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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag für Lagerartikel Gly-Sar - Moligand™, ≥98% , Peptide transporter 1;Peptide transporter 2, CAS No.29816-01-1, Peptide transporter 1;Peptide transporter 2
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98% Synonyms
GLYCINE, GLYCYL-N-METHYL- | [(ammonioacetyl)(methyl)amino]acetate | 2JE8SG6VDT | tritiated glycylsarcosine | L168049 | G0138 | [(Aminoacetyl)(methyl)amino]acetic acid | 19Z49HUF4G | GTPL4659 | GTPL9505 | N-glycyl-N-methylglycine | NSC 206288 | Gly-Sarcosi
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Why this grade Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Übersicht Amino Acid Sequence Gly-Sar
Specifications Synonyme
GLYCINE, GLYCYL-N-METHYL- | [(ammonioacetyl)(methyl)amino]acetate | 2JE8SG6VDT | tritiated glycylsarcosine | L168049 | G0138 | [(Aminoacetyl)(methyl)amino]acetic acid | 19Z49HUF4G | GTPL4659 | GTPL9505 | N-glycyl-N-methylglycine | NSC 206288 | Gly-Sarcosi
Spezifikationen & Reinheit
Moligand™, ≥98%
Verschickt in
Wet ice
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Mechanismus der Wirkung
Peptide transporter 1;Peptide transporter 2
Namen und Kennungen Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504756172
Kanonisches Lächeln
CN(CC(=O)O)C(=O)CN
IUPAC Name
2-[(2-aminoacetyl)-methylamino]acetic acid
InChIKey
VYAMLSCELQQRAE-UHFFFAOYSA-N
INCHI
1S/C5H10N2O3/c1-7(3-5(9)10)4(8)2-6/h2-3,6H2,1H3,(H,9,10)
Isomere SMILES
CN(CC(=O)O)C(=O)CN
Alternative CAS-Nummer
29816-01-1
MeSH-Eintrag
Gly-Sar;glycylsarcosine
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1768450&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic acids and derivatives Klasse Peptidomimetics Subclass Peptoid-peptide hybrids Intermediate Tree Nodes Not available Direct Parent Peptoid-peptide hybrids Alternative Parents Dipeptides N-acyl-alpha amino acids Alpha amino acid amides Tertiary carboxylic acid amides Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents Peptoid/peptide hybrid - Alpha-dipeptide - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Tertiary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Amino acid - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Primary aliphatic amine - Organic nitrogen compound - Carbonyl group - Amine - Organic oxygen compound - Primary amine - Hydrocarbon derivative - Aliphatic acyclic compound Beschreibung This compound belongs to the class of organic compounds known as peptoid-peptide hybrids. These are compounds containing a peptoid-peptide backbone, which consists alternating amino acid and n-substituted amino acids linked to each other by a peptide bond. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Empfindlichkeit Heat Sensitive Schmelzpunkt (°C) 198-202°C Molekulargewicht 146.140 g/mol XLogP3 -3.900 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 3 Exact Mass 146.069 Da Monoisotopic Mass 146.069 Da Topological Polar Surface Area 83.600 Ų Heavy Atom Count 10 Formal Charge 0 Complexity 146.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 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
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