Samixogrel , CAS No.133276-80-9

CAS: 133276-80-9 Cat. No.: S668965 Formule: C25H25ClN2O4S Poids moléculaire: 485
DISPONIBLE À COMMANDE
Synonyms
Samixogrel|Samixogrel [INN]|(E)-6-(4-(2-((4-chlorophenyl)sulfonamido)ethyl)phenyl)-6-(pyridin-3-yl)hex-5-enoic acid|dttx30|(E)-6-[4-[2-[(4-chlorophenyl)sulfonylamino]ethyl]phenyl]-6-pyridin-3-ylhex-5-enoic acid|(E)-6-{4-[2-(4-Chloro-benzenesulfonylamino)-ethyl]-phenyl}-6-pyridin-3-yl-hex-5-enoic acid|(E)-6-(p-(2-(p-Chlorobenzenesulfonamido)ethyl)phenyl)-6-(3-pyridyl)-5-hexenoic acid|6-(4-(2-(((4-Chlorophenyl)sulfonyl)amino)ethyl)phenyl)-6-(3-pyridyl)hex-5-enoic acid
Storage
Room temperature
★
Taille
Allemagne (EU)
USA*
Prix
Qté
1mg
S668965-1mg
Sur commande · 8–12 semaines

496,26€

744,43€
Enregistrer 248,17 € (33.34%)
5mg
S668965-5mg
Sur commande · 8–12 semaines

1 735,39€

2 603,13€
Enregistrer 867,74 € (33.33%)
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Spécifications

Synonymes
Samixogrel | Samixogrel [INN] | (E)-6-(4-(2-((4-chlorophenyl)sulfonamido)ethyl)phenyl)-6-(pyridin-3-yl)hex-5-enoic acid | dttx30 | (E)-6-[4-[2-[(4-chlorophenyl)sulfonylamino]ethyl]phenyl]-6-pyridin-3-ylhex-5-enoic acid | (E)-6-{4-[2-(4-Chloro-benzenesulfonylamino)-ethyl]-phenyl}-6-pyridin-3-yl-hex-5-enoic acid | (E)-6-(p-(2-(p-Chlorobenze Afficher plus
Conditions de stockage de stockage
Room temperature
Propriétés du produit
ALogP
5
Noms et identifiants
Sourires canoniques
C1=CC(=CN=C1)C(=CCCCC(=O)O)C2=CC=C(C=C2)CCNS(=O)(=O)C3=CC=C(C=C3)Cl
IUPAC Name
(E)-6-[4-[2-[(4-chlorophenyl)sulfonylamino]ethyl]phenyl]-6-pyridin-3-ylhex-5-enoic acid
InChIKey
LGHLGTHRJNIRCA-ZXKDJJQISA-N
INCHI
1S/C25H25ClN2O4S/c26-22-11-13-23(14-12-22)33(31,32)28-17-15-19-7-9-20(10-8-19)24(5-1-2-6-25(29)30)21-4-3-16-27-18-21/h3-5,7-14,16,18,28H,1-2,6,15,17H2,(H,29,30)/b24-5+
Isomères SMILES
C1=CC(=CN=C1)/C(=C/CCCC(=O)O)/C2=CC=C(C=C2)CCNS(=O)(=O)C3=CC=C(C=C3)Cl
Poids moléculaire
485
Reaxy-Rn
6692061
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6692061&ln=

Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassBenzenesulfonamides
Intermediate Tree Nodes Not available
Direct ParentBenzenesulfonamides
Alternative Parents Benzenesulfonyl compounds  Styrenes  Medium-chain fatty acids  Heterocyclic fatty acids  Halogenated fatty acids  Chlorobenzenes  Unsaturated fatty acids  Pyridines and derivatives  Organosulfonamides  Aryl chlorides  Aminosulfonyl compounds  Heteroaromatic compounds  Azacyclic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Carbonyl compounds  Hydrocarbon derivatives  Organic oxides  Organochlorides  Organonitrogen compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Benzenesulfonamide - Benzenesulfonyl group - Styrene - Medium-chain fatty acid - Chlorobenzene - Halobenzene - Halogenated fatty acid - Heterocyclic fatty acid - Fatty acid - Aryl halide - Aryl chloride - Fatty acyl - Unsaturated fatty acid - Pyridine - Organosulfonic acid amide - Aminosulfonyl compound - Heteroaromatic compound - Sulfonyl - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Azacycle - Carboxylic acid - Carboxylic acid derivative - Hydrocarbon derivative - Organic nitrogen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organosulfur compound - Organic oxygen compound - Organic oxide - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzenesulfonamides. These are organic compounds containing a sulfonamide group that is S-linked to a benzene ring.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
TBXAS1 Tchem Thromboxane-A synthase (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TBXA2R Tclin Thromboxane A2 receptor (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TBXAS1 Tchem Thromboxane-A synthase (3355 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriétés chimiques et physiques
Poids moléculaire485.000 g/mol
XLogP35.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count11
Exact Mass484.122 Da
Monoisotopic Mass484.122 Da
Topological Polar Surface Area105.000 Ų
Heavy Atom Count33
Formal Charge0
Complexity736.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Calculateurs de solution
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