CCK-33, Agonist of CCK 1 receptor;Agonist of CCK 2 receptor, CAS No.rp173630, Agonist of CCK 1 receptor;Agonist of CCK 2 receptor

CAS: rp173630 Cat. No.: rp173630 PubChem CID: 16129670
Disponibile su ordine
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
Germania (EU)
USA*
Price
Qty
500μg
rp173630-500μg
Su ordinazione · 8–12 settimane
2.082,49€
1mg
rp173630-1mg
Su ordinazione · 8–12 settimane
3.470,87€
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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
CCK-33, Agonist of CCK 1 receptor;Agonist of CCK 2 receptor, CAS No.rp173630
Sinonimi
CCRIS 3307 | Cholecystokinin 33 | SCHEMBL3045554 | 00XI8W60QF | CCK-33 | Cecekin vitrum | CHOLECYSTOKININ | GTPL860 | UNII-00XI8W60QF
Grado
Moligand™
Specifiche e purezza
Moligand™
Tipo di azione
AGONIST
Meccanismo d'azione
Agonist of CCK 1 receptor;Agonist of CCK 2 receptor
CAS
rp173630
Tipo di molecola
Peptidi
Stoccaggio e spedizione
Condizioni di conservazione di stoccaggio
Room temperature

Documentazione

📋 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
ClassePolypeptides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPolypeptides
Alternative Parents Peptides  Phenylalanine and derivatives  Arginine and derivatives  Histidine and derivatives  Glutamine and derivatives  Leucine and derivatives  Methionine and derivatives  Isoleucine and derivatives  Asparagine and derivatives  Aspartic acid and derivatives  Proline and derivatives  Valine and derivatives  Tetracarboxylic acids and derivatives  N-acyl-alpha amino acids and derivatives  Alpha amino acid amides  Tryptamines and derivatives  Serine and derivatives  Phenylsulfates  Phenylacetamides  Amphetamines and derivatives  3-alkylindoles  Imidazolyl carboxylic acids and derivatives  Pyrrolidinecarboxamides  Phenoxy compounds  N-acylpyrrolidines  Sulfuric acid monoesters  Substituted pyrroles  N-acyl amines  Tertiary carboxylic acid amides  Heteroaromatic compounds  Primary carboxylic acid amides  Secondary carboxylic acid amides  Guanidines  Amino acids  Sulfenyl compounds  Dialkylthioethers  Azacyclic compounds  Carboximidamides  Carboxylic acids  Hydrocarbon derivatives  Primary alcohols  Organic oxides  Carbonyl compounds  Monoalkylamines  Imines  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Polypeptide - Alpha peptide - Arginine or derivatives - Phenylalanine or derivatives - Histidine or derivatives - Glutamine or derivatives - Methionine or derivatives - Asparagine or derivatives - Aspartic acid or derivatives - Leucine or derivatives - Isoleucine or derivatives - Tetracarboxylic acid or derivatives - N-acyl-alpha amino acid or derivatives - Valine or derivatives - Proline or derivatives - Alpha-amino acid amide - Serine or derivatives - Triptan - Phenylsulfate - Arylsulfate - Alpha-amino acid or derivatives - N-substituted-alpha-amino acid - 3-alkylindole - Amphetamine or derivatives - Phenylacetamide - Indole - Indole or derivatives - Phenoxy compound - Imidazolyl carboxylic acid derivative - N-acylpyrrolidine - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Benzenoid - Sulfuric acid ester - Monocyclic benzene moiety - Fatty acyl - Fatty amide - N-acyl-amine - Sulfate-ester - Sulfuric acid monoester - Substituted pyrrole - Azole - Imidazole - Tertiary carboxylic acid amide - Organic sulfuric acid or derivatives - Heteroaromatic compound - Pyrrole - Pyrrolidine - Amino acid or derivatives - Primary carboxylic acid amide - Secondary carboxylic acid amide - Amino acid - Carboxamide group - Guanidine - Dialkylthioether - Carboximidamide - Sulfenyl compound - Carboxylic acid derivative - Carboxylic acid - Thioether - Azacycle - Organoheterocyclic compound - Organic oxide - Imine - Alcohol - Organic nitrogen compound - Primary aliphatic amine - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Hydrocarbon derivative - Amine - Primary alcohol - Primary amine - Organooxygen compound - Organosulfur compound - Aromatic heteropolycyclic compound
DescrizioneThis 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
Obiettivi associati (umani)
CCKAR Tclin Cholecystokinin receptor type A (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CCKBR Tclin Gastrin/cholecystokinin type B receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Informazioni genetiche
Alternate NamesCCRIS 3307 | Cholecystokinin 33 | SCHEMBL3045554 | 00XI8W60QF | CCK-33 | Cecekin vitrum | CHOLECYSTOKININ | GTPL860 | UNII-00XI8W60QF
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
Calcolatori di soluzioni
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