Vernakalant of wild-type and mutant Kv1.5 channels Fractional block is 13.35±0.93 μM, 0.61±0.03 μM, and 1.63±0.09 μM for Kv1.5 channel wt, Kv1.5 channel I508F, Kv1.5 channel T479A, respectively.
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