货号:A293531 同义名: 非尼拉敏马来酸盐 / Prophenpyridamine maleate;Tripoton maleate
Pheniramine maleate can acts as an antihistamine and vasoconstrictor.
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产品名称 | H1 receptor ↓ ↑ | H2 receptor ↓ ↑ | H3 receptor ↓ ↑ | H4 receptor ↓ ↑ | Histamine receptor ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Hydroxyzine 2HCl | {[allProObj[0].p_purity_real_show]} | ||||||||||||||||||
Cyclizine | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Loratadine |
+
B(0)AT2, IC50: 4 μM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Desloratadine |
++
Histamine H1 receptor, IC50: 51 nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Doxylamine succinate | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Ebastine | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Tripelennamine HCl |
+
H1 receptor, IC50: 30 μM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Meclizine dihydrochloride | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Chlorpheniramine maleate |
+++
Histamine H1 receptor, IC50: 12 nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Diphenhydramine HCl | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Alcaftadine |
++++
H1 receptor, pKi: 8.5 |
++
H2 receptor, pKi: 7.2 |
{[allProObj[0].p_purity_real_show]} | ||||||||||||||||
Fexofenadine HCl |
++
Histamine H1 receptor, IC50: 246 nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Bilastine |
+++
H1 receptor, Ki: 44.15 nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Pemirolast potassium | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Bepotastine besilate |
+
Histamine H1 receptor, pIC50: 5.7 |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Mizolastine |
+++
Histamine H1 receptor, IC50: 47 nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Brompheniramine maleate | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Carbinoxamine maleate salt | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Clemastine fumarate |
++++
Histamine H1 receptor, IC50: 3 nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Ketotifen fumarate salt | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Rupatadine Fumarate |
++
Histamine H1 receptor, Ki: 102 nM |
PAFR | {[allProObj[0].p_purity_real_show]} | ||||||||||||||||
Famotidine | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Roxatidine Acetate HCl |
+
Histamine H2 receptor, IC50: 3.2 μM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Lafutidine | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Cimetidine | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Nizatidine |
++++
Histamine H2 receptor, IC50: 0.9 nM |
AChE | {[allProObj[0].p_purity_real_show]} | ||||||||||||||||
Ranitidine | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Betahistine |
+
Histamine H3 receptor, IC50: 1.9 μM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Ciproxifan maleate |
+++
Histamine H3 receptor, IC50: 9.2 nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
S 38093 |
++
human H3 receptor, Ki: 1.2 μM rat H3 receptor, Ki: 1.44 μM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
JNJ-7777120 |
++++
Histamine H4 receptor, Ki: 4.5 nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Azelastine HCl | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Epinastine HCl | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Levodropropizine | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Cyproheptadine hydrochloride | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Hesperetin | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Olopatadine HCl | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Mianserin hydrochloride | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Buclizine 2HCl | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Latrepirdine 2HCl | ✔ | GluR | {[allProObj[0].p_purity_real_show]} | ||||||||||||||||
Cetirizine 2HCl | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | Pheniramine Maleate is an antihistamine that also has some anti-inflammatory effects. Histological examination demonstrated that Ph (pheniramine maleate) had protective effects against I/R injury developing in the brain tissue. Ph has a protective effect against ischemia/reperfusion injury created experimentally in rat brains[3]. Pheniramine Maleate 45.5 mg is better than placebo and as effective as lidocaine to prevent fentanyl induced cough[4]. Use of Dexamethasone and Pheniramine hydrogen maleate prior to surgical skin incision helps to reduce both postoperative pain and acute physiological stress[5]. After rats were injected intrathecally with diphenhydramine and pheniramine, the dose-response curves were obtained. Diphenhydramine and pheniramine produced dose-dependent spinal blockades in motor function, proprioception, and nociception[6]. |
NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
NCT02477787 | Acute Myelogenous Leukemia | Phase 2 | Recruiting | December 2019 | Korea, Republic of ... 展开 >> Asan Medical Center Recruiting Seoul, Korea, Republic of Contact: Kyoo-Hyung Lee, MD 82-2-3010-3213 khlee2@amc.seoul.kr Contact: Inpyo Choi, PhD 82-42-860-4223 ipchoi@kribb.re.kr 收起 << |
NCT02731560 | Rheumatoid Arthritis | Phase 4 | Completed | - | - |
NCT01380275 | Sarcoma | Phase 2 | Unknown | December 2014 | Korea, Republic of ... 展开 >> National Cancer Center Recruiting Goyang-si, Gyeonggi, Korea, Republic of Contact: Soon Mi Kim, RN 82-31-920-0425 ksm@ncc.re.kr Principal Investigator: Byung-Kiu Park, M.D., Ph.D. 收起 << |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.81mL 0.56mL 0.28mL |
14.03mL 2.81mL 1.40mL |
28.06mL 5.61mL 2.81mL |
CAS号 | 132-20-7 |
分子式 | C20H24N2O4 |
分子量 | 356.416 |
别名 | 非尼拉敏马来酸盐 ;Prophenpyridamine maleate;Tripoton maleate |
运输 | 蓝冰 |
存储条件 |
粉末 Sealed in dry,Room Temperature 液体 -20°C:3-6个月-80°C:12个月 |
溶解度 |
H2O: 35 mg/mL(98.2 mM) |
动物实验配方 |
PO 0.5% CMC-Na 80 mg/mL suspension |