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L6006
Leu-Pro trifluoroacetate salt
powder
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Empirische Formel (Hill-System):
C11H20N2O3 · C2HF3O2
CAS-Nummer:
Molekulargewicht:
342.31
UNSPSC Code:
12352202
PubChem Substance ID:
MDL number:
form
powder
color
white
storage temp.
−20°C
SMILES string
OC(=O)C(F)(F)F.CC(C)C[C@H](N)C(=O)N1CCC[C@H]1C(O)=O
InChI
1S/C11H20N2O3.C2HF3O2/c1-7(2)6-8(12)10(14)13-5-3-4-9(13)11(15)16;3-2(4,5)1(6)7/h7-9H,3-6,12H2,1-2H3,(H,15,16);(H,6,7)/t8-,9-;/m0./s1
InChI key
AUVSSRGHMVVWPD-OZZZDHQUSA-N
Biochem/physiol Actions
L-leucyl-L-proline (Leu-Pro) and its retro variant Pro-Leu may be used along with other proline dipeptides to study imprinting and chemotaxis in tetrahymena.
Lagerklasse
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Fengxia Zhang et al.
Molecular bioSystems, 6(5), 852-861 (2010-06-23)
A novel metabonomic method based on fast liquid chromatography coupled with ion trap-time of flight mass spectrometry (UFLC/MS-IT-TOF) was applied to study the metabolic changes of plasma and urine in depression and excess fatigue rats. Principal component analysis (PCA) and
L Köhidai et al.
Cell biology international, 21(6), 341-345 (1997-06-01)
Our investigations demonstrate that proline-containing dipeptides can provoke a chemosensory response from the unicellular Tetrahymena pyriformis. The chemotactic effects of the dipeptides have a close relationship with the side chain and the lipophilicity of the amino-terminal amino acid. Comparison of
G Csaba et al.
Bioscience reports, 17(6), 537-542 (1998-04-30)
Proline-glycine, proline-leucine and proline-valine dipeptides and their retro variants were used in the experiments to study the effects of pretreatment (imprinting) in Tetrahymena, by investigating fluorescein isothiocyanate (FITC)-conjugated peptide binding. The protozoan organism could differentiate between the proline-dipeptides containing different
Global Trade Item Number
| SKU | GTIN |
|---|---|
| L6006-250MG | 04061832888804 |
| L6006-25MG | 04061832888811 |