teduglutide, Agonist of GLP-2 receptor, CAS No.197922-42-2, Agonist of GLP-2 receptor

CAS: 197922-42-2 Cat. No.: rp175268 EC Number: 812-261-5 PubChem CID: 16139605
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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.
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Size
Status
Price
Qty
500μg
rp175268-500μg
1-2 wks(?)
Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$2,399.90
1mg
rp175268-1mg
1-2 wks(?)
Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$3,999.90
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Why this grade

Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships 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.

Specifications

Product Name
teduglutide, Agonist of GLP-2 receptor, CAS No.197922-42-2
Synonyms
s9935 | revefenacinum | HOVEYDA-GRUBBS CATALYST M72 | GLP2-2G | (Gly2)GLP-2 | teduglutidum | [Gly2]GLP-2 | Teduglutide-d8 (Phe-d8) | HSDB 8337 | revestive | DTXSID30471901 | Teduglutide [USAN:INN:BAN] | ALX 0600 | Teduglutide | ALX-0600 | Gly(2)-GLP-2 | G
Grade
Moligand™
Specifications & Purity
Moligand™
Action Type
AGONIST
Mechanism of action
Agonist of GLP-2 receptor
CAS
197922-42-2
Molecule Type
Peptide
Storage and Shipping
Storage
Room temperature

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.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic Polymers
ClassPolypeptides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPolypeptides
Alternative Parents Peptides  Arginine and derivatives  Phenylalanine and derivatives  Histidine and derivatives  Glutamic acid and derivatives  Glutamine and derivatives  Aspartic acid and derivatives  Asparagine and derivatives  Methionine and derivatives  Leucine and derivatives  Isoleucine and derivatives  Acyl L-homoserines  N-acyl-L-alpha-amino acids  Serine and derivatives  Tryptamines and derivatives  Alpha amino acid amides  Alanine and derivatives  3-alkylindoles  Amphetamines and derivatives  Imidazolyl carboxylic acids and derivatives  Aralkylamines  N-acyl amines  Substituted pyrroles  Heteroaromatic compounds  Amino acids  Guanidines  Primary carboxylic acid amides  Secondary alcohols  Secondary carboxylic acid amides  Sulfenyl compounds  Dialkylthioethers  Carboxylic acids  Carboximidamides  Azacyclic compounds  Carbonyl compounds  Hydrocarbon derivatives  Imines  Monoalkylamines  Organic oxides  Organopnictogen compounds  Primary alcohols  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Polypeptide - Alpha peptide - Arginine or derivatives - Phenylalanine or derivatives - Histidine or derivatives - Glutamic acid or derivatives - Glutamine or derivatives - Methionine or derivatives - Asparagine or derivatives - Aspartic acid or derivatives - Leucine or derivatives - Isoleucine or derivatives - Acyl-l-homoserine - N-acyl-l-alpha-amino acid - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Acyl-homoserine - Alpha-amino acid amide - Serine or derivatives - Triptan - Alanine or derivatives - Alpha-amino acid or derivatives - 3-alkylindole - N-substituted-alpha-amino acid - Amphetamine or derivatives - Indole - Indole or derivatives - Imidazolyl carboxylic acid derivative - Aralkylamine - Fatty amide - N-acyl-amine - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Imidazole - Pyrrole - Azole - Guanidine - Secondary carboxylic acid amide - Carboxamide group - Secondary alcohol - Primary carboxylic acid amide - Amino acid - Amino acid or derivatives - Organoheterocyclic compound - Azacycle - Carboximidamide - Dialkylthioether - Thioether - Carboxylic acid derivative - Sulfenyl compound - Carboxylic acid - Primary amine - Alcohol - Imine - Hydrocarbon derivative - Primary aliphatic amine - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organosulfur compound - Organic oxide - Primary alcohol - Amine - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as polypeptides. These are peptides containing ten or more amino acid residues.
External Descriptors polypeptide
Associated Targets(Human)
GLP2R Tclin Glucagon-like peptide 2 receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Genetic information
Alternate Namess9935 | revefenacinum | HOVEYDA-GRUBBS CATALYST M72 | GLP2-2G | (Gly2)GLP-2 | teduglutidum | [Gly2]GLP-2 | Teduglutide-d8 (Phe-d8) | HSDB 8337 | revestive | DTXSID30471901 | Teduglutide [USAN:INN:BAN] | ALX 0600 | Teduglutide | ALX-0600 | Gly(2)-GLP-2 | G
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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