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T21674LPKA inhibitor fragment (6-22) amide AcetatePKA inhibitor fragment (6-22) amide Acetate(121932-06-7 F
PKA Inhibitor Fragment (6-22) amide Acetate is a PKA inhibitor with a Ki of 2.8 nM. It can significantly reverse low-level morphine antinociceptive tolerance in mice.
价 格：￥电议型 号：T21674L产 地：中国大陆
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T14496BAMB-4ITPKA-IN-C14
Bamb-4 is a highly membrane-permeable inhibitor of inositol-1,4,5-trisphosphate-3-kinase A (ITPKA). It acts by suppressing the metastasis-promoting effect of ITPKA in lung tumor cells(with IC50 of 37 μM in ADP-Glo Assay).
价 格：￥电议型 号：T14496产 地：中国大陆
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T76381H1-7 (histone H1 phosphorylation site), PKA Substrate；化合物 H1-7 (histone H1 phosphorylation site), PK
H1-7 (histone H1 phosphorylation site), a synthetic polypeptide serving as a PKA substrate, demonstrates utility in PKA substrate applications [1] [2].
价 格：￥电议型 号：T76381产 地：中国大陆
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T75888PKA Inhibitor Fragment (6-22) amide TFA；PKA Inhibitor Fragment (6-22) amide三氟乙酸盐PKI-(6-22)-amide TFA
PKA Inhibitor Fragment (6-22) amide TFA (PKA Inhibitor Fragment (6-22) amide TFA) is an inhibitor of the highly potent cAMP-dependent protein kinase A (PKA) inhibitor (Ki: 2.8 nM).PKA Inhibitor Fragment (6-22) amide TFA reverses the pain-relieving effects of low levels of morphine in mice.
价 格：￥电议型 号：T75888产 地：中国大陆
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T72886Akt1&PKA-IN-2；化合物 Akt1&PKA-IN-2Akt1&PKA-IN-2
Akt1&PKA-IN-2 ((R)-29), a compound with specificity towards PKB/AKT and notable selectivity for cyclin-dependent kinase 2 (CDK2), effectively inhibits AKT1, PKAa, and CDK2a with IC50 values of 0.007 ?M, 0.01 ?M, and 0.69 ?M, respectively.
价 格：￥电议型 号：T72886产 地：中国大陆
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T72885Akt1&PKA-IN-1；化合物 Akt1&PKA-IN-1Akt1&PKA-IN-1
Akt1&PKA-IN-1 is a potent dual inhibitor targeting Akt and PKA, exhibiting IC50 values of 0.11 μM for Akt, 0.03 μM for PKAα, and 9.8 μM for CDK2. Notably, it demonstrates selectivity for cyclin-dependent kinase 2 (CDK2).
价 格：￥电议型 号：T72885产 地：中国大陆
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T39217PKA-IN-1；PKA抑制剂4PKA-IN-1
PKA-IN-1 is a selective and potent cyclic AMP-dependent protein kinase (PKA) catalytic subunit (cAK) inhibitor (IC50: 0.03 μM).PKA-IN-1 can be used to study diseases of the immune system.
价 格：￥电议型 号：T39217产 地：中国大陆
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T36019PKA Inhibitor (5-24) (trifluoroacetate salt)；PKA Inhibitor (5-24) (trifluoroacetate salt)PKA Inhibit
PKI PKA Inhibitor (5-24) is a synthetic peptide inhibitor of PKA (cAMP-dependent protein kinase) (Ki= 2.3 nM) derived from the active site of the skeletal muscle inhibitor protein.1It mimics the protein substrate by binding to the catalytic site through the arginine-cluster basic subsite.1The prominent enzyme-substrate interaction site occurs where PKA catalytic subunit residues Tyr235and Phe239form a sandwich-like structure with residue Phe10of PKI (5-24).2
价 格：￥电议型 号：T36019产 地：中国大陆
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T21674LPKA inhibitor fragment (6-22) amide Acetate；化合物T21674LPKA inhibitor fragment (6-22) amide Acetate(12
PKA inhibitor fragment (6-22) amide Acetate is a synthetic peptide which selectively inhibits PKA activity by binding to its substrate site (IC50 < 2 nM).
价 格：￥电议型 号：T21674L产 地：中国大陆
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T14496BAMB-4；化合物BAMB-4ITPKA-IN-C14；ITPKA-IN-C14
BAMB-4 (ITPKA-IN-C14) is a highly membrane-permeable inhibitor of inositol-1,4,5-trisphosphate-3-kinase A (ITPKA). It acts by suppressing the metastasis-promoting effect of ITPKA in lung tumor cells(with IC50 of 37 μM in ADP-Glo Assay).
价 格：￥电议型 号：T14496产 地：中国大陆
