cas 1007635-27-9|| where to buy 19-ethyl-18-hydroxy-6,8-dimethyl-15-oxa-3-thia-5,11-diazapentacyclo[11.8.0.0^{2,10}.0^{4,9}.0^{16,21}]henicosa-1(13),2(10),4(9),5,7,11,16,18,20-nonaen-14-one

Nombre del producto:19-ethyl-18-hydroxy-6,8-dimethyl-15-oxa-3-thia-5,11-diazapentacyclo[11.8.0.0^{2,10}.0^{4,9}.0^{16,21}]henicosa-1(13),2(10),4(9),5,7,11,16,18,20-nonaen-14-one

IUPAC Name:19-ethyl-18-hydroxy-6,8-dimethyl-15-oxa-3-thia-5,11-diazapentacyclo[11.8.0.0²,¹⁰.0⁴,⁹.0¹⁶,²¹]henicosa-1(13),2(10),4(9),5,7,11,16,18,20-nonaen-14-one

: CAS：1007635-27-9; Fórmula molecular：C21H16N2O3S; Pureza：95%+

: Número de catálogo：CM799808; Peso molecular：376.43

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: Núm. De CAS :1007635-27-9; Fórmula molecular:C21H16N2O3S; Punto de fusión:-; Código de sonrisas:CCC1=C(O)C=C2OC(=O)C3=C(C4=C(N=C3)C3=C(S4)N=C(C)C=C3C)C2=C1; Densidad:

: Número de catálogo:CM799808; Peso molecular:376.43; Punto de ebullición:; Nº Mdl:; Almacenamiento:

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: Coumarins; Coumarin occurs naturally in a variety of plants, such as lentils, sweet sawdust, vanilla grass, and sweet grass. Coumarin has a simple structure, benzopyrone, associated with different reaction centers. Coumarins are further subdivided into different classes: simple coumarins, pyranocoumarins, furanocoumarins, dicoumarins and isocoumarins. Coumarin derivatives are an important class of natural plant metabolites with various biological activities. They can also be synthesized artificially, and various synthetic coumarin derivatives (azoles, sulfonyls, furans, pyrazoles, etc.) have shown good anticancer, antitumor and antiproliferative activities. Coumarin derivatives are not only effective anticancer agents, but also possess minimum side effects. Based on different substitution patterns, these potential active substances show a great ability to modulate potential anticancer activities.

: Thienopyridines; Thienopyridines are similar in structure to quinoline and isoquinoline, and are a class of heterocyclic compounds with important physiological activity and medicinal value. Thienopyridines are a subclass of antiplatelet drugs that prevent platelet aggregation by binding to selected extracellular cysteine residues on the P2Y12 receptor located on the platelet membrane.

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