199 Results for "

rats model

" in MedChemExpress (MCE) Product Catalog:
Products (199)

199 Results for "rats model" in MCE Product Catalog:

Cat. No.: HY-156618
CAS No.: 2230974-62-4
Purity:  99.63%
Synonyms: ABSK011
Target:  

FGFR

Research Areas:  

Cancer

Irpagratinib (ABSK011) is an orally active FGFR4 inhibitor (IC50<10 nM). Irpagratinib inhibits FGFR4 autophosphorylation and blocks signaling from FGFR4 to downstream pathway activation. Irpagratinib has shown high exposure in PK studies in mice, rats, and dogs, and also demonstrated antitumor activity in a subcutaneous xenograft tumor model .
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Cat. No.: HY-B2141
CAS No.: 621-72-7
Bendazol is an orally effective antihypertensive agent. Bendazol acts directly on vascular smooth muscle to dilate blood vessels and reduce peripheral resistance, thereby improving blood circulation. Bendazol significantly inhibits the development of myopia in rabbit models. Bendazol can regulate kidney function by increasing the activity of NO synthase in the rat model of nephrogenic hypertension. In addition, Bendazol has an effect on sexual behavior and spermatogenesis in male rats .
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Cat. No.: HY-107482
CAS No.: 34562-97-5
Purity:  98.25%
Synonyms: Nicotinoyl-GABA; Nicotinoyl-γ-aminobutyric acid
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

Picamilon is an orally active derivative of γ-aminobutyric acid that has nootropic effect. Picamilon improves the epilepsy model in rats and promotes correction of functional disorders of the pancreas during Alloxan (HY-W017227)-induced diabetes mellitus in rats .
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Cat. No.: HY-P3662
CAS No.: 82188-67-8
Target:  

Tyrosinase

Research Areas:  

Cancer

Ac-[Nle4,D-Phe7]-α-MSH (4-10)-NH2 is a melanotropin, a melanocyte-stimulating hormone. Ac-[Nle4,D-Phe7]-α-MSH (4-10)-NH2 stimulates tyrosinase and exhibits thermoregulatory effect in rats model .
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Cat. No.: HY-101481
CAS No.: 91503-79-6
Purity:  99.85%
Flurbiprofen axetil is a non-selective COX inhibitor and a nonsteroidal anti-inflammatory agent with anti-inflammatory and analgesic effects. Flurbiprofen axetil inhibits basal-like breast cancer metastasis by inhibiting the MEK/ERK signaling pathway. Flurbiprofen axetil can promote neuroprotection after focal cerebral ischemia in rats by partially activating PPAR-γ. Flurbiprofen axetil alleviates cerebral ischemia/reperfusion injury by reducing inflammation in a transient global cerebral ischemia/reperfusion rat model. Flurbiprofen axetil can alleviate inflammatory responses and cognitive function in a mild cognitive impairment (MCI) SD rat model through the AMPKα/NF-κB signaling pathway .
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Cat. No.: HY-W116576
CAS No.: 934-00-9
Target:  

Drug Intermediate

Research Areas:  

Cancer

3-Methoxycatechol is intermediate for the antivascular agents combretastatin A-1 (HY-121993) and combretastatin B-1. 3-Methoxycatechol promotes esophageal carcinogenesis in rats models .
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Cat. No.: HY-105495
CAS No.: 137214-72-3
Target:  

Glycosyltransferase

Research Areas:  

Cardiovascular Disease

Iliparcil has a potent antithrombotic activity in the Wessler model in rats. Iliparcil has oral activity .
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Cat. No.: HY-P1555
CAS No.: 22006-64-0
Synonyms: Adrenocorticotropic Hormone (1-13)
Target:  

Inhibitory Antibodies

Research Areas:  

Inflammation/Immunology

ACTH (1-13) is a 13-aa peptide, with cytoprotective effects in the model of ethanol induced gastric lesions in rats.
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Cat. No.: HY-W098792
CAS No.: 139481-69-9
Target:  

Angiotensin Receptor

Research Areas:  

Cardiovascular Disease

Candesartan methyl ester (compound 14) is an antagonist for angiotensin II (AII) receptor with an IC50 of 66 nM. Candesartan methyl ester exhibits blood pressure lowering activity in rats models .
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Cat. No.: HY-149316
CAS No.: 1824708-03-3
Purity:  99.47%
Target:  

E1/E2/E3 Enzyme

Research Areas:  

Cardiovascular Disease

Smurf1-IN-1 is an orally active and selective inhibitor of specific E3 ubiquitin protein ligase 1 (SMURF1) with an IC50 of 92 nM. Smurf1-IN-1 has significant efficacy in rats model of pulmonary hypertension .
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Cat. No.: HY-164605
CAS No.: 300552-09-4
Research Areas:  

Metabolic Disease

(6S)-CP-470711 (Compound 8) is an inhibitor for sorbitol dehydrogenase, that inhibits human and rat SDH with IC50 of 19 nM and 27 nM. (6S)-CP-470711 ameliorates the Streptozotocin (HY-13753)-induced diabetes in rats models .
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Cat. No.: HY-175741
CAS No.: 3094992-69-2
Target:  

Topoisomerase Parasite

Research Areas:  

Infection

IID432 is a potent, orally active, and covalent inhibitor of Trypanosoma cruzi topoisomerase II. IID432 shows an EC50 of 8 nM against T. cruzi intracellular amastigotes, exhibits excellent oral bioavailability (52% in rats), favorable ADME properties, and no S1P pathway modulation. IID432 achieves relapse-free cure in a chronic T. cruzi infection mouse model, can be used for the study of Chagas disease .
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Cat. No.: HY-118383
CAS No.: 28441-98-7
Purity:  99.62%
Agathisflavone is a flavonoid with antioxidant, anti-inflammatory, antiviral, antiparasitic, cytotoxic, neuroprotective, and hepatoprotective activities. Agathisflavone can improve tissue repair in a spinal cord injury model in rats .
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Cat. No.: HY-115597
CAS No.: 2413939-89-4
Purity:  98.90%
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

BTT-266 is an antagonist forcalcium channel, through suppression of the CaVα1-AID-CaVβ3 interaction, with a Ki of 1.4 μM. BTT-266 modulates the activation of voltage-dependent CaV2.2. BTT-266 exhibits analgesic efficacy against neuropathic pain in rats model .
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Cat. No.: HY-107482A
CAS No.: 62936-56-5
Synonyms: Nicotinoyl-GABA sodium; Nicotinoyl-γ-aminobutyric acid sodium
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

Picamilon sodium is an orally active derivative of γ-aminobutyric acid that has nootropic effect. Picamilon sodium improves the epilepsy model in rats and promotes correction of functional disorders of the pancreas during Alloxan (HY-W017227)-induced diabetes mellitus in rats .
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Cat. No.: HY-103232
CAS No.: 258282-23-4
Target:  

mGluR

Research Areas:  

Neurological Disease

IEM-1925 bromide is an orally active glutamate receptor antagonist, increases the latent period and decreases the duration of status epilepticus in rats in a lithium-pilocarpine model of epilepsy .
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Cat. No.: HY-144289
CAS No.: 1001419-18-6
Purity:  99.75%
Target:  

Glucokinase

Research Areas:  

Metabolic Disease

BMS-820132 is an orally active and partial glucokinase (GK) activator with a AC50 of 29 nM. BMS-820132 decreases the glucose levels in glucose tolerance test (OGTT) model in normal rats, but not Zucker diabetic fatty (ZDF) rats. BMS-820132 exhibits pharmacological toxicity secondary to strong GK activation .
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Cat. No.: HY-W116576R
CAS No.: 934-00-9
Research Areas:  

Cancer

3-Methoxycatechol is intermediate for the antivascular agents combretastatin A-1 (HY-121993) and combretastatin B-1. 3-Methoxycatechol promotes esophageal carcinogenesis in rats models .
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Cat. No.: HY-B0235R
CAS No.: 133-67-5
Research Areas:  

Metabolic Disease

Trichlormethiazide (Standard) is the analytical standard of Trichlormethiazide. This product is intended for research and analytical applications. Trichlormethiazide is an orally active thiazide diuretic, with antihypertensive effect. Trichlormethiazide increases urine volume (UV), Na and K excretion and tends to improve the depressed creatinine clearance (CCRE) in acute renal failure rats model .
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Cat. No.: HY-153369
CAS No.: 1609342-18-8
Synonyms: BAY 1165747
BAY-747 (BAY 1165747) is an orally active and brain-penetrant stimulator of soluble guanylate cyclase (sGC). BAY-747 reverses L-NAME induced memory impairments and enhances cognition of rats in the object location task (OLT). BAY-747 also decreases blood pressure in both conscious normotensive and spontaneously hypertensive rats (SHR). BAY-747 improves function of the skeletal muscle associated with Duchenne muscular dystrophy (DMD) in mdx/mTRG2 mice model .
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