Nom du produit:rel-((1R,8S)-bicyclo[6.1.0]non-4-yn-9-yl)methyl (2-(2-hydroxyethoxy)ethyl)carbamate
IUPAC Name:[(1R,8S)-bicyclo[6.1.0]non-4-yn-9-yl]methyl N-[2-(2-hydroxyethoxy)ethyl]carbamate
- CAS：1395786-21-6
- Formule moléculaire：C15H23NO4
- Pureté：95%+
- Numéro de catalogue：CM563669
- Poids moléculaire：281.35
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Détails du produit
- N° CAS:1395786-21-6
- Formule moléculaire:C15H23NO4
- Point de fusion:-
- Code SMILES:O=C(OCC1[C@@]2([H])CCC#CCC[C@@]12[H])NCCOCCO
- Densité:
- Numéro de catalogue:CM563669
- Poids moléculaire:281.35
- Point d'ébullition:
- N° Mdl:
- Stockage:
Category Infos
- Bridged Compounds
- Bridged ring compound refers to any two rings in the compound, which share two non-directly connected carbon atoms, and are classified into bicyclic hydrocarbons, tricyclic hydrocarbons, tetracyclic hydrocarbons, etc. Carbon atoms used in two or more rings are bridgehead carbon atoms, and the bond connecting the bridgehead carbon atoms is called a bridge. Bridged ring compounds are a class of organic compounds that are widely present in nature and usually have important physiological activities, such as the famous anticancer drug paclitaxel and antimalarial drug artemisinin.
- bridged compounds,bridged bicyclic compounds
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- Cyclopropanes
- Cyclopropane is the smallest cyclic compound with unique structural features and physicochemical properties, which is widely used in the design of small molecule drugs. In drug design, it is often used to increase activity, fix conformation and improve PK and water solubility. The introduction of cyclopropyl groups into drugs can change various properties of molecules, such as improving metabolic stability; increasing biological activity; enhancing drug efficacy; limiting polypeptide conformation and slowing down its hydrolysis; reducing plasma clearance; improving drug dissociation and many more. Cyclopropane rings are widely found in marketed drugs, including cardiovascular drugs, central nervous system (CNS) drugs, anticancer drugs, autoimmune and anti-inflammatory drugs.
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