Alverine citrate
CAS No. 5560-59-8
Alverine citrate ( NSC 35459 )
产品货号. M15021 CAS No. 5560-59-8
Alverine Citrate(NSC35459)是一种用于治疗功能性胃肠道疾病的化合物。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 50MG | ¥127 | 有现货 |
|
| 100MG | ¥167 | 有现货 |
|
| 500MG | ¥356 | 有现货 |
|
| 1G | ¥521 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥429 | 有现货 |
|
生物学信息
-
产品名称Alverine citrate
-
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Alverine Citrate(NSC35459)是一种用于治疗功能性胃肠道疾病的化合物。
-
产品描述Alverine Citrate(NSC35459) is a drug used for functional gastrointestinal disorders.(In Vitro):Alverine is a drug used for functional gastrointestinal disorders. Alverine acts directly on the muscle in the gut, causing it to relax. Alverine Citrate (20 mg/kg) suppresses the effect of 5-HTP, but not that of 8-OH-DPAT. However, when injected intracerebroventricularly (75 μg/rat) alverine citrate reduces 8-OH-DPAT-induced enhancement of rectal distension-induced abdominal contractions. In-vitro binding studies reveal that Alverine citrate has a high affinity for 5-HT1A receptors and a weak affinity for 5-HT3 and 5-HT4 subtypes. Alverine may increase Ca influx during action potentials due to inhibition of the inactivation of L-type Ca channels, but may also suppress evoked activity by inhibiting the sensitivity of contractile proteins to Ca2+.
-
体外实验Alverine is a drug used for functional gastrointestinal disorders. Alverine acts directly on the muscle in the gut, causing it to relax. Alverine Citrate (20 mg/kg) suppresses the effect of 5-HTP, but not that of 8-OH-DPAT. However, when injected intracerebroventricularly (75 μg/rat) alverine citrate reduces 8-OH-DPAT-induced enhancement of rectal distension-induced abdominal contractions. In-vitro binding studies reveal that Alverine citrate has a high affinity for 5-HT1A receptors and a weak affinity for 5-HT3 and 5-HT4 subtypes. Alverine may increase Ca influx during action potentials due to inhibition of the inactivation of L-type Ca channels, but may also suppress evoked activity by inhibiting the sensitivity of contractile proteins to Ca2+.
-
体内实验——
-
同义词NSC 35459
-
通路Endocrinology/Hormones
-
靶点5-HT Receptor
-
受体5-HT
-
研究领域Metabolic Disease
-
适应症——
化学信息
-
CAS Number5560-59-8
-
分子量473.57
-
分子式C26H35NO7
-
纯度>98% (HPLC)
-
溶解度DMSO: 95 mg/mL (200.6 mM)
-
SMILESOC(=O)CC(O)(CC(O)=O)C(O)=O.CCN(CCCC1=CC=CC=C1)CCCC1=CC=CC=C1
-
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.Coelho AM, et al. J Pharm Pharmacol. 2001 Oct; 53(10):1419-26.
产品手册
关联产品
-
MDL 100009
MDL 100009 是 MDL 100151 的 S-对映体,也是 MDL 100907 的相反对映体,是 5-HT2A 的选择性拮抗剂。
-
MM 77 dihydrochlorid...
MM 77 diHClide 是一种有效的 5-HT1A 受体突触后拮抗剂,具有抗焦虑样活性。
-
Chlorprothixene hydr...
Chlorprothixene hydrochloride 是一种多巴胺 (dopamine) 和组胺 (histamine) 受体拮抗剂,高亲和力地结合人 D1,D2,D3,D5,H1 受体,Ki 分别为 18 nM,2.96 nM,4.56 nM,9 nM 和 3.75 nM。具有抗精神病作用。
021-51111890
购物车()
sales@molnova.cn

