Hello Bio/MMPX/HB0092/10mg
商品编号：
HB0092-10mg
品牌：
hellobio
市场价：
¥3588.00
美元价：
2760.00
产品分类：
酸碱缓冲液
联系Q Q：
3392242852
电话号码：
4000-520-616
电子邮箱：
info@ebiomall.com
商品介绍
Product overview
-
NameMMPX
-
Short descriptionSelective calmodulin-dependent PDE-1 inhibitor
-
Biological descriptionSelective calmodulin-dependent phosphodiesterase 1 (PDE-1) inhibitor. Increases Ca2+-activated K+ (BK) channel activity in the urinary bladder and shows smooth muscle relaxing actions. Also shows vasodilator actions.
-
Alternative names8-Methoxymethyl-IBMX
-
Biological actionInhibitor
-
Purity>98%
-
Our products in actionSubmit Your Citation Now
Properties
-
Molecular Weight266.3
-
Chemical structure
![8-Methoxymethyl-IBMX [78033-08-6]](images/hellobio/201710/hb0092.png "8-Methoxymethyl-IBMX [78033-08-6]")
-
Molecular FormulaC12H18N4O3
-
CAS Number78033-08-6
-
PubChem identifier155806
-
SMILESCC(C)CN1C2=C(C(=O)N(C1=O)C)NC(=N2)COC
Storing and Using Your Product
-
Storage instructionsroom temperature
-
Solubility overviewsoluble in ethanol or DMOS (5mg/ml)
-
ImportantThis product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.
References for MMPX
Effects of selective inhibitors on cyclic nucleotide phosphodiesterases of rabbit aorta.
Ahn HS et al (1989) Biochem Pharmacol 38(19) : 3331-9.PubMedID: 2554921Selective inhibition of phosphodiesterase 1 relaxes urinary bladder smooth muscle: role for ryanodine receptor-mediated BK channel activation.
Xin W et al (2012) Am J Physiol Cell Physiol 303(10) : C1079-89.PubMedID: 22992675In vivo effects of phosphodiesterase inhibition on basal cyclic guanosine monophosphate levels in the prefrontal cortex, hippocampus and cerebellum of freely moving rats.
Marte A et al (2008) J Neurosci Res 86(15) : 3338-47.PubMedID: 18655195Lung vasodilatory response to inhaled iloprost in experimental pulmonary hypertension: amplification by different type phosphodiesterase inhibitors.
Schermuly RT et al (2005) Respir Res 6 : 76PubMedID: 16033645
品牌介绍
Hello Bio是由一群经验丰富的科学家和化学家们创立的充满活力的生物企业，总部位于英国布里斯托尔，在美国普林斯顿设有分公司，主旨在于提供质优价廉的生命科学研究工具，主要产品线为小分子化合物，如激动剂、拮抗剂、抑制剂等，部分产品价格甚至低至其他供应商的50%。热销产品线：酶抑制剂和激动剂ROCK inhibitor Y-27632, PKA inhibitor KT 5720 , adenylyl cyclase activator Forskolin, and novel GRK2/3 inhibitor Cmpd101等。 离子通道调节剂NMDA antagonist D-AP5, sodium channel blocker tetrodotoxin citrate, TRP antagonist capsazepine, and GABAA antagonist SR 95531 等。信号通路工具各种信号通路抑制剂、激动剂表观遗传学研究工具potent HDAC inhibitor Trichostatin A, DNA methyltransferase inhibitor 5-aza-2'-deoxycytidine,BET bromodomain inhibitor (+)-JQ1 and potent,selective GLP / G9a HMTase inhibitor BIX 01294 等受体配体novel selective GRK2/3 inhibitor, NMDA antagonist D-AP5, Group I mGlu agonist (S)-3,5-DHPG, and GABAA antagonist SR 95531.等干细胞调节剂ROCK inhibitor Y-27632, SB 431542 DAPT.
联络我们
