L-Anserine

L-Anserine Suppliers list
Company Name: Shanghai Yurlic Chemical S&T Co.Ltd.  Gold
Tel: 021-37285141 15618858630
Email: yancf@yulibiotech.com
Company Name: Hangzhou Sinoda Pharmaceutical Technology Co. LTD  Gold
Tel: 0571-87213919 17306812703
Email: 3007955328@qq.com
Company Name: Zhejiang Jiekun Biotechnology Co., Ltd  Gold
Tel: 0571-88211921 15397062932
Email: sales1@gotopbio.com
Company Name: Nanjing Leon Biological Technology Co., Ltd.  Gold
Tel: 025-84523390 -127; 17705183659
Email: sales@njleonbiotech.com
Company Name: Chongqing Botao Biotechnology Co., LTD  Gold
Tel: 15223382610
Email: danny@chemdad.com

L-Anserine manufacturers

  • L-Anserine
  • L-Anserine pictures
  • $10.00
  • 2026-09-13
  • CAS:584-85-0
  • Min. Order: 1ASSAYS
  • Purity: 99%
  • Supply Ability: 1 ton
  • L-Anserine
  • L-Anserine pictures
  • $1.10
  • 2026-08-25
  • CAS:584-85-0
  • Min. Order: 1KG
  • Purity: 99%min
  • Supply Ability: 100KG
  • Anserine
  • Anserine pictures
  • $29.00
  • 2026-07-15
  • CAS:584-85-0
  • Purity: 99.91%
  • Supply Ability: 10g
L-Anserine Basic information
Product Name:L-Anserine
Synonyms:L-Anserine;N-beta-alanyl-3-methyl-L-histidine;2-(3-aminopropanoylamino)-3-(3-methylimidazol-4-yl)-propanoic acid;Nα-β-Alanyl-1-dehydro-3-methyl-L-histidine;L-N-beta-Alanyl-3-methylhistidine;H-β-Ala-His(3-Me)-OH;(S)-2-(4-Aminobutanamido)-3-(1-methyl-1H-imidazol-5-yl)propanoic acid;Anserin
CAS:584-85-0
MF:C10H16N4O3
MW:240.26
EINECS:209-545-0
Product Categories:Chiral heterocyclic compounds;cosmestic
Mol File:584-85-0.mol
L-Anserine Structure
L-Anserine Chemical Properties
Melting point 268℃ (decomposition)
Boiling point 611.3±55.0 °C(Predicted)
density 1.38±0.1 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
solubility Methanol (Slightly, Heated), Water (Slightly)
form Solid
pka3.02±0.10(Predicted)
color White to Off-White
Cosmetics Ingredients FunctionsANTIOXIDANT
HUMECTANT
SKIN CONDITIONING
InChIInChI=1/C10H16N4O3/c1-14-6-12-5-7(14)4-8(10(16)17)13-9(15)2-3-11/h5-6,8H,2-4,11H2,1H3,(H,13,15)(H,16,17)/t8-/s3
InChIKeyMYYIAHXIVFADCU-SBYBRXNCNA-N
SMILESC(C1=CN=CN1C)[C@@H](C(=O)O)NC(=O)CCN |&1:7,r|
LogP-2.220 (est)
Safety Information
HS Code 2933299090
MSDS Information
L-Anserine Usage And Synthesis
UsesAnserine, a methylated form of Carnosine, is an orally active, natural Histidine-containing dipeptide found in skeletal muscle of vertebrates. Anserine is not cleaved by serum carnosinase and act as biochemical buffers, chelators, antioxidants, and anti-glycation agents. Anserine improves memory functions in Alzheimer's disease (AD)-model mice[1][2].
DefinitionChEBI: Anserine is a dipeptide comprising of beta-alanine and 3-methyl-L-histidine units. It has a role as an animal metabolite and a mouse metabolite. It is a beta-alanine derivative and a dipeptide. It is a tautomer of an anserine zwitterion.
Synthesis
L-Histidine, N-[3-[[(1,1-dimethylethoxy)carbonyl]amino]-1-oxopropyl]-3-methyl-, methyl ester

952739-81-0

L-Anserine

584-85-0

The general procedure for the synthesis of (S)-2-(3-aminopropionamido)-3-(1-methyl-1H-imidazol-5-yl)propionic acid, using the compound (CAS: 952739-81-0) as a starting material, was as follows: to a solution of methanol (1 mL) containing the ester 14 (18.8 mg, 53.0 μmol), 1 M aqueous sodium hydroxide was added to adjust the pH to >11. The reaction was carried out by stirring the reaction mixture for 16 h at room temperature. reaction mixture was stirred for 16 h at room temperature. Upon completion of the reaction, the solvent was removed by evaporation to give a colloidal residue. This residue was dissolved in distilled water (1 mL) and the reaction mixture was subsequently acidified with 1 M aqueous hydrochloric acid.

in vivo

Anserine (drinking water at a concentration of 2.0 g/L (equivalent to 10 mg/mouse); for 8 weeks) completely recoveres the memory deficits, improves pericyte coverage on endothelial cells in the brain, and diminishes chronic glial neuroinflammatory reactions in AβPPswe/PSEN1dE9 Alzheimer's disease (AD) model mice over 18-months old[2].

IC 50Human Endogenous Metabolite
Purification MethodsCrystallise anserine from aqueous EtOH. It is hygroscopic and is best stored as the nitrate salt (see below). Purify it by shaking the nitrate salt with Dowex 3 (x4 free base) and washing with H2O, evaporating the filtrate and removing H2O by 3 distillations with 10mL of propan-2-ol. Dissolve the crystals in MeOH and add H2O dropwise until one phase is obtained and cool. Dry the crystals at 60o over P2O5 in a vacuum. The picrate has m 145o (from H2O). [Rinderknecht et al. J Org Chem 29 1968 1964, Beilstein 25 II 408, 25 IV 4383.]
References[1] Boldyrev AA, et al. The histidine-containing dipeptides, carnosine and anserine: distribution, properties and biological significance. Adv Enzyme Regul. 1990;30:175-94. DOI:10.1016/0065-2571(90)90017-v
[2] Jun Kaneko, et al. Anserine (beta-alanyl-3-methyl-L-histidine) improves neurovascular-unit dysfunction and spatial memory in aged AβPPswe/PSEN1dE9 Alzheimer's-model mice. Sci Rep. 2017 Oct 3;7(1):12571. DOI:10.1038/s41598-017-12785-7
Tag:L-Anserine(584-85-0) Related Product Information
Atrial natriuretic factor (4-28) (human) Nonathymulin Urodilatin (human) Secretin (human) Secretin Palmitoyl tetrapeptide-7 L-Carnosine L-Anserine nitrate 3-Methyl-L-histidine L-Anserine