Ethamsylate - 10mM in DMSO , CAS No.2624-44-4

CAS: 2624-44-4 Cat. No.: E422928 Summenformel: C6H6O5S·C4H11N Molekulargewicht: 263.31 EG-Nummer: 220-090-7
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QUALITÄT & REINHEIT 10mM in DMSO
Synonyms
Etamsylate|ETHAMSYLATE|2624-44-4|Cyclonamine|Aglumin|Dicynene|Ciclonamina|Eselin|Etamsylatum|Etamsilate|Etamsilato|MD 141|Ethamsylate [USAN]|Diethylamine dobesilate|E 141|Etamsylatum [INN-Latin]|diethylamine 2,5-dihydroxybenzenesulfonate|Etamsilato [INN-S
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Preis
Menge
1ml
E422928-1ml
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30,28€
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Warum diese Qualität

10mM in DMSO für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Store at -80°C Versand Dry ice packs + Cold packs. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Qualitätsdokumente

SDS, COA, Datenblatt und Spezifikationsblatt stehen zum Download bereit. Chargenspezifische COA über Chargennummernsuche abrufbar.

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Literaturbeleg

In 2 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

Antifibrinolytic agent. Increases capillary endothelial resistance. Promotes platelet adhesion. Inhibits platelet disaggregating and vasodilatory prostaglandin biosynthesis and function. Enhances P-selectin membrane expression. Shows angioprotective and proaggregant effects in vivo. Orally active.

Spezifikationen

Synonyme
Etamsylate | ETHAMSYLATE | 2624-44-4 | Cyclonamine | Aglumin | Dicynene | Ciclonamina | Eselin | Etamsylatum | Etamsilate | Etamsilato | MD 141 | Ethamsylate [USAN] | Diethylamine dobesilate | E 141 | Etamsylatum [INN-Latin] | diethylamine 2,5-dihydroxybenzenesulfonate | Etamsilato [INN-S
Spezifikationen & Reinheit
10mM in DMSO
Biochemische und physiologische Mechanismen
Antifibrinolytic agent. Increases capillary endothelial resistance. Promotes platelet adhesion. Inhibits platelet disaggregating and vasodilatory prostaglandin biosynthesis and function. Enhances P-selectin membrane expression.
Storage
Store at -80°C
Verschickt in
Dry ice packs + Cold packs
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Aktionsart
INHIBITOR
Namen und Kennungen
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/528775941
Kanonisches Lächeln
CCNCC.C1=CC(=C(C=C1O)S(=O)(=O)O)O
IUPAC Name
2,5-dihydroxybenzenesulfonic acid;N-ethylethanamine
InChIKey
HBGOLJKPSFNJSD-UHFFFAOYSA-N
INCHI
1S/C6H6O5S.C4H11N/c7-4-1-2-5(8)6(3-4)12(9,10)11;1-3-5-4-2/h1-3,7-8H,(H,9,10,11);5H,3-4H2,1-2H3
Isomere SMILES
CCNCC.C1=CC(=C(C=C1O)S(=O)(=O)O)O
RTECS
DB6145000
Molekulargewicht
263.31
Reaxy-Rn
4166074
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4166074&ln=

Dokumentation

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✅ Analysezertifikat (COA)

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🔬 Spezifikationsblatt

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
KlasseBenzene and substituted derivatives
SubclassBenzenesulfonic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentBenzenesulfonic acids and derivatives
Alternative Parents Benzenesulfonyl compounds  1-sulfo,2-unsubstituted aromatic compounds  Hydroquinones  1-hydroxy-2-unsubstituted benzenoids  Sulfonyls  Organosulfonic acids  Dialkylamines  Organopnictogen compounds  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkNot available
Substituents Benzenesulfonate - Arylsulfonic acid or derivatives - Benzenesulfonyl group - 1-sulfo,2-unsubstituted aromatic compound - Hydroquinone - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Secondary aliphatic amine - Secondary amine - Amine - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as benzenesulfonic acids and derivatives. These are organic compounds containing a sulfonic acid or a derivative thereof that is linked to a benzene ring.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasma (328 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemische und physikalische Eigenschaften
Schmelzpunkt (°C)130 °C
Molekulargewicht263.310 g/mol
XLogP3
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count3
Exact Mass263.083 Da
Monoisotopic Mass263.083 Da
Topological Polar Surface Area115.000 Ų
Heavy Atom Count17
Formal Charge0
Complexity252.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Citations of This Product
Lösungsrechner
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