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Kynurenic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 90411-17-9 Structure
  • Basic information

    1. Product Name: Kynurenic acid methyl ester
    2. Synonyms: Kynurenic acid methyl ester
    3. CAS NO:90411-17-9
    4. Molecular Formula:
    5. Molecular Weight: 222.244
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90411-17-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Kynurenic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Kynurenic acid methyl ester(90411-17-9)
    11. EPA Substance Registry System: Kynurenic acid methyl ester(90411-17-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 90411-17-9(Hazardous Substances Data)

90411-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90411-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,1 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90411-17:
(7*9)+(6*0)+(5*4)+(4*1)+(3*1)+(2*1)+(1*7)=99
99 % 10 = 9
So 90411-17-9 is a valid CAS Registry Number.

90411-17-9Downstream Products

90411-17-9Relevant articles and documents

Discovery of kynurenines containing oligopeptides as potent opioid receptor agonists

Benyhe, Sándor,Dimmito, Marilisa Pia,Mollica, Adriano,Nalli, Marianna,Pieretti, Stefano,Stefanucci, Azzurra,Sz?cs, Edina,Vécsei, László,Zádor, Ferenc,Zengin, Gokhan

, (2020)

Kynurenine (kyn) and kynurenic acid (kyna) are well-defined metabolites of tryptophan catabolism collectively known as “kynurenines”, which exert regulatory functions in host-microbiome signaling, immune cell response, and neuronal excitability. Kynurenine containing peptides endowed with opioid receptor activity have been isolated from natural organisms; thus, in this work, novel opioid peptide analogs incorporating L-kynurenine (L-kyn) and kynurenic acid (kyna) in place of native amino acids have been designed and synthesized with the aim to investigate the biological effect of these modifications. The kyna-containing peptide (KA1) binds selectively the μ-opioid receptor with a Ki = 1.08 ± 0.26 (selectivity ratio μ/δ/? = 1:514:10000), while the L-kyn-containing peptide (K6) shows a mixed binding affinity for μ, δ, and ?-opioid receptors, with efficacy and potency (Emax = 209.7 + 3.4%; LogEC50 = ?5.984 + 0.054) higher than those of the reference compound DAMGO. This novel oligopeptide exhibits a strong antinociceptive effect after i.c.v. and s.c. administrations in in vivo tests, according to good stability in human plasma (t1/2 = 47 min).

Kynurenic acid derivatives, their preparation and pharmaceutical compositions containing them

-

, (2008/06/13)

Kynurenic acid derivatives useful as therapeutic agents in treating neurological disorders, for example, thiokynurenic acid, 7-chloro-thio-kynurenic acid, 7-trifluoromethyl-thiokynurenic acid, 7-methoxy-thiokynurenic acid and 5-fluoro-thiokynurenic acid.

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