Nom du produit:N-{[1-(1,3-benzoxazol-2-yl)pyrrolidin-2-yl]methyl}-3-methoxy-2-methyl-2H-indazole-6-carboxamide
IUPAC Name:N-{[1-(1,3-benzoxazol-2-yl)pyrrolidin-2-yl]methyl}-3-methoxy-2-methyl-2H-indazole-6-carboxamide
- CAS:1795477-24-5
- Formule moléculaire:C22H23N5O3
- Pureté:95%+
- Numéro de catalogue:CM995976
- Poids moléculaire:405.46
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Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:1795477-24-5
- Formule moléculaire:C22H23N5O3
- Point de fusion:-
- Code SMILES:COC1=C2C=CC(=CC2=NN1C)C(=O)NCC1CCCN1C1=NC2=C(O1)C=CC=C2
- Densité:
- Numéro de catalogue:CM995976
- Poids moléculaire:405.46
- Point d'ébullition:
- N° Mdl:
- Stockage:
Category Infos
- Indazoles
- Indazoles are a class of organic heterocyclic compounds, also known as 1,2-diazaindene and benzopyrazole. Indazole is a good bioisomer of phenol, which is more lipophilic than phenol and less prone to phase I and II metabolism. Indazole derivatives have a wide range of biological activities, and it has been confirmed that indazole compounds have anti-tumor, analgesic, anti-inflammatory and other drug activities. Anticancer is the most important application field of indazole drugs. Renal cell carcinoma, solid tumor, nausea and vomiting caused by chemotherapy and leukemia are the main indications of this structural backbone drug.
- Pyrrolidines
- Pyrrolidine, also known as tetrahydropyrrole, is a saturated five-membered heterocyclic ring, which is miscible with water. Pyrrolidine exists in many alkaloids and drug molecules, such as kappa opioids, antagonists of dopamine D4 receptors, and HIV reverse transcriptase inhibitors.
- Benzoxazoles
- Benzoxazole is an aromatic organic compound with a molecular formula of C7H5NO, a benzoxazole ring structure, and an odor similar to pyridine. Although benzoxazole itself has little practical value, many benzoxazole derivatives are commercially important. As heterocyclic compounds, benzoxazoles are used in research as starting materials for the synthesis of larger, often biologically active structures. Its aromaticity makes it relatively stable, although as a heterocycle it has an active site that enables it to be functionalized.