V7878
Val-Pro hydrochloride
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About This Item
Empirical Formula (Hill Notation):
C10H18N2O3 · HCl
CAS Number:
Molecular Weight:
250.72
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
InChI
1S/C10H18N2O3.ClH/c1-6(2)8(11)9(13)12-5-3-4-7(12)10(14)15;/h6-8H,3-5,11H2,1-2H3,(H,14,15);1H
SMILES string
Cl.CC(C)C(N)C(=O)N1CCCC1C(O)=O
InChI key
IIQAHNBGJJXSGP-UHFFFAOYSA-N
technique(s)
ligand binding assay: suitable
storage temp.
−20°C
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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M Sjölund et al.
Differentiation; research in biological diversity, 32(2), 173-180 (1986-01-01)
Early in primary culture, arterial smooth-muscle cells undergo a transition from a contractile to a synthetic phenotype. This process includes the loss of myofilaments and of contractility. At the same time, an extensive rough endoplasmic reticulum and a large Golgi
S H Moolenaar et al.
Journal of inherited metabolic disease, 24(8), 843-850 (2002-03-28)
Three urine samples from two prolidase-deficient patients were analysed using 1H NMR spectroscopy. One-dimensional 1H NMR spectra showed a characteristic pattern of overlapping resonances of the proline and hydroxyproline protons of the imidodipeptides. The model compounds Ala-Pro, Gly-Pro, Phe-Pro, Leu-Pro
H Kodama et al.
Journal of chromatography, 527(2), 279-288 (1990-05-18)
Analyses of standard iminodipeptides and iminodipeptides in the urine of patients with prolidase deficiency have been demonstrated using liquid chromatography-mass spectrometry with an atmospheric pressure ionization interface system. The separation was carried out on a reversed-phase column using 0.1% aqueous
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