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已选条件
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T24626PF-249;化合物PF-249PF-06685249|||PF 06685249|||PF06685249;PF-06685249|||PF 06685249|||PF06685249
PF-249 (PF-06685249) is a β1-selective AMPK with an EC50 of 12 nM for AMPK α1β1γ1 and can be used in studies about diabetic nephropathy.
价 格:¥电议型 号:T24626产 地:中国大陆
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T24625PF-184563;化合物 T24625PF184563|||PF 184563;PF184563|||PF 184563
PF-184563 is an effective and selective non-peptidic V1a receptor antagonist.
价 格:¥电议型 号:T24625产 地:中国大陆
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T24624PF-06815189;化合物 T24624PF-06815189
PF-06815189 is a phosphodiesterase 2A inhibitor. PF-06815189 also has good selectivity over other phosphodiesterases with a 1000-fold margin (PDE5/2 selectivity: 2439 nM/0.4 nM).
价 格:¥电议型 号:T24624产 地:中国大陆
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T24623PF-06807656;化合物 T24623PF 06807656;PF 06807656
PF-06807656 is insensitive to the introduction of the N171D mutation in the ROMK conduction pore that greatly diminishes the activity of other small-molecule inhibitors. PF-06807656 is an effective ROMK inhibitor (Tl+ flux IC50 = 160 nM).
价 格:¥电议型 号:T24623产 地:中国大陆
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T24622PF-06679142;化合物 T24622PF06679142|||PF-6679142|||PF6679142|||PF 6679142;PF06679142|||PF-6679142|||PF6
PF-06679142 is an effective AMPK activator. PF-06679142 exhibited robust activation of AMPK in rat kidneys as well as desirable oral absorption.
价 格:¥电议型 号:T24622产 地:中国大陆
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T24621PF-06648671;化合物 T24621PF 6648671|||PF 06648671|||PF6648671|||PF-6648671;PF 6648671|||PF 06648671|||P
PF-06648671 is a γ-secretase modulator for the treatment of neurodegenerative and/or neurological disorders.
价 格:¥电议型 号:T24621产 地:中国大陆
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T24620PF-06372222;化合物 T24620PF-0637222|||PF0637222|||PF 0637222;PF-0637222|||PF0637222|||PF 0637222
PF-06372222 is a small-molecule negative allosteric modulator of the glucagon receptor (GCGR). PF-06372222 is also an antagonist for glucagon-like peptide-1 receptor GLP-1R, which inhibits glucagon secretion and glucose-dependent insulin secretion.
价 格:¥电议型 号:T24620产 地:中国大陆
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T24619PF-05388169;化合物 T24619PF05388169|||PF 05388169;PF05388169|||PF 05388169
PF-05388169 is an effective and selective inhibitor of IRAK4.
价 格:¥电议型 号:T24619产 地:中国大陆
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T24618PF-05387252;化合物 T24618PF-05387252
PF-05387252 is an effective and selective inhibitor of the IRAK4.
价 格:¥电议型 号:T24618产 地:中国大陆
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T24617PF-04859989;化合物 T24617PF-04859989
PF-04859989 is a brain-penetrable irreversible inhibitor of kynurenine amino transferase II. PF-04859989 is ~1000-fold selective for KAT II over human KAT I, KAT III, and KAT IV. PF-04859989 has IC50 values of 23 nM for hKAT II and 263 nM for rKAT II.
价 格:¥电议型 号:T24617产 地:中国大陆
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T24616PF-04781340;化合物 T24616PF-04781340
PF-04781340 is an effective, selective, and CNS penetrant agonist of 5-HT2C receptor.
价 格:¥电议型 号:T24616产 地:中国大陆
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T24615PF04677490;化合物 T24615PF-04677490|||PF 04677490;PF-04677490|||PF 04677490
PF04677490 is an effective PDE1 inhibitor. PF04677490 efficaciously inhibits cAMP- and cGMP-hydrolytic activity in preparations from human myocardium at concentrations selective for PDE1.
价 格:¥电议型 号:T24615产 地:中国大陆
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T24614PF04471141 HCl;化合物 T24614PF04471141 hydrochloride|||PF04471141|||PF 04471141|||PF-04471141;PF0447114
PF-04471141 is an effective and selective inhibitor of the calcium-activated phosphodiesterase PDE1 (IC50 = 35 nM).
价 格:¥电议型 号:T24614产 地:中国大陆
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T24613PF-00217830;化合物PF-00217830PF-217830;PF-217830
PF-00217830 is a serotonin 1A receptor agonist, dopamine D2 receptor agonist, and serotonin 2A receptor antagonist.PF-00217830 may be used in the study of schizophrenia.
价 格:¥电议型 号:T24613产 地:中国大陆
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T2455PFK-015;化合物PFK-015PFK15|||PFK 015;PFK15|||PFK 015
PFK-015 (PFK15) is an effective inhibitor of PFKFB3 (IC50: 110 nM) and inhibits PFKFB3 activity in Y cells (IC50: 20 nM).
价 格:¥电议型 号:T2455产 地:中国大陆
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T23987DGJ-pFPhT;化合物 T23987DGJ pFPhT;DGJ pFPhT
DGJ-pFPhT is a ligand of human α-galactosidase A.
价 格:¥电议型 号:T23987产 地:中国大陆
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T23141PF-998425化合物 T23141PF 998425
non-steroidal androgen receptor (AR) antagonist
价 格:¥电议型 号:T23141产 地:中国大陆
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T2314PF-431396;化合物PF 431396PF-431396
PF-431396 is a dual PYK2/FAK inhibitor (IC50: 11/2 nM).
价 格:¥电议型 号:T2314产 地:中国大陆