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| Product | Description | |
|---|---|---|
| Bestatin | Bestatin is a natural, broad-spectrum, and competitive CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase inhibitor. Bestatin has anticancer effects [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Ubenimex. CAS No. 58970-76-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0134. |  |
| Bestatin | Bestatin is a specific aminopeptidase B inhibitor produced by Streptomyces olivoreticuli. Bestatin is a potent aminopeptidase-B and leukotriene (LT) A4 hydrolase inhibitor used in the treatment of acute myelocytic leukemia. It exhibits potential immunomodulatory and antitumor activities. Uses: The treatment of acute myelocytic leukemia. Synonyms: Ubenimex. Grades: >98%. CAS No. 58970-76-6. Molecular formula: C16H24N2O4. Mole weight: 308.37. |  |
| Bestatin | Bestatin is "pseudo"-dipeptide isolated from Streptomyces olivreticuli in 1976. Bestatin is potent aminopeptidase B inhibitor with no carboxypeptidase activity. Bestatin acts as an immunomodulator by activation of macrophages and T-lymphocytes. Bestatin also exhibits good antitumor activity and is under clinical investigation. Group: Biochemicals. Grades: Highly Purified. CAS No. 58970-76-6. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| Bestatin-d7 | Bestatin-d7 is the isotope labelled analog of Bestatin. Bestatin based inhibitors have novel binding mode in S1 pocket of essential malaria M1 metalloaminopeptidase. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C16H17D7N2O4, Molecular Weight: 315.42. US Biological Life Sciences. | Worldwide |
| Bestatin hydrochloride | Bestatin hydrochloride is a competitive aminopeptidase inhibitor, which is studied for use in the treatment of acute myelocytic leukemia. It has become a useful tool in elucidating the physiological role of some mammalian exopeptidases in the regulation of the immune system, in the growth of tumors and their invasion of surrounding tissues, and in the degradation of cellular proteins. Synonyms: Aminopeptidase inhibitor; leucine aminopeptidase; aminopeptidase B; NK-421. Grades: >98%. CAS No. 65391-42-6. Molecular formula: C16H24N2O4.HCl. Mole weight: 344.83. | |
| Bestatin hydrochloride | Bestatin hydrochloride is an inhibitor of CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase , used for cancer research. Uses: Scientific research. Group: Natural products. Alternative Names: Ubenimex hydrochloride. CAS No. 65391-42-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0134A. | |
| Bestatin Impurity 1 | Bestatin Impurity 1. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C16H19D5N2O4. Mole Weight: 313.41. Catalog: APB11450. |  |
| Bestatin trifluoroacetate | Bestatin, also known as Ubenimex (INN), is a competitive protease inhibitor. It is an inhibitor of aminopeptidase B, leukotriene A4 hydrolase, aminopeptidase N. It is being studied for use in the treatment of acute myelocytic leukemia. Bestatin can be administered, with low toxicity, to cultured cells, intact animals and humans. It has become a useful tool in elucidating the physiological role of some mammalian exopeptidases in the regulation of the immune system, in the growth of tumors and their invasion of surrounding tissues, and in the degradation of cellular proteins. Synonyms: Ubenimex trifluoroacetate. Grades: >98%. CAS No. 223763-80-2. Molecular formula: C18H25F3N2O6. Mole weight: 422.4. | |
| (2S,3R)-3-Amino-2-hydroxy-4-phenylbutanoic Acid | (2S,3R)-3-Amino-2-hydroxy-4-phenylbutanoic acid is a component of a renin inhibitor and bestatin. Group: Biochemicals. Grades: Highly Purified. CAS No. 59554-14-2. Pack Sizes: 50mg, 100mg. Molecular Formula: C10H13NO3, Molecular Weight: 195.22. US Biological Life Sciences. | Worldwide |
| (2S,3R)-3-Amino-2-hydroxy-4-phenylbutanoic acid-d7 | (2S,3R)-3-Amino-2-hydroxy-4-phenylbutanoic acid-d7 is labelled (2S,3R)-3-Amino-2-hydroxy-4-phenylbutanoic acid which is a component of a renin inhibitor and bestatin. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C10H6D7NO3, Molecular Weight: 202.26. US Biological Life Sciences. | Worldwide |
| Arphamenine B | Arphamenine B is a specific inhibitor of aminopeptidase B, which is first isolated from bacteria. Arphamenine B shares the same properties as the aminopeptidase inhibitors bestatin and amastatin, both of which enhance the immune response. Synonyms: Benzenepropanoic acid, α-[(3S)-3-amino-6-[(aminoiminomethyl)amino]-2-oxohexyl]-4-hydroxy-, (αR)-; (αR)-α-[(3S)-3-Amino-6-[(aminoiminomethyl)amino]-2-oxohexyl]-4-hydroxybenzenepropanoic acid; Benzenepropanoic acid, α-[3-amino-6-[(aminoiminomethyl)amino]-2-oxohexyl]-4-hydroxy-, [S-(R*,S*)]-; Arphamenin B. Grades: 95%. CAS No. 103900-19-2. Molecular formula: C16H24N4O4. Mole weight: 336.39. | |
| Arphamenine B hemisulfate | Arphamenine B is a specific inhibitor of aminopeptidase B, which is first isolated from bacteria. Arphamenine B Hemisulfate is the hemisulfate form. Arphamenine B share the same property with aminopeptidase inhibitors bestatin and amastatin, they all enhance imune responses. Synonyms: Benzenepropanoic acid, α-[(3S)-3-amino-6-[(aminoiminomethyl)amino]-2-oxohexyl]-4-hydroxy-, (αR)-, sulfate (2:1) (salt); Benzenepropanoic acid, α-[3-amino-6-[(aminoiminomethyl)amino]-2-oxohexyl]-4-hydroxy-, monohydrochloride, [S-(R*,S*)]-, sulfate (2:1) (salt); Arphamenine B sulfate; (αR)-α-[(3S)-3-Amino-6-[(aminoiminomethyl)amino]-2-oxohexyl]-4-hydroxybenzenepropanoic acid, sulfate (2:1) (salt). Grades: ≥95%. CAS No. 144110-38-3. Molecular formula: C16H24N4O4·1/2H2SO4. Mole weight: 385.43. | |
| ATRA-hydroxyimino | ATRA-hydroxyimino (CRABP-II ligand 1), the Retinoic acid (ATRA)-based moiety, binds to cIAP1 ligand (Bestatin) via a linker to form SNIPER to degrade CRABP-II in IMR-32 cells. Synonyms: ATRA-hydroxyimino; CRABP-II ligand 1. CAS No. 135325-47-2. Molecular formula: C20H27NO3. Mole weight: 329.43. | |
| cytosol nonspecific dipeptidase | A zinc enzyme with broad specificity, varying somewhat with source species. Activated and stabilized by dithiothreitol and Mn2+. Inhibited by bestatin and leucine. Group: Enzymes. Synonyms: N2-β-alanylarginine dipeptidase; glycyl-glycine dipeptidase; glycyl-leucine dipeptidase; iminodipeptidase; peptidase A; Pro-X dipeptidase; prolinase; prolyl dipeptidase; prolylglycine dipeptidase; iminodipeptidase; prolinase; L-prolylglycine dipe. Enzyme Commission Number: EC 3.4.13.18. CAS No. 9025-31-4. 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-4032; cytosol nonspecific dipeptidase; EC 3.4.13.18; 9025-31-4; N2-β-alanylarginine dipeptidase; glycyl-glycine dipeptidase; glycyl-leucine dipeptidase; iminodipeptidase; peptidase A; Pro-X dipeptidase; prolinase; prolyl dipeptidase; prolylglycine dipeptidase; iminodipeptidase; prolinase; L-prolylglycine dipeptidase; prolylglycine dipeptidase; diglycinase; Gly-Leu hydrolase; glycyl-L-leucine dipeptidase; glycyl-L-leucine hydrolase; glycyl-L-leucine peptidase; L-amino-acyl-L-amino-acid hydrolase; glycylleucine peptidase; glycylleucine hydrolase; glycylleucine dipeptide hydrolase; non-specific dipeptidase; human cytosolic non-specific dipeptidase; glycyl-L-leucine hydrolase; glycyl-glycine dipeptidase. Cat No: EXWM-4032. |  |
| membrane dipeptidase | A membrane-bound, zinc enzyme with broad specificity. Abundant in the kidney cortex. Inhibited by bestatin and cilastatin. Type example of peptidase family M19. Group: Enzymes. Synonyms: renal dipeptidase; dehydropeptidase I (DPH I); dipeptidase (ambiguous); aminodipeptidase; dipeptide hydrolase (ambiguous); dipeptidyl hydrolase (ambiguous); nonspecific dipeptidase; glycosyl-phosphatidylinositol-anchored renal dipeptidase; MDP. Enzyme Commission Number: EC 3.4.13.19. CAS No. 9031-99-6. 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-4033; membrane dipeptidase; EC 3.4.13.19; 9031-99-6; renal dipeptidase; dehydropeptidase I (DPH I); dipeptidase (ambiguous); aminodipeptidase; dipeptide hydrolase (ambiguous); dipeptidyl hydrolase (ambiguous); nonspecific dipeptidase; glycosyl-phosphatidylinositol-anchored renal dipeptidase; MDP. Cat No: EXWM-4033. | |
| nardilysin | Enzyme of 133 kDa from rat brain and testis. A homologue of pitrilysin containing the His-Phe-Leu-Glu-His zinc-binding sequence, and a highly acidic stretch of 71 residues. Unusually for a metalloendopeptidase, inhibited by bestatin, amastatin and N-ethylmaleimide. In peptidase family M16 (pitrilysin family). Group: Enzymes. Synonyms: N-arginine dibasic convertase; NRD-convertase. Enzyme Commission Number: EC 3.4.24.61. CAS No. 292850-69-2. 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-4344; nardilysin; EC 3.4.24.61; 292850-69-2; N-arginine dibasic convertase; NRD-convertase. Cat No: EXWM-4344. | |
| Native Aeromonas proteolytica Aminopeptidase | Aminopeptidase from Aeromonas proteolytica is a metalloenzyme, which contains 2 atoms of Zn2+ in a single polypeptide with an approximate molecular weight of 29.5 kDa as determined by sedimentation. This enzyme has a high degree of stability, being stable even at tempeRatures of 70°C for several hours. Partial inactivation occurs in 8 M urea. Maximum stability and activity are between pH 8.0-8.5. Aminopeptidase from Aeromonas proteolytica can function as an esterase. Applications: Aminopeptidases are a family of widely distributed proteases, which may be used to study many significant biological processes such as protein maturation, hormone production, and peptide digestion. the enzyme has been used to measure the kinetic rate constant for the binding of bestatin, a general protease inhibitor, to aminopeptidase. Group: Enzymes. Synonyms: Aminopeptidase; 37288-67-8; EC 3.4.11.10; Aeromonas proteolytica aminopeptidase. Enzyme Commission Number: EC 3.4.11.10. CAS No. 37288-67-8. Aminopeptidase. Storage: -20°C. Form: lyophilized powder, 50-150 units/mg protein. Source: Aeromonas proteolytica. Aminopeptidase; 37288-67-8; EC 3.4.11.10; Aeromonas proteolytica aminopeptidase. Cat No: NATE-0071. | |
| Native Porcine Aminopeptidase M | Native amino peptidase M from porcine kidney. Metalloprotease that hydrolyzes N-terminal amino acids from almost all unsubstituted oligopeptides. Does not cleave X-Pro bonds or N-blocked amino acids. Useful in peptide sequencing. Inhibited by EDTA, bestatin, and amastatin. Group: Enzymes. Synonyms: Aminopeptidase M. Enzyme Commission Number: EC 3.4.11.2. CAS No. 9054-63-1. Aminopeptidase M. Activity: > 50 units/ml. Stability: Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 4 months at -20°C. Appearance: White crystalline suspension. Storage: 2 - 8°C. Source: Porcine kidney. Species: Porcine. Aminopeptidase M. Cat No: NATE-1912. | |
| Ubenimex | Ubenimex (INN), also known more commonly as bestatin, is a competitive, reversible protease inhibitor. It is an inhibitor of arginyl aminopeptidase (aminopeptidase B), leukotriene A4 hydrolase (a zinc metalloprotease that displays both epoxide hydrolase and aminopeptidase activities), alanyl aminopeptidase (aminopeptidase M/N), leucyl/cystinyl aminopeptidase (oxytocinase/vasopressinase), and membrane dipeptidase (leukotriene D4 hydrolase). It is being studied for use in the treatment of acute myelocytic leukemia. It is derived from Streptomyces olivoreticuli. Ubenimex has been found to inhibit the enzymatic degradation of oxytocin, vasopressin, enkephalins, and various other peptides and compounds. Alternative Names: 3-(r)-amino-2-(s)-hydroxy-4-phenylbutanoyl-(s)-leucine;n-(3-amino-2-hydroxy-1-oxo-4-phenylbutyl)-,(s-(r*,s*))-l-leucin;nk421;UBENIMEX;N-[(2S,3R)-3-AMINO-2-HYDROXY-1-OXO-4-PHENYLBUTYL]-L-LEUCINE;N-((2S,3R)-3-AMINO-2-HYDROXY-4-PHENYLBUTYRYL)-L-LEUCINE;[(2S,3R)-3-AMINO-2-HYDROXY-4-PHENYLBUTYRYL]-L-LEUCINE;[(2S,3R)-3-AMINO-2-HYDROXY-4-PHENYLBUTANOYL]-LEU. CAS No. 58970-76-6. Molecular formula: C16H24N2O4. Mole weight: 308.37. Appearance: White crystalline powder. Purity: 0.99. IUPACName: (2S)-2-[[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanoyl]amino]-4-methylpentanoicacid. Canonical SMILES: CC (C)CC (C (=O)O)NC (=O)C (C (CC1=CC=CC=C1)N)O. Density: 1.197 g/cm³. ECNumber: 261-529-2. Catalog: ACM58970766. |  |
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