C3, Agonist of MCH 1 receptor, CAS No.rp173605, Agonist of MCH 1 receptor

CAS: rp173605 Cat. No.: rp173605 PubChem CID: 268
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
rp173605-500μg
Su ordinazione · 8–12 settimane
2.082,49€
1mg
rp173605-1mg
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
C3, Agonist of MCH 1 receptor, CAS No.rp173605
Grado
Moligand™
Specifiche e purezza
Moligand™
Tipo di azione
AGONIST
Meccanismo d'azione
Agonist of MCH 1 receptor
CAS
rp173605
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 acids and derivatives
ClasseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Peptides
Direct ParentOligopeptides
Alternative Parents Pyrimidine nucleotide sugars  Pyrimidine ribonucleoside diphosphates  Pentose phosphates  Glutamic acid and derivatives  N-acyl-alpha-hexosamines  N-acyl-alpha amino acids  Alpha amino acid amides  Alanine and derivatives  Glycosylamines  Monosaccharide phosphates  Organic pyrophosphates  Monoalkyl phosphates  Pyrimidones  Dicarboxylic acids and derivatives  Hydropyrimidines  N-acyl amines  Oxanes  Acetamides  Tetrahydrofurans  Heteroaromatic compounds  Vinylogous amides  Lactams  Amino acids  Secondary carboxylic acid amides  Secondary alcohols  Ureas  Oxacyclic compounds  Dialkyl ethers  Carboxylic acids  Azacyclic compounds  Hydrocarbon derivatives  Organic oxides  Organopnictogen compounds  Carbonyl compounds  Monoalkylamines  Primary alcohols  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Alpha-oligopeptide - Pyrimidine nucleotide sugar - Pyrimidine ribonucleoside diphosphate - Pentose phosphate - Pentose-5-phosphate - N-acyl-alpha-hexosamine - Glutamic acid or derivatives - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Glycosyl compound - N-glycosyl compound - Alanine or derivatives - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Organic pyrophosphate - Monosaccharide phosphate - Pyrimidone - Monoalkyl phosphate - Alkyl phosphate - Dicarboxylic acid or derivatives - Hydropyrimidine - Organic phosphoric acid derivative - Oxane - Pyrimidine - Fatty amide - Phosphoric acid ester - N-acyl-amine - Monosaccharide - Fatty acyl - Acetamide - Vinylogous amide - Tetrahydrofuran - Heteroaromatic compound - Secondary alcohol - Secondary carboxylic acid amide - Urea - Lactam - Amino acid or derivatives - Carboxamide group - Amino acid - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid - Dialkyl ether - Ether - Organonitrogen compound - Primary amine - Organooxygen compound - Amine - Hydrocarbon derivative - Primary alcohol - Carbonyl group - Alcohol - Organic nitrogen compound - Organic oxide - Organopnictogen compound - Primary aliphatic amine - Organic oxygen compound - Aromatic heteromonocyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
MCHR1 Tchem Melanin-concentrating hormone receptor 1 (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
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
Recensioni

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