DX600, Inhibitor of Angiotensin-converting enzyme 2, CAS No.rp173930, Inhibitor of Angiotensin-converting enzyme 2

CAS: rp173930 Cat. No.: rp173930 PubChem CID: 16138722
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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
Deutschland (EU)
USA*
Price
Qty
500μg
rp173930-500μg
Auf Bestellung · 8–12 Wochen
2.082,49€
1mg
rp173930-1mg
Auf Bestellung · 8–12 Wochen
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
DX600, Inhibitor of Angiotensin-converting enzyme 2, CAS No.rp173930
Synonyme
DX-600
Note
Moligand™
Spezifikationen & Reinheit
Moligand™
Aktionsart
INHIBITOR
Mechanismus der Wirkung
Inhibitor of Angiotensin-converting enzyme 2
CAS
rp173930
Molekültyp
Peptide
Lagerung und Versand
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
KlassePolypeptides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPolypeptides
Alternative Parents Peptides  Tyrosine and derivatives  Arginine and derivatives  Phenylalanine and derivatives  Histidine and derivatives  Glutamic acid and derivatives  Aspartic acid and derivatives  Leucine and derivatives  N-acyl-alpha amino acids and derivatives  Proline and derivatives  Tryptamines and derivatives  Cysteine and derivatives  Alpha amino acid amides  Serine and derivatives  Amphetamines and derivatives  3-alkylindoles  Tricarboxylic acids and derivatives  Pyrrolidinecarboxamides  N-acylpyrrolidines  Imidazolyl carboxylic acids and derivatives  1-hydroxy-2-unsubstituted benzenoids  N-acyl amines  Substituted pyrroles  Acetamides  Heteroaromatic compounds  Tertiary carboxylic acid amides  Primary carboxylic acid amides  Secondary carboxylic acid amides  Amino acids  Secondary alcohols  Guanidines  Carboximidamides  Carboxylic acids  Azacyclic compounds  Alkylthiols  Carbonyl compounds  Hydrocarbon derivatives  Imines  Monoalkylamines  Organic oxides  Primary alcohols  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Polypeptide - Alpha peptide - Tyrosine or derivatives - Arginine or derivatives - Phenylalanine or derivatives - Histidine or derivatives - Glutamic acid or derivatives - Aspartic acid or derivatives - Leucine or derivatives - N-acyl-alpha amino acid or derivatives - Proline or derivatives - Alpha-amino acid amide - Triptan - Serine or derivatives - Cysteine or derivatives - Alpha-amino acid or derivatives - Amphetamine or derivatives - N-substituted-alpha-amino acid - 3-alkylindole - Tricarboxylic acid or derivatives - Indole - Indole or derivatives - Pyrrolidine carboxylic acid or derivatives - N-acylpyrrolidine - Imidazolyl carboxylic acid derivative - Pyrrolidine-2-carboxamide - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Substituted pyrrole - Fatty amide - N-acyl-amine - Fatty acyl - Benzenoid - Azole - Heteroaromatic compound - Imidazole - Acetamide - Tertiary carboxylic acid amide - Pyrrolidine - Pyrrole - Amino acid or derivatives - Primary carboxylic acid amide - Secondary carboxylic acid amide - Secondary alcohol - Amino acid - Carboxamide group - Guanidine - Carboximidamide - Carboxylic acid derivative - Carboxylic acid - Alkylthiol - Organoheterocyclic compound - Azacycle - Primary amine - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Hydrocarbon derivative - Alcohol - Organooxygen compound - Organosulfur compound - Primary alcohol - Amine - Organic nitrogen compound - Organic oxide - Imine - Organic oxygen compound - Aromatic heteropolycyclic compound
BeschreibungThis 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
Zugehörige Ziele (menschlich)
ACE2 Tchem Angiotensin-converting enzyme 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Genetische Informationen
Alternate NamesDX-600
Referenz
  • 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
Lösungsrechner
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