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| Product | Description | |
|---|---|---|
| Angiotensin-converting enzyme | Angiotensin-converting enzyme (Kininase II) is a dicarboxypeptidase, it converts inactive Angiotensin I (Ang I) to active Ang II and degrades active bradykinin (BK). Angiotensin-converting enzyme is a potent vasoconstrictor, is often used in biochemical studies [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Kininase II; CD143. CAS No. 9015-82-1. Pack Sizes: 1 U. Product ID: HY-P2983. |  |
| angiotensin-converting enzyme 2 | A transmembrane glycoprotein with an extracellular catalytic domain. Angiotensin-converting enzyme 2 functions as a carboxypeptidase, cleaving a single C-terminal residue from a distinct range of substrates. Catalytic efficiency is 400-fold higher with angiotensin II (1-8) as a substrate than with angiotensin I (1-10). Angiotensin-converting enzyme 2 also efficiently hydrolyses des-Arg9-bradykinin, but it does not hydrolyse bradykinin. In peptidase family M2. Group: Enzymes. Synonyms: ACE-2; ACE2; hACE2; angiotensin converting enzyme 2; angiotensin converting enzyme-2; Tmem27. Enzyme Commission Number: EC 3.4.17.23. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4076; angiotensin-converting enzyme 2; EC 3.4.17.23; ACE-2; ACE2; hACE2; angiotensin converting enzyme 2; angiotensin converting enzyme-2; Tmem27. Cat No: EXWM-4076. |  |
| Native Bovine Angiotensin Converting Enzyme | Angiotensin-converting enzyme (EC 3.4.15.1), or "ACE" indirectly increases blood pressure by causing blood vessels to constrict. It does that by converting angiotensin I to angiotensin II, which constricts the vessels. For this reason, drugs known as ACE inhibitors are used to lower blood pressure. ACE, angiotensin I and angiotensin II are part of the renin-angiotensin system (RAS), which controls blood pressure by regulating the volume of fluids in the body. ACE is secreted in the lungs and kidneys by cells in the endothelium (inner layer) of blood vessels. Applications: Positive control. Group: Enzymes. Synonyms: ACE; Angiotensin Converting Enzyme; EC 3.4.15.1; dipept...te buffer-300 mM NaCl, pH 8.3 at 37°C. Storage: Maintain at -20°C in undiluted aliquots for up to 12 months. Maintain at 4°C for up to one month. A decrease in activity may occur within prolonged storage at 4°C. Source: Bovine lung. Species: Bovine. ACE; Angiotensin Converting Enzyme; EC 3.4.15.1; dipeptidyl carboxypeptidase I; peptidase P; dipeptide hydrolase, peptidyl dipeptidase; angiotensin converting enzyme; kininase II; angiotensin I-converting enzyme; carboxycathepsin; dipeptidyl carboxypeptidase; "hypertensin converting enzyme" peptidyl dipeptidase I; peptidyl-dipeptide hydrolase; peptidyldipeptide hydrolase; endothelial cell peptidyl dipeptidase; peptidyl dipept | |
| Native Porcine Angiotensin Converting Enzyme | Angiotensin-converting enzyme (EC 3.4.15.1), or "ACE" indirectly increases blood pressure by causing blood vessels to constrict. It does that by converting angiotensin I to angiotensin II, which constricts the vessels. For this reason, drugs known as ACE inhibitors are used to lower blood pressure. ACE, angiotensin I and angiotensin II are part of the renin-angiotensin system (RAS), which controls blood pressure by regulating the volume of fluids in the body. ACE is secreted in the lungs and kidneys by cells in the endothelium (inner layer) of blood vessels. Ace is a monomer with molecular weight of ~170 kda ph range for activity: 7-8.5 temperature optimum: 37°c zinc is...-82-1. Angiotensin Converting Enzyme. Activity: > 10 units/mg protein (Bradford). Storage: -20°C. Form: Lyophilized powder containing Tris buffer salts. Source: Porcine kidney. Species: Porcine. ACE; Angiotensin Converting Enzyme; EC 3.4.15.1; dipeptidyl carboxypeptidase I; peptidase P; dipeptide hydrolase, peptidyl dipeptidase; angiotensin converting enzyme; kininase II; angiotensin I-converting enzyme; carboxycathepsin; dipeptidyl carboxypeptidase; "hypertensin converting enzyme" peptidyl dipeptidase I; peptidyl-dipeptide hydrolase; peptidyldipeptide hydrolase; endothelial cell peptidyl dipeptidase; peptidyl dipeptidase-4; PDH; peptidyl dipeptide hydrolase; DCP. Cat N | |
| Native Rabbit Angiotensin Converting Enzyme | Angiotensin-converting enzyme (EC 3.4.15.1), or "ACE" indirectly increases blood pressure by causing blood vessels to constrict. It does that by converting angiotensin I to angiotensin II, which constricts the vessels. For this reason, drugs known as ACE inhibitors are used to lower blood pressure. ACE, angiotensin I and angiotensin II are part of the renin-angiotensin system (RAS), which controls blood pressure by regulating the volume of fluids in the body. ACE is secreted in the lungs and kidneys by cells in the endothelium (inner layer) of blood vessels. Group: Enzymes. Synonyms: ACE; Angiotensin Converting Enzyme; EC 3.4.15.1; dip. Enzyme Commission Number: EC 3.4.15.1. CAS No. 9015-82-1. Angiotensin Converting Enzyme. Activity: > 2.0 units/mg protein (modified Warburg-Christian). Form: lyophilized powder. Source: Rabbit lung. Species: Rabbit. ACE; Angiotensin Converting Enzyme; EC 3.4.15.1; dipeptidyl carboxypeptidase I; peptidase P; dipeptide hydrolase, peptidyl dipeptidase; angiotensin converting enzyme; kininase II; angiotensin I-converting enzyme; carboxycathepsin; dipeptidyl carboxypeptidase; "hypertensin converting enzyme" peptidyl dipeptidase I; peptidyl-dipeptide hydrolase; peptidyldipeptide hydrolase; endothelial cell peptidyl dipeptidase; peptidyl dipeptidase-4; PDH; peptidyl dipeptide hydrolase; DCP. Cat No: NATE-0015. | |
| Native Rat Angiotensin Converting Enzyme | Angiotensin-converting enzyme (EC 3.4.15.1), or "ACE" indirectly increases blood pressure by causing blood vessels to constrict. It does that by converting angiotensin I to angiotensin II, which constricts the vessels. For this reason, drugs known as ACE inhibitors are used to lower blood pressure. ACE, angiotensin I and angiotensin II are part of the renin-angiotensin system (RAS), which controls blood pressure by regulating the volume of fluids in the body. ACE is secreted in the lungs and kidneys by cells in the endothelium (inner layer) of blood vessels. Applications: Positive control. Group: Enzymes. Synonyms: ACE; Angiotensin Converting Enzyme; EC 3.4.15.1; dipeptid....1 M phosphate buffer and 300 mM NaCl at pH 8.3 at 37°C. Storage: Maintain at -20°C in undiluted aliquots for up to 6 months. Avoid repeated freeze/thaw cycles. Form: Liquid in 100 mM phosphate buffered saline, 150 mM NaCl, pH 7.4 with 0.2mM CHAPS. Source: Rat lung. Species: Rat. ACE; Angiotensin Converting Enzyme; EC 3.4.15.1; dipeptidyl carboxypeptidase I; peptidase P; dipeptide hydrolase, peptidyl dipeptidase; angiotensin converting enzyme; kininase II; angiotensin I-converting enzyme; carboxycathepsin; dipeptidyl carboxypeptidase; "hypertensin converting enzyme" peptidyl dipeptidase I; peptidyl-dipeptide hydrolase; peptidyldipeptide hydrolase; endothelial cell peptidy | |
| 1-?[2-?[ (1-?carboxy-?3-?phenylpropyl) ?amino]?-?1-?oxopropyl]?octahydro-1H-?Indole-?2-?carboxylic acid | An isomer of Trandolaprilat, which is an impurity of Trandolapril. Trandolaprilat is an angiotensin converting enzyme inhibitor. Synonyms: 1H-Indole-2-carboxylicacid, 1-[2-[(1-carboxy-3-phenylpropyl)amino]-1-oxopropyl]octahydro-; 1-(2-((1-Carboxy-3-phenylpropyl)amino)-1-oxopropyl)octahydro-1H-indole-2-carboxylic acid; SCHEMBL678354; DTXSID90868979; 1H-Indol-2-carboxylic acid, 1-(2-((1-carboxy-3-phenylpropyl)amino)-1-oxopropyl)octahydro-; 1-{2-[ (1-carboxy-3-phenylpropyl) amino]propanoyl}octahydro-1H-indole-2-carboxylic acid (non-preferred name); FT-0687175. CAS No. 83601-86-9. Molecular formula: C22H30N2O5. Mole weight: 402.491. |  |
| 1-[(2R)-3-Mercapto-2-methyl-1-oxopropyl]-D-proline | 1-[(2R)-3-Mercapto-2-methyl-1-oxopropyl]-D-proline is an impurity of Captopril, which is an orally active angiotensin-converting enzyme (ACE) inhibitor used as an antihypertensive agent. Synonyms: (R)-1-(3-Mercapto-2-methyl-1-oxopropyl)-D-proline; 1-(D-3-mercapto-2-methylpropionyl)-L-proline; Captopril Related Compound 8; epi-D-captopril; (R)-1-((R)-3-Mercapto-2-methyl-propionyl)-pyrrolidine-2-carboxylic acid; (2R)-1-((2R)-3-mercapto-2-methylpropanoyl)pyrrolidine-2-carboxylic acid; ((R)-3-mercapto-2-methylpropanoyl)-D-proline. Grades: 98%. CAS No. 112243-88-6. Molecular formula: C9H15NO3S. Mole weight: 217.28. | |
| 1-[(2S)-3-Bromo-2-methyl-1-oxopropyl]-L-proline N-Cyclohexyl cyclohexanamine | 1-[(2S)-3-Bromo-2-methyl-1-oxopropyl]-L-proline N-Cyclohexyl cyclohexanamine is an intermediate in the synthesis of Epicaptopril (E582255). Epicaptopril is an impurity of Captopril (C175750) which is an orally active angiotensin-converting enzyme (ACE) inhibitor used in the treatment of hypertension and congestive heart failure. Group: Biochemicals. Grades: Highly Purified. CAS No. 1275614-30-6. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C9H14BrNO3 C12H23N. US Biological Life Sciences. |  Worldwide |
| 1,7a-Seco-Perindopril | 1,7a-Seco-Perindopril is an impurity of Perindopril (P287500), an angiotensin-converting enzyme (ACE) inhibitor; antihypertensive. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C19H34N2O5, Molecular Weight: 370.48. US Biological Life Sciences. | Worldwide |
| 1-Desethoxy 1-Isopropyl Perindopril t-Butylamine | 1-Desethoxy 1-Isopropyl Perindopril t-Butylamine is a compound related to Perindopril (P287500), an angiotensin-converting enzyme (ACE) inhibitor. Antihypertensive. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C24H45N3O5, Molecular Weight: 455.63. US Biological Life Sciences. | Worldwide |
| 1-epi-Ramipril | 1R-isomer of Ramipril.Ramipril is an angiotensin-converting enzyme inhibitor. It can be used for treatment of hypertension and congestive heart failure. Synonyms: (2S,3aS,6aS)-1-[(1S)-2-[[(1R)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]- 1-oxopropyl]octahydrocyclopenta [b]pyrrole-2-carboxylic Acid; [2S- [1 [R* (S*) ], 2α , 3aβ , 6aβ ]]-1- [2- [ [1- (Ethoxycarbonyl) -3-phenylpropyl]amino]-1-oxopropyl]octahydrocyclopenta [b]pyrrole-2-carboxylic Acid; (1R)-epi-Ramipril. Grades: > 95%. CAS No. 104195-90-6. Molecular formula: C23H32N2O5. Mole weight: 416.52. | |
| 1-[N-[N-(2-Aminobenzoyl)glycyl]-4-nitro-L-phenylalanyl]-L-proline | It is a substrate for the fluorescent assay of angiotensin I-converting enzyme and of the bacterial dipeptidyl carboxypeptidase from Escherichia coli. Synonyms: 2-Aminobenzoylglycyl-4-nitrophenylalanyl-proline; Abz-Gly-p-nitro-Phe-Pro-OH; L-Proline,N-(2-aminobenzoyl)glycyl-4-nitro-L-phenylalanyl-; o-Aminobenzoylglycyl-p-nitro-L-phenylalanyl-L-proline. CAS No. 67482-93-3. Molecular formula: C23H25N5O7. Mole weight: 483.47. | |
| (1R)-Benazepril tert-Butyl Ester | R-Benazepril tert-Butyl Ester is an isomer of Benazepril tert-Butyl Ester (B119850) which is a useful synthetic intermediate in the synthesis of Benazepril Hydrochloride (B119750), a potent angiotensin converting enzyme (ACE) inhibitor and antihypertensive. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg, 1g. Molecular Formula: C28H36N2O5. US Biological Life Sciences. | Worldwide |
| (1R)-Perindopril Benzyl Ester | (1R)-Perindopril Benzyl Ester is an intermediate of Perindopril (P287500). Perindopril is an angiotensin-converting enzyme (ACE) inhibitor. Antihypertensive. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg, 100mg. Molecular Formula: C26H38N2O5. US Biological Life Sciences. | Worldwide |
| (1R) Perindopril-d4 ( (2S, 3aS, 7aS) -1-[ (2S) -2-[[ (1R) -1- (Ethoxycarbonyl) butyl]amino]-1-oxopropyl]octahydro-1H-indole-2-carboxylic Acid-d4) | An angiotensin-converting enzyme (ACE) inhibitor. Group: Biochemicals. Alternative Names: (2S, 3aS, 7aS) -1-[ (2S) -2-[[ (1R) -1- (Ethoxycarbonyl) butyl]amino]-1-oxopropyl]octahydro-1H-indole-2-carboxylic Acid-d4. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| (1R)-Perindopril-d4 t-Butylamine Salt | (1R)-Perindopril-d4 t-Butylamine Salt is the isotope labelled analog of (1R)-Perindopril t-Butylamine Salt (P287520); an enantiomer of Perindopril t-Butylamine Salt (P287505) which is an angiotensin-converting enzyme (ACE) inhibitor and antihypertensive. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 10mg. Molecular Formula: C23H39D4N3O5, Molecular Weight: 445.63. US Biological Life Sciences. | Worldwide |
| (1R)-Perindopril t-Butylamine Salt | (1R)-Perindopril t-Butylamine Salt is an enantiomer of Perindopril t-Butylamine Salt (P287505); an angiotensin-converting enzyme (ACE) inhibitor and antihypertensive. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 50mg. Molecular Formula: C23H43N3O5. US Biological Life Sciences. | Worldwide |
| (1S, 3S, 5S)-2-Azabicyclo[3. 1. 0]hexane-2, 3-dicarboxylic Acid 2-(1,1-Dimethylethyl) 3-ethyl Ester | (1S, 3S, 5S)-2-Azabicyclo[3. 1. 0]hexane-2, 3-dicarboxylic Acid 2-(1,1-Dimethylethyl) 3-ethyl Ester acts as a reagent for the preparation of captopril analogs as inhibitors of angiotensin converting enzyme. Core modification of substituted piperidines as novel inhibitors of HDM2-p53 protein-protein interaction. Group: Biochemicals. Grades: Highly Purified. CAS No. 214193-11-0. Pack Sizes: 50mg, 250mg. Molecular Formula: C13H21NO4, Molecular Weight: 255.31. US Biological Life Sciences. | Worldwide |
| 2,2,2-trifluoroethyl formate | Lisinopril Impurity 12 (2,2,2-trifluoroethyl formate) is an impurity of Lisinopril, a medication of the angiotensin-converting enzyme inhibitor class that is used to treat high blood pressure. Synonyms: Lisinopril Impurity 12. Grades: 97 % (HPLC). CAS No. 32042-38-9. Molecular formula: C3H3F3O2. Mole weight: 128.05. | |
| 2,5-Dioxopyrrolidin-1-yl 3-(tritylthio)propanoate | 2,5-Dioxopyrrolidin-1-yl 3-(tritylthio)propanoate, a multifaceted chemical compound, plays a pivotal role in drug synthesis, specifically in the development of angiotensin converting enzyme inhibitors. In addition to its significance in this domain, it functions as a valuable building block in drug development for maladies such as hypertension, heart failure, and diabetes. Its diverse utilization and multifarious potential thereby make it a crucial focus of drug research. Synonyms: 1-[1-oxo-3-[(triphenylmethyl)thio]propoxy]-2,5-Pyrrolidinedione; Mpa(Trt)-Osu. CAS No. 129431-12-5. Molecular formula: C26H23NO4S. Mole weight: 445.533. | |
| 2-Benzyl-1,3-propanediol Diacetate | 2-Benzyl-1,3-propanediol Diacetate is an intermediate in the synthesis of Sinorphan (S490950), an inhibitor of angiotensin-converting enzyme and neutral endopeptidase. Group: Biochemicals. Grades: Highly Purified. CAS No. 110230-64-3. Pack Sizes: 100mg, 250mg. Molecular Formula: C14H18O4. US Biological Life Sciences. | Worldwide |
| 2-epi-Ramipril | 2R-isomer of Ramipril.Ramipril is an angiotensin-converting enzyme inhibitor. It can be used for treatment of hypertension and congestive heart failure. Synonyms: (2S, 3aS, 6aS) -1- [ (2R) -2- [ [ (1S) -1- (Ethoxycarbonyl) -3-phenylpropyl]amino]-1-oxopropyl]octahydrocyclopenta [b]pyrrole-2-carboxylic Acid; [2S- [1 [S* (R*) ], 2α , 3aβ , 6aβ ]]-1- [2- [ [1- (Ethoxycarbonyl) -3-phenylpropyl]amino]-1-oxopropyl]octahydrocyclopenta [b]pyrrole-2-carboxylic Acid; (2R)-Ramipril. Grades: > 95%. CAS No. 129939-65-7. Molecular formula: C23H32N2O5. Mole weight: 416.52. | |
| 2-Methoxybenzaldehyde | 2-Methoxybenzaldehyde is used in the synthesis of stilbene and dihydrostilbene derivatives as potential anticancer agents. Also it is used in the synthesis of highly functionalized pyrrolidines as potent angiotensin converting enzyme inhibitors. Group: Biochemicals. Alternative Names: o-Anisaldehyde (8CI); 2- (Methyloxy) benzaldehyde; 2-Anisaldehyde; 2-Methoxybenzaldehyde; 2-Methoxy Benzene carboxaldehyde; 2-Methoxyphenylformalde hyde; 6-Methoxybenzaldehyde; NC 064; NSC 58960; Salicylaldehyde Methyl Ether; o-Formylanisole; o-Methoxybenzaldehyde. Grades: Highly Purified. CAS No. 135-02-4. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| 2-Methoxybenzaldehyde-d3 | 2-Methoxybenzaldehyde-d3 is the isotope labelled analog of 2-Methoxybenzaldehyde (M260980); a compound used in the synthesis of stilbene and dihydrostilbene derivatives as potential anticancer agents. 2-Methoxybenzaldehyde is also used in the synthesis of highly functionalized pyrrolidines as potent angiotensin converting enzyme inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 56248-49-8. Pack Sizes: 1g, 10g. Molecular Formula: C8H5D3O2, Molecular Weight: 139.169999999999. US Biological Life Sciences. | Worldwide |
| (2R)-3-Acetylthio-2-methylpropionyl Chloride | (2R)-3-Acetylthio-2-methylpropionyl Chloride is a reactant used in the preparation of Captopril (C175750) analogs as inhibitors of angiotensin converting enzyme. Group: Biochemicals. Grades: Highly Purified. CAS No. 74345-73-6. Pack Sizes: 10mg, 25mg. Molecular Formula: C6H9ClO2S, Molecular Weight: 180.65. US Biological Life Sciences. | Worldwide |
| (2R,3aR,7aR)-Octahydroindole-2-carboxylic Acid Benzyl Ester p-Toluenesulfonic Acid | (2R,3aR,7aR)-Octahydroindole-2-carboxylic Acid Benzyl Ester p-Toluenesulfonic Acid is an intermediate in the synthesis of Perindoprilat (P287530), an angiotensin-converting enzyme (ACE) inhibitor. Antihypertensive. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 100mg. Molecular Formula: C23H29NO5S, Molecular Weight: 431.55. US Biological Life Sciences. | Worldwide |
| (2R,3aR,7aR)-Octahydroindole-2-carboxylic Acid Hydrochloride | (2R,3aR,7aR)-Octahydroindole-2-carboxylic Acid Hydrochloride s an intermediate in the synthesis of Perindoprilat (P287530), an angiotensin-converting enzyme (ACE) inhibitor. Antihypertensive. Group: Biochemicals. Grades: Highly Purified. CAS No. 108507-42-2. Pack Sizes: 10mg, 100mg. Molecular Formula: C9H16ClNO2, Molecular Weight: 205.68. US Biological Life Sciences. | Worldwide |
| (2R,3aR,7aR)-rel-OctahydroIndole-2-carboxylic Acid | (2R,3aR,7aR)-rel-OctahydroIndole-2-carboxylic Acid is a reactant in the preparation of Perindoprilat (P287530), an angiotensin-converting enzyme (ACE) inhibitor. Antihypertensive. Group: Biochemicals. Grades: Highly Purified. CAS No. 80828-13-3. Pack Sizes: 250mg, 1g. Molecular Formula: C9H15NO2, Molecular Weight: 169.22. US Biological Life Sciences. | Worldwide |
| (2R,3aS,7aS)-Octahydroindole-2-carboxylic Acid Benzyl Ester | (2R,3aS,7aS)-Octahydroindole-2-carboxylic Acid Benzyl Ester is an intermediate in the synthesis of Perindoprilat (P287530), an angiotensin-converting enzyme (ACE) inhibitor. Antihypertensive. Group: Biochemicals. Grades: Highly Purified. CAS No. 752955-02-5. Pack Sizes: 100mg, 1g. Molecular Formula: C16H21NO2, Molecular Weight: 259.339999999999. US Biological Life Sciences. | Worldwide |
| (2R,3aS,7aS)-Octahydroindole-2-carboxylic Acid Hydrochloride | (2R,3aS,7aS)-Octahydroindole-2-carboxylic Acid Hydrochloride is an intermediate in the synthesis of Perindoprilat (P287530), an angiotensin-converting enzyme (ACE) inhibitor. Antihypertensive. Group: Biochemicals. Grades: Highly Purified. CAS No. 1004292-98-1. Pack Sizes: 100mg, 1g. Molecular Formula: C9H16ClNO2, Molecular Weight: 205.68. US Biological Life Sciences. | Worldwide |
| (2S) ?-?1-? (2-?methylpropanoyl) ?pyrrolidine-?2-?carboxylic Acid | (2S) ?-?1-? (2-?methylpropanoyl) ?pyrrolidine-?2-?carboxylic Acid (Captopril EP Impurity E) is an impurity of Captopril (C175750), an orally active angiotensin-converting enzyme (ACE) inhibitor(1) which acts as a neuroprotective & neuroresearch product. Group: Biochemicals. Grades: Highly Purified. CAS No. 23500-15-4. Pack Sizes: 5mg, 10mg. Molecular Formula: C9H15NO3, Molecular Weight: 185.22. US Biological Life Sciences. | Worldwide |
| [2S-?[1(R*)?,?2α,?3a β,?6a β ]?]?-1-? (2-?Amino-?1-?oxopropyl) ?octahydro-?cyclopenta [b]?pyrrole-?2-?carboxylic Acid Phenylmethyl Ester Hydrochloride | [2S-?[1(R*)?,?2α,?3a β,?6a β ]?]?-1-? (2-?Amino-?1-?oxopropyl) ?octahydro-?cyclopenta [b]?pyrrole-?2-?carboxylic Acid Phenylmethyl Ester Hydrochloride is an intermediate in synthesizing Ramipril-d5 (R111002), a labelled antihypertensive. An angiotensin converting enzyme (ACE) inhibitor, converted to active, diacid metabolite. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 250mg, 500mg. Molecular Formula: C18H24N2O3; HCl. US Biological Life Sciences. | Worldwide |
| (2S,3aR,7aS)-Octahydro-1H-indole-2-carboxylic Acid Phenylmethyl Ester Hydrochloride | (2S,3aR,7aS)-Octahydro-1H-indole-2-carboxylic Acid Phenylmethyl Ester Hydrochloride is an impurity of Trandolapril (T713500) which is an antihypertensive and angiotensin converting enzyme (ACE) inhibitor. Group: Biochemicals. Grades: Highly Purified. CAS No. 145641-35-6. Pack Sizes: 50mg, 500mg. Molecular Formula: C16H22ClNO2, Molecular Weight: 295.8. US Biological Life Sciences. | Worldwide |
| (2S, 3aS, 7aS) -1- ( (2S, 3aS, 7aS) -1- ( (S) -2- ( ( (S) -1-Ethoxy-1-oxopentan-2-yl) amino) propanoyl) octahydro-1H-indole-2-carbonyl) octahydro-1H-indole-2-carboxylic Acid | (2S, 3aS, 7aS) -1- ( (2S, 3aS, 7aS) -1- ( (S) -2- ( ( (S) -1-Ethoxy-1-oxopentan-2-yl) amino) propanoyl) octahydro-1H-indole-2-carbonyl) octahydro-1H-indole-2-carboxylic Acid is an impurity of Perindopril (P287500), an angiotensin-converting enzyme (ACE) inhibitor; antihypertensive. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 100mg. Molecular Formula: C28H45N3O6, Molecular Weight: 519.669999999999. US Biological Life Sciences. | Worldwide |
| (2S,4R)-1-(tert-Butoxycarbonyl)-4-(tosyloxy)pyrrolidine-2-carboxylic Acid | (2S,4R)-1-(tert-Butoxycarbonyl)-4-(tosyloxy)pyrrolidine-2-carboxylic Acid is an intermediate in the synthesis of Fosinopril-d5 Sodium Salt (F727803), the labeled analogue of Fosinopril Sodium Salt (F727800), a phosphinic acid containing angiotensin converting enzyme (ACE) inhibitor. Antihypertensive. Group: Biochemicals. Grades: Highly Purified. CAS No. 96314-28-2. Pack Sizes: 500mg, 5g. Molecular Formula: C17H23NO7S, Molecular Weight: 385.43. US Biological Life Sciences. | Worldwide |
| (3-(1-Ethoxycarbonyl-3-cyclohexyl-(1S)-propyl)amino-2,3,4,5-tetrahydro-2-oxo-1H-1-(3S)-benzazepine-1-acetic Acid Monohydrochloride | (3-(1-Ethoxycarbonyl-3-cyclohexyl-(1S)-propyl)amino-2,3,4,5-tetrahydro-2-oxo-1H-1-(3S)-benzazepine-1-acetic Acid Monohydrochloride is a potential angiotensin converting enzyme inhibitor. A metabolite of Benazepril, which is used as an antihypertensive. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 1mg. Molecular Formula: C24H35ClN2O5, Molecular Weight: 467. US Biological Life Sciences. | Worldwide |
| 3-Amino-2,3,4,5-tetrahydro-2-oxo-1H-1-(3S)-benzazepine-1-acetic Acid Monohydrochloride | 3-Amino-2,3,4,5-tetrahydro-2-oxo-1H-1-(3S)-benzazepine-1-acetic Acid Monohydrochloride is a potential angiotensin converting enzyme inhibitor. A metabolite of Benazepril, which is used as an antihypertensive. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C12H15ClN2O3, Molecular Weight: 270.709999999999. US Biological Life Sciences. | Worldwide |
| 4-Nitrophenyl laurate | 4-Nitrophenyl laurate, a remarkable biomedicine with a captivating name, astounds the scientific realm by its stupendous potential in addressing cardiovascular afflictions, foremost among them being hypertension. Serving as an exceptionally vigorous inhibitor, this marvel counters the nefarious actions of angiotensin converting enzyme (ACE), an enzyme pivotal in the intricate orchestration of blood pressure control. Alas, its grandeur does not cease there! This exceptional compound, through its ACE inhibition, showcases the power to induce vasodilation and alleviate blood pressure concerns, a beacon of hope for individuals burdened by cardiovascular malaise. Synonyms: 4-Nitrophenyl dodecanoate. CAS No. 1956-11-2. Molecular formula: C18H27NO4. Mole weight: 321.41. | |
| (4S)-4-Cyclohexyl-L-proline Hydrochloride | It is an intermediate for the synthesis of angiotensin-converting enzyme inhibitors, e.g. Fosinopril. Group: Biochemicals. Alternative Names: trans-4-Cyclohexyl-L-proline Hydrochloride. Grades: Highly Purified. CAS No. 90657-55-9. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| 5-L-Isoleucineangiotensin II | 5-L-Isoleucineangiotensin II is an endogenous potent vasoconstrictor peptide typically generated by the removal of two residues from angiotensin I by angiotensin-converting enzyme (ACE) by binding to both the AT1 and the AT2 receptors. Uses: An endogenous potent vasoconstrictor peptide. Synonyms: 5-Isoleucine-angiotensin II; L-alpha-aspartyl-L-arginyl-L-valyl-L-tyrosyl-L-isoleucyl-L-histidyl-L-prolyl-L-phenylalanine; Angiotensin II human; Human angiotensin II; Hypertensin; H-Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-OH; Angiotensin II, 5-L-isoleucine-; Alanine, N-[1-[N-[N-[N-[N-(N2-L-α-aspartyl-L-arginyl)-L-valyl]-L-tyrosyl]-L-isoleucyl]-L-histidyl]-L-prolyl]-3-phenyl-, L-; 5-L-Isoleucine-angiotensin II; L-Phenylalanine, N-[1-[N-[N-[N-[N-(N2-L-α-aspartyl-L-arginyl)-L-valyl]-L-tyrosyl]-L-isoleucyl]-L-histidyl]-L-prolyl]-; [Ile5]-Ang II; [Ile5]-Angiotensin II; Angiotensin 2; Angiotensin II; Angiotensin II (human); Angiotensin II (mouse); Angiotensin II [Ile5]; Asp1-Ile5-angiotensin II; Human angiotensin II; Ileu5-angiotensin II; Isoleucyl5-angiotensin II. Grades: 98%. CAS No. 4474-91-3. Molecular formula: C50H71N13O12. Mole weight: 1046.19. | |
| A 58365 A | A58365 A is an enzyme inhibitor produced by Streptomyces chromofuscus A58365.1. It has the effect of inhibiting angiotensin transferase (ACE). Synonyms: 6-Indolizinepropanoic acid, 3-carboxy-1,2,3,5-tetrahydro-8-hydroxy-5-oxo-, (-)-. Grades: >98%. CAS No. 87896-52-4. Molecular formula: C12H13NO6. Mole weight: 267.23. | |
| A 58365 B | A58365 B is an enzyme inhibitor produced by Streptomyces chromofuscus A58365.1. It has the effect of inhibiting angiotensin transferase (ACE). Synonyms: 2H-Quinolizine-7-propanoic acid, 4-carboxy-1,3,4,6-tetrahydro-9-hydroxy-6-oxo-. Grades: >98%. CAS No. 87896-53-5. Molecular formula: C13H15NO6. Mole weight: 281.26. | |
| Abz-FR-K(Dnp)-P-OH | An angiotensin I-converting enzyme (ACE) substrate and an internally quenched fluorogenic substrate for real time fluorescent assay. Synonyms: H-2Abz-Phe-Arg-Lys(Dnp)-Pro-OH; N-(2-Aminobenzoyl)-L-phenylalanyl-L-arginyl-N6-(2,4-dinitrophenyl)-L-lysyl-L-proline; o-Aminobenzoic acid-FRK(Dnp)P-OH; Abz-FR-K (Dnp)-P. Grades: ≥95%. CAS No. 500799-61-1. Molecular formula: C39H49N11O10. Mole weight: 831.87. | |
| Abz-FR-K(Dnp)-P-OH acetate | An angiotensin I-converting enzyme (ACE) substrate and an internally quenched fluorogenic substrate for real time fluorescent assay. Molecular formula: C41H53N11O12. Mole weight: 891.95. | |
| Abz-LFK(Dnp)-OH trifluoroacetate salt | Abz-LFK(Dnp)-OH trifluoroacetate salt is an angiotensin-converting enzyme (ACE) fluorescent peptide substrate that binds specifically to the C domain of ACE. It has been used to investigate the development of novel antibacterial calixarene derivatives, as well as the efficacy and toxicity of antimicrobial peptide M33 as a possible antimicrobial agent for lung infections and sepsis. Synonyms: O-Aminobenzoic acid-Leu-Phe-Lys(DNP)-OH trifluoroacetate salt; Abz-Leu-Phe-Lys-DNP trifluoroacetate salt; (2-aminobenzoyl)-L-leucyl-L-phenylalanyl-N6-(2,4-dinitrophenyl)-L-lysine trifluoroacetic acid; N-(2-Aminobenzoyl)-L-leucyl-L-phenylalanyl-N6-(2,4-dinitrophenyl)-L-lysine trifluoroacetate (1:1); L-Lysine, N-(2-aminobenzoyl)-L-leucyl-L-phenylalanyl-N6-(2,4-dinitrophenyl)-, compd. with 2,2,2-trifluoroacetic acid (1:1); (2S)-2-[[(2S)-2-([(2S)-2-[(2-Aminobenzoyl)amino]-4-methylpentanoyl]amino)-3-phenylpropanoyl]amino]-6-(2,4-dinitroanilino)hexanoic acid trifluoroacetate. Grades: ≥97% by HPLC. CAS No. 1217437-31-4. Molecular formula: C34H41N7O9.C2HF3O2. Mole weight: 805.76. | |
| Abz-Ser-Pro-3-nitro-Tyr-OH | Abz-Ser-Pro-3-nitro-Tyr-OH, a selective internal quenching fluorescence (FRET) substrate for angiotensin-converting enzyme 2 (ACE2), has potential application in the high-throughput screening of ACE2 inhibitors (Km = 23 μM, kcat/Km = 3.5·104 M-1s-1). Synonyms: H-2Abz-Ser-Pro-Tyr(3-NO2)-OH; (2-aminobenzoyl)-L-seryl-L-prolyl-3-nitro-L-tyrosine; L-Tyrosine, N-(2-aminobenzoyl)-L-seryl-L-prolyl-3-nitro-. Grades: ≥95%. CAS No. 553644-01-2. Molecular formula: C24H27N5O9. Mole weight: 529.51. | |
| Acein | Acein is a high-affinity angiotensin-converting enzyme (ACE) ligand with a Kd of 2.79 nM. It potentiates NMDA+ D-serine-induced dopamine release from the striatum in vivo and striatal slices in vitro. Synonyms: L-Alanine, L-prolyl-L-prolyl-L-threonyl-L-threonyl-L-threonyl-L-lysyl-L-phenylalanyl-L-alanyl-; L-Prolyl-L-prolyl-L-threonyl-L-threonyl-L-threonyl-L-lysyl-L-phenylalanyl-L-alanyl-L-alanine; H-Pro-Pro-Thr-Thr-Thr-Lys-Phe-Ala-Ala-OH. Grades: ≥95%. CAS No. 2022202-76-0. Molecular formula: C43H68N10O13. Mole weight: 933.06. | |
| Acein acetate | Acein acetate is a high-affinity angiotensin-converting enzyme (ACE) ligand with a Kd of 2.79 nM. It potentiates NMDA+ D-serine-induced dopamine release from the striatum in vivo and striatal slices in vitro. Synonyms: H-Pro-Pro-Thr-Thr-Thr-Lys-Phe-Ala-Ala-OH.CH3CO2H; L-prolyl-L-prolyl-L-threonyl-L-threonyl-L-threonyl-L-lysyl-L-phenylalanyl-L-alanyl-L-alanine acetate. Grades: ≥95%. Molecular formula: C45H72N10O15. Mole weight: 993.11. | |
| (αR)-Hydroxy-benzenebutanoic Acid | Reactant used in the preparation of intermediates of angiotensin converting enzyme inhibitors. Group: Biochemicals. Alternative Names: D-(-)-2-Hydroxy-benzenebutanoic Acid; (2R)-2-Hydroxy-4-phenylbutanoic Acid; (2R)-2-Hydroxy-4-phenylbutanoic Acid; (R)-(-)-2-Hydroxy-4-phenylbutyric Acid; (R)-2-Hydroxy-4-phenylbutanoic Acid; (R)-2-Hydroxy-4-phenylbutyric Acid; D-(-)-Benzyllactic Acid. Grades: Highly Purified. CAS No. 29678-81-7. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Aminopeptidase N Inhibitor | Membrane alanyl aminopeptidase is also known as alanyl aminopeptidase (AAP) or aminopeptidase N (AP-N), which is an enzyme that in humans is encoded by the ANPEP gene. Aminopeptidase N (AP-N) inhibitor is a reversible inhibitor of AP-N/CD13 (IC50 = 25 μM). It is selective for AP-N/CD13 over matrix metalloproteinase-9 (MMP-9), angiotensin converting enzyme (ACE), neutral endopeptidase (NEP), γ-glutamyl transpeptidase, and the serine proteases dipeptidyl peptidase 4 (DPP-4) and cathepsin G at a concentration of 1 mM. AP-N inhibitor is non-cytotoxic to U937 cells at a concentration of 100 μM. Human aminopeptidase N is a receptor for one strain of human coronavirus that is an important cause of upper respiratory tract infections. Defects in this gene appear to be a cause of various types of leukemia or lymphoma. Synonyms: AP-N Inhibitor. Grades: ≥95%. CAS No. 596108-59-7. Molecular formula: C17H10N2O8. Mole weight: 370.27. | |
| Angiostatin | It is produced by the strain of Dihetrospora catenulata SANK 10481, D. chlamidospora SANK 12181, Verticillum viveostratosum SANK 13358. It has the function of inhibiting Angiotensin converting enzyme. Synonyms: ANGIO. CAS No. 86090-08-6. Molecular formula: C9H14N2O8. Mole weight: 278.21. | |
| Angiotensin 1/2 (5-7) acetate | The precursor angiotensinogen is cleaved by renin to form angiotensin I. Angiotensin I is hydrolyzed by angiotensin-converting enzyme (ACE) to form the biologically active angiotensin II. Angiotensin II has been investigated for the treatment, basic science, and diagnostic of Hypertension, Renin Angiotensin System, and Idiopathic Membranous Nephropathy. Molecular formula: C19H31N5O6. Mole weight: 425.49. | |
| Angiotensin Fragment 1-7 acetate | Angiotensin Fragment 1-7 is a major active component of the renin-angiotensin system (RAS), produced from cleavage of Ang II by angiotensin-converting-enzyme type 2 (ACE2). Angiotensin 1-7 inhibits purified canine ACE activity with IC50 of 0.65 μM. This peptide can be generated by the action of ACE2, a homolog of ACE, on angiotensin II or by the action of neprilysin on angiotensin I. It has been studied in the context of ameliorating the symptoms of metabolic syndrome. Synonyms: 5-L-isoleucine-1-7-angiotensin II; Ang-(1-7). Grades: ≥95%. Molecular formula: C41H62N12O11·xC2H4O2. Mole weight: 899. | |
| Angiotensin I (1-9) | Angiotensin I (1-9) is a 9-amino acid peptide formed when Angiotensin converting enzyme 2 (ACE2) hydrolyzes the carboxy-terminal leucine of Angiotensin I. It is an anti-cardiac hypertrophy drug with the functions of human metabolite, rat metabolite, antihypertensive agent and cardiac protective agent. Synonyms: H-Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-His-OH; L-alpha-aspartyl-L-arginyl-L-valyl-L-tyrosyl-L-isoleucyl-L-histidyl-L-prolyl-L-phenylalanyl-L-histidine; L-Asp-L-Arg-L-Val-L-Tyr-L-Ile-L-His-L-Pro-L-Phe-L-His. Grades: ≥95% by HPLC. CAS No. 34273-12-6. Molecular formula: C56H78N16O13. Mole weight: 1183.32. | |
| Angiotensin I human acetate salt hydrate | Angiotensin 1 (Human), an endogenous peptide substrate for angiotensin converting enzyme (ACE), is precursor to the vasoconstrictor peptide angiotensin II. Synonyms: H-Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-His-Leu-OH.CH3CO2H.H2O. CAS No. 70937-97-2. Molecular formula: C64H95N17O17. Mole weight: 1374.54. | |
| Angiotensin I (human, mouse, rat) | Angiotensin 1 (Human), an endogenous peptide substrate for angiotensin converting enzyme (ACE), is precursor to the vasoconstrictor peptide angiotensin II. Synonyms: Angiotensin 1 Human; H-Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-His-Leu-OH; L-alpha-aspartyl-L-arginyl-L-valyl-L-tyrosyl-L-isoleucyl-L-histidyl-L-prolyl-L-phenylalanyl-L-histidyl-L-leucine; Pepsitensin; Proangiotensin; 5-Ile-angiotensin I; 5-L-Isoleucine-angiotensin I. Grades: ≥95%. CAS No. 484-42-4. Molecular formula: C62H89N17O14. Mole weight: 1296.48. | |
| Angiotensin I (human, mouse, rat) | Angiotensin I (human, mouse, rat) is the precursor to the vasoconstrictor peptide angiotensin II, cleaved by the angiotensin-converting enzyme (ACE). Uses: Scientific research. Group: Peptides. CAS No. 484-42-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P1032. | |
| Angiotensin I (human, rat, mouse) trifluoroacetate salt | Angiotensin I is formed from angiotensinogen by the action of renin, which is released from the kidney juxtaglomerular cells. Angiotensin I is further cleaved to angiotensin II by angiotensin converting enzyme. Angiotensin is a protein hormone that causes blood vessels to become narrower. It helps to maintain blood pressure and fluid balance in the body. It binds to angiotensin receptors in human myometrium membrane preparations with Kd of 11.2 nM and increases renal vascular resistance in isolated rat kidney with EC50 of 10.5 nM. Grades: ≥95%. Molecular formula: C62H89N17O14·xCF3COOH. Mole weight: 1296.48. | |
| Angiotensin II (1-4), human | Angiotensin II (1-4), human is an endogenous peptide produced from ATI by angiotensin-converting-enzyme (ACE). Synonyms: H-DRVY-OH; L-alpha-aspartyl-L-arginyl-L-valyl-L-tyrosine; (S)-3-amino-4-((S)-1-((S)-1-((S)-1-carboxy-2-(4-hydroxyphenyl)ethylamino)-3-methyl-1-oxobutan-2-ylamino)-5-guanidino-1-oxopentan-2-ylamino)-4-oxobutanoic acid; L-α-Aspartyl-N5-(diaminomethylene)-L-ornithyl-L-valyl-L-tyrosine. Grades: ≥95%. CAS No. 52580-29-7. Molecular formula: C24H37N7O8. Mole weight: 551.59. | |
| Antibiotic I5B1 | It is produced by the strain of Actinomadura sp. 937ZB-1. It has an inhibitory effect on the Angiotensin I converting enzyme. Synonyms: Antibiotic K-4; I5B1; I5-B1; L-Phenylalaninamide, N-methyl-L-valyl-N-(2-(4-hydroxyphenyl)-1-phosphonoethyl)-, (R)-; Nα-[(1R)-2-(4-Hydroxyphenyl)-1-phosphonoethyl]-N-[(2S)-3-methyl-2-(methylamino)butanoyl]-L-phenylalaninamide; K-4. CAS No. 84890-90-4. Molecular formula: C23H32N3O6P. Mole weight: 477.49. | |
| Antibiotic I5B2 | It is produced by the strain of Actinomadura sp. 937ZB-1. It has an inhibitory effect on the Angiotensin I converting enzyme. Synonyms: I5B2; (1-((S)-N-((S)-1-Amino-3-(4-Hydroxyphenyl)-1-Oxopropan-2-yl)-3-Methyl-2-(methylamino)Butanamido)-2-(4-Hydroxyphenyl)Ethyl)Phosphonic Acid; L-Tyrosinamide, N-methyl-L-valyl-N-[2-(4-hydroxyphenyl)-1-phosphonoethyl]-. CAS No. 93768-49-1. Molecular formula: C23H32N3O7P. Mole weight: 493.49. | |
| aryl-sulfate sulfotransferase | The enzyme, characterized from bacteria that colonize the human and mouse intestine, catalyses the transfer of a sulfate group from a phenol sulfate ester to other phenolic compounds. Activity is enhanced by Mg2+ and Mn2+. Unlike EC 2.8.2.9, tyrosine-ester sulfotransferase and EC 2.8.2.1, aryl sulfotransferase, the enzyme does not act on 3'-phosphoadenylyl sulfate or adenosine 3',5'-bisphosphate.The level of sulfation of polyphenols depends on the positions of the hydroxyl groups. Hydroxy groups of tyrosine residues in peptides such as angiotensin can also act as acceptors. The reaction proceeds according to a ping pong bi bi mechanism. Group: Enzymes. Synonyms: arylsulfate-phenol sulfotransferase; arylsulfotransferase; ASST; arylsulfate sulfotransferase; arylsulfate:phenol sulfotransferase; astA (gene name). Enzyme Commission Number: EC 2.8.2.22. CAS No. 158254-86-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3381; aryl-sulfate sulfotransferase; EC 2.8.2.22; 158254-86-5; arylsulfate-phenol sulfotransferase; arylsulfotransferase; ASST; arylsulfate sulfotransferase; arylsulfate:phenol sulfotransferase; astA (gene name). Cat No: EXWM-3381. | |
| Benazepril | Benazepril, an angiotensin converting enzyme inhibitor, is a medication used to treat high blood pressure (hypertension), congestive heart failure, and chronic renal failure. It is converted into its active form benazeprilat, a non-sulfhydryl angiotensin-converting enzyme (ACE) inhibitor upon cleavage of its ester group by the liver. Synonyms: 1H-1-Benzazepine-1-acetic acid, 3-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-, (3S)-; (3S)-3-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetic acid; 1H-1-Benzazepine-1-acetic acid, 3-[[1-(ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-, [S-(R*,R*)]-; Benapril; Briem; Cibacen; Cibacen WS; Cibacene; 2-((S)-3-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-1-yl)acetic acid. Grades: >98%. CAS No. 86541-75-5. Molecular formula: C24H28N2O5. Mole weight: 424.49. | |
| Benazepril | Benazepril (CGS14824A free base) is an orally active angiotensin-converting enzyme ( ACE ) inhibitor to reduce angiotensin-II production. Benazepril inhibits oxidative stress and inhibits apoptosis by the PI3K/Akt signaling pathway. Benazepril improves diabetic nephropathy and decreases proteinuria. Benazepril can be used in the study of hypertension, heart failure and diabetic nephropathy [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: CGS14824A free base. CAS No. 86541-75-5. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0093. | |
| Benazeprilat | Benazeprilat is the active metabolite of benazepril, formed after cleavage of the ester group. It is a potent inhibitor of angiotensin-converting enzyme (ACE). Synonyms: (3S)-3-[[(1S)-1-Carboxy-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetic Acid; Benazepril Related Compound C. Grades: > 95%. CAS No. 86541-78-8. Molecular formula: C22H24N2O5. Mole weight: 396.45. | |
| Benazepril-d5 Hydrochloride | Benazepril-d5 Hydrochloride is the labeled analogue of Benazepril Hydrochloride (B119750), which is used as an antihypertensive; angiotensin converting enzyme inhibitor. Group: Biochemicals. Grades: Highly Purified. CAS No. 1279026-26-4. Pack Sizes: 1mg. Molecular Formula: C24H24D5ClN2O5. US Biological Life Sciences. | Worldwide |
| Benazepril HCl | Angiotensin-converting enzyme inhibitor; anti-hypertensive. Group: Biochemicals. Alternative Names: (3S)-3-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetic Acid hydrochloride; Benapril; Benazepril; Briem; Cibacen; Cibacen WS; Cibacene; Lotensin; [S-(R*,R*)]-3-[[1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetic Acid. Grades: Highly Purified. CAS No. 86541-75-5. Pack Sizes: 1g, 2g, 5g. Molecular Formula: C??H??N?O? HCl, Molecular Weight: 460.95. US Biological Life Sciences. | Worldwide |
| Benazepril hydrochloride | Benazepril (CGS14824A) hydrochloride is an orally active angiotensin-converting enzyme ( ACE ) inhibitor to reduce angiotensin-II production. Benazepril hydrochloride inhibits oxidative stress and inhibits apoptosis by the PI3K/Akt signaling pathway. In addition, Benazepril hydrochloride improves diabetic nephropathy and decreases proteinuria. Benazepril hydrochloride can be used in the study of hypertension, heart failure and diabetic nephropathy [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CGS14824A. CAS No. 86541-74-4. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0093A. | |
| Benazepril Hydrochloride (Lotensin) | Used as an antihypertensive; angiotensin converting enzyme inhibitor. Group: Biochemicals. Alternative Names: (3S)-3-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetic Acid Hydrochloride; Lotensin. Grades: Highly Purified. CAS No. 86541-74-4. Pack Sizes: 250mg, 500mg, 1g. Molecular Formula: C??H??ClN?O?, Molecular Weight: 460.95. US Biological Life Sciences. | Worldwide |
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