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21.
Swen C. Renner John H. Rappole Pamela C. Rasmussen Thein Aung Myint Aung Nay Myo Shwe John P. Dumbacher Robert C. Fleischer 《Journal of Ornithology》2008,149(3):439-450
We collected several individuals of the Slaty-bellied Tesia Tesia olivea in the temperate rain forest of the sub-Himalayan region of northeastern Burma/Myanmar in February/March 2004 and March 2006.
Subsequent comparison of these with T. olivea from northeastern India and northern Thailand revealed that while our northeastern Burma/Myanmar birds were similar to those
from northeastern India, specimens of both populations were distinctly different from T. olivea from Chiang Mai Province of northern Thailand and northern Vietnam. Herein, we designate the latter populations as members
of a new subspecies of T. olivea based on analyses of variations in morphometric characters, plumage, song, and mitochondrial (mt)DNA sequence. 相似文献
22.
Htay Htay Shwe Mye Aye Myint Myint Sein Khin Than Htay Peter Kreitmeier Jürg Gertsch Oliver Reiser Jörg Heilmann 《化学与生物多样性》2010,7(3):610-622
Three new steroid saponins (3β,25R)‐spirost‐5‐en‐3‐yl 6‐deoxy‐α‐L ‐mannopyranosyl‐(1→2)‐[β‐D ‐glucopyranosyl‐(1→4)‐6‐deoxy‐α‐L ‐mannopyranosyl‐(1→3)]‐β‐D ‐glucopyranoside ( 1 ), (3β,22R,25R)‐26‐(β‐D ‐glucopyranosyloxy)‐22‐hydroxyfurost‐5‐en‐3‐yl 6‐deoxy‐α‐L ‐mannopyranosyl‐(1→2)‐[6‐deoxy‐α‐L ‐mannopyranosyl‐(1→3)]‐β‐D ‐glucopyranoside ( 3 ), and (3β,22R,25R)‐26‐(β‐D ‐glucopyranosyloxy)‐22‐hydroxyfurost‐5‐en‐3‐yl 6‐deoxy‐α‐L ‐mannopyranosyl‐(1→2)‐[β‐D ‐glucopyranosyl‐(1→4)‐6‐deoxy‐α‐L ‐mannopyranosyl‐(1→3)]‐β‐D ‐glucopyranoside ( 5 ), as well as the new pregnane glycoside (3β,16β)‐3‐{[6‐deoxy‐α‐L ‐mannopyranosyl‐(1→2)‐[6‐deoxy‐α‐L ‐mannopyranosyl‐(1→3)]‐β‐D ‐glucopyranosyl]oxy}‐20‐oxopregn‐5‐en‐16‐yl (4R)‐5‐(β‐D ‐glucopyranosyloxy)‐4‐methylpentanoate ( 6 ), were isolated from the rhizomes of Tacca integrifolia together with two known (25R) configurated steroid saponins (3β,25R)‐spirost‐5‐en‐3‐yl 6‐deoxy‐α‐L ‐mannopyranosyl‐(1→2)‐[6‐deoxy‐α‐L ‐mannopyranosyl‐(1→3)]‐β‐D ‐glucopyranoside ( 2 ) and (3β,22R,25R)‐26‐(β‐D ‐glucopyranosyloxy)‐22‐methoxyfurost‐5‐en‐3‐yl 6‐deoxy‐α‐L ‐mannopyranosyl‐(1→2)‐[6‐deoxy‐α‐L ‐mannopyranosyl‐(1→3)]‐β‐D ‐glucopyranoside ( 4 ). The cytotoxic activity of the isolated compounds was evaluated in HeLa cells and showed the highest cytotoxicity value for compound 2 with an IC50 of 1.2±0.4 μM . Intriguingly, while compounds 1 – 5 exhibited similar cytotoxic properties between 1.2±0.4 ( 2 ) and 4.0±0.6 μM ( 5 ), only compound 2 showed a significant microtubule‐stabilizing activity in vitro. 相似文献
23.
Aye Thida Sai Thein Than Tun Sai Ko Ko Zaw Andrew A. Lover Philippe Cavailler Jennifer Chunn Mar Mar Aye Par Par Kyaw Win Naing Kaung Nyunt Zan Myint Shwe Thar Tun Kyaw Zaw Htoon Waing Philippe Clevenbergh 《PloS one》2014,9(9)