L-DAB HBR
CAS No. 1758-80-1
L-DAB HBR( L-24-Diaminobutyric acid )
Catalog No. M20932 CAS No. 1758-80-1
L-DAB HBR is an inhibitor of GABA transaminase ?(IC50 > 500 μM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameL-DAB HBR
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NoteResearch use only, not for human use.
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Brief DescriptionL-DAB HBR is an inhibitor of GABA transaminase ?(IC50 > 500 μM).
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DescriptionL-DAB HBR is an inhibitor of GABA transaminase ?(IC50 > 500 μM).
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In VitroThe tumor cells are irreversibly and totally damaged by incubation with 10 mM L-2,4-Diaminobutyric acid for 24 h at 37°C. The cell-destructive effect by L-DABA is probably due to an osmotic lysis induced by the non-saturated intracellular accumulation of L-DABA. The harmful effect of L-DABA could be abolished by concomitant incubation with L-alanine and L-methionine. Kinetic studies indicates that L-DABA is a non-linear, non-competitive inhibitor of GABA transaminase activity. The L-DABA-induced elevation of GABA levels parallels the inhibition of GABA transaminase activity. L-2,4-Diaminobutyric acid, an amino acid analogue, produceS a cytolytic effect with a human glioma cell line, SKMG-1, and normal human fibroblasts. The concentrations of L-DABA necessary to reduce the cell count to 50% of control following a 24-h incubation at 37°C are 12.5 mM for the human fibroblasts and 20 mM for the glioma cell line.
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In VivoTreatment with L-DABA results in 43.4% reduction of tumor growth. L-DABA is a more effective inhibitor of GABA transaminase in vivo than in vitro.
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SynonymsL-24-Diaminobutyric acid
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PathwayOthers
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TargetOther Targets
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RecptorGABA|Human Endogenous Metabolite
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Research Area——
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Indication——
Chemical Information
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CAS Number1758-80-1
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Formula Weight118.13
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Molecular FormulaC4H10N2O2
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Purity>98% (HPLC)
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SolubilityH2O:34 mg/mL (287.82 mM)
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SMILESNCC[C@H](N)C(=O)O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Beart P M Bilal K . l-24-Diaminobutyric acid and the GABA system[J]. Neuroscience Letters 1977 5(3-4):193-198.
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