O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE
- CAS NO.：118021-35-5
- Empirical Formula: C5H13ClN2O3
- Molecular Weight: 184.62
- MDL number: MFCD01631149
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-07-02 08:54:57
What is O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE?
Biological Activity
L-4-Oxalysine hydrochloride is a natural substance isolated from the culture medium of Streptomyces in China and has anticancer activity.
in vitro
L-4-oxalysine functionally antagonizes the a-fetoprotein-induced suppression of the mitogen- and one-way mixed lymphocyte culture-induced proliferation of spleen lymphocytes and interleukin-6 production by these cells in mice bearing the hepatoma-22 tumor.
in vivo
L-4-oxalysine inhibits the proliferation of some mouse implanted tumors and pulmonary metastasis of mouse Lewis lung carcinoma.
Properties of O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE
| Melting point: | 212-216 °C(lit.) |
| alpha | +4.0～+8.0°(c=10,dilHCl)(D/20) |
| storage temp. | Store at -20°C |
| solubility | Soluble in DMSO |
| form | Solid |
| color | White to off-white |
Safety information for O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE
Computed Descriptors for O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE
New Products
4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Mefenamic Acid IP/BP/EP/USP Diclofenac Sodium IP/BP/EP/USP Ornidazole IP Diclofenac Potassium SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
![BOC-LYS[*4(<-O),CL-Z]-OH](https://img.chemicalbook.in/StructureFile/ChemBookStructure9/GIF/CB1146505.gif)
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