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T31377Demiditraz；化合物 T31377PF 3814927|||PF-3814927|||PF3814927；PF 3814927|||PF-3814927|||PF3814927
Demiditraz(PF-3814927) is an acaricide (veterinary use).
价 格：￥电议型 号：T31377产 地：中国大陆
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T31086CPFPX；化合物 T31086[18F]CPFPX；[18F]CPFPX
CPFPX is a highly selective radioactive ligand for the A1 adenosine receptor (A1AR).
价 格：￥电议型 号：T31086产 地：中国大陆
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T3105PFK-158；化合物PFK-158PFK-158
PFK-158 is an effective and specific inhibitor PFKFB3.
价 格：￥电议型 号：T3105产 地：中国大陆
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T30966Clenpirin；化合物 T30966UNII-PFM79PGI92|||Clempirina|||BRN 1540697；UNII-PFM79PGI92|||Clempirina|||BRN 15
Clenpirin is a bio-active chemical.
价 格：￥电议型 号：T30966产 地：中国大陆
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T30939Cindunistat HCl maleate；化合物 T30939PHA 728669F|||SD 6010|||PHA-728669F|||SD6010 PF-00572986|||SD-6010
Cindunistat( PHA-728669F, PF-00572986, PHA-84250, SD-6010, and SC-084250) is a potent and oral selective iNOS inhibitor which is expected to be used in patients with symptomatic osteoarthritis of the knee.
价 格：￥电议型 号：T30939产 地：中国大陆
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T30798Cerlapirdine；化合物CerlapirdinePF05212365|||P -05212365|||SAM-531|||SAM531|||PF-05212365|||SAM 531|||WA
Cerlapirdine (PF-05212365) is a selective, potent, full antagonist of the 5-hydroxytryptamine 6 (5-HT6) receptor. Cerlapirdine is already in clinical development for the treatment of cognitive disorders related to Alzheimer´s disease and schizophrenia. It works by acting as a selective 5-HT6 receptor antagonist.
价 格：￥电议型 号：T30798产 地：中国大陆
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T3073PF-670462化合物PF670462PF670462
PF-670462 is a potent (IC50 = 7.7 ± 2.2 nM) and selective (>30-fold with respect to 42 additional kinases) inhibitor of CK1ε in isolated enzyme preparations.
价 格：￥电议型 号：T3073产 地：中国大陆
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T3061Lorlatinib；劳拉替尼PF-6463922|||PF-06463922|||Loratinib；劳拉替尼|||PF-6463922|||PF-06463922|||Loratinib
Lorlatinib (PF-6463922) is an orally available, ATP-competitive inhibitor of the receptor tyrosine kinases, anaplastic lymphoma kinase (ALK) and C-ros oncogene 1 (Ros1), with potential antineoplastic activity.
价 格：￥电议型 号：T3061产 地：中国大陆
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T30476LBisoxatin acetate；化合物 T30476LWY 8138|||WY-8138|||WY8138|||Exodol|||Kritel Tropfen；WY 8138|||WY-8138|
Bisoxatin acetate is a contact laxative in pearl form.
价 格：￥电议型 号：T30476L产 地：中国大陆
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T29001Tranterol hydrochloride；化合物 T29001SPFF；SPFF
Tranterol, a β2-adrenergic receptor agonist, is used potentially for the treatment of asthma.
价 格：￥电议型 号：T29001产 地：中国大陆
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T28785Sisapronil；化合物 T28785PF-0241851|||PF 0241851|||PF0241851；PF-0241851|||PF 0241851|||PF0241851
Sisapronil is a member of the phenylpyrazole class of antiparasitics.
价 格：￥电议型 号：T28785产 地：中国大陆
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T28393Pfn1-IN-C2；化合物 T28393Pfn1 inhibitor C2；Pfn1 inhibitor C2
Pfn1-IN-C2, an inhibitor of Profilin1 (Pfn1), has been shown to reduce the overall level of cellular filamentous (F)-actin, slow EC migration and proliferation, and inhibit the angiogenic ability of EC both in vitro and ex vivo.
价 格：￥电议型 号：T28393产 地：中国大陆
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T28392Pfn1-IN-C1；化合物 T28392Pfn1INC1|||Pfn1 IN C1|||Pfn1 inhibitor C1；Pfn1INC1|||Pfn1 IN C1|||Pfn1 inhibito
Pfn1-IN-C1, an inhibitor of Profilin1 (Pfn1), has been shown to reduce the overall level of cellular filamentous (F)-actin, slow EC migration and proliferation, and inhibit the angiogenic ability of EC both in vitro and ex vivo.
价 格：￥电议型 号：T28392产 地：中国大陆
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T28391PF-9404C；化合物 T28391PF9404C；PF9404C
PF-9404C is the S-S diesteroisomer of a beta adrenergic receptors blocker with vasodilatory properties. PF9404C increased the formation of cyclic GMP from 3 pmol mg?1 protein in basal conditions, to 53 pmol mg?1 protein in 10 μM in rat aorta smooth muscle cells.
价 格：￥电议型 号：T28391产 地：中国大陆
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T28390PF9238；化合物 T28390PF 9238|||PF-9238；PF 9238|||PF-9238
PF9238 is an inhibitor of beta-secretase I. PF9238 has a CatD potency of 12 uM in vivo.
价 格：￥电议型 号：T28390产 地：中国大陆
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T28389PF-6422899；化合物 T28389PF6422899|||PF 6422899；PF6422899|||PF 6422899
PF-6422899 irreversibly inhibits EGFR kinase activity by binding covalently to active-site cysteine residues in the ATP binding pocket of EGFR.
价 格：￥电议型 号：T28389产 地：中国大陆
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T28388PF-5274857 mseylate (1373615-35-0 free base)；化合物 T28388PF5274857 HCl|||PF 5274857|||PF-5274857|||PF-
PF-5274857 is a potent, orally active and selective inhibitor of hedgehog (Hh) signaling pathway (IC50 = 5.8 nM, Ki = 4.6 nM) . PF-5274857 effectively penetrates the blood-brain barrier and inhibits Smo activity in the brain of primary medulloblastoma mice, resulting in improved animal survival rates.
价 格：￥电议型 号：T28388产 地：中国大陆
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T28387PF-4950834；化合物 T28387PF 4950834|||PF4950834；PF 4950834|||PF4950834
PF-4950834, a ATP-competitive, selective Rho kinase inhibitor, provides therapeutic benefits in chronic inflammatory diseases.
价 格：￥电议型 号：T28387产 地：中国大陆
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T28386PF-46396；化合物 T28386PF 46396；PF 46396
PF-46396 is a HIV maturation inhibitor and can be used against HIV-1 clade B and C.
价 格：￥电议型 号：T28386产 地：中国大陆
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T28385PF-462991；化合物 T28385PF-991|||PF991|||PF 991|||PF 462991；PF-991|||PF991|||PF 991|||PF 462991
PF-462991 is a S1P1 agonist.
价 格：￥电议型 号：T28385产 地：中国大陆
