100 Results for "

Constipation

" in MedChemExpress (MCE) Product Catalog:
Products (100)

100 Results for "Constipation" in MCE Product Catalog:

Cat. No.: HY-B0679S
CAS No.: 1217675-13-2
Synonyms: RU-0211-d7; SPI-0211-d7
Lubiprostone-d7 (RU-0211-d7) is the deuterium labeled Lubiprostone. Lubiprostone (SPI-0211) increases intestinal fluid secretion through generation of CIC-2/CFTR and activation of cAMP signaling pathway. Lubiprostone inhibits myeloperoxidase (MPO) activity, downregulates Indomethacin (HY-14397)-induced iNOS and TNFα expression. Lubiprostone can be used for chronic constipation research .
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Cat. No.: HY-106761
CAS No.: 90729-41-2
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease Others

Oxodipine, a dihydropyridine-type calcium antagonist, inhibits KCl-induced aortic contraction in rabbits and reduces cardiac force in less potent rat ventricular test-paper contractions. In rat cultured neonatal ventricular myocytes, Oxodipine reduces L-type Ca currents (I) with an IC50 of 0.24 μM, and against T-type Ca currents (I) with an IC50 of 0.41 μM. Oxodipine causes constipation in mice and gingival hyperplasia in dogs .
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Cat. No.: HY-15790S
Synonyms: A 3309-d5; AZD 7806-d5
Elobixibat-d5 is the deuterium labeled Elobixibat (HY-15790). Elobixibat (A 3309; AZD 7806) is orally active, bile acid transporter (IBAT) inhibitor with IC50 values ??of 0.53 nM (human IBAT), 0.13 nM (mouse IBAT), and 5.8 nM (canine IBAT). Elobixibat can lower LDL cholesterol, increase serum GLP-1, promote colonic motility, and has the potential to treat metabolic syndrome. Elobixibat can be used in the study of chronic functional constipation (CIC), dyslipidemia, non-alcoholic hepatitis, and liver tumors in the elderly .
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Cat. No.: HY-159924
CAS No.: 2131200-75-2
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

DBPR116 is a prodrug of BPRMU191 (HY-159923) with blood-brain barrier penetration capability. DBPR116 significantly improves the delivery of centrally targeted drugs. In combination with the antagonist Naltrexone (HY-76711), DBPR116 demonstrated superior safety and analgesic efficacy compared to morphine in various in vivo pharmacological studies, including thermal pain models, cancer pain models, constipation, sedation, psychological dependence, heart rate, and respiratory frequency. As a prodrug strategy for peripheral administration, DBPR116 effectively alleviates pain while reducing adverse effects, showing potential as a safer opioid analgesic .
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Cat. No.: HY-N0886R
CAS No.: 28371-16-6
Synonyms: Isobarbaloin (Standard)
Aloin B (Isobarbaloin) (Standard) is the analytical standard of Aloin B. This product is intended for research and analytical applications. Aloin B is an orally active SARS-CoV-2 papain-like protease (PLpro) inhibitor with an IC50 of 16.08 μM (hydrolytic activity) and 17.51 μM (deubiquitinase activity). Aloin B is metabolized by rat intestinal flora into aloe-emodin-9-anthrone to exert laxative effects. Aloin B inhibits TPA (HY-18739)-induced ear edema, putrescine elevation, and tumor promotion in mouse skin. Aloin B can be used in research related to anti-inflammation, tumor promotion inhibition, coronavirus disease 2019 (COVID-19) and constipation .
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Cat. No.: HY-N6082R
CAS No.: 34298-86-7
Rhein 8-O-β-D-Glucopyranoside (Standard) is the analytical standard of Rhein 8-O-β-D-Glucopyranoside (HY-N6083). This product is intended for research and analytical applications. Rhein 8-O-β-D-Glucopyranoside is an orally active glycoside found in Rhubarb. Rhein 8-O-β-D-Glucopyranoside attenuates high glucose-induced apoptosis, recovers altered lincRNA ANRIL and let-7a expression, reverses high glucose-altered Bcl-2 and cleaved caspase-3 protein expression, and inhibits TGF-β1/Smad signaling. Rhein 8-O-β-D-Glucopyranoside accelerates Sennoside A (HY-N0365) metabolism, stimulates sennoside A purgative activity. Rhein 8-O-β-D-Glucopyranoside inhibits bacterial biofilm formation, suppresses its virulence gene expression, and exerts antibacterial activity. Rhein 8-O-β-D-Glucopyranoside can be used for the research of diabetic nephropathy, constipation, and infection .
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Cat. No.: HY-109065A
CAS No.: 1184661-33-3
Synonyms: DSP-6952 hydrobromide
Target:  

5-HT Receptor

Research Areas:  

Endocrinology

Minesapride hydrobromide (DSP-6952 hydrobromide) is an orally active, selective 5-HT4 receptor partial agonist. Minesapride hydrobromide enhances gastrointestinal motility, colonic transit and defecation function, and inhibits visceral hypersensitivity. Minesapride hydrobromide does not inhibit/induce cytochrome P450 isozymes, has no significant affinity for hERG, and does not trigger the risk of cardiac ischemia via coronary vasoconstriction. Minesapride hydrobromide can be used in research related to constipation-predominant irritable bowel syndrome, chronic constipation, atonic constipation, spastic constipation, functional constipation and functional dyspepsia .
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Cat. No.: HY-183487
CAS No.: 2257498-40-9
Target:  

mAChR

Research Areas:  

Endocrinology

M1R modulator-1 is an orally effective positive allosteric modulator of muscarinic M1R, with an IP value of 0.88 nM. M1R modulator-1 can be used in constipation-related research .
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Cat. No.: HY-124706
CAS No.: 858747-13-4
Target:  

OAT

DRAinh-A250 is an orally active inhibitor of mouse and human SLC26A3 (DRA). DRAinh-A250 inhibits SLC26A3-mediated anion transport, blocks colonic fluid absorption, reduces luminal fluid alkalization in the distal colonic loops of mice, and alleviates Loperamide (HY-156131)-induced constipation in wild-type and cystic fibrosis mice. DRAinh-A250 can be used in the research of constipation and cystic fibrosis-related constipation .
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Cat. No.: HY-182340
CAS No.: 143394-68-7
Target:  

Adenosine Receptor

Research Areas:  

Endocrinology

KF20274 is an orally active adenosine A1 receptor antagonist. KF20274 increases the fecal pellet output in rats, and does not affect small intestinal propulsion or gastric emptying at defecation-increasing doses. KF20274 does not induce diarrhea at defecation-increasing doses. KF20274 can be used for the research of constipation .
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Cat. No.: HY-N18653
CAS No.: 100084-89-7
Category:  

Extract

Target:  

Others

Aloe capensis extract is rich in bioactive compounds such as aloe-emodin, plant minerals, vitamins, amino acids, and polysaccharides. It has a strong laxative effect and can be used in research on constipation.
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Cat. No.: HY-N18652
CAS No.: 85187-05-9
Category:  

Extract

Target:  

Bacterial

Senna extract contains anthraquinone compounds, such as sennosides A and B, which have laxative properties. Sennosides in senna extract can stimulate colon muscles, promote intestinal peristalsis, and relieve constipation.
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Cat. No.: HY-N18746
CAS No.: 93348-59-5
Category:  

Extract

Target:  

Others

Cassia tora extract is derived from the Cassia tora and is rich in bioactive constituents such as flavonoids, saponins, and polysaccharides. Cassia tora extract can be utilized in research on various conditions, including skin infections, liver diseases, and constipation.
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Cat. No.: HY-N18781
CAS No.: 92202-07-8
Category:  

Extract

Target:  

Bacterial

Chitrakmool extract contains a variety of key active ingredients, including the potent naphthoquinone compound pampinidin, as well as various alkaloids, flavonoids, and terpenoids. Chitrakmool extract helps stimulate appetite, improve digestion, and relieve indigestion, bloating, and constipation.
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Cat. No.: HY-10457AR
CAS No.: 866933-51-9
Synonyms: TD-5108 hydrochloride (Standard)
Velusetrag hydrochloride (Standard) is the analytical standard of Velusetrag hydrochloride (HY-10457A). This product is intended for research and analytical applications. Velusetrag (TD-5108) hydrochloride is an orally active, potent and selective agonist of serotonin 5-HT4 receptor (5-HT4R), with a pKi of 7.7. Velusetrag hydrochloride exhibits no affinity (Ki>10 μM) for 5-HT2A and 5-HT2B receptors. Velusetrag hydrochloride can be used for the research of gastrointestinal diseases and Parkinson's disease .
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Cat. No.: HY-10457R
CAS No.: 866933-46-2
Synonyms: TD-5108 (Standard)
Velusetrag (Standard) is the analytical standard of Velusetrag (HY-10457). This product is intended for research and analytical applications. Velusetrag (TD-5108) is an orally active, potent and selective agonist of serotonin 5-HT4 receptor (5-HT4R), with a pKi of 7.7. Velusetrag exhibits no affinity (Ki>10 μM) for 5-HT2A and 5-HT2B receptors. Velusetrag can be used for the research of gastrointestinal diseases and Parkinson's disease .
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Cat. No.: HY-101907R
CAS No.: 1190217-35-6
Research Areas:  

Neurological Disease

ASP7663 (Standard) is the analytical standard of ASP7663 (HY-101907). This product is intended for research and analytical applications. ASP7663 is an orally active and selective TRPA1 agonist. ASP7663 exerts both anti-constipation and anti-abdominal pain actions .
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Cat. No.: HY-N17361
CAS No.: 160954-12-1
Methylgerambullone is a constitutional isomer of Methylisogerambullone. Methylgerambullone can be isolated from the methanolic leaf extract of Glycosmis angustifolia. Methylgerambullone shows the relaxatory effect on guinea-pig isolated ileum precontracted with Acetylcholine .
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Cat. No.: HY-N18676
CAS No.: 93348-15-3
Category:  

Extract

Target:  

Others

Dolichos Biflorus Extract, derived from the Dolichos biflorus plant (commonly known as horse gram), is a nutrient-dense herb widely used in Ayurvedic and traditional medicine for its numerous health benefits. Dolichos biflorus extract contains alkaloids, saponins, flavonoids, carbohydrates, proteins, and tannins. It is known for its digestive support, as it promotes healthy digestion, alleviates bloating, and helps with constipation, along with mild diuretic effects that aid detoxification by eliminating excess fluids and waste products from the body.
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Cat. No.: HY-181103
CAS No.: 2059904-64-0
Research Areas:  

Neurological Disease

ERG-IN-6 (compound (+)-(S)-5a) is a μ-opioid receptor activator with an EC50 of 0.12 nM. ERG-IN-6 also is a hERG (Kv11.1) potassium channel inhibitor with an IC50 of 0.681 μM. ERG-IN-6 can be used for the research of pain .
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