021-51111890
购物车（）
sales@molnova.cn
首页-
Products -
Others -
Other Targets -
3-O-β-D-Xylopyranosyl-(1-3)-α-L-Rhamnopyranosyl-(1-4)-α-L-arabinopyranosyl hederagenin-28-O-β-D-glucopyranosyl-(1-6)-β-D-glucopyranosyl ester
3-O-β-D-Xylopyranosyl-(1-3)-α-L-Rhamnopyranosyl-(1-4)-α-L-arabinopyranosyl hederagenin-28-O-β-D-glucopyranosyl-(1-6)-β-D-glucopyranosyl ester
CAS No. ———
3-O-β-D-Xylopyranosyl-(1-3)-α-L-Rhamnopyranosyl-(1-4)-α-L-arabinopyranosyl hederagenin-28-O-β-D-glucopyranosyl-(1-6)-β-D-glucopyranosyl ester ( 3-O-β-D-吡喃木糖基(1→3)-α-L-吡喃鼠李糖基(1→4)-α-L-吡喃阿拉伯糖基常春藤皂苷元-28-O-β-D-吡喃葡萄糖基(1→6)-β-D-吡喃葡萄糖酯苷 )
产品货号. M38315 CAS No. ———
3-O-β-D-Xylopyranosyl-(1→3)-α-L-Rhamnopyranosyl-(1→4)-α-L-arabinopyranosyl hederagenin-28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 25MG | 获取报价 | 有现货 |
|
| 50MG | 获取报价 | 有现货 |
|
| 100MG | 获取报价 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称3-O-β-D-Xylopyranosyl-(1-3)-α-L-Rhamnopyranosyl-(1-4)-α-L-arabinopyranosyl hederagenin-28-O-β-D-glucopyranosyl-(1-6)-β-D-glucopyranosyl ester
-
注意事项本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断
-
产品简述3-O-β-D-Xylopyranosyl-(1→3)-α-L-Rhamnopyranosyl-(1→4)-α-L-arabinopyranosyl hederagenin-28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester
-
产品描述3-O-β-D-Xylopyranosyl-(1→3)-α-L-Rhamnopyranosyl-(1→4)-α-L-arabinopyranosyl hederagenin-28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester
-
体外实验———
-
体内实验———
-
同义词3-O-β-D-吡喃木糖基(1→3)-α-L-吡喃鼠李糖基(1→4)-α-L-吡喃阿拉伯糖基常春藤皂苷元-28-O-β-D-吡喃葡萄糖基(1→6)-β-D-吡喃葡萄糖酯苷
-
通路Others
-
靶点Other Targets
-
受体———
-
研究领域———
-
适应症———
化学信息
-
CAS Number———
-
分子量———
-
分子式———
-
纯度>98% (HPLC)
-
溶解度———
-
SMILES———
-
化学全称———
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
产品手册
关联产品
-
(S/R)-Orteronel
TAK-700 (Orteronel) 是一种有效且高度选择性的人类 17, 20-裂解酶抑制剂，IC50 为 38 nM，其选择性比其他 CYP（例如 11-羟化酶和 CYP3A4）高 1000 倍。
-
Adenosine Dialdehyde...
腺苷二醛是一种嘌呤核苷类似物。腺苷二醛是 S-腺苷高半胱氨酸水解酶 (SAHH) 的有效抑制剂 (Ki=3.3 nM)。腺苷二醛在体内表现出有效的抗肿瘤活性。
-
Picrotoxinin
Picrotoxinin is a blocker of chloride channel and a noncompetitive antagonist of GABAA with an IC50 of 1.15 μM for α1β2γ2L GABAA. Picrotoxinin shows convulsant properties.
