5-amino-1,2-dihydroisoquinolin-1-one
CAS No. 93117-08-9
5-amino-1,2-dihydroisoquinolin-1-one ( —— )
产品货号. M28409 CAS No. 93117-08-9
5-aminoisoquinolin-1(2H)-one 是小牛胸腺 PARP1 的抑制剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 50MG | ¥129 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥94 | 有现货 |
|
生物学信息
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产品名称5-amino-1,2-dihydroisoquinolin-1-one
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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
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产品简述5-aminoisoquinolin-1(2H)-one 是小牛胸腺 PARP1 的抑制剂。
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产品描述5-aminoisoquinolin-1(2H)-one is the inhibitor of calf thymus PARP1.
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体外实验5-AIQ (5000 μg) significantly reduces the number of colonies of TA 98 without metabolic activation, and TA 98 and TA 1537 with metabolic activation.
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体内实验5-AIQ (150 and 250 mg/kg; p.o.; once) possess no significantly genotoxic in vivo system by micronucleus test.5-AIQ (3 mg/kg; p.o.; 5 min prior to onset of liver ischemia) reduces the tissue injury associated with ischemia-reperfusion of the liver. Animal Model:Male mice Dosage:150 and 250 mg/kg Administration:Oral administration; 150 and 250 mg/kg; once Result:Showed no increase of micronucleated polychromatic erythrocytes (MNPCE) in both 24 h and 48 h after both 125 and 250 mg/kg duration exposure as compared to the corresponding control.Animal Model:Anesthetised male Wistar rats with liver ischemia (for 30 minutes) and reperfusion (for 2 hours) Dosage:3 mg/kg Administration:Intravenous injection; 3 mg/kg; 5 min prior to onset of liver ischemiaResult:Reduced PARP activation and showed less staining for ICAM-1.
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同义词——
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通路Cell Cycle/DNA Damage
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靶点PARP
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受体TRPV1
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研究领域——
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适应症——
化学信息
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CAS Number93117-08-9
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分子量160.176
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分子式C9H8N2O
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (624.34 mM)
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SMILESNc1cccc2c(O)nccc12
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Giovanni Appendino, et al. Development of the first ultra-potent "capsaicinoid" agonist at transient receptor potential vanilloid type 1 (TRPV1) channels and its therapeutic potential. J Pharmacol Exp Ther. 2005 Feb;312(2):561-70.
产品手册
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