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| Product | Description | |
|---|---|---|
| Leucyl-lysine | Leucyl-lysine is a dipeptide composed of leucine and lysine. It is an incomplete breakdown product of protein digestion or protein catabolism. Alternative Names: L-Lysine, L-Leucyl-; (S)-6-Amino-2-((S)-2-amino-4-methylpentanamido)hexanoic acid; L-leucyl-L-lysine; H-LK-OH; Leu-Lys; L-Leu-L-Lys. Grades: ≥95%. CAS No. 6416-76-8. Molecular formula: C12H25N3O3. Mole weight: 259.35. |  |
| Leucyl-phenylalanine | Leucyl-phenylalanine belongs to the class of organic compounds known as dipeptides. Uses: Scientific research. Category: Signaling pathways. CAS No. 3063-5-6. Pack Sizes: 10 mM * 1 mL in Water; 50 mg. Product ID: HY-113278. |  |
| Leucyl-phenylalanine | Leucyl-phenylalanine is a competitive inhibitor of both the peptidase and the esterase activities of carboxy peptidase Y. Alternative Names: L-leucyl-L-Phenylalanine. CAS No. 3063-5-6. Molecular formula: C15H22N2O3. Mole weight: 278.35. | |
| Leucylproline | Leucylproline, a dipeptide, plays important roles in the medium-dependent regulation of proteinase activity[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 6403-35-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-114729. | |
| Leucyl-serine | Leucyl-serine is a dipeptide composed of leucine and serine. It is an incomplete breakdown product of protein digestion or protein catabolism. Alternative Names: L-leucyl-L-serine; H-LS-OH; Leu-Ser; N-Leucylserine; L-Leu-L-Ser; Leu-Ser-OH; N-L-leucyl-L-serine; L-Serine, L-leucyl-. Grades: ≥95% by HPLC. CAS No. 6209-12-7. Molecular formula: C9H18N2O4. Mole weight: 218.25. | |
| Leucyl-threonine | Leucyl-threonine. Alternative Names: L-leucyl-L-threonine. CAS No. 38062-82-7. Molecular formula: C10H20N2O4. Mole weight: 232.28. | |
| leucyltransferase | Also transfers phenylalanyl groups. Requires a univalent cation. Peptides and proteins containing an N-terminal arginine, lysine or histidine residue can act as acceptors. Group: Enzymes. Synonyms: leucyl, phenylalanine-tRNA-protein transferase; leucyl-phenylalanine-transfer ribonucleate-protein aminoacyltransferase; leucyl-phenylalanine-transfer ribonucleate-protein transferase; L-leucyl-tRNA:protein leucyltransferase. Enzyme Commission Number: EC 2.3.2.6. CAS No. 37257-22-0. 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-2306; leucyltransferase; EC 2.3.2.6; 37257-22-0; leucyl, phenylalanine-tRNA-protein transferase; leucyl-phenylalanine-transfer ribonucleate-protein aminoacyltransferase; leucyl-phenylalanine-transfer ribonucleate-protein transferase; L-leucyl-tRNA:protein leucyltransferase. Cat No: EXWM-2306. |  |
| Leu-D-Leu | Leu-D-Leu is a specific substrate for D-peptidase S, an intracellular carboxypeptidase-like enzyme that preferentially hydrolyzes dipeptides containing hydrophobic D-amino acids. Alternative Names: l-Leucyl-d-leucine; D-Leucine, L-leucyl-; N-L-Leucyl-D-leucine; (R)-2-((S)-2-amino-4-methylpentanamido)-4-methylpentanoic acid. CAS No. 17665-02-0. Molecular formula: C12H24N2O3. Mole weight: 244.33. | |
| Leu-Gly-Gly | Leu-Gly-Gly. Alternative Names: Leucyl-glycyl-glycine; N-(N-L-Leucylglycyl)glycine; (S)-2-(2-(2-Amino-4-methylpentanamido)acetamido)acetic acid. Grades: 95%. CAS No. 1187-50-4. Molecular formula: C10H19N3O4. Mole weight: 245.28. | |
| Leu-Gly-Gly-Gly | Leu-Gly-Gly-Gly is a tetrapeptide consisting of L-leucine and three glycine residues. L-leucine is a branched-chain amino acid critical for protein synthesis, muscle repair, and energy production. Glycine plays a role in various physiological processes, including neurotransmission and collagen synthesis. This peptide may support muscle recovery and overall metabolic functions, with L-leucine driving protein synthesis and glycine contributing to structural and functional roles in the body. Alternative Names: LGGG; Leucyl-glycyl-glycyl-glycine; L-Leucylglycylglycylglycine; H-Leu-Gly-Gly-Gly-OH; L-leucyl-glycyl-glycyl-glycine; H-LGGG-OH; Glycine, N-(N-(N-L-leucylglycyl)glycyl)-; N-(N-(N-L-Leucylglycyl)glycyl)-glycine. Grades: ≥90%. CAS No. 14857-78-4. Molecular formula: C12H22N4O5. Mole weight: 302.33. | |
| Leu-Gly-Leu-OH | Leu-Gly-Leu-OH. Alternative Names: L-Leucylglycyl-L-leucine; H2N-LGL-OH. Grades: ≥ 98% (TLC). CAS No. 19408-48-1. Molecular formula: C14H27N3O4. Mole weight: 301.39. | |
| Leu-Gly-Leu-OH | Leu-Gly-Leu-OH. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg. US Biological Life Sciences. |  Worldwide |
| Leu-Gly -naphthylamide | Leu-Gly -naphthylamide. Alternative Names: Leu-Gly beta-naphthylamide; (S)-2-Amino-4-methyl-N-(2-(naphthalen-2-ylamino)-2-oxoethyl)pentanamide. Grades: 95%. CAS No. 100930-00-5. Molecular formula: C18H23N3O2. Mole weight: 313.39. | |
| Leu-Gly-NH2 HBr | Leu-Gly-NH2 HBr. Alternative Names: L-Leucylglycine amide hydrobromide. Grades: ≥ 99% (TLC). CAS No. 28671-28-5. Molecular formula: C8H17N3O2·HBr. Mole weight: 268.15. | |
| Leu-Gly-OH | This dipeptide inhibits the ubiquitin-mediated proteolysis. Alternative Names: Leu Gly OH; L-Leucyl-glycine; (S)-2-(2-Amino-4-methylpentanamido)acetic acid. Grades: ≥ 99% (HPLC). CAS No. 686-50-0. Molecular formula: C8H16N2O3. Mole weight: 188.22. | |
| Leu-Gly-OH | Leu-Gly-OH. Group: Biochemicals. Alternative Names: L-Leucyl-glycine. Grades: Highly Purified. CAS No. 686-50-0. Pack Sizes: 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| Leu-Gly-OH hydrochloride | Leu-Gly-OH hydrochloride. Group: Biochemicals. Grades: Reagent Grade. CAS No. 686-50-0(net). Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Leu-Gly-Tyr | Leu-Gly-Tyr is a tripeptide composed of L-leucine, L-glycine, and L-tyrosine. L-leucine is a branched-chain amino acid essential for protein synthesis and muscle repair, L-glycine is a small amino acid involved in protein structure and neurotransmission, and L-tyrosine is an aromatic amino acid important for synthesizing neurotransmitters like dopamine and norepinephrine. This tripeptide may be studied for its impact on peptide stability, structure-function relationships in proteins, and potential roles in neurotransmitter-related pathways. It could also be relevant in research focused on amino acid interactions and therapeutic peptide development. Alternative Names: LGY; L-Leucylglycyl-L-tyrosine; L-Tyrosine, N-(N-L-leucylglycyl)-; Tyrosine, N-(N-L-leucylglycyl)-; H-Leu-Gly-Tyr-OH; H-LGY-OH; L-Leucyl-glycyl-L-tyrosine; Leucyl-glycyl-tyrosine. Grades: ≥90%. CAS No. 93993-14-7. Molecular formula: C17H25N3O5. Mole weight: 351.40. | |
| Leuhistin | It is produced by the strain of Bacillus laterosporus BMI 156-14F1. It inhibits aminopeptidase M with IC50 of 0.2 μg/mL. It has no antimicrobial effects (100 μg/mL). Alternative Names: Leuhistine; (2R,3S)-2-((1H-imidazol-4-yl)methyl)-3-amino-2-hydroxy-5-methylhexanoic acid; 1H-Imidazole-4-propanoic acid, alpha-(1-amino-3-methylbutyl)-alpha-hydroxy-, (R-(R*,S*))-. Grades: 95%. CAS No. 129085-76-3. Molecular formula: C11H19N3O3. Mole weight: 241.29. | |
| Leukadherin 1 | Leukadherin 1. Group: Biochemicals. Grades: Purified. CAS No. 344897-95-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Leukadherin-1 | Leukadherin-1, a specific agonist of the leukocyte surface integrin CD11b/CD18, increases CD11b/CD18-dependent cell adhesion to fibrinogen with an EC50 of 4 μM. Leukadherin-1 enhances leukocyte adhesion to ligands (such as ICAM-1) and vascular endothelium and thus reduces leukocyte transendothelial migration and influx to the injury sites. Leukadherin-1 suppresses innate inflammatory signaling[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 344897-95-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-15701. | |
| leukocyte elastase | Differs from pancreatic elastase in specificity on synthetic substrates and in inhibitor sensitivity. In peptidase family S1 (trypsin family). Formerly included in EC 3.4.21.11. Group: Enzymes. Synonyms: lysosomal elastase; neutrophil elastase; polymorphonuclear leukocyte elastase; elastase; elaszym; serine elastase; lysosomal elastase; granulocyte elastase. Enzyme Commission Number: EC 3.4.21.37. CAS No. 9004-6-2. ELA2. 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-4131; leukocyte elastase; EC 3.4.21.37; 9004-06-2; lysosomal elastase; neutrophil elastase; polymorphonuclear leukocyte elastase; elastase; elaszym; serine elastase; lysosomal elastase; granulocyte elastase. Cat No: EXWM-4131. | |
| Leukocyte Proteinase-3 (169-177) | Leukocyte Proteinase-3 (169-177) is amino acids 169 to 177 fragment of Leukocyte Proteinase-3. Proteinase-3 is a serine protease enzyme expressed mainly in neutrophil granulocytes. In human neutrophils, proteinase 3 contributes to the proteolytic generation of antimicrobial peptides. | |
| leukotriene-A4 hydrolase | This is a bifunctional zinc metalloprotease that displays both epoxide hydrolase and aminopeptidase activities. It preferentially cleaves tripeptides at an arginyl bond, with dipeptides and tetrapeptides being poorer substrates (see EC 3.4.11.6, aminopeptidase B). It also converts leukotriene A4 into leukotriene B4, unlike EC 3.3.2.10, soluble epoxide hydrolase, which converts leukotriene A4 into 5,6-dihydroxy-7,9,11,14-icosatetraenoic acid. In vertebrates, five epoxide-hydrolase enzymes have been identified to date: EC 3.3.2.6 (leukotriene A4 hydrolase), EC 3.3.2.7 (hepoxilin-epoxide hydrolase), EC 3.3.2.9 (microsomal epoxide hydrolase), EC 3.3.2.10 (soluble epoxide hydrolase) and EC 3.3.2.11 (cholesterol-5,6-oxide hydrolase). Group: Enzymes. Synonyms: LTA4 hydrolase; LTA4H; leukotriene A4 hydrolase. Enzyme Commission Number: EC 3.3.2.6. CAS No. 90119-07-6. LTA4H. 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-4003; leukotriene-A4 hydrolase; EC 3.3.2.6; 90119-07-6; LTA4 hydrolase; LTA4H; leukotriene A4 hydrolase. Cat No: EXWM-4003. | |
| Leukotriene A4 Hydrolase from Human, Recombinant | Leukotriene A4 Hydrolase human (LTA4H) is a bifunctional zinc metalloenzyme that converts LTA4 into Leukotriene B4, and also demonstrates aminopeptidase activity. Leukotriene B4 is a lipid chemoattractant that plays critical roles in inflammaton, immune responses, host defenses against infections, and lipid homeostasis. Inhibition of LTA4H in a mouse model decreases LTB4 in the airways and attenuates airway inflammation and airway hyperreactivity through modulation of T cell and dendritic cell function. Contains c-terminal his-tag. Applications: Leukotriene a4 hydrolase human (lta4h) is a drug target for anti-inflammation, and for cancer prevention and therapy. it is also suitable for screening inhibitors of leukotriene b4 synthesis. lta4h is used to study allergic asthma and airway hyperresponsiveness. Group: Enzymes. Synonyms: leukotriene-A4 hydrolase; LTA-4 hydrolase; LTA4; LTA4 hydrolase; LTA4H; leukotriene A4 hydrolase; EC 3.3.2.6; 90119-07-6. Enzyme Commission Number: EC 3.3.2.6. CAS No. 90119-07-6. LTA4H. Mole weight: mol wt ~69 kDa. Storage: -70°C. Form: Supplied as a solution in 100mM Tris, pH 8.0, containing 20% glycerol and 100mM potassium chloride. Source: E. coli. Species: Human. leukotriene-A4 hydrolase; LTA-4 hydrolase; LTA4; LTA4 hydrolase; LTA4H; leukotriene A4 hydrolase; EC 3.3.2.6; 90119-07-6. Cat No: NATE-0419. | |
| LEUKOTRIENE A5 METHYL ESTER | LEUKOTRIENE A5 METHYL ESTER. Alternative Names: leukotrieneA5methylester, 90121-06-5. CAS No. 90121-06-5. Purity: 96%. Product ID: ACM90121065-1. Molecular formula: C21H30O3. Mole weight: 330.461100 [g/mol]. IUPAC Name: methyl 4-[(2S,3S)-3-[(1E,3E,5Z,8Z,11Z)-tetradeca-1,3,5,8,11-pentaenyl]oxiran-2-yl]butanoate. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Leukotriene B4 | Leukotriene B4 (LTB4) is known as one of the most potent chemoattractants and activators of leukocytes and is involved in inflammatory diseases. Leukotriene B4 is also an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: LTB4; 5(S),12(R)-DiHETE. CAS No. 71160-24-2. Pack Sizes: 25 μg (297.2 μM * 250 μL in Ethanol). Product ID: HY-107608. | |
| leukotriene-B4 20-monooxygenase | A heme-thiolate protein (P-450). Not identical with EC 1.14.13.34, leukotriene-E4 20-monooxygenase. Group: Enzymes. Synonyms: leukotriene-B4 20-hydroxylase; leucotriene-B4 ω-hydroxylase; LTB4 20-hydroxylase; LTB4 ω-hydroxylase. Enzyme Commission Number: EC 1.14.13.30. CAS No. 90119-11-2. 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-0837; leukotriene-B4 20-monooxygenase; EC 1.14.13.30; 90119-11-2; leukotriene-B4 20-hydroxylase; leucotriene-B4 ω-hydroxylase; LTB4 20-hydroxylase; LTB4 ω-hydroxylase. Cat No: EXWM-0837. | |
| Leukotriene B4-d4 | Leukotriene B4-d4 is the deuterium labeled Leukotriene B4. Leukotriene B4 (LTB4) is known as one of the most potent chemoattractants and activators of leukocytes and is involved in inflammatory diseases. Leukotriene B4 is also an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: LTB4-d4; 5(S),12(R)-DiHETE-d4. CAS No. 124629-74-9. Pack Sizes: 10 μg (293.69 μM * 100 μL in Acetonitrile); 25 μg (293.69 μM * 250 μL in Acetonitrile). Product ID: HY-107608S. | |
| Leukotriene C4 | Leukotriene C4 is a eicosanoid lipid mediator and produced by immune cells during type 2 inflammation. Leukotriene C4 can mediate inflammation,allergy, bronchoconstriction, and vascular leakage[1][2]. Uses: Scientific research. Category: Induced disease models products. CAS No. 72025-60-6. Pack Sizes: 25 μg (159.8 μM * 250 μL in Ethanol). Product ID: HY-113446. | |
| LEUKOTRIENE C4 | LEUKOTRIENE C4. Alternative Names: Leukotriene C4 Lipid. CAS No. 72025-60-6. Purity: 97%. Product ID: ACM72025606. Molecular formula: C30H47N3O9S. Mole weight: 625.77. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Leukotriene C4-d5 | Leukotriene C4-d5 is the deuterium labeled Leukotriene C4. Leukotriene C4 is the parent cysteinyl leukotriene produced by the LTC4 synthase catalyzed conjugation of glutathione to LTA4. Uses: Scientific research. Category: Signaling pathways. CAS No. 1441421-73-3. Pack Sizes: 25 μg (158.53 μM * 250 μL in Ethanol); 1 mg; 5 mg. Product ID: HY-113446S. | |
| leukotriene-C4 hydrolase | The mouse enzyme is specific for leukotriene C4, while the human enzyme also has considerable activity towards glutathione and oxidized glutathione (cf. EC 3.4.19.13, glutathione hydrolase). Group: Enzymes. Synonyms: γ-glutamyl leukotrienase; GGT5. Enzyme Commission Number: EC 3.4.19.14. 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-4086; leukotriene-C4 hydrolase; EC 3.4.19.14; γ-glutamyl leukotrienase; GGT5. Cat No: EXWM-4086. | |
| leukotriene-C4 synthase | The reaction proceeds in the direction of addition. Not identical with EC 2.5.1.18, glutathione transferase. Group: Enzymes. Synonyms: leukotriene C4 synthetase; LTC4 synthase; LTC4 synthetase; leukotriene A4:glutathione S-leukotrienyltransferase; (7E,9E,11Z,14Z)-(5S,6R)-5,6-epoxyicosa-7,9,11,14-tetraenoate:glutathioneleukotriene-transferase (epoxide-ring-opening); (7E,9E,11Z,14Z)-(5S,6R)-6-(glutathion-S-yl)-5-hydroxyicosa-7,9,11,14-tetraenoate glutathione-lyase (epoxide-forming). Enzyme Commission Number: EC 4.4.1.20. CAS No. 90698-32-1. 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-5322; leukotriene-C4 synthase; EC 4.4.1.20; 90698-32-1; leukotriene C4 synthetase; LTC4 synthase; LTC4 synthetase; leukotriene A4:glutathione S-leukotrienyltransferase; (7E,9E,11Z,14Z)-(5S,6R)-5,6-epoxyicosa-7,9,11,14-tetraenoate:glutathioneleukotriene-transferase (epoxide-ring-opening); (7E,9E,11Z,14Z)-(5S,6R)-6-(glutathion-S-yl)-5-hydroxyicosa-7,9,11,14-tetraenoate glutathione-lyase (epoxide-forming). Cat No: EXWM-5322. | |
| Leukotriene D4 | Leukotriene D4 is a potent bronchoconstrictor. Leukotriene D4 has the potential for the research of asthma. Leukotriene D4 induces edema and increases capillary permeability[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 73836-78-9. Pack Sizes: 10 μg (201.34 μM * 100 μL in Ethanol); 50 μg (201.34 μM * 500 μL in Ethanol). Product ID: HY-113456. | |
| LEUKOTRIENE D4 METHYL ESTER | LEUKOTRIENE D4 METHYL ESTER. CAS No. 103476-23-9. Purity: 96%. Product ID: ACM103476239. Molecular formula: C26H42N2O6S. Mole weight: 510.68600. IUPAC Name: 7Z,9E,11E,14Z-LTD4 methyl ester. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Leukotriene E4 | Leukotriene E4 is a cysteinyl leukotriene produced by LTD4 and LTC4 in breath condensation, plasma, and urine. It is a constituent of slow-reacting substance of anaphylaxis (SRS-A). It is the final product of the pathway where 5-lipoxygenase converts arachidonic acid to cysteinyl leukotrienes, thus it can be used as an indicator in clinical diagnosis of asthma. Alternative Names: 5S-hydroxy-6R-(S-cysteinyl)-7E,9E,11Z,14Z-eicosatetraenoic acid; LTE4. Grades: ≥97%. CAS No. 75715-89-8. Molecular formula: C23H37NO5S. Mole weight: 439.61. | |
| Leukotriene E4 | Leukotriene E4 (LTE4) is produced by the action of dipeptidase on LTD4. Leukotriene E4 is one of the constituents of slow-reacting substance of anaphylaxis (SRS-A). Leukotriene E4 accumulates in both plasma and urine and urinary excretion of Leukotriene E4 is most often used as an indicator of asthma. Uses: Scientific research. Category: Signaling pathways. Alternative Names: LTE4. CAS No. 75715-89-8. Pack Sizes: 25 μg (227.47 μM * 250 μL in Ethanol); 50 μg (227.47 μM * 500 μL in Ethanol); 100 μg (227.47 μM * 1 mL in Ethanol). Product ID: HY-113465. | |
| leukotriene-E4 20-monooxygenase | Also acts on N-acetyl-leukotriene E4, but more slowly. Not identical with EC 1.14.13.30 leukotriene-B4 20-monooxygenase. Group: Enzymes. Synonyms: leukotriene-E4 ω-hydroxylase. Enzyme Commission Number: EC 1.14.13.34. CAS No. 111940-51-3. 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-0841; leukotriene-E4 20-monooxygenase; EC 1.14.13.34; 111940-51-3; leukotriene-E4 ω-hydroxylase. Cat No: EXWM-0841. | |
| Leukotriene E4-d5 | Leukotriene E4-d5 is the deuterium labeled Leukotriene E4. Leukotriene E4 (LTE4) is produced by the action of dipeptidase on LTD4. Leukotriene E4 is one of the constituents of slow-reacting substance of anaphylaxis (SRS-A). Leukotriene E4 accumulates in both plasma and urine and urinary excretion of Leukotriene E4 is most often used as an indicator of asthma. Uses: Scientific research. Category: Signaling pathways. Alternative Names: LTE4-d5. CAS No. 1240398-14-4. Pack Sizes: 25 μg (224.90 μM * 250 μL in Ethanol). Product ID: HY-113465S. | |
| Leu-Leu-Leu-OH | Leu-Leu-Leu-OH is a leucine derivative. Alternative Names: L-Leucyl-L-leucyl-L-leucine; Leu Leu Leu OH. Grades: 98%. CAS No. 10329-75-6. Molecular formula: C18H35N3O4. Mole weight: 357.49. | |
| Leu-Leu-Leu-OH | Leu-Leu-Leu-OH. Group: Biochemicals. Alternative Names: L-Leucyl-L-leucyl-L-leucine. Grades: Highly Purified. CAS No. 10329-75-6. Pack Sizes: 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| Leu-Leu-Leu-OH ≥96% | Leu-Leu-Leu-OH ≥96%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 10329-75-6. Pack Sizes: 250mg, 1g. US Biological Life Sciences. | Worldwide |
| Leu-Leu-OBzl | Leu-Leu-OBzl. Alternative Names: L-Leucyl-L-leucine phenylmethyl ester; L-Leu-Leu-Obzl; Benzyl L-leucyl-L-leucinate. CAS No. 77167-53-4. Molecular formula: C19H30N2O3. Mole weight: 334.45. | |
| Leu-Leu-OH | Leu-Leu-OH. Alternative Names: L-Leucyl-L-leucine; Leu Leu OH. Grades: ≥ 96% (HPLC). CAS No. 3303-31-9. Molecular formula: C12H24N2O3. Mole weight: 244.33. | |
| Leu-Leu-OH | Leu-Leu-OH (L-Leucyl-L-leucine), a Leu derivative, is a neutral dipeptide that can be used to study the functionality of dileucine motifs[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: L-Leucyl-L-leucine; Leu-Leu; H-Leu-Leu-OH. CAS No. 3303-31-9. Pack Sizes: 50 mg; 100 mg; 500 mg. Product ID: HY-W008642. | |
| Leu-Leu-OH | Leu-Leu-OH. Group: Biochemicals. Alternative Names: L-Leucyl-L-leucine. Grades: Highly Purified. CAS No. 3303-31-9. Pack Sizes: 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| Leu-Leu-OMe HCl | Leu-Leu-OMe has immunosuppressive activity. Alternative Names: LLME; LLOMe; L-Leucyl-L-Leucine methyl ester hydrochloride. Grades: ≥ 98%. CAS No. 6491-83-4. Molecular formula: C13H26N2O3·HCl. Mole weight: 294.82. | |
| Leu-Leu-Val-Phe-OH | Leu-Leu-Val-Phe-OH. Alternative Names: (Leu16)-Amyloid β-Protein (16-19); L-leucyl-L-leucyl-L-valyl-L-phenylalanine. Grades: ≥ 99%. CAS No. 24205-68-3. Molecular formula: C26H42N4O5. Mole weight: 490.64. | |
| Leu-Nle-NH2 HCl | Leu-Nle-NH2 HCl is an analog of Leupeptin. Alternative Names: L-leucyl-L-norleucinamide hydrochloride. Grades: ≥ 95%. CAS No. 68759-98-8. Molecular formula: C12H25N3O2·HCl. Mole weight: 279.81. | |
| Leupeptin | Leupeptin, a naturally occurring protease inhibitor, has potential applications in cosmetics due to its anti-inflammatory properties and ability to inhibit various proteases. It can be used in skincare products to help reduce inflammation and provide soothing effects to the skin. Additionally, Leupeptin's ability to inhibit proteases could contribute to the prevention of skin degradation and promote skin health by preserving the structural integrity of proteins in the skin matrix. Therefore, Leupeptin's applications in cosmetics may include anti-inflammatory and skin-protective effects, making it a valuable ingredient for products aimed at reducing skin irritation and promoting a healthy skin environment. It is a reversible, competitive inhibitor that targets serine and cysteine proteases, including trypsin, plasmin, calpain, papain, and cathepsins B, H, and L. Alternative Names: Ac-Leu-Leu-Arg-CHO; Acetyl Tripeptide; L-Leucinamide, N-acetyl-L-leucyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-, (S)-; N-Acetyl-L-leucyl-N-[(1S)-4-[(aminoiminomethyl)amino]-1-formylbutyl]-L-leucinamide; Acetyl-L-leucyl-L-leucyl-L-argininal; N-Acetyl-L-leucyl-L-leucyl-L-argininal; Ac-Leu-Leu-Arg-al; Ac-LLR-al. Grades: ≥95%. CAS No. 55123-66-5. Molecular formula: C20H38N6O4. Mole weight: 426.55. | |
| Leupeptin | Leupeptin Inhibitor. Uses: Scientific use. Product Category: T6564. CAS No. 103476-89-7. |  |
| Leupeptin | 25mg Pack Size. Group: Analytical Reagents, Antibiotics, Bioactive Small Molecules, Biochemicals, Research Organics & Inorganics. Formula: C20H38N6O4 ·HCl. CAS No. 24125-16-4. Prepack ID 89968247-25mg. Molecular Weight 463.01. See USA prepack pricing. |  |
| Leupeptin Ac-LL hydrochloride | Leupeptin Ac-LL (hydrochloride) is the hydrochloride form of Leupeptin Ac-LL (HY-18234B). Leupeptin Ac-LL (hydrochloride) has better inhibition than Leupeptin Ac-LL[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 24125-16-4. Pack Sizes: 5 mg; 10 mg. Product ID: HY-18234C. | |
| Leupeptin HCI | Leupeptin HCI. Group: Biochemicals. Grades: Highly Purified. CAS No. 24125-16-4. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C20H38N6O4·HCl. US Biological Life Sciences. | Worldwide |
| Leupeptin hemisulfate | Leupeptin Hemisulfate is a reversible inhibitor of serine and cysteine proteases. It can be used in skincare products to help reduce inflammation and provide soothing effects to the skin. Alternative Names: Ac-Leu-Leu-Arg-CHO.1/2H2SO4; Acetyl Tripeptide; L-Leucinamide, N-acetyl-L-leucyl-N-[(1S)-4-[(aminoiminomethyl)amino]-1-formylbutyl]-, sulfate (2:1); L-Leucinamide, N-acetyl-L-leucyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-, (S)-, sulfate (2:1); Leupeptin sulfate (2:1); N-Acetyl-L-leucyl-N-[(1S)-4-[(aminoiminomethyl)amino]-1-formylbutyl]-L-leucinamide hemisulfate; Acetyl-L-leucyl-L-leucyl-L-argininal hemisulfate; N-Acetyl-L-leucyl-L-leucyl-L-argininal hemisulfate; Ac-Leu-Leu-Arg-al.1/2H2SO4; Ac-LLR-al.1/2H2SO4. Grades: 95%. CAS No. 103476-89-7. Molecular formula: C20H38N6O4.1/2H2SO4. Mole weight: 475.59. | |
| Leupeptin hemisulfate | 25mg Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C20H38N6O4 · 0.5H2O4S. CAS No. 103476-89-7. Prepack ID 35875057-25mg. Molecular Weight 475.59. See USA prepack pricing. | |
| Leupeptin hemisulfate | 100mg Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C20H38N6O4 · 0.5H2O4S. CAS No. 103476-89-7. Prepack ID 35875057-100mg. Molecular Weight 475.59. See USA prepack pricing. | |
| Leupeptin hemisulfate | Leupeptin hemisulfate is a broad-spectrum, membrane-permeable protease inhibitor. Leupeptin hemisulfate potently inhibits serine, cysteine and threonine proteases. Leupeptin hemisulfate inhibits Mpro (the main protease of SARS-CoV-2) and also has anti-inflammatory activity[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 103476-89-7. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18234A. | |
| Leupeptin Hemisulfate | Leupeptin Hemisulfate is a reversible inhibitor of serine and cysteine proteases. It inhibits cathepsin B (Ki = 6 nM), calpain (Ki = 10 nM), trypsin (Ki = 35 nM), plasmin (Ki = 3.4 μM), and kallikrein (Ki = 19 μM), and has no effect against chymotrypsin, elastase, renin, or pepsin. Group: Inhibitors. CAS No. 103476-89-7. Pack Sizes: 10mg. Product ID: S7380. Formula: C20H38N6O4.1/2H2SO4. Smiles: CC(C)CC(C(=O)NC(CC(C)C)C(=O)NC(CCCN=C(N)N)C=O)NC(=O)C.CC(C)CC(C(=O)NC(CC(C)C)C(=O)NC(CCCN=C(N)N)C=O)NC(=O)C.OS(=O)(=O)O. Storage Conditions: 2 years -80 in solvent. |  United States; Europe |
| Leupeptin,HemisulfateSalt | Leupeptin,HemisulfateSalt. CAS No. 10347-89-7. Product ID: ACM10347897. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Leupeptin Trifluoroacetate | Leupeptin Trifluoroacetate. Group: Biochemicals. Grades: Highly Purified. CAS No. 147385-61-3. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C22H39F3N6O6. US Biological Life Sciences. | Worldwide |
| Leu-Pro-Ala-NH2 | Leu-Pro-Ala-NH2 is a simple tripeptide with a free amine group at the C-terminus. It consists of leucine (Leu), proline (Pro), and alanine (Ala) residues. The -NH2 at the C-terminus indicates that the peptide has a free amine group, which can be utilized for further reactions or modifications. This peptide sequence is used to study the effects of leucine, proline, and alanine in peptide structures and interactions, with potential applications in understanding peptide conformations or biological activities. Alternative Names: LPA; H-Leu-Pro-Ala-NH2; (S)-1-(L-Leucyl)-N-((S)-1-amino-1-oxopropan-2-yl)pyrrolidine-2-carboxamide. Grades: ≥95%. Molecular formula: C14H26N4O3. Mole weight: 298.39. | |
| Leuprolide Acetate | Leuprolide Acetate. Categories: leuprolide acetate; leuprorelin acetate. |  CA, FL & NJ |
| Leuprolide Acetate | Synthetic nonapeptide agonist analog of LH-RH. Antineoplastic (hormonal). Group: Biochemicals. Alternative Names: 6-D-Leucine-9- (N-ethyl-L-prolinamide ) -10-deglycinamide luteinizing Hormone-Releasing Factor Acetate(Pig); A 43818; Abbott 43818; Leuprorelin Acetate; Lupron; Procren Depot; Procrin; Prostap; TAP 144; TAP 144SR. Grades: Highly Purified. CAS No. 74381-53-6. Pack Sizes: 10mg, 25mg. Molecular Formula: C??H??N??O??, Molecular Weight: 1269.45. US Biological Life Sciences. | Worldwide |
| Leuprolide-d5 Acetate | Labeled synthetic nonapeptide agonist analog of LH-RH. Antineoplastic (hormonal). Group: Biochemicals. Alternative Names: 6-D-Leucine-9-(N-ethyl-L-prolinamide)-. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Leuprorelin EP Impurity A | Leuprorelin EP Impurity A. Uses: For analytical and research use. CAS No. 62621-13-0. Molecular formula: C59H84N16O12. Mole weight: 1209.42. Catalog: APB62621130. |  |
| Leuprorelin EP Impurity B | Leuprorelin EP Impurity B. Uses: For analytical and research use. CAS No. 112642-11-2. Molecular formula: C59H84N16O12. Mole weight: 1209.42. Catalog: APB112642112. | |
| Leuprorelin EP Impurity C | Leuprorelin EP Impurity C. Uses: For analytical and research use. CAS No. 54785-87-4. Molecular formula: C59H84N16O12. Mole weight: 1209.42. Catalog: APB54785874. | |
| Leuprorelin EP Impurity D | Leuprorelin EP Impurity D. Uses: For analytical and research use. CAS No. 1926163-25-8. Molecular formula: C61H86N16O13. Mole weight: 1251.46. Catalog: APB1926163258. | |
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