L-(-)-Histidinol dihydrochloride

L-(-)-Histidinol dihydrochloride Basic information
Product Name:L-(-)-Histidinol dihydrochloride
Synonyms:L(-)-Histidinol dihydrochloride,99%;(S)-β-amino-1H-imidazole-4-propanol dihydrochloride;L-HISTIDINOL 2 HCL;L-HISTIDINOL DIHYDROCHLORIDE;L-HISTIDINE DIHYDROCHLORIDE;L-BETA-AMINO-1H-IMIDAZOLE-4-PROPANOL DIHYDROCHLORIDE;(L)-2-AMINO-3-(4-IMIDAZOLYL)PROPANOL DIHYDROCHLORIDE;HISTIDINOL Dihydrochloride, L-(RG)
CAS:1596-64-1
MF:C6H13Cl2N3O
MW:214.09
EINECS:216-482-2
Product Categories:Chiral Reagents;Heterocycles;Amino hydrochloride;Metabolites & Impurities
Mol File:1596-64-1.mol
L-(-)-Histidinol dihydrochloride Structure
L-(-)-Histidinol dihydrochloride Chemical Properties
Melting point 198-201 °C (dec.)(lit.)
alpha -3 º (C=2, H2O 24 ºC)
storage temp. Inert atmosphere,2-8°C
solubility DMSO (Slightly), Methanol (Slightly), Water (Sparingly)
form Crystalline Powder
color White to slightly beige
BRN 3914853
InChIKeyFRCAFNBBXRWXQA-XRIGFGBMSA-N
CAS DataBase Reference1596-64-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-22
Safety Statements 26-36-37/39-36/37-22
WGK Germany 3
RTECS NI8260000
HS Code 29332900
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
L-(-)-Histidinol dihydrochloride Usage And Synthesis
DescriptionL-Histidinol is a natural amino alcohol that serves as an intermediate in the biosynthesis of the amino acid L-histidine in bacteria, archaebacteria, fungi, and plants. It is generated from its immediate precursor, L-histidinol phosphate, by a phosphatase. L-Histidinol is oxidized to L-histidinal, which in turn is oxidized to L-histidine, by a single enzyme, histidinol dehydrogenase.
Chemical Propertieswhite to slightly beige crystalline powder
UsesA metabolite within Histidine metabolism.
DefinitionChEBI: L-Histidinol dihydrochloride is an aralkylamine.
in vitropreliminary experiments were done to investigate the cytotoxic effect of l-histidinol on cultured eac cells. results showed that l-histidinol up to 4 mm had no cytotoxic effects on eac cells. doxorubicin alone showed concentration-dependent cytotoxic effects. l-histidinol combination with doxorubicin led to significant potentiation of doxorubicin cytotoxicity to eac cells compared to doxorubicin alone. the concentration that caused 50% growth inhibition in eac cells after 24 h incubation was about 0.2 μg/ml, whereas it was 0.1 μg/ml when l-histidinol was added to culture medium [1].
in vivol-histidinol at 250 mg/kg for five consecutive doses before doxorubicin single injection could enhance the antitumour activity of doxorubicin in eac-bearing mice as demonstrated by a significant increase in average life span and cure rate of mice. in normal mice, l-histidinol, in the same dose regimen, could not alter the acute cardiotoxicity and lethality of doxorubicin [1].
references[1] al-shabanah oa, badary oa, al-gharably nm, al-sawaf ha. effects of l-histidinol on the antitumour activity and acute cardiotoxicity of doxorubicin in mice. pharmacol res. 1998 sep;38(3):225-30.
L-(-)-Histidinol dihydrochloride Preparation Products And Raw materials
Ketorolac tromethamine N'-Methyl-L-histidine methyl ester L-HISTIDINE DIHYDROCHLORIDE ALTRENOGEST Glycinamide hydrochloride 6-Aminocaproic acid 1-METHYL-L-HISTIDINE DIHYDROCHLORIDE Glycine Imidazole L-(-)-Histidinol dihydrochloride Dihydrochloride Tris(hydroxymethyl)aminomethane L-HISTIDINE, 3-(PHENYLMETHYL)-, DIHYDROCHLORIDE AMINO ACIDS TRISTEARIN H-HIS(TRT)-OME 2HCL Fosfomycin tromethamine 1-Propanol

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