Aprotinin, CAS No.9087-70-1

CAS: 9087-70-1 Cat. No.: A274384 Summenformel: C284H432N84O79S7 Molekulargewicht: 6511.44 EG-Nummer: 232-994-9 PubChem CID: 22833874
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QUALITÄT & REINHEIT EnzymoPure™ ? EnzymoPure™ — Aladdin's line of high-quality enzymatic solutions. Use when enzyme purity and defined activity drive assay or process performance. High-purity ? High-purity grade with substantially reduced impurity levels. Use when trace contaminants would interfere with your measurement or process.
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10mg
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Warum diese Qualität

EnzymoPure™, high-purity High-purity,EnzymoPure™ für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Store at 2-8°C Versand Wet ice. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Qualitätsdokumente

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Literaturbeleg

In 16 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

Aprotinin (Traskolan) is a broad-spectrum serine protease (BPTI) inhibitor that inhibits the activity of a number of different esterases and proteases. Aprotinin is an antifibrinolytic agent used to minimize hemorrhage during complex surgical procedures.

Spezifikationen

Product Name
Aprotinin, CAS No.9087-70-1
Synonyme
Aprotinin from bovine lung | CCG-270718 | APROTININ | Traskolan | Antilysin | J-200086 | Bovine Pancreatic Trypsin Inhibitor | AKOS024457997
Note
High-purity, EnzymoPure™
Spezifikationen & Reinheit
EnzymoPure™, high-purity
CAS
9087-70-1
Molekültyp
Enzyme
Lagerung und Versand
Storage
Store at 2-8°C
Verschickt in
Wet ice
Definition der Einheit
1 U corresponds to 1 biological kallikrein inhibitor unit (KIU)

Dokumentation

📋 Sicherheitsdatenblatt (SDS)

Umfassendes Dokument zu Gefahren, Handhabung, Lagerung und Einhaltung regulatorischer Vorschriften.

<<<<<<< HEAD SDS herunterladen → ======= SDS herunterladen → >>>>>>> release248-p3

✅ Analysezertifikat (COA)

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📊 Datenblatt

Kurzübersicht über Produktspezifikationen und Anwendungen.

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🔬 Spezifikationsblatt

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic Polymers
KlassePolypeptides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPolypeptides
Alternative Parents Cyclic peptides  Phenylalanine and derivatives  Pentacarboxylic acids and derivatives  Aspartic acid and derivatives  N-acyl-alpha amino acids  Proline and derivatives  Alpha amino acid amides  Alanine and derivatives  Amphetamines and derivatives  Pyrrolidinecarboxamides  N-acylpyrrolidines  1-hydroxy-2-unsubstituted benzenoids  N-acyl amines  Tertiary carboxylic acid amides  Secondary alcohols  Guanidines  Amino acids  Organic disulfides  Secondary carboxylic acid amides  Lactams  Primary carboxylic acid amides  Sulfenyl compounds  Azacyclic compounds  Carboximidamides  Carboxylic acids  Dialkylthioethers  Primary alcohols  Imines  Carbonyl compounds  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  Monoalkylamines  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Polypeptide - Cyclic alpha peptide - Phenylalanine or derivatives - Pentacarboxylic acid or derivatives - Aspartic acid or derivatives - N-acyl-alpha amino acid or derivatives - N-acyl-alpha-amino acid - Proline or derivatives - Alpha-amino acid amide - Alanine or derivatives - Amphetamine or derivatives - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - N-acylpyrrolidine - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Fatty acyl - Benzenoid - N-acyl-amine - Fatty amide - Pyrrolidine - Tertiary carboxylic acid amide - Organic disulfide - Amino acid or derivatives - Primary carboxylic acid amide - Carboxamide group - Amino acid - Secondary alcohol - Secondary carboxylic acid amide - Lactam - Guanidine - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Dialkylthioether - Sulfenyl compound - Carboximidamide - Thioether - Hydrocarbon derivative - Organic oxide - Amine - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Alcohol - Imine - Primary aliphatic amine - Primary amine - Primary alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen 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
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
PLG Tclin Plasminogen (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:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot NumberCertificate TypeDatumArtikel
D2418123D2418123Certificate of AnalysisAug 04, 2026 A274384
J2429171J2429171Certificate of AnalysisMay 20, 2026 A274384
J2429173J2429173Certificate of AnalysisMay 20, 2026 A274384
F2221118F2221118Certificate of AnalysisApr 03, 2026 A274384
J2327212J2327212Certificate of AnalysisApr 02, 2026 A274384
J2327215J2327215Certificate of AnalysisFeb 04, 2026 A274384
E2120018E2120018Certificate of AnalysisSep 20, 2023 A274384
F2221119F2221119Certificate of AnalysisJun 04, 2022 A274384
C2223049C2223049Certificate of AnalysisMay 11, 2022 A274384
Genetische Informationen
Alternate NamesAprotinin from bovine lung | CCG-270718 | APROTININ | Traskolan | Antilysin | J-200086 | Bovine Pancreatic Trypsin Inhibitor | AKOS024457997
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
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