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TAK-448, Agonist of kisspeptin receptor, CAS No.rp175259, Agonist of kisspeptin receptor

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Item Number
rp175259
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rp175259-500μg
500μg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,334.90
rp175259-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$2,334.90
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kisspeptin receptor Agonist (16)

Basic Description

Product Name TAK-448, Agonist of kisspeptin receptor, CAS No.rp175259
Synonyms analogue 24;RVT-602;TAK448
Grade Moligand™
Specifications & Purity Moligand™
Action Type AGONIST
Mechanism of action Agonist of kisspeptin receptor

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Carboxylic acids and derivatives
Subclass Amino acids, peptides, and analogues
Intermediate Tree Nodes Peptides
Direct Parent Oligopeptides
Alternative Parents Arginine and derivatives  Phenylalanine and derivatives  Leucine and derivatives  Asparagine and derivatives  N-acyl-alpha amino acids and derivatives  N-carbamoyl-alpha amino acids and derivatives  Proline and derivatives  Tryptamines and derivatives  Alpha amino acid amides  3-alkylindoles  Amphetamines and derivatives  N-acylpyrrolidines  Pyrrolidinecarboxamides  1-hydroxy-2-unsubstituted benzenoids  Substituted pyrroles  N-acyl amines  Heteroaromatic compounds  Hydrazinecarboxamides  Semicarbazides  Tertiary carboxylic acid amides  Acetamides  Secondary carboxylic acid amides  Secondary alcohols  Primary carboxylic acid amides  Organic carbonic acids and derivatives  Carboxylic acid hydrazides  Guanidines  Azacyclic compounds  Propargyl-type 1,3-dipolar organic compounds  Carboximidamides  Carbonyl compounds  Organopnictogen compounds  Organic oxides  Imines  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Alpha-oligopeptide - Arginine or derivatives - Phenylalanine or derivatives - Leucine or derivatives - Asparagine or derivatives - N-carbamoyl-alpha-amino acid or derivatives - N-acyl-alpha amino acid or derivatives - Proline or derivatives - Alpha-amino acid amide - Triptan - N-substituted-alpha-amino acid - 3-alkylindole - Alpha-amino acid or derivatives - Amphetamine or derivatives - Indole or derivatives - Indole - Pyrrolidine carboxylic acid or derivatives - N-acylpyrrolidine - Pyrrolidine-2-carboxamide - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Fatty acyl - N-acyl-amine - Benzenoid - Substituted pyrrole - Fatty amide - Monocyclic benzene moiety - Heteroaromatic compound - Acetamide - Hydrazinecarboxamide - Pyrrole - Tertiary carboxylic acid amide - Semicarbazide - Pyrrolidine - Secondary carboxylic acid amide - Secondary alcohol - Primary carboxylic acid amide - Carbonic acid derivative - Carboxamide group - Carboxylic acid hydrazide - Guanidine - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Organoheterocyclic compound - Alcohol - Organooxygen compound - Organic oxygen compound - Carbonyl group - Organonitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Imine - Organic nitrogen compound - Organic oxide - Aromatic heteropolycyclic compound
Description This 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

Associated Targets(Human)

KISS1R Tchem KiSS-1 receptor (0 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)

Storage and Shipping

CAS rp175259

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

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

Genetic information

Alternate Names analogue 24;RVT-602;TAK448
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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