CAS 103476-89-7

L-Leucinamid, N-acetyl-L-leucyl-N-[(1S)-4-[(aminoiminomethyl)amino]-1-formylbutyl]-, sulfat (2:1)

Beschreibung:

L-Leucinamid, N-acetyl-L-leucyl-N-[(1S)-4-[(aminoiminomethyl)amino]-1-formylbutyl]-, sulfat (2:1) ist eine komplexe organische Verbindung, die durch ihre strukturellen Komponenten gekennzeichnet ist, zu denen ein Aminosäurederivat (L-Leucin) und eine Sulfatgruppe gehören. Diese Verbindung weist eine einzigartige Anordnung funktioneller Gruppen auf, einschließlich Amid- und Acylfunktionen, die zu ihrer biologischen Aktivität und Löslichkeitseigenschaften beitragen. Die Anwesenheit der Sulfatgruppe verstärkt ihren ionischen Charakter, was potenziell ihre Wechselwirkung mit biologischen Systemen und die Löslichkeit in wässrigen Umgebungen beeinflussen kann. Als Derivat von L-Leucin kann es Eigenschaften aufweisen, die mit der Proteinsynthese und dem Stoffwechsel zusammenhängen. Die Stereochemie der Verbindung, insbesondere die (1S)-Konfiguration, weist auf spezifische räumliche Anordnungen hin, die ihre biologischen Wechselwirkungen beeinflussen können. Insgesamt dürfte diese Substanz von Interesse in der biochemischen Forschung sein, insbesondere in Studien zur Peptidsynthese, Arzneimitteldesign und therapeutischen Anwendungen, obwohl spezifische biologische Aktivitäten und pharmakologische Eigenschaften weitere Untersuchungen erfordern würden.

Formel: C₂₀H₃₈N₆O₄H₂O₄S

InChl: InChI=1S/C20H38N6O4.H2O4S/c1-12(2)9-16(24-14(5)28)19(30)26-17(10-13(3)4)18(29)25-15(11-27)7-6-8-23-20(21)22;1-5(2,3)4/h11-13,15-17H,6-10H2,1-5H3,(H,24,28)(H,25,29)(H,26,30)(H4,21,22,23);(H2,1,2,3,4)/t15-,16-,17-;/m0./s1

InChI Key: InChIKey=IBDASEYBOOUHFZ-FRKSIBALSA-N

SMILES: [C@@H](NC([C@H](CC(C)C)NC(C)=O)=O)(C(N[C@@H](CCCNC(=N)N)C=O)=O)CC(C)C.S(=O)(=O)(O)O

Synonyme:

• (2S)-2-(acetylamino)-N-[(2S)-2-({4-[(diaminomethylidene)amino]-1-formylbutyl}amino)-4-methylpentanoyl]-4-methylpentanamide (non-preferred name)
• 2-(2-Acetamido-4-methylvaleramido)-N-(1-formyl-4-guanidinobutyl)-4-methylvaleramide
• <span class="text-smallcaps">L</smallcap>-Leucinamide, N-acetyl-<smallcap>L</span>-leucyl-N-[(1S)-4-[(aminoiminomethyl)amino]-1-formylbutyl]-, sulfate (2:1)
• <span class="text-smallcaps">L</smallcap>-Leucinamide, N-acetyl-<smallcap>L</span>-leucyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-, (S)-, sulfate (2:1)
• Acetyl-L-leucyl-L-leucylargininal
• L-Leucinamide, N-acetyl-L-leucyl-N-(4-((aminoiminomethyl)amino)-1-formylbutyl)-
• Leupeptin Ac-LL
• Leupeptin Hemisulfate From Microbial*Source
• Leupeptin hemisulfate
• N-Acetyl-L-leucyl-L-leucyl-L-argininal
• N-acetyl-L-leucyl-N-{(2S)-5-[(diaminomethylidene)amino]-1-oxopentan-2-yl}-L-leucinamide
• Nk-381
• Valeramide, 2-(2-acetamido-4-methylvaleramido)-N-(1-formyl-4-guanidinobutyl)-4-methyl-
• L-Leucinamide, N-acetyl-L-leucyl-N-[(1S)-4-[(aminoiminomethyl)amino]-1-formylbutyl]-, sulfate (2:1)

Leupeptin

CAS: 103476-89-7

A reversible compeptitive protease inhibitor, which was shown to inhibit cathepsins B, H, L, and S, calpain and trypsin. Ac-LLR-CHO inhibits the trypsin-like activity of the proteasome endopeptidase complex. CAS Number (hemisulfate): 103476-89-7.

Formel: C₂₀H₃₈N₆O₄·H₂SO₄

Reinheit: 97.8380%

Farbe und Form: White

Molekulargewicht: 951.2

Ref: 01-4013467

Leupeptin

CAS: 103476-89-7

Formel: C₄₀H₇₈N₁₂O₁₂S

Reinheit: 97%

Farbe und Form: Solid

Molekulargewicht: 951.1855

Ref: IN-DA00ILJA

Leupeptin Hemisulfate

CAS: 103476-89-7

Leupeptin Hemisulfate

Reinheit: ≥90%

Molekulargewicht: 475.59g/mol

Ref: 54-BUP13431

Leupeptin hemisulphate

CAS: 103476-89-7

Leupeptin hemisulphate

Formel: C₂₀H₃₈N₆O₄·H₂SO₄

Reinheit: >90%

Farbe und Form: white to off white powder

Molekulargewicht: 951.18552g/mol

Ref: 54-BIMI2183

Leupeptin Hemisulfate

CAS: 103476-89-7

Leupeptin hemisulfate is a protease inhibitor with cell membrane-permeable, reversible, competitive, and oral activities.

Formel: C₂₀H₃₈N₆O₄H₂SO₄

Reinheit: 90% - ≥98%

Farbe und Form: White Solid

Molekulargewicht: 475.59

Ref: TM-T6564

Leupeptin Hemisulfate

CAS: 103476-89-7

Formel: C₂₀H₃₈N₆O₄H₂O₄S

Molekulargewicht: 426.56 1/2*98.07

Ref: 4Z-L-175001

Leupeptin hemisulfate

CAS: 103476-89-7

Formel: C₂₀H₃₈N₆O₄·5H₂SO₄

Reinheit: ≥ 95%

Farbe und Form: White to off-white powder

Molekulargewicht: 475.59

Ref: 7W-GE7125

Leupeptin hemisulfate anhydrous

CAS: 103476-89-7

Leupeptin is a protease inhibitor that inhibits the activity of proteases in cells. It has been shown to inhibit transcriptional regulation and apoptosis pathway, as well as possessing anti-inflammatory properties. Leupeptin has been shown to have inhibitory properties against a variety of proteases, including group P2 metalloproteases, cathepsin D, and proteinase 3. This drug has also been shown to prevent neuronal death in experimental models by inhibiting cell lysis. Leupeptin binds to the active site of the enzyme by forming hydrogen bonds with conserved amino acid residues and steric interactions with nearby amino acid residues. The redox potentials of leupeptin are not known, but it is assumed that they are low enough for its antioxidant properties to be effective.

Formel: C₂₀H₃₈N₆O₄H₂SO

Reinheit: Min. 90 Area-%

Molekulargewicht: 475.6 g/mol

Ref: 3D-ILP-4041

Leupeptin hemisulfate anhydrous (vial)

CAS: 103476-89-7

Leupeptin is an ion channel blocker that belongs to the group of protease inhibitors. It blocks the passage of ions across cell membranes by binding to the active site of a variety of enzymes in the membrane. Leupeptin is used as a research tool for studying protein interactions, and can be used for antibody production. Leupeptin is also useful in cell biology studies, because it inhibits the activation of many proteins involved in signal transduction and cell division.

Formel: C₂₀H₃₈N₆O₄

Reinheit: Min. 95%

Molekulargewicht: 426.55 g/mol

Ref: 3D-ILP-4041-V

Leupeptin hemisulfate

CAS: 103476-89-7

Leupeptin is a protein inhibitor that binds to the ubiquitin ligases and inhibits their activity. It has been shown to inhibit the transcriptional regulation of gene expression, which is important in cancer, chronic oral administration, and experimental models. Leupeptin also blocks the binding of proteins to DNA in cell culture and animal models. This leads to decreased production of fatty acids, which are needed for cellular growth and function. Leupeptin also has an anti-depressant effect by blocking the transcriptional regulation of gene expression for serotonin receptors.

Formel: C₂₀H₃₈N₆O₄•(H₂SO₄)₀

Reinheit: Min. 90.0 Area-%

Farbe und Form: White Powder

Molekulargewicht: 475.59 g/mol

Ref: 3D-FL29627