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T11483GSK256066 Trifluoroacetate化合物 T11483GSK 256066 Trifluoroacetate|||GSK256066 (2,2,2-trifluoroacetic a
GSK 256066 Trifluoroacetate is a selective and high-affinity phosphodiesterase 4 (PDE) inhibitor (IC50: 3.2 pM for PDE4B). It can be used for the treatment of chronic obstructive pulmonary disease.
价 格：￥电议型 号：T11483产 地：中国大陆
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T11466GSK-2793660；化合物 T11466GSK-2793660
GSK-2793660 is an orally active and irreversible inhibitor of Cathepsin C (CTSC). GSK-2793660 is a bioactive dipeptide that can be used for the research of bronchiectasis [1] [2].
价 格：￥电议型 号：T11466产 地：中国大陆
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T11460GPR4 antagonist 1；化合物 T11460GPR4 antagonist 1
GPR4 antagonist 1 is a GPR4 antagonist (IC50: 189 nM).
价 格：￥电议型 号：T11460产 地：中国大陆
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T11412IPN60090；化合物IPN60090GLS1-IN-1；GLS1-IN-1
IPN60090 is a novel, potent, orally bioavailable, renal-type glutaminase (GLS1)-specific inhibitor with an IC50 value of 31 nM for GLS1. IPN60090 has potential anticancer and immunostimulant/immunomodulatory activity, selectively targets, binds, and inhibits human glutaminase, and can be used to study GLS1-mediated diseases.
价 格：￥电议型 号：T11412产 地：中国大陆
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T11360gamma-secretase modulator 3；化合物 T11360gamma-secretase modulator 3
gamma-secretase modulator 3 is a gamma-secretase modulator.
价 格：￥电议型 号：T11360产 地：中国大陆
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T11318Dopexamine hydrochloride；盐酸多培沙明FPL60278AR；盐酸多培沙明|||FPL60278AR
Dopexamine hydrochloride (FPL60278AR) is a β2-adrenergic receptor agonist. Dopexamine can attenuate the inflammatory response and protect against organ injury in the absence of significant effects on hemodynamics or regional microvascular flow.
价 格：￥电议型 号：T11318产 地：中国大陆
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T11267FASN-IN-1；化合物FASN-IN-1TVB-2460；TVB-2460
FASN-in-1 is an effective, specific inhibitor of fatty acid synthase (FASN), a compound specifically designed to target and inhibit the activity of the enzyme involved in fatty acid synthesis, potentially disrupting fatty acid production and affecting various cellular processes.
价 格：￥电议型 号：T11267产 地：中国大陆
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T11260FAK inhibitor 2；化合物 T11260FAK inhibitor 2
FAK inhibitor 2, antitumor and anti-angiogenesis activitiesis ,is a potent focal adhesion kinase (FAK) inhibitor with an IC50 of 0.07 nM .
价 格：￥电议型 号：T11260产 地：中国大陆
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T11177Elinogrel；化合物ElinogrelPRT060128；PRT060128
Elinogrel (PRT060128) is a competitive and reversible antagonist of platelet P2Y12 with IC50 of 20 nM and exhibits potent antiplatelet effects.
价 格：￥电议型 号：T11177产 地：中国大陆
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T11175Elenbecestat；化合物ElenbecestatE2609；E2609
Elenbecestat (E2609) is an effective oral bioutilization and CNS penetrating ACE-1 inhibitor for the treatment of Alzheimer´s disease.
价 格：￥电议型 号：T11175产 地：中国大陆
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T11160EGFR-IN-5；化合物EGFR-IN-5EGFR-IN-5|||inhibit|||Epidermal growth factor receptor|||HER1|||ErbB-1|||Inhib
EGFR-IN-5 is a selective inhibitor of EGFR. The IC50s for EGFR, EGFR(L858R), EGFR(L858R/T790M), and EGFR(L858R/T790M/C797S) are 10.4, 1.1, 34, 7.2 nM, respectively.
价 格：￥电议型 号：T11160产 地：中国大陆
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T11104DS21360717；化合物 T11104DS21360717
DS21360717 is an effective oral tyrosine kinase inhibitor with anticancer activity and IC50 of 0.49 nM.
价 格：￥电议型 号：T11104产 地：中国大陆
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T11060DMAPT；化合物DMAPTDimethylamino Parthenolide；Dimethylamino Parthenolide
DMAPT (Dimethylamino Parthenolide) is a water-soluble analogue of Parthenolide (PTL). It is an orally active NF-κB inhibitor with an LD50 of 1.7 μM on primary acute myeloid leukemia cells.
价 格：￥电议型 号：T11060产 地：中国大陆
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T1105Penfluridol；五氟利多R-16341|||TLP-607；五氟利多|||R-16341|||TLP-607
Penfluridol (TLP-607) is a highly potent antipsychotic.
价 格：￥电议型 号：T1105产 地：中国大陆
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T11011Dexpramipexole dihydrochloride；右旋普拉克索二盐酸盐KNS-760704 dihydrochloride|||R-(+)-Pramipexole dihydrochlor
Dexpramipexole dihydrochloride (KNS-760704 dihydrochloride) ((R)-Pramipexole dihydrochloride) is a neuroprotective agent and is a weak non-ergoline dopamine agonist.
价 格：￥电议型 号：T11011产 地：中国大陆
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T10960LDarbufelone mesylate；达布非龙甲磺酸盐CI-1004 mesylate；CI-1004 mesylate
Darbufelone mesylate (CI-1004 mesylate) inhibited PGF2α and LTB4 in cells. Darbufelone mesylate inhibited PGHS-2 with IC50 value of 0.19 μM and PGHS-1 with IC50 value of 20 μM.
价 格：￥电议型 号：T10960L产 地：中国大陆
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T10960Darbufelone；达布非酮CI-1004；达布非酮|||CI-1004
Darbufelone (CI-1004) is a non-competitive dual inhibitor of PGF2α and LTB4. Dabfilon effectively inhibits PGHS-2 with a Ki of 10 μM and IC50s of 0.19 μM and 20 μM for PGHS-2 and PGHS-1.
价 格：￥电议型 号：T10960产 地：中国大陆
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T10883LCRA-026440 hydrochloride；化合物CRA-026440盐酸盐CRA-026440 hydrochloride（847460-34-8 Free base）；CRA-026440
CRA-026440 hydrochloride is a potent and broad-spectrum HDAC inhibitor. CRA-026440 hydrochloride exhibits Ki values against recombinant HDAC isoenzymes HDAC1, HDAC2, HDAC3, HDAC6, HDAC8, and HDAC10 are 4 nM, 14 nM, 11 nM, 15 nM, 7 nM, and 20 nM, respectively. CRA-026440 hydrochloride exhibits antitumor and antiangiogenic activities.
价 格：￥电议型 号：T10883L产 地：中国大陆
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T10874CP-060；化合物CP-060CP-060
CP-?060 is a potent Ca2+ antagonist and inhibits Ca2+ overload with antioxidant and cardioprotective activities.
价 格：￥电议型 号：T10874产 地：中国大陆
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T10872LCP 96021；化合物CP 96021CP 96021
CP 96021 is a group of 5-HT1 receptors and 5-HT2 receptors antagonists that have anti-inflammatory properties and are non-non-self anti-ulcer compounds for the treatment of gastrointestinal tract and respiratory asthma.
价 格：￥电议型 号：T10872L产 地：中国大陆
