Đang chuẩn bị liên kết để tải về tài liệu:
Synthesis of acyl oleanolic acid-uracil conjugates and their anti-tumor activity

Không đóng trình duyệt đến khi xuất hiện nút TẢI XUỐNG

Oleanolic acid, which can be isolated from many foods and medicinal plants, has been reported to possess diverse biological activities. It has been found that the acylation of the hydroxyl groups of the A-ring in the triterpene skeleton of oleanolic acid could be favorable for biological activities. The pyrimidinyl group has been con‑ structured in many new compounds in various anti-tumor studies. | Synthesis of acyl oleanolic acid-uracil conjugates and their anti-tumor activity

TÀI LIỆU LIÊN QUAN

Báo cáo Y học: Concerted regulation of free arachidonic acid and hormone-induced steroid synthesis by acyl-CoA thioesterases and acyl-CoA synthetases in adrenal cells

Comparative study of microwave-assisted and conventional synthesis of ibuprofen-based acyl hydrazone derivatives

Self-condensation reactions of acyl phosphonates: synthesis of tertiary O-protected α-hydroxyphosphonates

Synthesis and molecular modeling studies of naproxen-based acyl hydrazone derivatives

Synthesis of acyl oleanolic acid-uracil conjugates and their anti-tumor activity

Synthesis of tertiary propargylic phosphonates by addition of trialkynylaluminum reagents to acyl phosphonates and investigation of their antimicrobial activities

Báo cáo khoa học: Fatty acid synthesis Role of active site histidines and lysine in Cys-His-His-type b-ketoacyl-acyl carrier protein synthases

Lipases of germinating jojoba seeds efficiently hydrolyze triacylglycerols and wax esters and display wax estersynthesizing activity

Two different pathways of phosphatidylcholine synthesis, the Kennedy Pathway and the Lands Cycle, differentially regulate cellular triacylglycerol storage

Novel N-acyl/aroyl-2-(5-phenyl-2H-tetrazol-2-yl)acetohydrazides: synthesis and characterization
Đã phát hiện trình chặn quảng cáo AdBlock
Trang web này phụ thuộc vào doanh thu từ số lần hiển thị quảng cáo để tồn tại. Vui lòng tắt trình chặn quảng cáo của bạn hoặc tạm dừng tính năng chặn quảng cáo cho trang web này.