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产品数：86101
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T23764AZ3976；化合物AZ3976AZ 3976|||AZ-3976；AZ 3976|||AZ-3976
AZ3976 is an inhibitor of PAI-1 with an IC50 of 16 μM in a plasma clot lysis assay. AZ3976 displays profibrinolytic activities.
价 格：￥电议型 号：T23764产 地：中国大陆
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T23715Amb21795397；化合物 T23715Amb 21795397|||PPxY Budding Inhibitor 5|||Amb-21795397；Amb 21795397|||PPxY Bud
Amb21795397 is a blocker of the MARV VP40 PPxY-host Nedd4 interaction.
价 格：￥电议型 号：T23715产 地：中国大陆
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T23697AL-8417；化合物 T23697J1.090.276B|||AL8417|||(2R)-AL-5898；J1.090.276B|||AL8417|||(2R)-AL-5898
AL-8417 is an enzyme inhibitor. It acting as an antioxidant, anti-inflammatory, and cytostatic agent. It also has the ability to suppress vitrectomy-induced posterior lens fiber changes.
价 格：￥电议型 号：T23697产 地：中国大陆
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T23678AHR-11797；化合物 T23678AHR-11797
AHR-11797 is a novel benzodiazepine antagonist.
价 格：￥电议型 号：T23678产 地：中国大陆
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T23597A-940894；化合物 T23597A940894|||A 940894；A940894|||A 940894
A-940894 is a histamine H4 receptor antagonist with anti-inflammatory properties. A-940894 potently binds to both human and rat histamine H4 receptors and exhibits considerably lower affinity for the human histamine H1, H2, or H3 receptors. A-940894 has good pharmacokinetic properties.
价 格：￥电议型 号：T23597产 地：中国大陆
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T23541Y-29794 oxalate；化合物 T23541Y-29794 oxalate
Inhibitor of prolyl endopeptidase
价 格：￥电议型 号：T23541产 地：中国大陆
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T23497UK 78282 hydrochloride；UK-78282盐酸盐UK 78282 hydrochloride
UK 78282 hydrochloride, a novel potent and selective Kv1.3 blocker.UK 78282 hydrochloride inhibits Kv1.3 voltage-gated potassium channels and suppresses human T cell activation.
价 格：￥电议型 号：T23497产 地：中国大陆
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T23471TRAM 39；化合物TRAM 392-Chloro-alpha,alpha-diphenylbenzeneacetonitrile|||TRAM-39|||ZINC27105797|||2-(2-c
TRAM 39 (2-Chloro-α,α-diphenylbenzeneacetonitrile) is a selective blocker of intermediate-conductance Ca2+-activated K+channels.
价 格：￥电议型 号：T23471产 地：中国大陆
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T23397ST 91；化合物ST 91ST 91
ST-91 is an agonist of α2-adrenoceptor with a mixed α-adrenergic receptor type/subtype selection profile.
价 格：￥电议型 号：T23397产 地：中国大陆
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T23395SSR 146977 hydrochloride；化合物 T23395SSR 146977 hydrochloride
NK3 receptor antagonist
价 格：￥电议型 号：T23395产 地：中国大陆
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T23361SKF 81297 hydrobromide；化合物 T23361SKF 81297 hydrobromide
SKF 81297 hydrobromide is a Dopamine D1-like receptor agonist.
价 格：￥电议型 号：T23361产 地：中国大陆
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T23297(S)-(+)-Dimethindene maleate；(S)-(+)-Dimethindene 马来酸盐(S)-(+)-Dimethindene maleate
(S)-(+)-Dimethindene maleate is an orally available, selective muscarinic M2 receptor and histamine H1 receptor antagonist that inhibits muscarinic M1, M3, and M4 receptors.
价 格：￥电议型 号：T23297产 地：中国大陆
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T23255RS 23597-190 hydrochloride化合物 T23255RS 23597190 hydrochloride|||RS 23597 190 hydrochloride
RS 23597-190 hydrochloride is a 5-HT4 receptor antagonist.
价 格：￥电议型 号：T23255产 地：中国大陆
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T23128PD180970；化合物PD180970PD 180970；PD 180970
PD180970 is an inhibitor of Bcr-Abl with IC50s of 5 nM, 0.8 nM and 50 nM for the autophosphorylation of p210Bcr-Abl, Src and Kit. PD180970 can be used in studies about chronic myelogenous leukemia.
价 格：￥电议型 号：T23128产 地：中国大陆
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T23097O-1602；化合物O-1602O1602|||O 1602；O1602|||O 1602
O-1602 is a novel GPR55 agonist, an atypical cannabinoid associated with the central nervous system and obesity, and is a candidate compound for the treatment of cystitis.O-1602 promotes hepatic steatosis through GPR55 and PI3 kinase / Akt / SREBP-1c signalling in mice.O-1602 induces, in a GPR3-independent manner, in Hep55B cells with elevated intracellular calcium.
价 格：￥电议型 号：T23097产 地：中国大陆
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T23087NPY 5RA972；化合物NPY 5RA972NPY 5RA972
NPY 5RA972 is a neuropeptide Y Y5 receptor antagonist
价 格：￥电议型 号：T23087产 地：中国大陆
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T23000ML289；化合物ML289VU0463597|||ML 289；VU0463597|||ML 289
ML289 (VU0463597) is a potent, selective, and CNS-penetrant negative allosteric modulator of mGlu3 (IC50=0.66 μM), demonstrating over 15-fold selectivity compared to mGlu2 and showing no activity against mGlu5.
价 格：￥电议型 号：T23000产 地：中国大陆
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T22979Milameline hydrochloride；化合物 T22979Milameline hydrochloride
Milameline hydrochloride is a Muscarinic receptor agonist.
价 格：￥电议型 号：T22979产 地：中国大陆
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T22978MI-2 (hydrochloride)；化合物 T22978MI-2 (hydrochloride)
MI-2 (Menin-MLL Inhibitor) is an effective menin-MLL interaction inhibitor (IC50: 446 ± 28 nM).
价 格：￥电议型 号：T22978产 地：中国大陆
