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[¹²⁵I]GLP-1-(7-36)-amide, Agonist of GLP-1 receptor, CAS No.rp175107, Agonist of GLP-1 receptor

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Item Number
rp175107
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rp175107-1mg
1mg
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$1,668.90
rp175107-5mg
5mg
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$3,001.90
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GLP-1 receptor Agonist (16)

Basic Description

Product Name [¹²⁵I]GLP-1-(7-36)-amide, Agonist of GLP-1 receptor, CAS No.rp175107
Synonyms [¹²⁵I]GLP-1;[¹²⁵I]GLP-1(7-36)amide;[¹²⁵I]glucagon-like peptide 1 (7-36)
Grade Moligand™
Specifications & Purity Moligand™
Action Type AGONIST
Mechanism of action Agonist of GLP-1 receptor

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic Polymers
Class Polypeptides
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Polypeptides
Alternative Parents Peptides  Tyrosine and derivatives  Phenylalanine and derivatives  Arginine and derivatives  Histidine and derivatives  Glutamine and derivatives  Glutamic acid and derivatives  Aspartic acid and derivatives  Isoleucine and derivatives  Leucine and derivatives  Tetracarboxylic acids and derivatives  N-acyl-alpha amino acids and derivatives  Valine and derivatives  Alpha amino acid amides  Tryptamines and derivatives  Serine and derivatives  Alanine and derivatives  Amphetamines and derivatives  3-alkylindoles  Imidazolyl carboxylic acids and derivatives  1-hydroxy-2-unsubstituted benzenoids  Aralkylamines  Substituted pyrroles  N-acyl amines  Heteroaromatic compounds  Secondary carboxylic acid amides  Secondary alcohols  Amino acids  Primary carboxylic acid amides  Guanidines  Azacyclic compounds  Carboximidamides  Carboxylic acids  Organic oxides  Primary alcohols  Hydrocarbon derivatives  Imines  Carbonyl compounds  Monoalkylamines  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Polypeptide - Alpha peptide - Tyrosine or derivatives - Arginine or derivatives - Phenylalanine or derivatives - Histidine or derivatives - Glutamic acid or derivatives - Glutamine or derivatives - Aspartic acid or derivatives - Isoleucine or derivatives - Leucine or derivatives - Valine or derivatives - N-acyl-alpha amino acid or derivatives - Tetracarboxylic acid or derivatives - Alpha-amino acid amide - Serine or derivatives - Triptan - Alanine or derivatives - Alpha-amino acid or derivatives - N-substituted-alpha-amino acid - Amphetamine or derivatives - 3-alkylindole - Indole or derivatives - Indole - Imidazolyl carboxylic acid derivative - Aralkylamine - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Fatty acyl - Substituted pyrrole - N-acyl-amine - Fatty amide - Benzenoid - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Imidazole - Pyrrole - Primary carboxylic acid amide - Amino acid or derivatives - Secondary alcohol - Secondary carboxylic acid amide - Amino acid - Carboxamide group - Guanidine - Carboximidamide - Carboxylic acid derivative - Carboxylic acid - Organoheterocyclic compound - Azacycle - Organooxygen compound - Primary alcohol - Primary amine - Carbonyl group - Hydrocarbon derivative - Alcohol - Primary aliphatic amine - Organonitrogen compound - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Amine - Imine - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as polypeptides. These are peptides containing ten or more amino acid residues.
External Descriptors Not available

Associated Targets(Human)

GLP1R Tclin Glucagon-like peptide 1 receptor (0 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)

Storage and Shipping

CAS rp175107

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

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

Genetic information

Alternate Names [¹²⁵I]GLP-1;[¹²⁵I]GLP-1(7-36)amide;[¹²⁵I]glucagon-like peptide 1 (7-36)
Reference
  • 1. Kinetics and inhibition of recombinant human cystathionine gamma-lyase. Toward the rational control of transsulfuration., The Journal of biological chemistry, Steegborn, C C and 7 more authors.
  • 2. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences., Proceedings of the National Academy of Sciences of the United States of America, Strausberg, Robert L RL and 83 more authors.
  • 3. Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH)., Human genetics, Wang, Jian J and Hegele, Robert A RA.
  • 4. Cloning and nucleotide sequence of human liver cDNA encoding for cystathionine gamma-lyase., Biochemical and biophysical research communications, Lu, Y Y, O'Dowd, B F BF, Orrego, H H and Israel, Y Y.
  • 5. Single nucleotide polymorphism in CTH associated with variation in plasma homocysteine concentration., Clinical genetics, Wang, J J, Huff, A M AM, Spence, J D JD and Hegele, R A RA.
  • 6. Cystathionine gamma-lyase overexpression inhibits cell proliferation via a H2S-dependent modulation of ERK1/2 phosphorylation and p21Cip/WAK-1., The Journal of biological chemistry, Yang, Guangdong G, Cao, Kun K, Wu, Lingyun L and Wang, Rui R.
  • 7. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)., Genome research, Gerhard, Daniela S DS and 115 more authors.
  • 8. Towards a proteome-scale map of the human protein-protein interaction network., Nature, Rual, Jean-François JF and 37 more authors.
  • 9. The DNA sequence and biological annotation of human chromosome 1., Nature, Gregory, S G SG and 178 more authors.
  • 10. Polymorphisms in one-carbon metabolism and trans-sulfuration pathway genes and susceptibility to bladder cancer., International journal of cancer, Moore, Lee E LE and 14 more authors. more

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