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| Product | Description | |
|---|---|---|
| Amiloride hydrochloride | Amiloride hydrochloride (MK-870 hydrochloride) is an inhibitor of both epithelial sodium channel ( ENaC [1] ) and urokinase-type plasminogen activator receptor ( uTPA [2] ). Amiloride hydrochloride is a blocker of polycystin-2 (PC2; TRPP2 [3] ) channel. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-870 hydrochloride. CAS No. 2016-88-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0285A. |  |
| Amiloride Hydrochloride | Sodium channel blocker. Diuretic. Group: Biochemicals. Alternative Names: 3,5-Diamino-N-(aminoiminomethyl)-6-chloro-2-pyrazinecarboxamide Hydrochloride; N-Amidino-3, 5-diamino-6-chloro cyrazinecarboxamide Monohydrochloride; N-Amidino-3,5-diamino-6-chloropyrazinamide Hydrochloride; Amipramidine; Amipramizide; Amiprazide; Colectril; Midamor; Nilurid. Grades: Highly Purified. CAS No. 2016-88-8. Pack Sizes: 1g. US Biological Life Sciences. |  Worldwide |
| Amiloride Hydrochloride | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Amiloride Hydrochloride Dihydrate, 2-Pyrazinecarboxamide, 3,5-diamino-N-(aminoiminomethyl)-6-chloro-, hydrochloride, hydrate (1:1:2), N-Amidino-3,5-diamino-6-chloropyrazinamide hydrochloride dihydrate, Pyrazinecarboxamide, N-amidino-3,5-diamino-6-chloro-, monohydrochloride, dihydrate (8CI), Pyrazinecarboxamide, 3,5-diamino-N-(aminoiminomethyl)-6-chloro-, monohydrochloride, dihydrate (9CI). |  |
| Amiloride hydrochloride dihydrate | Amiloride hydrochloride dihydrate. Group: Biochemicals. Alternative Names: 3,5-Diamino-N-(aminoiminomethyl)-6-chloro-2-pyrazinecarboxamide hydrochloride; N-Amidino-3, 5-diamino-6-chloro cyrazinecarboxamide monohydrochloride; N-Amidino-3,5-diamino-6-chloropyrazinamide hydrochloride. Grades: Highly Purified. CAS No. 2016-88-8. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C6H9Cl2N7O. US Biological Life Sciences. | Worldwide |
| Amiloride hydrochloride dihydrate | Amiloride hydrochloride dihydrate (MK-870 hydrochloride dihydrate) is an inhibitor of both epithelial sodium channel ( ENaC [1] ) and urokinase-type plasminogen activator receptor ( uTPA [2] ). Amiloride hydrochloride dihydrate is a blocker of polycystin-2 (PC2; TRPP2 [3] ) channel. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-870 hydrochloride dihydrate. CAS No. 17440-83-4. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B0285B. | |
| Amiloride Hydrochloride Dihydrate | Amiloride precludes the alkalinization and in parallel inhibit cellular proliferation. Synonyms: Amiloride HCl dihydrate; MK-870 hydrochloride dihydrate; N-Amidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride dihydrate. Grade: >98%. CAS No. 17440-83-4. Molecular formula: C6H13Cl2N7O3. Mole weight: 302.12. |  |
| Amiloride hydrochloride hydrate | ?98% (HPLC), powder. Group: Fluorescence/luminescence spectroscopy. | |
| 5-(N,N-Dimethyl)amiloride hydrochloride | 5-(N,N-dimethyl)-amiloride (DMA) inhibits NHE1, NHE2, and NHE3 with Ki values of 0.02, 0.25, and 14 μM, respectively. Synonyms: 2-Pyrazinecarboxamide, 3-amino-N-(aminoiminomethyl)-6-chloro-5-(dimethylamino)-, hydrochloride (1:1); Pyrazinecarboxamide, 3-amino-N-(aminoiminomethyl)-6-chloro-5-(dimethylamino)-, monohydrochloride; Pyrazinecarboxamide, N-amidino-3-amino-6-chloro-5-(dimethylamino)-, monohydrochloride; (3-Amino-5-dimethylamino-6-chloropyrazinoyl)guanidine hydrochloride; Dimethylamiloride hydrochloride. Grade: ≥98%. CAS No. 2235-97-4. Molecular formula: C8H12ClN7O.HCl. Mole weight: 294.14. | |
| Amiloride-15N3 Hydrochloride | Labelled Amiloride. Sodium channel blocker. Diuretic. Synonyms: 3,5-Diamino-N-(aminoiminomethyl)-6-chloro-2-pyrazinecarboxamide-15N3 Hydrochloride; N-Amidino-3,5-diamino-6-chloropyrazinamide-15N3 Hydrochloride; Amipramidine-15N3; Amipramizide-15N3; Colectril-15N3; Midamor-15N3; Nilurid-15N3. CAS No. 1216796-18-7. Molecular formula: C6H9Cl2N4[15N]3O. Mole weight: 269.07. | |
| Amiloride, Hydrochloride - CAS 2016-88-8 | An inhibitor of angiogenesis. Group: Fluorescence/luminescence spectroscopy. | |
| Amiloride (hydrochloride) (Standard) | Amiloride (hydrochloride) (Standard) is the analytical standard of Amiloride (hydrochloride). This product is intended for research and analytical applications. Amiloride hydrochloride (MK-870 hydrochloride) is an inhibitor of both epithelial sodium channel ( ENaC [1] ) and urokinase-type plasminogen activator receptor ( uTPA [2] ). Amiloride hydrochloride is a blocker of polycystin-2 (PC2; TRPP2 [3] ) channel. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-870 hydrochloride (Standard). CAS No. 2016-88-8. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-B0285AR. | |
| Amiloride EP Impurity B | An impurity of Amiloride. Amiloride is a medication typically used with other medications to treat high blood pressure or swelling due to heart failure or cirrhosis of the liver. Synonyms: 3,5-Diamino-6-chloro-pyrazine acid; 3,5-Diamino-6-chloropyrazinecarboxylic acid; 3,5-Diamino-6-chloro-2-pyrazinecarboxylic acid; Amiloride Impurity B; Amiloride Hydrochloride Dihydrate Impurity B; Amiloride Hydrochloride Dihydrate EP Impurity B. Grade: ≥95%. CAS No. 4878-36-8. Molecular formula: C5H5ClN4O2. Mole weight: 188.57. | |
| Amiloride HCl | Amiloride HCl is a relatively selective inhibitor of the epithelial sodium channel, used in the management of hypertension and congestive heart failure. Uses: Acid sensing ion channel blockers. Synonyms: Amiloride HCl anhydrous; Amiloride (hydrochloride); Amiloride hydrochloride anhydrous; MK-870 hydrochloride; N-Amidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride. Grade: ≥ 98%. (HPLC). CAS No. 2016-88-8. Molecular formula: C6H9Cl2N7O. Mole weight: 266.09. | |
| Benzamil hydrochloride | Benzamil hydrochloride (Benzylamiloride hydrochloride), an Amiloride analogue, is a Na + /Ca 2+ exchanger (NCX) inhibitor ( IC 50 ~100 nM). Benzamil hydrochloride also is a non-selective Deg/epithelial sodium channels (ENaC) blocker, and can potentiate myogenic vasoconstriction. Benzamil hydrochloride inhibits TRPP3-mediated Ca 2+ -activated currents, with an IC 50 of 1.1 μM [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Benzylamiloride hydrochloride. CAS No. 161804-20-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B1546A. | |
| Benzamil hydrochloride | Benzamil hydrochloride is a Na+/Ca2+ exhanger (NCX) inhibitor (IC50 ~ 100 nM) and an epithelial sodium channel (ENaC) blocker. Benzamil is an analogue of amiloride, and it is potentially used for the treatment of cystic fibrosis. Uses: Potential treatment of cystic fibrosis. Synonyms: N-(Benzylamidino)-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride. Grade: ≥98% by HPLC. CAS No. 161804-20-2. Molecular formula: C13H14ClN7O.HCl. Mole weight: 356.21. | |
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