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| Product | Description | |
|---|---|---|
| Hippuric acid | 100g Pack Size. Group: Amino Acids, Analytical Reagents, Biochemicals, Building Blocks, Diagnostic Raw Materials. Formula: C9H9NO3. CAS No. 495-69-2. Prepack ID 24771195-100g. Molecular Weight 179.17. See USA prepack pricing. |  |
| Hippuric acid | 1kg Pack Size. Group: Amino Acids, Analytical Reagents, Biochemicals, Building Blocks, Diagnostic Raw Materials. Formula: C9H9NO3. CAS No. 495-69-2. Prepack ID 24771195-1kg. Molecular Weight 179.17. See USA prepack pricing. | |
| Hippuric acid | Hippuric Acid is an orally active metabolite. Hippuric Acid can be produced by intestinal microorganisms from the metabolism of polyphenols, benzoic acid. Hippuric Acid decreases NRF2 , MMP9 and leads to ROS accumulation. Hippuric Acid activates TGFβ/SMAD signaling. Hippuric Acid improves hyperuricemia and colitis. Hippuric Acid can also be used in cardiovascular disease research [1] [2] [3] [4]. [5] [6] [7] [8] [9]. Uses: Scientific research. Group: Natural products. Alternative Names: Benzoylglycine. CAS No. 495-69-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g. Product ID: HY-W016562. |  |
| Hippuric acid | Hippuric acid. Uses: For analytical and research use. Group: Impurity standards. CAS No. 495-69-2. Molecular Formula: C9H9NO3. Mole Weight: 179.18. Catalog: APB495692. |  |
| Hippuric Acid | N-Benzoylglycine also known as Hippuric Acid is the glycine conjugate of benzoic acid commonly found in ruminant urine. Hippuric acid is synthesized in the liver and its production is greatly increased following consumption of benzoic acid. In itself it does not have a direct biological function, however p-hydroxy-hippurica acid can be used as an inhibitor of Ca2+ ATPase. Group: Biochemicals. Grades: Highly Purified. CAS No. 495-69-2. Pack Sizes: 1g, 10g, 100g, 500g. Molecular Formula: C?H?NO?. US Biological Life Sciences. |  Worldwide |
| Hippuric Acid | Synonyms: N-Benzoylglycine; 2-(Benzoylamino)acetic Acid; (Benzoylamino)-acetic Acid; Benzamidoacetic Acid; Benzoyl Glycocoll; Benzoylglycine; NSC 9982; Phenylcarbonylaminoacetic Acid; Bz-Gly-OH; N-(phenylcarbonyl)glycine. Grades: ≥95%. CAS No. 495-69-2. Molecular formula: C9H9NO3. Mole weight: 179.17. |  |
| Hippuric acid 99+% | Hippuric acid 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100g, 250g, 1Kg, 5Kg, 10Kg. US Biological Life Sciences. | Worldwide |
| Hippuric Acid-d5 | Labeled Hippuric Acid. N-Benzoylglycine also known as Hippuric Acid is the glycine conjugate of benzoic acid commonly found in ruminant urine. Hippuric acid is synthesized in the liver and its production is greatly increased following consumption of benzoic acid. In itself it does not have a direct biological function, however p-hydroxy-hippurica acid can be used as an inhibitor of Ca2+ ATPase. Group: Biochemicals. Alternative Names: N-(Benzoyl-d5)glycine; 2-(Benzoylamino)acetic Acid-d5; 2-Benzamidoacetic Acid-d5; (Benzoylamino)acetic Acid-d5; Benzamidoacetic Acid-d5; Benzoyl-d5 Glycocoll; (Benzoyl-d5)glycine; NSC 9982-d5; Phenyl carbonyl aminoacetic Acid-d5. Grades: Highly Purified. CAS No. 53518-98-2. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Hippuric acid sodium salt | 100g Pack Size. Group: Amino Acids, Analytical Reagents, Biochemicals, Phenols. Formula: C9H8NNaO3. CAS No. 532-94-5. Prepack ID 56699544-100g. Molecular Weight 201.16. See USA prepack pricing. | |
| Hippuric acid sodium salt | Hippuric acid sodium salt. Group: Biochemicals. Alternative Names: N-Benzoylglycine sodium salt; Benzoylaminoacetic acid sodium salt. Grades: Highly Purified. CAS No. 532-94-5. Pack Sizes: 100g, 250g, 500g, 1kg. US Biological Life Sciences. | Worldwide |
| Hippuric acid sodium salt 99+% | Hippuric acid sodium salt 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| Hippuric acid (Standard) | Hippuric acid (Standard) is the analytical standard of Hippuric acid. This product is intended for research and analytical applications. Hippuric Acid is an orally active metabolite. Hippuric Acid can be produced by intestinal microorganisms from the metabolism of polyphenols, benzoic acid. Hippuric Acid decreases NRF2 , MMP9 and leads to ROS accumulation. Hippuric Acid activates TGFβ/SMAD signaling. Hippuric Acid improves hyperuricemia and colitis. Hippuric Acid can also be used in cardiovascular disease research [1] [2] [3] [4]. [5] [6] [7] [8] [9]. Uses: Scientific research. Group: Natural products. CAS No. 495-69-2. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-W016562R. | |
| 2-Chloro Hippuric Acid | 2-Chlorohippuric Acid is an N-benzoyl derivative with anticonvulsant and cardiotonic activity. 2-Chlorohippuric Acid is a metabolite of Isoprophenamine and Ticlopidine. Group: Biochemicals. Alternative Names: (2-Chlorobenzoylamino) acetic Acid; N-(2-Chlorobenzoyl)glycine; N-(o-Chlorobenzoyl)glycine; o-Chlorobenzoylglycine; o-Chlorohippuric Acid. Grades: Highly Purified. CAS No. 16555-60-5. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 2-Chloro Hippuric Acid-d3 | 2-Chlorohippuric Acid is an N-benzoyl derivative with anticonvulsant and cardiotonic activity. 2-Chlorohippuric Acid is a metabolite of Isoprophenamine and Ticlopidine. Group: Biochemicals. Alternative Names: (2-Chlorobenzoylamino) acetic Acid-d3; N-(2-Chlorobenzoyl)glycine-d3; N-(o-Chlorobenzoyl)glycine-d3; o-Chlorobenzoylglycine-d3; o-Chlorohippuric Acid-d3. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| 2-Hydroxy hippuric acid | 2-Hydroxy hippuric acid. Group: Biochemicals. Alternative Names: N- (2-Hydroxybenzoyl) glycine; o-Hydroxy-hippuric acid; Salicyluric acid. Grades: Highly Purified. CAS No. 487-54-7. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C9H9NO4. US Biological Life Sciences. | Worldwide |
| 2-Hydroxy hippuric acid-13C2,15N | 13C Labeled Compounds. Alternative Names: N-(2-Hydroxybenzoyl)glycine-13C2,15N; o-Hydroxy-hippuric Acid; Salicyluric Acid-13C2,15N; (2-Hydroxybenzoyl)glycine-13C2,15N; 2-Hydroxyhippuric Acid-13C2,15N; NSC 524135-13C2,15N; Salicyloylglycine-13C2,15N; o-Hydroxyhippuric Acid-13C2,15N. CAS No. 1286521-95-6. Molecular formula: C713C2H915NO4. Mole weight: 198.15. Catalog: ACM1286521956. |  |
| 2-Hydroxy Hippuric Acid-13C2,15N | Metabolite of Salicylic Acid. Group: Biochemicals. Alternative Names: N-(2-Hydroxybenzoyl)glycine-13C2,15N; o-Hydroxy-hippuric Acid; Salicyluric Acid-13C2,15N; (2-Hydroxybenzoyl)glycine-13C2,15N; 2-Hydroxyhippuric Acid-13C2,15N; NSC 524135-13C2,15N; Salicyloylglycine-13C2,15N; o-Hydroxyhippuric Acid-13C2,15N. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 2-Methyl hippuric acid | 2-Methyl hippuric acid. Group: Biochemicals. Alternative Names: N-(2-Methylbenzoyl)glycine; NSC 163983; o-Methylhippuric acid. Grades: Highly Purified. CAS No. 42013-20-7. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C10H11NO3. US Biological Life Sciences. | Worldwide |
| 3-Methylhippuric acid | Α substituted hippurate analog as a substrate and inhibitor of peptidylglycine α-hydroxylating monooxygenase (PHM). Synonyms: [(3-Methylbenzoyl)amino]acetic acidm-Toluric acid; N-(3-Methylbenzoyl)glycine. Grades: > 98.0 % (T). CAS No. 27115-49-7. Molecular formula: C10H11NO3. Mole weight: 193.20. | |
| 3-Methyl Hippuric Acid | Α substituted hippurate analog as substrates and inhibitor of peptidylglycine α-hydroxylating monooxygenase (PHM). Group: Biochemicals. Alternative Names: N-(3-Methylbenzoyl)glycine. Grades: Highly Purified. CAS No. 27115-49-7. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 4-Aminohippuric Acid | 4-Aminohippuric Acid. Group: Biochemicals. Alternative Names: N-(4-Aminobenzoyl)-glycine; p-Amino-hippuric Acid; (4-Aminobenzoylamino) acetic Acid; (p-Aminobenzoyl)glycine; 2-[ (4-Aminobenzoyl) amino]acetic Acid; 4-Aminobenzoylglycine; 4-Aminohippuric Acid; N- (4-Aminobenzoyl) aminoacetic Acid; N-(4-Aminobenzoyl)glycine; N-(p-Aminobenzoyl)glycine; NSC 13064; NSC 7550; PAH; PAH (amino acid); p-Aminohippuric Acid. Grades: Highly Purified. CAS No. 61-78-9. Pack Sizes: 10g. Molecular Formula: C9H10N2O3, Molecular Weight: 194.19. US Biological Life Sciences. | Worldwide |
| 4-Aminohippuric-d4 Acid | 4-Aminohippuric-d4 Acid. Group: Biochemicals. Alternative Names: N-(4-Aminobenzoyl)glycine-d4; p-Amino-hippuric-d4 Acid; (4-Aminobenzoylamino) acetic-d4 Acid; (p-Aminobenzoyl)glycine-d4; 2-[ (4-Aminobenzoyl) amino]acetic-d4 Acid; 4-Aminobenzoylglycine-d4; 4-Aminohippuric-d4 Acid; N- (4-Aminobenzoyl) aminoacetic-d4 Acid; N-(4-Aminobenzoyl)glycine-d4; N-(p-Aminobenzoyl)glycine-d4; NSC 13064-d4; NSC 7550-d4; PAH-d4; PAH (Amino Acid)-d4; p-Aminohippuric-d4 Acid. Grades: Highly Purified. CAS No. 1219805-41-0. Pack Sizes: 2.5mg. Molecular Formula: C9H6D4N2O3, Molecular Weight: 198.21. US Biological Life Sciences. | Worldwide |
| 4-Methylhippuric acid | A substituted hippurate analog as a substrate and inhibitor of peptidylglycine α-hydroxylating monooxygenase (PHM). Synonyms: [(4-Methylbenzoyl)amino]acetic acid; N-(p-Toluoyl)glycinep-Toluric acid. Grades: > 98.0 % (HPLC) (T). CAS No. 27115-50-0. Molecular formula: C10H11NO3. Mole weight: 193.20. | |
| 4-Methyl Hippuric Acid | A substituted hippurate analog as substrate and inhibitor of peptidylglycine α-hydroxylating monooxygenase (PHM). Group: Biochemicals. Alternative Names: N-(4-Methylbenzoyl)glycine; N-(p-Methylbenzoyl)glycine; NSC 126814; p-Methylhippuric Acid; p-Toluric Acid. Grades: Highly Purified. CAS No. 27115-50-0. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Glycine, N-Benzoyl (Hippuric acid ) (Ring-13C6) | Isotope-labeled Amino Acids13C Labeled Compounds. Alternative Names: Hippuric acid-13C6. CAS No. 1163160-18-6. Molecular formula: 13C6C3H9NO3. Appearance: White powder. IUPACName: 2- ( (1, 5, 6-13C3) cyclohexatrienecarbonylamino) acetic acid. Canonical SMILES: C1=C[13C] (=[13CH][13CH]=C1)[13C] (=O)N[13CH2][13C] (=O)O. Catalog: ACM1163160186. | |
| m-Chloro Hippuric Acid | m-Chloro Hippuric Acid. Group: Biochemicals. Alternative Names: (3-Chlorobenzoylamino) acetic Acid; N-(3-Chlorobenzoyl)glycine; NSC 201882; m-Chlorohippuric Acid; N-(3-Chlorobenzoyl)glycine. Grades: Highly Purified. CAS No. 57728-59-3. Pack Sizes: 1g. Molecular Formula: C9H8ClNO3, Molecular Weight: 218.62. US Biological Life Sciences. | Worldwide |
| m-Chloro Hippuric Acid-d2,15N | m-Chloro Hippuric Acid-d2,15N. Group: Biochemicals. Alternative Names: (3-Chlorobenzoylamino) acetic Acid-d2,15N; N-(3-Chlorobenzoyl)glycine-d2,15N; NSC 201882-d2,15N; m-Chlorohippuric Acid-d2,15N; N-(3-Chlorobenzoyl)glycine-d2,15N. Grades: Highly Purified. Pack Sizes: 2.5mg. Molecular Formula: C9H6D2Cl15NO3, Molecular Weight: 216.62. US Biological Life Sciences. | Worldwide |
| Acylase I from Aspergillus sp., Immobilized on Eupergit C | In enzymology, an aminoacylase (EC 3.5.1.14) is an enzyme that catalyzes the chemical reaction:N-acyl-L-amino acid + H2O<-> carboxylate + L-amino acid. Thus, the two substRates of this enzyme are N-acyl-L-amino acid and H2O, whereas its two products are carboxylate and L-amino acid. This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. This enzyme participates in urea cycle and metabolism of amino groups. Moist pearls (dried substance ~30%, pearl diameter 50-100 μm), covalent fixation of the acylase. Group: Enzymes. Synonyms: aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α. Enzyme Commission Number: EC 3.5.1.14. CAS No. 9012-37-7. ACY1. Activity: > 50 U/g moist material. Storage: 2-8°C. Source: Aspergillus sp. aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase; EC 3.5.1.14; 9012-37-7. Cat No: NATE-0030. |  |
| AminoAcylase-1 from Human, Recombinant | Aminoacylase-1 is a cytosolic, homodimeric, zinc-binding enzyme that catalyzes the hydrolysis of acylated L-amino acids to L-amino acids and acyl group, and has been postulated to function in the catabolism and salvage of acylated amino acids. ACY1 has been assigned to chromosome 3p21.1, a region reduced to homozygosity in small-cell lung cancer (SCLC), and its expression has been reported to be reduced or undetectable in SCLC cell lines and tumors. The amino acid sequence of human aminoacylase-1 is highly homologous to the porcine counterpart, and ACY1 is the first member of a new family of zinc-binding enzymes. Acy1 recombinant human produced in e. coli is a single, non-... SDS-PAGE. ACY1. Mole weight: 48 kDa. Stability: Store at 4°C if entire vial will be used within 2-4 weeks. Store, frozen at -20°C for longer periods of time. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA). Avoid multiple freeze-thaw cycles. Appearance: Sterile Filtered clear solution. Source: E. coli. Species: Human. N-acyl-L-amino-acid amidohydrolase; ACY-1, ACY1D; ACYLASE; ACY1; aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short | |
| AminoAcylase (Industry grade) | In enzymology, an aminoacylase (EC 3.5.1.14) is an enzyme that catalyzes the chemical reaction:N-acyl-L-amino acid + H2O<-> carboxylate + L-amino acid. Thus, the two substRates of this enzyme are N-acyl-L-amino acid and H2O, whereas its two products are carboxylate and L-amino acid. This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. This enzyme participates in urea cycle and metabolism of amino groups. Group: Enzymes. Enzyme Commission Number: EC 3.5.1.14. CAS No. 9012-37-7. Purity: 0.98. ACY1. Storage: at -4-25°C, dry, dark conditions for 3 years. Form: Lyophilized powder. aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase; EC 3.5.1.14; 9012-37-7. Cat No: NATE-1620. | |
| Benzoylglycine methyl ester | Heterocyclic Organic Compound. Alternative Names: Hippurate methyl ester;Hippuric acid, methyl ester;Methyl (benzoylamino)acetate;Methyl ester of Hippuric acid;Methyl hippurate;Methyl N-benzoylglycinate;N-BENZOYLGLYCINE METHYL ESTER;BENZOYLGLYCINE METHYL ESTER. CAS No. 1205-08-9. Molecular formula: C10H11NO3. Mole weight: 193.2. Purity: 0.96. IUPACName: methyl 2-benzamidoacetate. Canonical SMILES: COC(=O)CNC(=O)C1=CC=CC=C1. Catalog: ACM1205089. | |
| Isopropyl Hippurate | Isopropyl Hippurate is the isopropyl derivative of Hippuric Acid (H356700); the glycine conjugate of benzoic acid commonly found in ruminant urine. Hippuric acid is synthesized in the liver and its production is greatly increased following consumption of benzoic acid. On itself it does not have a direct biological function, however p-hydroxy-hippuric acid can be used as an inhibitor of Ca2+ ATPase. Group: Biochemicals. Grades: Highly Purified. CAS No. 1776-56-3. Pack Sizes: 1g, 10g. Molecular Formula: C12H15NO3, Molecular Weight: 221.25. US Biological Life Sciences. | Worldwide |
| L-Aminoacylase (Crude Enzyme) | This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Synthesis; medicine. Group: Enzymes. Synonyms: aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase. Enzyme Commission Number: EC 3.5.1.14. CAS No. 9012-37-7. ACY1. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase. Pack: 100ml. Cat No: NATE-1835. | |
| Methyl hippurate | Synonyms: Methyl N-Benzoylglycinate; Methyl Benzoylaminoacetate; Methyl Benzoylglycinate; N-Benzoylglycine Methyl Ester; Bz-Gly-OMe; Glycine, N-benzoyl-, methyl ester; Hippuric acid, methyl ester; methyl 2-(phenylformamido)acetate; N-benzoyl-Glycine methyl ester. Grades: 95%. CAS No. 1205-08-9. Molecular formula: C10H11NO3. Mole weight: 193.20. | |
| N-acyl-aliphatic-L-amino acid amidohydrolase | Contains Zn2+. The enzyme is found in animals and is involved in the hydrolysis of N-acylated or N-acetylated amino acids (except L-aspartate). It acts on mercapturic acids (S-conjugates of N-acetyl-L-cysteine) and neutral aliphatic N-acyl-α-amino acids. Some bacterial aminoacylases demonstrate substrate specificity of both EC 3.5.1.14 and EC 3.5.1.114. cf. EC 3.5.1.15, aspartoacylase and EC 3.5.1.114, N-acyl-aromatic-L-amino acid amidohydrolase. Group: Enzymes. Synonyms: aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoa. Enzyme Commission Number: EC 3.5.1.14. CAS No. 9012-37-7. ACY1. 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-4403; N-acyl-aliphatic-L-amino acid amidohydrolase; EC 3.5.1.14; 9012-37-7; aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase. Cat No: EXWM-4403. | |
| Native Aspergillus genus Acylase I | In enzymology, an aminoacylase (EC 3.5.1.14) is an enzyme that catalyzes the chemical reaction:N-acyl-L-amino acid + H2O<-> carboxylate + L-amino acid. Thus, the two substRates of this enzyme are N-acyl-L-amino acid and H2O, whereas its two products are carboxylate and L-amino acid. This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. This enzyme participates in urea cycle and metabolism of amino groups. Group: Enzymes. Synonyms: aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase; EC 3.5.1.14; 9012-37-7. CAS No. 9012-37-7. ACY1. Storage: 0-10°C. Source: Aspergillus genus. aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase; EC 3.5.1.14; 9012-37-7. Cat No: NATE-1593. | |
| Native Aspergillus melleus Acylase I | In enzymology, an aminoacylase (EC 3.5.1.14) is an enzyme that catalyzes the chemical reaction:N-acyl-L-amino acid + H2O<-> carboxylate + L-amino acid. Thus, the two substRates of this enzyme are N-acyl-L-amino acid and H2O, whereas its two products are carboxylate and L-amino acid. This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. This enzyme participates in urea cycle and metabolism of amino groups. Enzyme activity: the optimum temperature is 40-45 oc, the optimum ph is 8.0 (stable form ph 6-10). the enzyme is activated by cocl2 in the range of 10-4 to 10-3 m. Group: Enzymes. Synonyms: aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; . Enzyme Commission Number: EC 3.5.1.14. CAS No. 9012-37-7. ACY1. Activity: >0.5 units/mg. Storage: 2-8°C. Form: powder. Source: Aspergillus melleus. aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase; EC 3.5.1.14; 9012-37-7. Cat No: NATE-0029. | |
| Native Porcine Acylase I | In enzymology, an aminoacylase (EC 3.5.1.14) is an enzyme that catalyzes the chemical reaction:N-acyl-L-amino acid + H2O<-> carboxylate + L-amino acid. Thus, the two substRates of this enzyme are N-acyl-L-amino acid and H2O, whereas its two products are carboxylate and L-amino acid. This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. This enzyme participates in urea cycle and metabolism of amino groups. Protein determined by biuret. Applications: Acylase i from porcine kidney has been used to study the acylase i-catalyzed deacetylation of various s-alkyl-n-acetyl-l-cysteines and their carb...ort acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase; EC 3.5.1.14; 9012-37-7. Enzyme Commission Number: EC 3.5.1.14. CAS No. 9012-37-7. ACY1. Activity: > 2,000 units/mg protein; 500-1,500 units/mg protein. Storage: -20°C. Form: lyophilized powder. Source: Porcine kidney. Species: Porcine. aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase; EC 3.5.1.14; 9012-37-7. Cat No: NATE-0031. | |
| N-Benzoyl-L-phenylalanine | N-Benzoyl-L-phenylalanine. Group: Biochemicals. Alternative Names: L-N-benzoyl-3-phenylalanine; N-Benzoyl-3-phenyl-L-alanine; (+)-N-Benzoylphenylalanine; (2S)-2-(Benzoylamino)-3-phenylpropanoic Acid; (S)-2-Benzoylamino-3-phenylpropanoic Acid; (S)-N-Benzoylphenylalanine; (S)-α-(Phenylmethyl)hippuric Acid; Benzoyl-L-phenylalanine; L-Bz-Phenylalanine; N-Benzoyl-3-phenylalanine; N-Benzoyl-L-phenylalanine; N-Benzoylphenylalanine; NSC 167264. Grades: Highly Purified. CAS No. 2566-22-5. Pack Sizes: 5g. Molecular Formula: C16H15NO3, Molecular Weight: 269.3. US Biological Life Sciences. | Worldwide |
| (Benzamido)oxy Acetic Acid | Hippurate analog. Inhibitor of peptidylglycine α-hydroxylating monooxygenase (PHM). Pesticide. Group: Biochemicals. Alternative Names: 2-[(Benzoylamino)oxy]-acetic Acid; (Benzamidooxy)acetic Acid; Benzadox; N-Benzoyl-O-(carboxymethyl)-hydroxylamine; NSC 75601; S 6173. Grades: Highly Purified. CAS No. 5251-93-4. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| (Benzamido)oxy Acetic Acid-d2 | Hippurate analog. Inhibitor of peptidylglycine α-hydroxylating monooxygenase (PHM). Pesticide. Group: Biochemicals. Alternative Names: 2-[(Benzoylamino)oxy]-acetic Acid-d2; (Benzamidooxy)acetic Acid-d2; Benzadox-d2; N-Benzoyl-O-(carboxymethyl)-hydroxylamine-d2; NSC 75601-d2; S 6173 -d2. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| hippurate hydrolase | Acts on various N-benzoylamino acids. Group: Enzymes. Enzyme Commission Number: EC 3.5.1.32. CAS No. 37278-43-6. 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-4422; hippurate hydrolase; EC 3.5.1.32; 37278-43-6. Cat No: EXWM-4422. | |
| Hippuryl-his-leu acetate | Heterocyclic Organic Compound. Alternative Names: N-Benzoyl-Gly-His-Leu, Hippuryl-His-Leu acetate salt, 103404-54-2. CAS No. 103404-54-2. Molecular formula: C21H27N5O5. Mole weight: 429.47. Purity: 0.96. IUPACName: acetic acid;(2S)-2-[[(2S)-2-[(2-benzamidoacetyl)amino]-3-(1H-imidazol-5-yl)propanoyl]amino]-4-methylpentanoic acid. Catalog: ACM103404542. | |
| Hippuryl-L-lysine | Hippuryl-L-lysine is a substrate for carboxypeptidase B and carboxypeptidase N. Synonyms: Hippuryl-Lys-OH; Bz-GK-OH; L-Lysine,N-benzoylglycyl-; (S)-6-Amino-2-(2-benzamidoacetamido)hexanoic acid. CAS No. 740-63-6. Molecular formula: C15H21N3O4. Mole weight: 307.34. | |
| Hippuryl-L-phenylalanine | Hippuryl-L-phenylalanine is used as a substrate for the determination of carboxypeptidase A and mast cell carboxypeptidase activities. Synonyms: (S)-2-(2-Benzamidoacetamido)-3-phenylpropanoic acid; Benzoyl-Gly-Phe; Hippuryl-Phe-OH; Bz-GF-OH. Grades: >99%. CAS No. 744-59-2. Molecular formula: C18H18N2O4. Mole weight: 326.36. | |
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