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127060-75-7

中文名稱 CGP 42112;NΑ-NICOTINOYL-TYR-(NΑ-CBZ-ARG)-LYS-HIS-PRO-ILE
英文名稱 CGP 42112
CAS 127060-75-7
分子式 C52H69N13O11
分子量 1052.18
MOL 文件 127060-75-7.mol
更新日期 2025/01/21 16:31:09
127060-75-7 結(jié)構(gòu)式 127060-75-7 結(jié)構(gòu)式

基本信息

中文別名
CGP 42112
NΑ-NICOTINOYL-TYR-(NΑ-CBZ-ARG)-LYS-HIS-PRO-ILE
英文別名
CGP 42112
CGP-42112A
CGP42112A, CGP42112
CGP-42112 (CGP42112
ANGIOTENSIN II ANTAGONIST
ANGIOTENSIN II RECEPTOR LIGAND
NIC-TYR-LYS(Z-ARG)-HIS-PRO-ILE
CGP-42112A >=95%, synthetic, solid
NICOTINOYL-TYR-LYS(CBZ-ARG)-HIS-PRO-ILE
NICOTINOYL-TYR-LYS(Z-ARG)-HIS-PRO-ILE-OH

物理化學(xué)性質(zhì)

儲存條件-20°C
溶解度DMSO:350.0(Max Conc. mg/mL);332.64(Max Conc. mM)
形態(tài)solid
顏色white
水溶解性Soluble to 1 mg/ml in water
BRN8184948

安全數(shù)據(jù)

安全說明22-24/25
WGK Germany3
WGK Germany3
CGP 42112;NΑ-NICOTINOYL-TYR-(NΑ-CBZ-ARG)-LYS-HIS-PRO-ILE價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2024/11/08HY-12405CGP 42112;NΑ-NICOTINOYL-TYR-(NΑ-CBZ-ARG)-LYS-HIS-PRO-ILE
CGP-42112
127060-75-71mg1260元
2024/11/08HY-12405CGP 42112;NΑ-NICOTINOYL-TYR-(NΑ-CBZ-ARG)-LYS-HIS-PRO-ILE
CGP-42112
127060-75-75mg3780元
2024/11/08HY-12405CGP 42112;NΑ-NICOTINOYL-TYR-(NΑ-CBZ-ARG)-LYS-HIS-PRO-ILE
CGP-42112
127060-75-710mM * 1mLin DMSO7083元

常見問題列表

生物活性
CGP-42112(CGP-42112A)是血管緊張素受體AT2激動劑。
體外研究

CGP-42112 (≥1 nM) significantly inhibits cGMP production from the basal value. CGP-42112 (≥1 nM) significantly inhibits TH-enzyme activity from the basal value. These inhibitory effects of CGP-42112 on TH-enzyme activity and-cGMP production are abolished by PD123319 (AT(2)-R antagonist) while CV-11974 (AT(1)-R antagonist) is ineffective. [ 125 I]CGP-42112 binds selectively to the AT2 angiotensin II receptor subtype. [ 125 I]CGP-42112 binds with higher affinity in the brain than in the adrenal. beta-Mercaptoethanol enhanced [ 125 I]CGP-42112 binding in the brain, but does not alter its binding in the adrenal. [ 125 I]CGP-42112 binds with high affinity (Kd = 0.07-0.3 nM, depending on the area studied). [ 125 I]CGP-42112 binding is selective for AT2 receptors, as determined by lack of competition with the AT1 ligand losartan, and competition by the AT2 ligands PD 123177 and unlabeled CGP-42112 and the non-selective peptides Ang II and angiotensin III (Ang III).

體內(nèi)研究

Intravenous infusions of CGP-42112 (0.1 and 1 mg kg-1 min-1) and PD 123319 (0.36 and 1 mg kg-1 min-1) shifted the upper limit of CBF autoregulation toward higher blood pressures without affecting baseline CBF.

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