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T27327FKGK11；化合物 T27327FKGK-11|||FKGK 11；FKGK-11|||FKGK 11
FKGK11 is a potent inhibitor of GVIA iPLA2.
价 格：￥电议型 号：T27327产 地：中国大陆
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T27326FK960；化合物 T27326FK 59960|||FK-960|||FK-59960|||FK59960；FK 59960|||FK-960|||FK-59960|||FK59960
FK962 is an enhancer of somatostatin release, which exerts cognitive-enhancing actions in rats. FK960 increases synaptic density in the hippocampal CA3 region of aged rats.
价 格：￥电议型 号：T27326产 地：中国大陆
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T27325FK-739 free acid；化合物 T27325FK-739|||FK 739|||FK739；FK-739|||FK 739|||FK739
FK-739 is an angiotensin type 1 receptor antagonist. FK 739 inhibits the specific binding of [125I]-angiotensin II to rat aortic smooth muscle cell membrane (IC50 = 8.6 nM) without displacing the specific binding of [125I]-angiotensin II to bovine cerebellum membrane.
价 格：￥电议型 号：T27325产 地：中国大陆
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T27323FK-453；化合物FK-453FK453|||FK 453；FK453|||FK 453
FK-453 is a potent antagonist of non-xanthine adenosine A1 receptor with diuretic and renal vasodilatory activity.
价 格：￥电议型 号：T27323产 地：中国大陆
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T26730AZ-PFKFB3-67；化合物 T26730AZ-PFKFB3-67
AZ-PFKFB3-67 is a novel, potent and selective inhibitor of PFKFB3.
价 格：￥电议型 号：T26730产 地：中国大陆
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T25420FK 33-824；化合物 T25420FK-33-824|||Sandoz FK 33-824|||FK33-824|||SAN 33-824|||Damme；FK-33-824|||Sandoz
FK 33-824 ,with similar actions to those of methionine enkephalin(ENKEPHALIN, METHIONINE),is a stable synthetic analog of that. Its effects can be reversed by narcotic antagonists such as naloxone.
价 格：￥电议型 号：T25420产 地：中国大陆
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T25419FK 224；化合物 T25419FK-224|||FK224；FK-224|||FK224
FK 224 is an antagonist of tachykinin receptor.
价 格：￥电议型 号：T25419产 地：中国大陆
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T2481Ascomycin；子囊霉素FK520|||Immunomycin|||FR-900520；FK520|||Immunomycin|||子囊霉素|||FR-900520
Ascomycin (Immunomycin)(Immunomycin, FR-900520, FK520) is an ethyl analog of tacrolimus (FK506) with strong immunosuppressant properties.
价 格：￥电议型 号：T2481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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T24449Mepacrine；米帕林Haffkinine|||Erion；Haffkinine|||Erion
Mepacrine (Erion) is an acridine derivative formerly widely used as an antimalarial. It is used in cell biological experiments as an inhibitor of phospholipase A2.
价 格：￥电议型 号：T24449产 地：中国大陆
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T24348L 708286；化合物 T24348L708286|||L-708286|||DFKi；L708286|||L-708286|||DFKi
L 708286 is an agent of peptide-based phenethylcarbamoyldifluoromethylene. It is a slow-binding inhibitor of human leucocyte elastase (HLE).
价 格：￥电议型 号：T24348产 地：中国大陆
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T24065FK-3657；化合物 T24065FK 3657|||FK3657|||FR-173657|||FR 173657|||FR173657；FK 3657|||FK3657|||FR-173657||
FK-3657 is a non-peptide antagonist of bradykinin (BK)-B2 receptor.
价 格：￥电议型 号：T24065产 地：中国大陆
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T23758ASP-6537；化合物 T23758FR 122047|||FK 881|||ASP 6537|||FK-881；FR 122047|||FK 881|||ASP 6537|||FK-881
ASP-6537 is a selective and reversible inhibitor of cyclooxygenase-1.
价 格：￥电议型 号：T23758产 地：中国大陆
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T22785FK 866 hydrochloride (658084-64-1 free base)；化合物 T22785FK 866 hydrochloride；FK 866 hydrochloride
FK 866 hydrochloride is an inhibitor of nicotinamide phosphoribosyltransferase (IC50: 0.09nM and 27.2nM).
价 格：￥电议型 号：T22785产 地：中国大陆
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T2144Tacrolimus；他克莫司Fujimycin|||FK506|||FR900506；他克莫司|||Fujimycin|||FK506|||FR900506
Tacrolimus (Fujimycin) is a macrolide antibiotic that binds to FKBP12 to form a high-affinity complex (Ki=0.2 nM) that inhibits calcium/calmodulin-dependent protein phosphatase activity. Tacrolimus is an immunosuppressant that inhibits the overall suppression of T-lymphocytes by inhibiting the release of IL-2.
价 格：￥电议型 号：T2144产 地：中国大陆
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T21119Cevimeline西维美林AF-102B|||西维美林|||FKS 508|||SNI 2011|||HSDB 7286
Cevimeline, a parasympathomimetic and muscarinic agonist, affects M1 and M3 receptors. Cevimeline has been shown to treat dry mouth and Sj gren´s syndrome. It is also used to reduce Xerostomia symptoms and increase salivary flow in head and neck cancer survivors after radiotherapy.
价 格：￥电议型 号：T21119产 地：中国大陆
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T20879Tacrolimus monohydrate；他克莫司一水合物FK-506|||FR 900506|||Prograf|||FR900506|||Tacrolimus hydrate|||LCP-Ta
Tacrolimus monohydrate (LCP-Tacro) is a macrolide from the culture broth of a strain of Streptomyces tsukubaensis, binds to FK506 binding protein (FKBP) to form a complex. Tacrolimus inhibits calcineurin phosphatase, which inhibits T-lymphocyte signal transduction and IL-2 transcription. Immunosuppressive properties. It prevents the activation of T-lymphocytes in response to antigenic or mitogenic stimulation in vitro and has strong immunosuppressive activity in vivo.
价 格：￥电议型 号：T20879产 地：中国大陆
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T19322FKK；化合物 T19322FKK
FKK is an indazole derivative and also a novel bronchodilator.
价 格：￥电议型 号：T19322产 地：中国大陆
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T18611AP1867-2-(carboxymethoxy)；化合物 T18611PROTAC FKBP12-binding moiety 2；PROTAC FKBP12-binding moiety 2
AP1867-2-(carboxymethoxy), a moiety based on the synthetic FKBP12F36V-directed ligand AP1867, connects to the CRBN ligand through a linker to generate dTAG molecules[1].
价 格：￥电议型 号：T18611产 地：中国大陆
