Leucyl-leucine-methyl ester
Grundinformationen
- CAS
13022-42-9- Standard-SMILES
COC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC(C)C- InChIKey
AJMOLNFDYWTVQW-QWRGUYRKSA-N- Summenformel
- C13H26N2O3
- Durchschnittliche Molmasse
- 258,36 g/mol
Überblick
L-leucyl-l-leucine methyl ester is a peptide.
Namen und Bezeichner
- Bevorzugter Name
- Leucyl-leucine-methyl ester
- IUPAC
- methyl (2S)-2-[[(2S)-2-amino-4-methylpentanoyl]amino]-4-methylpentanoate
- Englischer Name
- leucyl-leucine-methyl ester
- Summenformel
- C13H26N2O3
- Molmasse
- 258.36
Namen und Synonyme
13022-42-9Leu-leu-omeLeucyl-leucine-methyl ester74SY3EEM9RRefChem:924678Leucylleucine methyl esterl-leucyl-l-leucine methyl esterL-Leucine, L-leucyl-, methyl esterL-Leucine, N-L-leucyl-, methyl esterMethyl L-leucyl-L-leucinatemethyl (2S)-2-[[(2S)-2-amino-4-methylpentanoyl]amino]-4-methylpentanoateN-L-Leucyl-L-leucine methyl ester
Weitere Namen anzeigen
LeuLeuOMe
AJMOLNFDYWTVQW-QWRGUYRKSA-Nstarbld0037349leucylleucine-methyl-esterUNII-74SY3EEM9RMETHYL LEUCYLLEUCINATESCHEMBL56187orb1700158CHEBI:184067
Datenbank-Bezeichner
- CAS
13022-42-9- PubChem CID
- 7016877
- ChEBI
CHEBI:184067- UNII
- 74SY3EEM9R
- Nikkaji
- J1.330.955H
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 1,1
- Polarare Oberfläche (TPSA)
- 81,4 Ų
- H-Brücken-Donoren
- 2
- H-Brücken-Akzeptoren
- 4
- Frei drehbare Bindungen
- 8
- Schwere Atome
- 18
- Formalladung
- 0
- Komplexität
- 277
Physikochemische Eigenschaften
- Siedepunkt
- 375.9 · 375.9±22.0 °C(Predicted)
- Dichte
- 1.002 · 1.002±0.06 g/cm3(Predicted)
- pka
- 13.79 · 13.79±0.46(Predicted)
Chemie und Industrie
Pharmakologische Informationen
MeSH Pharmacological Classification
Agents that suppress immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-CELLS or by inhibiting the activation of HELPER CELLS. While immunosuppression has been brought about in the past primarily to prevent rejection of transplanted organs, new applications involving mediation of the effects of INTERLEUKINS and other CYTOKINES are emerging.
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