ChemicalBook > CAS DataBase List > O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE

O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE

Product Name
O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE
CAS No.
118021-35-5
Chemical Name
O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE
Synonyms
L-4-OXALYSINE HCL;H-SER(ETNH2)-OH HCL;H-LYS[*4(<-O)]-OH HCL;4-OXY-L-LYSINE HYDROCHLORIDE;L-4-Oxalysine (hydrochloride);O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE;O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE USP/EP/BP;(2S)-2-amino-3-(2-aminoethoxy)propanoicacid,hydrochloride;(S)-(+)-2-AMINO-3-(2-AMINOETHOXY)PROPANOIC ACID, MONOHYDROCHLORIDE;(S)-(+)-2-AMINO-3-(2-AMINOETHOXY)-PROPAN OIC ACID HYDROCHLORIDE, 98%
CBNumber
CB0297079
Molecular Formula
C5H13ClN2O3
Formula Weight
184.62
MOL File
118021-35-5.mol
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O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE Property

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
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P321Specific treatment (see … on this label).

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

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N-Bromosuccinimide Price

ChemScene
Product number
CS-7133
Product name
L-4-Oxalysinehydrochloride
Purity
97.10%
Packaging
1mg
Price
$104
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
AAA0007225
Product name
O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE
Purity
95.00%
Packaging
5MG
Price
$503.66
Updated
2021/12/16
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O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE Chemical Properties,Usage,Production

Uses

L-4-Oxalysine hydrochloride is a natural product isolated from the culture media of Streptomyces roseovirdofuscus in China which has shown antitumor activities.

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.

References

[1] Dai ZQ, et al. Effect of L-4-oxalysine on ultrastructures of liver cells in mice. Zhongguo Yao Li Xue Bao. 1991 Jul;12(4):336-40. PMID:1807083
[2] Wang XW, et al. Immunostimulatory action of L-4-oxalysine counteracts immunosuppression induced by alpha-fetoprotein. Eur J Pharmacol. 1998 Jun 12;351(1):105-11. DOI:10.1016/s0014-2999(98)00277-5

O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE Suppliers

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118021-35-5, O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDERelated Search:


  • H-SER(ETNH2)-OH HCL
  • H-LYS[*4(<-O)]-OH HCL
  • L-4-OXALYSINE HCL
  • (S)-(+)-2-AMINO-3-(2-AMINOETHOXY)PROPANOIC ACID, MONOHYDROCHLORIDE
  • O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE
  • L-4-Oxalysine (hydrochloride)
  • (S)-(+)-2-AMINO-3-(2-AMINOETHOXY)-PROPAN OIC ACID HYDROCHLORIDE, 98%
  • 4-OXY-L-LYSINE HYDROCHLORIDE
  • (2S)-2-amino-3-(2-aminoethoxy)propanoicacid,hydrochloride
  • O-(2-AMINOETHYL)-L-SERINE HYDROCHLORIDE USP/EP/BP
  • 118021-35-5
  • C5H13ClN2O3
  • H2NCH2CH2OCH2CHNH2CO2HHCl
  • C5H12N2O3HCl
  • Peptide Synthesis
  • Others
  • Unnatural Amino Acid Derivatives
  • Specialty Synthesis
  • Others
  • Peptide Synthesis
  • Unnatural Amino Acid Derivatives