![Spiro[6,16-(epithiopropanoxymethano)-7,13-imino-12H-1,3-dioxolo[7,8]isoquino[3,2-b][3]benzazocine-…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F490956-spiro-616-epithiopropanoxymethano-713-imino-12h-13-dioxolo-78-isoquino-32-b-3-benzazocine-201-2-h-isoquinoline-14-carbonitrile-5-acetyloxy-3-4-66a-7131416-octahydro-6-8-dihydroxy-7-9-dimethoxy-41023-trimethyl-19-oxo-1-r-6r-6ar-7r.webp&w=3840&q=75)
CAS 114899-80-8
:Spiro[6,16-(epithiopropanoxymethano)-7,13-imino-12H-1,3-dioxolo[7,8]isoquino[3,2-b][3]benzazocine-20,1'(2'H)-isoquinoline]-14-carbonitrile,5-(acetyloxy)-3',4',6,6a,7,13,14,16-octahydro-6',8-dihydroxy-7',9-dimethoxy-4,10,23-trimethyl-19-oxo-,(1'R,6R,6aR,7R
Description:
The chemical substance known as Spiro[6,16-(epithiopropanoxymethano)-7,13-imino-12H-1,3-dioxolo[7,8]isoquino[3,2-b][3]benzazocine-20,1'(2'H)-isoquinoline]-14-carbonitrile,5-(acetyloxy)-3',4',6,6a,7,13,14,16-octahydro-6',8-dihydroxy-7',9-dimethoxy-4,10,23-trimethyl-19-oxo-,(1'R,6R,6aR,7R) is a complex organic compound characterized by its intricate molecular structure, which includes multiple functional groups such as carbonitrile, acetyloxy, and methoxy. This compound features a spirocyclic framework, indicating the presence of two or more rings that share a common atom, contributing to its unique three-dimensional shape. The presence of hydroxyl groups suggests potential for hydrogen bonding, which may influence its solubility and reactivity. Additionally, the compound's multiple chiral centers imply that it may exist in different stereoisomeric forms, which can affect its biological activity and pharmacological properties. Overall, this substance is likely to exhibit significant chemical diversity and potential applications in medicinal chemistry or related fields.
Formula:C40H42N4O10S
Synonyms:- Spiro[6,16-(epithiopropanoxymethano)-7,13-imino-12H-1,3-dioxolo[7,8]isoquino[3,2-b][3]benzazocine-20,1'(2'H)-isoquinoline]-14-carbonitrile,5-(acetyloxy)-3',4',6,6a,7,13,14,16-octahydro-6',8-dihydroxy-7',9-dimethoxy-4,10,23-trimethyl-19-oxo-,[6R-(6a,6ab,7b,13b,14b,16a,20R*)]-
- Ecteinascidin 770
- Ecteinascidine 770
- Et 770
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Found 7 products.
(1′R,6R,6aR,7R,13S,14R,16R)-5-(Acetyloxy)-3′,4′,6,6a,7,13,14,16-octahydro-6′,8-dihydroxy-7′,9-dimethoxy-4,10,23-trimethyl-19-oxospiro[6,16-(epithiopropanoxymethano)-7,13-imino-12H-1,3-dioxolo[7,8]isoquino[3,2-b][3]benzazocine-20,1′(2′H)-isoquinoline]-14-carbonitrile
CAS:Formula:C40H42N4O10SPurity:99%Color and Shape:SolidMolecular weight:770.8473Ecteinascidin 770
CAS:<p>Ecteinascidin 770 inhibits SARS-CoV-2 and Mycobacterium tuberculosis by inhibiting cancer cell viability through RDRP1 (RNA-dependent RNA polymerase 1).</p>Formula:C40H42N4O10SPurity:99.84%Color and Shape:SolidMolecular weight:770.85Ecteinascidin 770
CAS:Controlled ProductFormula:C40H42N4O10SColor and Shape:NeatMolecular weight:741.786Ecteinascidin 770
CAS:<p>Ecteinascidin 770 is a linker that is used to connect drugs and diagnostic agents to form conjugates. This compound possesses a ring structure with a carbonyl group at the 3-position and hydroxyl groups at the 2- and 4-positions, which provides it with nucleophilic properties. Ecteinascidin 770 has been used in the synthesis of ecteinascidins, which are synthetic compounds that are degradable by microorganisms into natural products. Ecteinascidin 770 also has diagnostic applications for detecting cancer cells and can be used as a drug linker for attaching therapeutic molecules such as antibiotics, antivirals, or antifungals to antibodies.</p>Formula:C40H42N4O10SPurity:Min. 95%Molecular weight:770.8 g/molRef: 4Z-T-298004
Discontinued product
