157 Results for "

fraction

" in MedChemExpress (MCE) Product Catalog:
Products (157)

157 Results for "fraction" in MCE Product Catalog:

Cat. No.: HY-187661
CAS No.: 42408-79-7
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Pirandamine free base is a selective serotonin (5-HT) (HY-B1473A) uptake inhibitor with an IC50 of 250 nM. It exerts antidepressant-like effects by enhancing central serotonergic function, does not inhibit norepinephrine (HY-13715) uptake, and exhibits no central anticholinergic or monoamine oxidase inhibitory activity. Pirandamine free base is used in the study of depression .
loading...
    loading...
Cat. No.: HY-W040264
CAS No.: 911660-54-3
Synonyms: Lanostenol
24,25-Dihydrolanosterol is a naturally occurring tetracyclic Δ 8-triterpene alcohol that can be found in the seeds of Capsicum annuum. 24,25-Dihydrolanosterol is the initial carbocyclic sterol precursor in animals, fungi, and trypanosomatids, and participates in sterol synthesis .
loading...
    loading...
Cat. No.: HY-10486
CAS No.: 361444-66-8
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

JDTic is a blood-brain barrier-permeable κ-opioid receptor antagonist (Ki=0.02 nM) with favorable in vitro ADME properties. JDTic blocks agonist-mediated Gi and β-arrestin signaling pathways as well as analgesic effects by stabilizing the inactive conformation of hKOR and activating JNK. JDTic may also induce transient asymptomatic ventricular tachycardia. JDTic is widely applicable to studies related to depression, anxiety, stress-induced addictive behaviors, and nicotine withdrawal .
loading...
    loading...
Cat. No.: HY-182948
CAS No.: 2089135-65-7
Research Areas:  

Others

Dichloro-all-trans-retinone is a selective retinaldehyde dehydrogenase (RALDH) inhibitor, with an IC50 of 434.7 nM and a Ki of 194.4 nM against chicken RALDH1; an IC50 of 55 nM and a Ki of 5.1 nM against chicken RALDH2; an IC50 of 191.32 nM and a Ki of 64.35 nM against human RALDH2; and an IC50 of 161.27 nM and a Ki of 6.74 nM against chicken RALDH3. Dichloro-all-trans-retinone inhibits the synthesis of all-trans retinoic acid (ATRA). Dichloro-all-trans-retinone is applicable to research related to form-deprivation-induced myopia .
loading...
    loading...
Cat. No.: HY-B1803
CAS No.: 41094-88-6
Synonyms: ICI 136753
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

Tracazolate (ICI 136753) is an orally active non-benzodiazepine anxiolytic. Tracazolate significantly enhances the binding of the radioligand 3H-flunitrazepam ( 3H-FLU) to brain tissue benzodiazepine receptors. Tracazolate enhances the binding of γ-aminobutyric acid (GABA) to its receptors. Tracazolate exhibits anticonvulsant activity. Tracazolate can be used in anxiety-related research .
loading...
    loading...
Cat. No.: HY-116755
CAS No.: 55837-29-1
Synonyms: CR 605
Research Areas:  

Neurological Disease

Tiropramide (CR 605) is a tyrosine derivative with antispastic properties. Tiropramide hydrochloride inhibits phosphodiesterase activity involved in cAMP catabolism in rabbit colon homogenates. Tiropramide relaxes smooth muscle in rabbit isolated colon. Tiropramide can be used for the research of irritable colon and biliary dyskinesia .
loading...
    loading...
Cat. No.: HY-187231
CAS No.: 5080-22-8
Target:  

Drug Intermediate

Research Areas:  

Others

N-Isopropylhydroxylamine is an alkylhydroxylamine and also a synthetic precursor of N-hydroxypropranolol. N-Isopropylhydroxylamine can be used in studies on the synthesis of metabolic derivatives of β-adrenergic receptor antagonists .
loading...
    loading...
Cat. No.: HY-43934
CAS No.: 53567-47-8
Synonyms: CR 605 hydrochloride
Research Areas:  

Neurological Disease

Tiropramide (CR 605) hydrochloride is a tyrosine derivative with antispastic properties. Tiropramide hydrochloride inhibits phosphodiesterase activity involved in cAMP catabolism in rabbit colon homogenates. Tiropramide hydrochloride relaxes smooth muscle in rabbit isolated colon. Tiropramide hydrochloride can be used for the research of irritable colon and biliary dyskinesia .
loading...
    loading...
Cat. No.: HY-N21981
CAS No.: 87095-76-9
1,7-Diphenyl-6 (E)-hepten-3-ol is a diarylheptane compound that can be isolated from Curcuma comosa. 1,7-Diphenyl-6 (E)-hepten-3-ol effectively inhibits the motility of Caenorhabditis elegans, thereby causing paralysis or death of the nematodes as a nematicide. 1,7-Diphenyl-6 (E)-hepten-3-ol can be used in studies related to nematode infections .
loading...
    loading...
Cat. No.: HY-125954
CAS No.: 2616-64-0
Synonyms: UDP-α-D-glucuronic acid
Uridine diphosphate glucuronic acid (UDP-α-D-glucuronic acid) is a glucuronic acid donor. Uridine diphosphate glucuronic acid transfers its glucuronic acid moiety to acceptor molecules, thereby forming "ether" glucuronides, while being converted into uridine 5'-pyrophosphate. Uridine diphosphate glucuronic acid serves as a substrate for Arabidopsis UDP-GlcA 4-epimerase 1, and undergoes reversible 4-epimerization to generate UDP-α-D-galacturonic acid .
loading...
    loading...
Cat. No.: HY-120274
CAS No.: 1850385-64-6
Purity:  99.96%
Synonyms: AZD9977
Balcinrenone (AZD9977) is an orally active mineralocorticoid receptor modulator. Balcinrenone regulates mineralocorticoid receptor activity, inhibits aldosterone-induced target gene expression, and suppresses the activities of renal Toll-like receptor 4, MyD88 and NF-κB. Balcinrenone alleviates renal extracellular matrix remodeling, inflammatory cell infiltration, and the expression of renal injury markers. Balcinrenone restores myocardial perfusion reserve, regulates potassium homeostasis, and induces fecal potassium excretion. Balcinrenone is applicable to research on metabolism-related chronic kidney disease and heart failure .
loading...
    loading...
Cat. No.: HY-120274A
CAS No.: 1850385-65-7
Synonyms: (R)-AZD9977
(R)-Balcinrenone ((R)-AZD9977) is an isomer of Balcinrenone (HY-120274). Balcinrenone is an orally active mineralocorticoid receptor modulator. Balcinrenone regulates mineralocorticoid receptor activity, inhibits aldosterone-induced target gene expression, and suppresses the activities of renal Toll-like receptor 4, MyD88 and NF-κB. Balcinrenone alleviates renal extracellular matrix remodeling, inflammatory cell infiltration, and the expression of renal injury markers. Balcinrenone restores myocardial perfusion reserve, regulates potassium homeostasis, and induces fecal potassium excretion. Balcinrenone is applicable to research on metabolism-related chronic kidney disease and heart failure .
loading...
    loading...
Cat. No.: HY-45609
CAS No.: 150465-29-5
L-Cysteine S-sulfate sodium hydrate is an S-sulfated derivative of L-cysteine (HY-Y0337). L-Cysteine S-sulfate sodium hydrate is the substrate for cystine lyase, it can be used in mass spectrometry and chromatography analyses .
loading...
    loading...
Cat. No.: HY-NP0196I
Research Areas:  

Inflammation/Immunology

Rabbit IgG Fab fragment-AF488 is an AF488-labeled rabbit IgG Fab fragment .
loading...
    loading...
Cat. No.: HY-W127317
CAS No.: 102850-29-3
Inositol 1,3,4,5-tetraphosphate is an inositol tetraphosphate. Inositol 1,3,4,5-tetraphosphate is metabolically produced from Ins (1,4,5) P3 via 3-kinase, participates in intracellular signal transduction systems, and elevates intracellular calcium concentrations when present .
loading...
    loading...
Cat. No.: HY-W788040
CAS No.: 1246355-68-9
Target:  

Endogenous Metabolite

Research Areas:  

Others

Inositol 1,3,4,5-tetraphosphate tetraammonium is an inositol tetraphosphate. Inositol 1,3,4,5-tetraphosphate tetraammonium is metabolically produced from Ins (1,4,5) P3 via 3-kinase, participates in intracellular signal transduction systems, and elevates intracellular calcium concentrations when present .
loading...
    loading...
Cat. No.: HY-182566
CAS No.: 288246-59-3
Target:  

HIV

Research Areas:  

Infection

ITI-367 is a HIV-1 inhibitor that targets the nuclear localization signal 1 (NLS-1) of HIV-1 matrix protein and the interaction between HIV-1 pre-integration complex (PIC) and importin-β. ITI-367 inhibits HIV-1 replication at the pre-integration stage, reduces the formation of 2-LTR circles, and sequesters viral DNA in the cytoplasm. ITI-367 can be used for the research of HIV infection .
loading...
    loading...