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T11175ElenbecestatE2609
Elenbecestat 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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T0260Meclofenamic acid sodiumMeclofenamate Sodium；Meclomen；Movens；Meclonax；甲氯灭酸钠
Meclofenamate Sodium, a non-steroidal anti-inflammatory agent, has properties of antipyretic and antigranulation activities. It also inhibits prostaglandin biosynthesis.
价 格：￥电议型 号：T0260产 地：中国大陆
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T0260Meclofenamate SodiumMeclofenamate Sodium,Meclomen,Meclonax
Meclofenamate Sodium, a non-steroidal anti-inflammatory agent, has properties of antipyretic and antigranulation activities. It also inhibits prostaglandin biosynthesis.
价 格：￥电议型 号：T0260产 地：美洲
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T10260AglafolineAglafoline,Aglafolin,Rocaglamide U
Aglafoline inhibits in a concentration-dependent manner the aggregation and ATP release reaction induced in washed rabbit platelets by PAF (platelet-activating factor). The IC50 values of Aglafoline on PAF (3.6 nM)-induced platelet aggregation were about
价 格：￥电议型 号：T10260产 地：美洲
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T10543BIIL-260 hydrochlorideBIIL-260 hydrochloride
BIIL-260 hydrochloride is a potent and long-acting orally active antagonist of leukotriene B4 (LTB4) receptor with anti-inflammatory activity. It has a high affinity to the LTB4 receptor on isolated human neutrophil cell membranes (Ki: 1.7 nM).
价 格：￥电议型 号：T10543产 地：美洲
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T11175ElenbecestatElenbecestat,E2609,
Elenbecestat 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：美洲
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T14092AC260584AC260584
AC260584 is an M1 muscarinic receptor allosteric agonist (pEC50: 7.6).
价 格：￥电议型 号：T14092产 地：美洲
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T15260EvenamideEvenamide,NW-3509,
Evenamide is a sodium channel blocker. Which shows efficacy in a broad spectrum of rodent models of psychosis, mania, depression, and aggressiveness.
价 格：￥电议型 号：T15260产 地：美洲
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T16796RPR-260243RPR-260243
RPR-260243 is a novel activator of HERG and modifies HERG currents inhibited by dofetilide (IC50 = 58 nM).
价 格：￥电议型 号：T16796产 地：美洲
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T16841SAR-260301SAR-260301
SAR-260301 is an orally available and selective inhibitor of PI3Kβ (IC50: 23 nM).
价 格：￥电议型 号：T16841产 地：美洲
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T1856TPT-260TPT-260,TPT260,TPT 260
TPT-260 is a thiophene thiourea derivative with molecule weight 260.00 in free base form.
价 格：￥电议型 号：T1856产 地：美洲
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T1892Kobe2602Kobe2602
Kobe 2602 is an inhibitor of Ras that exhibits anticancer chemotherapeutic activities.
价 格：￥电议型 号：T1892产 地：美洲
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T2260GW 9662GW 9662,TIMTEC-BB SBB006523,
GW9662 is a specific PPARγ antagonist (IC50: 3.3 nM, in a cell-free assay), with 100 to 1000-fold functional selectivity for PPARγ than PPARα/δ in cells.
价 格：￥电议型 号：T2260产 地：美洲
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T2600AG-490AG-490,AG490,AG 490
AG-490 (Tyrphostin AG 490) is an inhibitor of EGFR (IC50: 0.1 μM). It is 135-fold more selective for EGFR than ErbB2, also inhibits JAK2 with no effect to Lyn, Lck, Syk, Btk, and Src.
价 格：￥电议型 号：T2600产 地：美洲
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T2601VidofludimusVidofludimus,SC12267,4sc-101
Vidofludimus (4SC-101, SC12267) is a novel small molecule inhibitor of dihydroorotate dehydrogenase (DHODH).
价 格：￥电议型 号：T2601产 地：美洲
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T2602BarasertibBarasertib,1H-Pyrazole-3-acetamide,AZD1152-HQPA
Barasertib (AZD1152-HQPA) is a highly selective Aurora B inhibitor (IC50: 0.37 nM) and demonstrates ~3,700-fold greater selectivity than Aurora A.
价 格：￥电议型 号：T2602产 地：美洲
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T2603SpebrutinibSpebrutinib,CC-292,AVL-292
Spebrutinib is an orally bioavailable, selective inhibitor of Bruton´s agammaglobulinemia tyrosine kinase (BTK), with potential antineoplastic activity.
价 格：￥电议型 号：T2603产 地：美洲
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T26041-Ethyl-2-benzimidazolinone1-Ethyl-2-benzimidazolinone,1-EBIO,
1-Ethyl-2-benzimidazolinone is a calium channel agonist.
价 格：￥电议型 号：T2604产 地：美洲
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T2605R788 DisodiumR788 Disodium,Fostamatinib Disodium,R788(Disodium)
Fostamatinib Disodium is an orally available Syk kinase inhibitor with potential anti-inflammatory and immunomodulating activities.
价 格：￥电议型 号：T2605产 地：美洲
