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T9688CC-90001CC90001,kinase,IPF,JNK,c-Jun,idiopathic,JNK1,Inhibitor,N-terminal,inhibit,CC-90001,CC 90001,
CC-90001 is an orally administered c-Jun N-terminal kinase (JNK) inhibitor with bias for JNK1 over JNK2.
价 格：￥电议型 号：T9688产 地：中国大陆
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T3153SerabelisibINK1117；MLN1117；TAK-117
MLN1117 (INK1117) is a p110α/β/γ/δ inhibitor (IC50: 15/4.5/1.9/13.39 μM).
价 格：￥电议型 号：T3153产 地：中国大陆
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T1988DuvelisibINK1197；IPI-145；度维利塞
Duvelisib is an orally bioavailable, highly selective and potent small molecule inhibitor of the delta and gamma isoforms of phosphoinositide-3 kinase (PI3K) with potential immunomodulating and antineoplastic activities.
价 格：￥电议型 号：T1988产 地：中国大陆
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T11129Duvelisib (R enantiomer)INK1197 R enantiomer；Duvelisib R enantiomer；IPI-145 R enantiomer
Duvelisib R enantiomer is an enantiomer of Duvelisib with lower activity. Duvelisib is a PI3K inhibitor.
价 格：￥电议型 号：T11129产 地：中国大陆
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T11129Duvelisib R enantiomerDuvelisib R enantiomer,IPI-145 R enantiomer,INK1197 R enantiomer
Duvelisib R enantiomer is an enantiomer with low activity of Duvelisib and is an inhibitor of PI3K.
价 格：￥电议型 号：T11129产 地：美洲
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T1988DuvelisibDuvelisib,INK1197,IPI-145
Duvelisib is an orally bioavailable, highly selective and potent small molecule inhibitor of the delta and gamma isoforms of phosphoinositide-3 kinase (PI3K) with potential immunomodulating and antineoplastic activities.
价 格：￥电议型 号：T1988产 地：美洲
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T6440CGP 57380CGP 57380,MNK1 Inhibitor,
CGP 57380 is a potent MNK1 inhibitor with IC50 of 2.2 μM, exhibiting no inhibitory activity on p38, JNK1, ERK1 and -2, PKC, or c-Src-like kinases.
价 格：￥电议型 号：T6440产 地：美洲
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T78268Anti-Mouse NK1.1 Antibody (PK136)；化合物 Anti-Mouse NK1.1 Antibody (PK136)Anti-Mouse NK1.1 Antibody (PK
Anti-Mouse NK1.1 Antibody (PK136) is an IgG2a class antibody of murine origin targeting NK1.1, which eliminates NK1.1 and NK1.1NKT cells and inhibits NK1.1 signaling in peripheral blood, spleen, and lung tissues, and can be used in the study of heart and lung failure.
价 格：￥电议型 号：T78268产 地：中国大陆
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T73295WNK1-IN-1；化合物 WNK1-IN-1WNK1-IN-1
WNK1-IN-1, a selective inhibitor of WNK1, exhibits an IC50 value of 1.6 μM and also inhibits OSR1 phosphorylation with an IC50 value of 4.3 μM, indicating its potential utility in the research of blood pressure regulation and cancer.
价 格：￥电议型 号：T73295产 地：中国大陆
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T72224NK1 receptor antagonist 2；化合物 NK1 receptor antagonist 2NK1 receptor antagonist 2
NK1 Receptor Antagonist 2, a compound targeting the NK1 receptor, holds potential for tinnitus and hearing loss research.
价 格：￥电议型 号：T72224产 地：中国大陆
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T6440CGP 57380；化合物CGP 57380MNK1 Inhibitor；N3-(4-氟苯基)-1H-吡唑并[3,4-D]嘧啶-3,4-二胺|||MNK1 Inhibitor
CGP 57380 (MNK1 Inhibitor) is a potent MNK1 inhibitor with IC50 of 2.2 μM, exhibiting no inhibitory activity on p38, JNK1, ERK1 and -2, PKC, or c-Src-like kinases.
价 格：￥电议型 号：T6440产 地：中国大陆
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T62686MNK1/2-IN-6；化合物 MNK1/2-IN-6MNK1/2-IN-6
MNK1/2-IN-6 is a potent and selective inhibitor of MNK1 (IC50: 2.3 nM), MNK2 (IC50: 3.4 nM), and MNK1/2-IN-6 induces apoptosis in a concentration-dependent manner.
价 格：￥电议型 号：T62686产 地：中国大陆
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T60733MNK1/2-IN-5；化合物 MNK1/2-IN-5MNK1/2-IN-5
MNK1/2-IN-5 is a potent and selective inhibitor of MNK1/2.
价 格：￥电议型 号：T60733产 地：中国大陆
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T33696NK-1145；化合物 T33696NK-1145 hydrocholdoride|||NK 1145|||NK1145；NK-1145 hydrocholdoride|||NK 1145|||NK1
Nk-1145 is a parasympathetic drug of the autonomic nervous system, which can cause behavioral stimulation and excitement.
价 格：￥电议型 号：T33696产 地：中国大陆
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T3153Serabelisib；化合物SerabelisibTAK-117|||INK1117|||MLN1117；TAK-117|||INK1117|||MLN1117
Serabelisib (INK1117) is a p110α/β/γ/δ inhibitor (IC50: 15/4.5/1.9/13.39 μM).
价 格：￥电议型 号：T3153产 地：中国大陆
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T29725AGN-191129；化合物 T29725AGN191129|||Prostaglandin F2α alcohol methyl ether|||PGF2α-OMe|||UNII-NK1168QB5
AGN-191129, also known as Prostaglandin F2α alcohol methyl ether (PGF2α-OMe), is an analog of PGF2α in which the C-1 carboxyl group has been replaced by an O-methyl ether. The compound is reported to retain ocular hypotensive properties, but the receptors which mediate this activity have not been clearly documented.
价 格：￥电议型 号：T29725产 地：中国大陆
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T26822Bisaramil hydrochloride；比沙雷米盐酸盐RGH-2957|||NK 1556|||NK1556|||Bisaramil|||NK-1556|||RGH 2957；RGH-2957
Bisaramil hydrochloride (Bisaramil) is a novel diazabicyclononane antiarrhythmic compound that inhibits the generation of free radicals.Bisaramil hydrochloride blocks sodium currents and inhibits the slow Ca(2+) action potential induced by isoproterenol in K(+)-depolarized muscle.
价 格：￥电议型 号：T26822产 地：中国大陆
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T1988Duvelisib；度维利塞INK1197|||IPI-145；INK1197|||IPI-145|||度维利塞
Duvelisib (INK1197) is an orally bioavailable, highly selective and potent small molecule inhibitor of the delta and gamma isoforms of phosphoinositide-3 kinase (PI3K) with potential immunomodulating and antineoplastic activities.
价 格：￥电议型 号：T1988产 地：中国大陆
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T11129Duvelisib (R enantiomer)化合物Duvelisib R entiomerDuvelisib R enantiomer|||IPI-145 R enantiomer|||INK11
Duvelisib R enantiomer (IPI-145 R enantiomer) is an enantiomer of Duvelisib with lower activity. Duvelisib is a PI3K inhibitor.
价 格：￥电议型 号：T11129产 地：中国大陆
