60 Results for "

Win 63843-d4

" in MedChemExpress (MCE) Product Catalog:
Products (60)

60 Results for "Win 63843-d4" in MCE Product Catalog:

33
33 Publications Verification
Cat. No.: HY-14252
CAS No.: 78415-72-2
Purity:  99.80%
Synonyms: Win 47203
Research Areas:  

Cardiovascular Disease

Milrinone is a PDE3 inhibitor, and also an inotrope and vasodilator.
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33
33 Publications Verification
Cat. No.: HY-14252A
CAS No.: 100286-97-3
Synonyms: Win 47203 lactate
Research Areas:  

Cardiovascular Disease

Milrinone lactate is a potent inotropic dilating agent. Milrinone lactate shows simultaneous positive inotropic and vasodilating activities. Milrinone lactate promotes reduction of SVR and PVR in patients with DCM and NYHA class III and IV of heart failure. Milrinone lactate has the potential for the research of cardiovascular function after cardiac surgery and in septic shock .
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15
15 Cited Publications
Cat. No.: HY-13767
CAS No.: 27314-97-2
Purity:  99.02%
Synonyms: SR259075; SR4233; Win59075; SML 0552; SR 259075; Tirazone
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Tirapazamine (SR259075) is an anticancer agent that shows selective cytotoxicity for hypoxic cells in solid tumors, thereby inducing single-and double-strand breaks in DNA, base damage, and cell death. Tirapazamine is an anticancer and bioreductive agent.Tirapazamine (SR259075) can enhance the cytotoxic effects of ionizing radiation in hypoxic cells .
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5
5 Cited Publications
Cat. No.: HY-111753
CAS No.: 2407457-36-5
Purity:  98.13%
Target:  

WDR5 Apoptosis

Research Areas:  

Cancer

WDR5-IN-4 (Compound C6) is a WIN site inhibitor of chromatin-associated WD repeat domain 5 protein (WDR5), Kd The value is 0.1 nM. WDR5-IN-4 is able to displace WDR5 from chromatin and reduce the expression of related genes, causing translation inhibition and nucleolar stress. Has anti-cancer effects .
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5
5 Cited Publications
Cat. No.: HY-111753A
CAS No.: 2749300-35-2
Purity:  99.87%
Target:  

WDR5 Apoptosis

Research Areas:  

Cancer

WDR5-IN-4 TFA (Compound C6) is an inhibitor of the WIN site of chromatin-associated WD repeat-containing protein 5 (WDR5), with a Kd of 0.1 nM. WDR5-IN-4 TFA displaces WDR5 from chromatin and decreases the expression of associated genes, causing translational inhibition, nucleolar stress. Anti-cancer activity .
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3
3 Cited Publications
Cat. No.: HY-W011094
CAS No.: 1477-57-2
Research Areas:  

Endocrinology

Win 18446 is an orally active testes-specific enzyme ALDH1a2 inhibitor, with an IC50 of 0.3 μM. Win 18446 reversibly inhibits spermatogenesis in many species and inhibits Retinoic acid (HY-14649) biosynthesis from Retinol (HY-B1342) within the testes .
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2
2 Cited Publications
Cat. No.: HY-14281
CAS No.: 13647-35-3
Purity:  99.81%
Synonyms: Win 24540
Target:  

3β-HSD

Research Areas:  

Endocrinology Cancer

Trilostane (Win 24540) is a competitive and orally active 3-β-hydroxysteroiddehydrogenase (3β-HSD) inhibitor. Trilostane is a synthetic nonhormonal steroid. Trilostane can be used for the research of breast cancer and prostate cancer .
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1
1 Cited Publications
Cat. No.: HY-19952
CAS No.: 153168-05-9
Synonyms: VP 63843; Win 63843
Target:  

Enterovirus

Research Areas:  

Infection

Pleconaril is a picornavirus capsid binding inhibitor that prevents attachment and/or virus uncoating. Pleconaril has potential for use in rhinoviruses and enteroviruses research .
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Cat. No.: HY-B0664
CAS No.: 52214-84-3
Synonyms: Win35833
Target:  

PPAR

Research Areas:  

Metabolic Disease

Ciprofibrate (Win35833) is a potent peroxisome proliferator and increases the phosphorylation level of the PPARalpha . Ciprofibrate acts as an orally active hypolipidaemic agent and can be used for the research of primary hyperlipidaemias .
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Cat. No.: HY-100919
CAS No.: 115-79-7
Purity:  96.18%
Synonyms: Win 8077 chloride
Target:  

Cholinesterase (ChE)

Research Areas:  

Others

Ambenonium (WIN 8077) chloride is an orally active and reversible inhibitor of Acetyicholinesterase (AChE) with high affinity. Ambenonium chloride inhibits human AChE with an IC50 value of 0.7 nM (hAChE) .
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Cat. No.: HY-119826
CAS No.: 62265-68-3
Purity:  99.69%
Synonyms: Win-40014
Target:  

Parasite

Research Areas:  

Infection

Quinfamide (WIN-40014) is an orally active class of dichloroacetyl derivative with significant anti-intestinal protozoan, particularly mmoeba histolytica activity. Quinfamide exhibits antiamoebic activity under solvent-free conditions with an IC50 of 28.15 μg/mL in a suspension condition. Quinfamide particles are actively engulfed by the amoebas, then cells are affected, and finally, amoebas are killed and lysed, and this process directly relies on the physical intake of the drug particles. Quinfamide can be used in the research of tropical parasitic infections such as amoebiasis and helminthiasis .
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Cat. No.: HY-154949
CAS No.: 326901-92-2
Purity:  99.83%
Target:  

WDR5

Research Areas:  

Cancer

WDR5-IN-6 is a WDR5 inhibitor, targeting to WBM site. WDR5-IN-6 inhibits cell proliferation of neuroblastoma cell lines with potent anti-tumor activity. WDR5-IN-6 shows high synergy with OICR-9429 (HY-16993), a WDR5 inhibitor targeting to WIN site. WDR5-IN-6 can be used for reasearch in neuroblastoma .
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Cat. No.: HY-150654
CAS No.: 2417012-26-9
Purity:  99.56%
Target:  

WDR5

Research Areas:  

Cancer

WDR5-IN-5 is an orally active and selective inhibitor of WIN site of WD repeat domain 5 (WDR5). WDR5-IN-5 exhibits anti-proliferative activity towards cancer cells and good pharmacokinetics profile in mice. WDR5-IN-5 shows high affinity to WDR5 and the binding affinity Ki value <0.02 nM .
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Cat. No.: HY-119677
CAS No.: 153-87-7
Purity:  99.84%
Synonyms: Win-18501-2
Research Areas:  

Neurological Disease

Oxypertine (WIN-18501-2) is a neuroprotective agent. Oxypertine shows high affinity for the 5-HT2 and dopamine D2 receptors with Kis of 8.6 nM and 30 nM, respectively. Oxypertine can be used in the research of neurological conditions, such as anxiety and schizophrenia .
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Cat. No.: HY-106296
CAS No.: 107355-45-3
Purity:  98.14%
Target:  

Enterovirus

Research Areas:  

Infection

WIN 54954 is an orally active and broad-spectrum antipicornavirus agent. WIN 54954 is effectiveness against human rhinovirus, echovirus 9 and enterovirus infections .
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Cat. No.: HY-U00221
CAS No.: 86393-37-5
Synonyms: Win49375
Target:  

Bacterial

Research Areas:  

Infection

Amifloxacin (Win49375) is a synthetic antibacterial agent of the quinolone class.
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Cat. No.: HY-105128
CAS No.: 80471-63-2
Synonyms: Win 32729
Target:  

3β-HSD

Research Areas:  

Endocrinology

Epostane (WIN 32729) is an orally active inhibitor for 3β-hydroxysteroid dehydrogenase, with IC50 of 1.45 nM. Epostane blocks ovulation and pregnancy in rats .
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Cat. No.: HY-16103
CAS No.: 30392-41-7
Synonyms: Win 32784; Bitolterol methanesulfonate; S-1540 mesylate
Target:  

Drug Derivative

Research Areas:  

Infection

Bitolterol mesylate (WIN 37284) is a diester-type agonist amine bronchodilator without significant cardiac side effects .
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Cat. No.: HY-116211
CAS No.: 15180-02-6
Synonyms: Win-25978
Research Areas:  

Neurological Disease

Amfonelic acid (WIN-25978) is a highly selective dopamine reuptake inhibitor. Amfonelic acid interferes with the in vitro neuronal uptake of norepinephrine in the iris of rats, but does not alter the concentrations of norepinephrine or dopamine in the whole mouse brain. Amfonelic acid can be used as a pharmacological tool to study the brain reward system, dopamine pathway and dopamine transporter .
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Cat. No.: HY-111233
CAS No.: 87495-31-6
Synonyms: Win-51711
Target:  

Enterovirus

Research Areas:  

Infection

Disoxaril (WIN-51711) is an antivirus agent with activity against poliovirus types 1 and 2. Disoxaril inserts into the hydrophobic interior of virus capsid protein VP1 to stabilize virion conformation, inhibits poliovirus uncoating, and prevents viral RNA release and synthesis. Disoxaril can be used for the research of poliovirus infection .
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