Antagonist G
CAS No. 115150-59-9
Antagonist G ( ——— )
产品货号. M41872 CAS No. 115150-59-9
Antagonist G是有效的后叶加压素 (vasopressin) 的拮抗剂。Antagonist G 也是弱的 GRP 和缓激肽的弱拮抗剂。Antagonist G 可诱导 AG-1 的转录,是癌细胞对化疗增敏。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1600 | 有现货 |
|
| 10MG | ¥2600 | 有现货 |
|
| 25MG | 获取报价 | 有现货 |
|
| 50MG | 获取报价 | 有现货 |
|
| 100MG | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Antagonist G
-
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Antagonist G是有效的后叶加压素 (vasopressin) 的拮抗剂。Antagonist G 也是弱的 GRP 和缓激肽的弱拮抗剂。Antagonist G 可诱导 AG-1 的转录,是癌细胞对化疗增敏。
-
产品描述Antagonist G is a potent vasopressin antagonist. Antagonist G is also a weak antagonist of GRP and Bradykinin. Antagonist G induces AP-1 transcription and sensitizes cells to chemotherapy.
-
体外实验———
-
体内实验Antagonist G (0-100 μM) induces apoptosis is redox-sensitive and caspase-dependently in SCLC cells.Antagonist G activates JNK1 in SCLC cells.Antagonist G is not intrinsically a free radical oxygen donor but stimulates free radical generation specifically within SCLC cells (6.2-fold) and increases the activity of the redox-sensitive transcription factor AP-1 by 61%.Cell Viability Assay Cell Line:SCLC cell lines NCI-H69, NCI-H510 and CHO-K1 cells.Concentration:0-100 μM.Incubation Time:24 h.
-
同义词———
-
通路Others
-
靶点Other Targets
-
受体———
-
研究领域———
-
适应症———
化学信息
-
CAS Number115150-59-9
-
分子量951.2
-
分子式C49H62O6N12S
-
纯度>98% (HPLC)
-
溶解度H2O : 50 mg/mL (52.57 mM; ultraphonic)
-
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
1. P J Woll, et al. A neuropeptide antagonist that inhibits the growth of small cell lung cancer in vitro. Cancer Res. 1990 Jul 1;50(13):3968-73.?
产品手册
关联产品
-
Somatostatin-28 a
Somatostatin-28 (sheep, human rat mouse) 是一种生物活性多肽,在近端肠上皮细胞中合成。Somatostatin-28 (sheep, human rat mouse) 抑制葡萄糖刺激的胰岛素分泌而不影响循环基础胰岛素浓度。Somatostatin-28 (sheep, human rat mouse) 也靶向生长抑素受体 5 亚型 (SSTR5) 调节 GLP-1 分泌。
-
10-Hydroxy mesaconit...
Beiwutine (10-Hydroxy mesaconitine) 是一种二酯二萜生物碱。
-
GIP (1-39)
Endogenous truncated form of the incretin hormone GIP. More potent at stimulating glucose-dependent insulin secretion from rat pancreatic β-cells than GIP.
021-51111890
购物车()
sales@molnova.cn

