Glycyl-L-leucine - 10mM in Water, high purity , CAS No.869-19-2

  • 10mM in Water
Item Number
G426493
Grouped product items
SKUSizeAvailabilityPrice Qty
G426493-1ml
1ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$69.90

Basic Description

SynonymsGlycyl-L-leucine | 869-19-2 | Gly-Leu | N-Glycyl-L-leucine | (S)-2-(2-Aminoacetamido)-4-methylpentanoic acid | L-Leucine, glycyl- | H-Gly-Leu-OH | Glycyl-leucine | L-Leucine, N-glycyl- | Leucine, N-glycyl-, L- | CHEMBL56119 | CHEBI:73514 | 8L97V505GU | Gly-L-Leu | MFCD00008127 | GLY-D
Specifications & Purity10mM in Water
Storage TempStore at -80°C
Shipped InIce chest + Ice pads

Associated Targets(Human)

ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC15A1 Tchem Oligopeptide transporter small intestine isoform (922 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Slc15a2 Oligopeptide transporter, kidney isoform (114 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc15a1 Solute carrier family 15 member 1 (124 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name (2S)-2-[(2-aminoacetyl)amino]-4-methylpentanoic acid
INCHI InChI=1S/C8H16N2O3/c1-5(2)3-6(8(12)13)10-7(11)4-9/h5-6H,3-4,9H2,1-2H3,(H,10,11)(H,12,13)/t6-/m0/s1
InChi Key DKEXFJVMVGETOO-LURJTMIESA-N
Canonical SMILES CC(C)CC(C(=O)O)NC(=O)CN
Isomeric SMILES CC(C)C[C@@H](C(=O)O)NC(=O)CN
PubChem CID 92843
Molecular Weight 188.22
Beilstein 4453
Reaxy-Rn 1726294

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

Specific Rotation[α]-35 ° (C=2, H2O)
Melt Point(°C)256°C

Safety and Hazards(GHS)

Reaxy-Rn 1726294

Related Documents

Citations of This Product

1. Yong-Yu Qi, Qian Gan, Ya-Xian Liu, Ya-Hong Xiong, Zong-Wan Mao, Xue-Yi Le.  (2018)  Two new Cu(II) dipeptide complexes based on 5-methyl-2-(2′-pyridyl)benzimidazole as potential antimicrobial and anticancer drugs: Special exploration of their possible anticancer mechanism.  EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,  154  (220).  [PMID:29803995] [10.1016/j.ejmech.2018.05.023]
2. Guangxin Yuan, Yongbo Peng, Zhenghua Liu, Jieya Hong, Yao Xiao, Jialiang Guo, Norman W. Smith, Jacques Crommen, Zhengjin Jiang.  (2013)  A facile and efficient strategy to enhance hydrophilicity of zwitterionic sulfoalkylbetaine type monoliths.  JOURNAL OF CHROMATOGRAPHY A,  1301  (88).  [PMID:23796416] [10.1016/j.chroma.2013.05.063]

References

1. Yong-Yu Qi, Qian Gan, Ya-Xian Liu, Ya-Hong Xiong, Zong-Wan Mao, Xue-Yi Le.  (2018)  Two new Cu(II) dipeptide complexes based on 5-methyl-2-(2′-pyridyl)benzimidazole as potential antimicrobial and anticancer drugs: Special exploration of their possible anticancer mechanism.  EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,  154  (220).  [PMID:29803995] [10.1016/j.ejmech.2018.05.023]
2. Guangxin Yuan, Yongbo Peng, Zhenghua Liu, Jieya Hong, Yao Xiao, Jialiang Guo, Norman W. Smith, Jacques Crommen, Zhengjin Jiang.  (2013)  A facile and efficient strategy to enhance hydrophilicity of zwitterionic sulfoalkylbetaine type monoliths.  JOURNAL OF CHROMATOGRAPHY A,  1301  (88).  [PMID:23796416] [10.1016/j.chroma.2013.05.063]

Solution Calculators