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Cat. No.	Product Name	Target	Signaling Pathways
T6250	H-89 dihydrochloride Protein kinase inhibitor H-89 dihydrochloride,H 89 2HCl,5-Isoquinolinesulfonamide	PKA; S6 Kinase; Autophagy	Autophagy; MAPK; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	H-89 dihydrochloride (5-Isoquinolinesulfonamide) 是一种选择性 cAMP 依赖性蛋白激酶A(PKA) 抑制剂，IC50值为 48 nM。也可轻微抑制 PKG、PKC 和酪蛋白激酶活性。
T11524	H-89 Protein kinase inhibitor H-89	Others	Others
	H-89 is a selective inhibitor of cyclic AMP-dependent protein kinase (protein kinase A; IC50: 48 nM). H-89 has weak inhibition on PKG, Casein Kinase, PKC, and other kinases.
T65656	H-Phe(2-Cl)-OH
	H-Phe(2-Cl)-OH 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T65656，CAS号为 103616-89-3。
T25394	ETB067 ETB-067,ETB 067
	ETB067, an H-89 analog, acts as a PKA and AKT1 inhibitor with specificity on no longer inhibiting CAMK2B and neither affecting viability of mice nor causing any detectable tissue damage at the dose given.
T37053	Z-(L-Arg)-AMC (hydrochloride)
	Z-(L-Arg)-AMC is a fluorogenic substrate for trypsin, cathepsin B, and cathepsin H.1,2Upon enzymatic cleavage by trypsin, cathepsin B, or cathepsin H, 7-amino-4-methylcoumarin (AMC) is released and its fluorescence can be used to quantify trypsin, cathepsin B, and cathepsin H activity. AMC displays excitation/emission maxima of 340-360/440-460 nm, respectively. 1.Zimmerman, M., Ashe, B., Yurewicz, E.C., et al.Sensitive assays for trypsin, elastase, and chymotrypsin using new fluorogenic substrat...

化合物

H-89 dihydrochloride

Cat.No: T6250

Synonym: Protein kinase inhibitor H-89 dihydrochloride,H 89 2HCl,5-Isoquinolinesulfonamide

Target: PKA, S6 Kinase, Autophagy

Cat.No: T11524

Synonym: Protein kinase inhibitor H-89

Target: Others

Cat.No: T65656

Cat.No: T25394

Synonym: ETB-067,ETB 067

Z-(L-Arg)-AMC (hydrochloride)

Cat.No: T37053

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