Hemorphin-7
CAS No. 152685-85-3
Hemorphin-7 ( —— )
产品货号. M30103 CAS No. 152685-85-3
Hemorphin-7 binds to the angiotensin IV receptor, triggering multiple effects including cellular proliferation and memory enhancement. Hemorphins are endogenous peptides belonging to the family of atypical opioid peptides released from hydrolyzed hemoglobin. Hemorphin-7 is investigated as a potential biomarker for breast cancer.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥2793 | 有现货 |
|
| 10MG | ¥5121 | 有现货 |
|
| 25MG | ¥8603 | 有现货 |
|
| 50MG | ¥12927 | 有现货 |
|
| 100MG | ¥18990 | 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Hemorphin-7
-
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Hemorphin-7 binds to the angiotensin IV receptor, triggering multiple effects including cellular proliferation and memory enhancement. Hemorphins are endogenous peptides belonging to the family of atypical opioid peptides released from hydrolyzed hemoglobin. Hemorphin-7 is investigated as a potential biomarker for breast cancer.
-
产品描述Hemorphin-7 binds to the angiotensin IV receptor, triggering multiple effects including cellular proliferation and memory enhancement. Hemorphins are endogenous peptides belonging to the family of atypical opioid peptides released from hydrolyzed hemoglobin. Hemorphin-7 is investigated as a potential biomarker for breast cancer.
-
体外实验——
-
体内实验——
-
同义词——
-
通路Endocrinology/Hormones
-
靶点Opioid Receptor
-
受体——
-
研究领域——
-
适应症——
化学信息
-
CAS Number152685-85-3
-
分子量997.11
-
分子式C49H64N12O11
-
纯度>98% (HPLC)
-
溶解度H2O : 12.5 mg/mL (12.54 mM; Need ultrasonic)
-
SMILES——
-
化学全称Sequence:Tyr-Pro-Trp-Thr-Gln-Arg-Phe
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
Dejouvencel T, et al. Hemorphin 7 reflects hemoglobin proteolysis in abdominal aortic aneurysm. Arterioscler Thromb Vasc Biol. 2010 Feb;30(2):269-75.
产品手册
关联产品
-
LY 2456302
LY 2456302 (CERC-501, JSPA 0658, Aticaprant) 是一种有效、选择性、短效的 κ-阿片受体 (KOR) 拮抗剂,Ki 为 0.81 nM。
-
Leuphasyl TFA
Leuphasyl TFA 是一种酰胺肽,一种 δ-阿片受体激动剂,是一种抗降解的长效亮氨酸脑啡肽类似物,用于研究 δ 阿片受体的信号通路。
-
CTAP
Potent and selective μ opioid receptor antagonist (IC50 = 3.5 nM). Displays > 1200-fold selectivity over δ opioid and somatostatin receptors. Brain penetrant and active in vivo.
021-51111890
购物车()
sales@molnova.cn

