
CAS 1000995-49-2: [(1aR,1bS,2R,2aS,5cR,9aR,10S,10aS,11aR,11bS,11cS,12aS,12bS)-1,1a,1b,2,2a,4,7,9,9a,10,10a,11,11a,11b,11c,12,12a,12b-Octadecahidro-2,2a,10,12a-tetrahidroxi-8-(hidroximetil)-1b,5,11b-trimetil-4,7-dioxobiscyclopropa[4′,5′]ciclopenta[1′,2′,3′:1,10;2′′,1′′:7,8]fenantreno[3,4-b:4b,5-b′]difurano-10-il]metil (2E)-2-metil-2-butenoato
Descripción:
La sustancia química con el nombre "[(1aR,1bS,2R,2aS,5cR,9aR,10S,10aS,11aR,11bS,11cS,12aS,12bS)-1,1a,1b,2,2a,4,7,9,9a,10,10a,11,11a,11b,11c,12,12a,12b-Octadecahidro-2,2a,10,12a-tetrahidroxi-8-(hidroximetil)-1b,5,11b-trimetil-4,7-dioxobiscyclopropa[4′,5′]ciclopenta[1′,2′,3′:1,10;2′′,1′′:7,8]fenantreno[3,4-b:4b,5-b′]difurano-10-il]metil (2E)-2-metil-2-butenoato" y el número CAS "1000995-49-2" es un compuesto orgánico complejo caracterizado por su intrincada estructura policíclica y múltiples estereocentros. Esta sustancia presenta una disposición única de grupos funcionales, incluyendo funcionalidades hidroxilo y éster, que contribuyen a su reactividad química y potencial actividad biológica. La presencia de múltiples anillos y configuraciones estereoquímicas sugiere que puede exhibir interacciones específicas con objetivos biológicos, lo que la hace de interés en la química medicinal. Su complejidad molecular indica que puede poseer propiedades físicas únicas, como solubilidad y estabilidad, que podrían influir en sus aplicaciones en farmacéuticos o ciencia de materiales. En general, la estereoquímica detallada y la funcionalización de este compuesto destacan su posible importancia en varios contextos químicos y biológicos.
Fórmula:C35H40O11
InChI:InChI=1S/C35H40O11/c1-6-13(2)26(37)44-12-33(42)20-7-17(20)30(4)21(33)9-16-15(11-36)28(39)45-34(16)22(30)10-32(41)19-8-18(19)31(5)25(32)24(34)23-14(3)27(38)46-35(23,43)29(31)40/h6,17-22,29,36,40-43H,7-12H2,1-5H3/b13-6+/t17-,18-,19+,20+,21-,22+,29-,30+,31+,32+,33+,34+,35+/m1/s1
Clave InChI:InChIKey=JDNYCIQWGHMSPJ-ANOWQDLRSA-N
SMILES:C[C@@]12[C@]3([C@]4(C5=C6[C@](O)(C3)[C@@]7([C@]([C@]6(C)[C@@H](O)[C@]8(O)C5=C(C)C(=O)O8)(C7)[H])[H])C(C[C@]1([C@@](COC(/C(=C/C)/C)=O)(O)[C@@]9([C@]2(C9)[H])[H])[H])=C(CO)C(=O)O4)[H]
Sinónimos:- Chloramultilide D
- [(1aR,1bS,2R,2aS,5cR,9aR,10S,10aS,11aR,11bS,11cS,12aS,12bS)-1,1a,1b,2,2a,4,7,9,9a,10,10a,11,11a,11b,11c,12,12a,12b-Octadecahydro-2,2a,10,12a-tetrahydroxy-8-(hydroxymethyl)-1b,5,11b-trimethyl-4,7-dioxobiscyclopropa[4′,5′]cyclopenta[1′,2′,3′:1,10;2′′,1′′:7,8]phenanthro[3,4-b:4b,5-b′]difuran-10-yl]methyl (2E)-2-methyl-2-butenoate
- Henriol B
- 2-Butenoic acid, 2-methyl-, [(1aR,1bS,2R,2aS,5cR,9aR,10S,10aS,11aR,11bS,11cS,12aS,12bS)-1,1a,1b,2,2a,4,7,9,9a,10,10a,11,11a,11b,11c,12,12a,12b-octadecahydro-2,2a,10,12a-tetrahydroxy-8-(hydroxymethyl)-1b,5,11b-trimethyl-4,7-dioxobiscyclopropa[4′,5′]cyclopenta[1′,2′,3′:1,10;2′′,1′′:7,8]phenanthro[3,4-b:4b,5-b′]difuran-10-yl]methyl ester, (2E)-
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Encontrado 3 productos.
Chloramultilide D
CAS:Chloramultilide D is a macrolide polyketide, which is a natural product typically derived from microorganisms, particularly certain strains of bacteria. It is synthesized through complex polyketide biosynthesis pathways involving polyketide synthases. The mode of action of Chloramultilide D involves disrupting bacterial protein synthesis by targeting the ribosomal machinery. This interference with protein production can inhibit bacterial growth, potentially classifying it within a valuable subset of antimicrobial compounds. Due to these properties, Chloramultilide D is of significant interest in the field of antibiotic research, especially as a candidate for combatting resistant bacterial strains. Its potential applications extend to exploring novel therapeutic strategies and designing new drugs that can overcome current antibiotic resistance challenges. Ongoing studies are focused on elucidating its biosynthetic pathways and optimizing its production, as well as evaluating its efficacy and safety in pharmacological contexts. Scientists are particularly interested in its structural features, which could aid in rational drug design and development of analogous compounds.Fórmula:C35H40O11Pureza:Min. 95%Peso molecular:636.7 g/molChloramultilide D
CAS:Chloramultilide D is a natural product from Chloranthus spicatus.Fórmula:C35H40O11Pureza:98%Forma y color:SolidPeso molecular:636.69