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T33947PF-06445974；化合物 T33947PF06445974|||PF6445974|||PF06445974|||PF-6445974|||PF 6445974|||PF-06445974|||
PF-06445974 has good selectivity for PDE4D, excellent brain permeability, and has a high level of specific binding in the "cold tracer" study.
价 格：￥电议型 号：T33947产 地：中国大陆
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T33946PF-06439015 mesylate；化合物 T33946PF 06439015|||PF-06439015|||PF06439015；PF 06439015|||PF-06439015|||PF
PF-06439015 overcomes clinical ALK (receptor tyrosine kinase anatropic lymphoma kinase) mutations resistant to krizotinib. Pf-06439015 is an effective selective inhibitor.
价 格：￥电议型 号：T33946产 地：中国大陆
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T33945PF-06260933 HCl；化合物 T33945PF06260933 dihydrochloride|||PF-06260933 dihydrochloride|||PF 06260933 dih
PF-06260933 Dihydrochloride is a MAP4K4 (HGK) inhibitor (IC50 = 140 nM). It can improve the fasting hyperglycemia in mice. In addition, it inhibited Mink and Tnik (IC50 values of 8 and 13 nM, respectively).
价 格：￥电议型 号：T33945产 地：中国大陆
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T33944PF-06260414；化合物 T33944PF 06260414|||PF06260414|||PF-6260414|||PF 6260414|||PF6260414；PF 06260414|||P
PF-06260414 is a selective androgen receptor modulator or SARM used to treat muscle weakness.
价 格：￥电议型 号：T33944产 地：中国大陆
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T33943PF-04856264化合物 T33943PF-4856264|||PF4856264|||PF 4856264
PF-04856264 is a potent and selective human Nav1.7 voltage-gated sodium channel inhibitor (IC50 = 28 nM).
价 格：￥电议型 号：T33943产 地：中国大陆
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T33942PF-0419789；化合物 T33942PF0419789；PF0419789
PF-0419789 is a bio-active chemical.
价 格：￥电议型 号：T33942产 地：中国大陆
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T33941PF-03635659；化合物PF-03635659PF03635659|||PF 03635659；PF03635659|||PF 03635659
PF-03635659 is a potent and long dissociative half-life muscarinic M3 antagonist (Ki: 0.2 nM) that shows potential for the treatment of chronic obstructive pulmonary disease (COPD).
价 格：￥电议型 号：T33941产 地：中国大陆
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T33940PF-03382792；化合物PF-03382792PF 03382792|||PF03382792；PF 03382792|||PF03382792
PF-03382792 is a small molecule 5-HT4 receptor activator for the study of Alzheimer´s disease.
价 格：￥电议型 号：T33940产 地：中国大陆
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T33939Dagrocorat hydrochloride；化合物 T33939PF-0251802|||PF 0251802|||PF-0251802 HCl|||PF0251802；PF-0251802||
PF-0251802 HCl is a bio-active chemical.
价 格：￥电议型 号：T33939产 地：中国大陆
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T3386Kaempferitrin；山奈苷Lespedin|||Kaempferol|||Lespenephryl|||Lespenefril|||Kaempferol 3,7-dirhamnoside；Le
Kaempferitrin (Lespenephryl) has antidepressant-like effect related to the serotonergic system, principally 5-HT1A. Kaempferitrin exerts cytotoxic and antitumor effects against HeLa cells. Kaempferitrin stimulates glucose-metabolizing enzymes, promotes glucose homeostasis. Kaempferitrin exerts immunostimulatory effects on immune responses mediated by splenocytes, macrophages, PBMC and NK cells. Kaempferitrin induces cytotoxic effects to include: cell cycle arrest in G1 phase and apoptosis via th
价 格：￥电议型 号：T3386产 地：中国大陆
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T33630Neo-cupferron；化合物 T33630Neo-cupferron
Neo-cupferron is an Agricultural Chemical.
价 格：￥电议型 号：T33630产 地：中国大陆
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T33493Mppf F-18；化合物 T33493J1.050.795B|||P-18FMPPF|||(18F) Mppf|||(18F)Mppf|||(18F)-Mppf；J1.050.795B|||P-18
Mppf F-18, which has been used as a radioactive ligand for positron emission tomography, is a compound that binds to the serotonin-1A receptor.
价 格：￥电议型 号：T33493产 地：中国大陆
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T3347PF3274167；化合物PF3274167PF 3274167|||Cligosiban|||PF-3274167；PF 3274167|||Cligosiban|||PF-3274167
PF3274167 (Cligosiban) is a potent and selective, high-affinity nonpeptide oxytocin receptor antagonist.
价 格：￥电议型 号：T3347产 地：中国大陆
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T3336Rg3039；化合物Rg3039PF-06687859；PF-06687859
Rg3039 (PF-06687859) is a potent DcpS inhibitor. DcpS is a therapeutic target for spinal muscular atrophy. Spinal muscular atrophy (SMA) is caused by deletion or mutation of both copies of the SMN1 gene which produces an essential protein known as SMN. RG3039 improves motor function in SMA mice. RG3039 also showed activity to improve survival, function and motor unit pathologies in two SMA mouse models.
价 格：￥电议型 号：T3336产 地：中国大陆
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T33288Mepramidil；化合物 T33288PF26|||PF-26|||PF 26；PF26|||PF-26|||PF 26
Mepramidil is a potential bioactive agent.
价 格：￥电议型 号：T33288产 地：中国大陆
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T3306PF-04418948；化合物PF04418948PF 04418948|||PF04418948；PF 04418948|||PF04418948
PF-04418948 is a potent EP2 receptor antagonist (IC50 = 16 nM for human EP2 receptors). Displays over 2000-fold selectivity for EP2 receptors over EP1, EP3, EP4, DP1 amd CRTH2 receptors; exhibits <30% binding at a diverse panel of GPCRs and ion channels at a concentration of 10 μM. Inhibits PGE2-induced increases in intracellular cAMP; reverses PGE2-invoked relaxation of mouse trachea (IC50 = 2.7 nM).
价 格：￥电议型 号：T3306产 地：中国大陆
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T32766Linifolin A；化合物 T32766NSC 153859|||NSC-153859|||NSC153859|||PF 57|||PF-57；NSC 153859|||NSC-153859|||
Linifolin A is a sesquiterpene lactone extracted from Helenium aromaticum.
价 格：￥电议型 号：T32766产 地：中国大陆
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T3217PF-CBP1 hydrochloride；化合物PF-CBP1 hydrochloridePF-CBP1 HCl；PF-CBP1 HCl
PF-CBP1 hydrochloride (PF-CBP1 HCl) is a highly selective inhibitor of the bromodomain of CREB-binding protein(CREBBP).It inhibits CREBBP and p300 bromodomains with IC50 of 125 and 363 nM respectively.
价 格：￥电议型 号：T3217产 地：中国大陆
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T31919Gdpflrfamide；化合物 T31919Gly-asp-pro-phe-leu-arg-phe-amide；Gly-asp-pro-phe-leu-arg-phe-amide
Gdpflrfamide is a neuropeptide that existed in the snail Lymnaea stagnalis.
价 格：￥电议型 号：T31919产 地：中国大陆
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T31594EA-230；化合物 T31594EA 230|||NMPF-46|||NMPF46|||NMPF 46；EA 230|||NMPF-46|||NMPF46|||NMPF 46
Ea-230 is an immunomodulator that may be used in the treatment of renal failure.
价 格：￥电议型 号：T31594产 地：中国大陆
