neuropeptide W-23, Agonist of NPBW1 receptor;Agonist of NPBW2 receptor, CAS No.383415-89-2, Agonist of NPBW1 receptor;Agonist of NPBW2 receptor

CAS: 383415-89-2 Cat. No.: rp174625 PubChem CID: 90472277
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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
rp174625-500μg
1-2 wks(?)
Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$2,399.90
1mg
rp174625-1mg
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
neuropeptide W-23, Agonist of NPBW1 receptor;Agonist of NPBW2 receptor, CAS No.383415-89-2
Synonyms
NPW-23
Grade
Moligand™
Specifications & Purity
Moligand™
Action Type
AGONIST
Mechanism of action
Agonist of NPBW1 receptor;Agonist of NPBW2 receptor
CAS
383415-89-2
Molecule Type
Peptide
Storage and Shipping
Storage
Room temperature

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ 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  Tyrosine and derivatives  Arginine and derivatives  Phenylalanine and derivatives  Histidine and derivatives  Leucine and derivatives  Methionine and derivatives  Valine and derivatives  N-acyl-L-alpha-amino acids  Proline and derivatives  Tryptamines and derivatives  Serine and derivatives  Alpha amino acid amides  Alanine and derivatives  Amphetamines and derivatives  3-alkylindoles  Pyrrolidinecarboxamides  N-acylpyrrolidines  Imidazolyl carboxylic acids and derivatives  Aralkylamines  1-hydroxy-2-unsubstituted benzenoids  N-acyl amines  Substituted pyrroles  Tertiary carboxylic acid amides  Heteroaromatic compounds  Guanidines  Secondary alcohols  Amino acids  Secondary carboxylic acid amides  Sulfenyl compounds  Monocarboxylic acids and derivatives  Azacyclic compounds  Carboximidamides  Carboxylic acids  Dialkylthioethers  Imines  Hydrocarbon derivatives  Organopnictogen compounds  Carbonyl compounds  Organic oxides  Primary alcohols  Monoalkylamines  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Polypeptide - Alpha peptide - Tyrosine or derivatives - Arginine or derivatives - Phenylalanine or derivatives - Histidine or derivatives - Methionine or derivatives - Leucine or derivatives - Proline or derivatives - N-acyl-alpha-amino acid - N-acyl-l-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Valine or derivatives - Alpha-amino acid amide - Triptan - Serine or derivatives - Alanine or derivatives - Amphetamine or derivatives - 3-alkylindole - Alpha-amino acid or derivatives - N-substituted-alpha-amino acid - Indole or derivatives - Indole - Imidazolyl carboxylic acid derivative - N-acylpyrrolidine - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Aralkylamine - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Fatty acyl - Monocyclic benzene moiety - Fatty amide - Substituted pyrrole - N-acyl-amine - Azole - Tertiary carboxylic acid amide - Imidazole - Heteroaromatic compound - Pyrrole - Pyrrolidine - Amino acid or derivatives - Secondary alcohol - Carboxamide group - Guanidine - Amino acid - Secondary carboxylic acid amide - Azacycle - Dialkylthioether - Thioether - Carboxylic acid derivative - Carboxylic acid - Sulfenyl compound - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboximidamide - Organonitrogen compound - Organosulfur compound - Primary alcohol - Primary amine - Organooxygen compound - Carbonyl group - Amine - Organopnictogen compound - Alcohol - Imine - Organic oxide - Organic nitrogen compound - Primary aliphatic amine - Organic oxygen compound - Hydrocarbon derivative - 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 Not available
Associated Targets(Human)
NPBWR2 Tbio Neuropeptides B/W receptor type 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
NPBWR1 Tchem Neuropeptides B/W receptor type 1 (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 NamesNPW-23
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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