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(S)-Willardiine - 99%, high purity , CAS No.21416-43-3

    Grade & Purity:
  • ≥99%
In stock
Item Number
W646211
Grouped product items
SKU Size
Availability
Price Qty
W646211-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$79.90
W646211-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$346.90

Basic Description

Synonyms 3-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)alanine | S(-)-Willardiine | SR-01000039436-1 | SCHEMBL13319907 | (2S)-2-amino-3-(2,4-dioxopyrimidin-1-yl)propanoic acid | CCG-205293 | 3-(Uracil-1-yl)-L-alanine | SCHEMBL401191 | 2-amino-3-(2,4-dioxo-3,4-dihydro
Specifications & Purity ≥99%
Biochemical and Physiological Mechanisms (S)-Willardiine is a potent agonist of AMPA/kainate receptors with EC50 of 44.8 uM.\nIC50 value: 44.8 uM(EC50) \nTarget: AMPA/kainate receptor agonist\nin vitro: The (S)- but not (R)-isomers of willardiine and 5-bromowillardiine were potent agonists, p
Storage Temp Store at -20°C
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Product Description

(S)-Willardiine is a potent agonist of AMPA/kainate receptors with EC50 of 44.8 uM.IC50 value: 44.8 uM(EC50)Target: AMPA/kainate receptor agonistin vitro: The (S)- but not (R)-isomers of willardiine and 5-bromowillardiine were potent agonists, producing rapidly but incompletely desensitizing responses. At a concentration of 1.8 mM, Ca2+ inhibited the currents induced by 100 microM willardiine by approximately 50%.in vivo: In newborn mice (P5, histopathology at P10), local injection of the AMPA receptor agonist S-bromo-willardiine at day 5 after birth induced cortical damage and white matter damage, which was reduced in a dose-dependent manner by the AMPA receptor antagonists

Form:Solid

IC50& Target:Kainate Receptor

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Carboxylic acids and derivatives
Subclass Amino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
Direct Parent L-alpha-amino acids
Alternative Parents Pyrimidones  Hydropyrimidines  Vinylogous amides  Heteroaromatic compounds  Ureas  Lactams  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aromatic heteromonocyclic compounds
Substituents L-alpha-amino acid - Pyrimidone - Hydropyrimidine - Pyrimidine - Vinylogous amide - Heteroaromatic compound - Lactam - Urea - Amino acid - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid - Azacycle - Carbonyl group - Amine - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
External Descriptors non-proteinogenic L-alpha-amino acid - L-alanine derivative

Associated Targets(Human)

GRIA4 Tclin Glutamate receptor 4 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
GRIA2 Tclin Glutamate receptor 2 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
GRIA1 Tclin Glutamate receptor 1 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
FOLH1 Tclin Glutamate carboxypeptidase II (711 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GRIA3 Tclin Glutamate receptor ionotropic, AMPA 3 (127 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GRIA1 Tclin Glutamate receptor ionotropic, AMPA 1 (277 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GRIA2 Tclin Glutamate receptor ionotropic, AMPA 2 (847 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GRIK5 Tclin Glutamate receptor ionotropic kainate 5 (45 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HEK293 (82097 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Gria4 Glutamate receptor ionotropic, AMPA 4 (112 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name (2S)-2-amino-3-(2,4-dioxopyrimidin-1-yl)propanoic acid
INCHI InChI=1S/C7H9N3O4/c8-4(6(12)13)3-10-2-1-5(11)9-7(10)14/h1-2,4H,3,8H2,(H,12,13)(H,9,11,14)/t4-/m0/s1
InChIKey FACUYWPMDKTVFU-BYPYZUCNSA-N
Smiles C1=CN(C(=O)NC1=O)CC(C(=O)O)N
Isomeric SMILES C1=CN(C(=O)NC1=O)C[C@@H](C(=O)O)N
PubChem CID 440053
Molecular Weight 199.166

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Solubility DMSO : <1 mg/mL (ultrasonic) (insoluble or slightly soluble)
Molecular Weight 199.160 g/mol
XLogP3 -4.400
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 3
Exact Mass 199.059 Da
Monoisotopic Mass 199.059 Da
Topological Polar Surface Area 113.000 Ų
Heavy Atom Count 14
Formal Charge 0
Complexity 312.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 1
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

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