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T4664ML297ML297
ML297 is a selective Kir3.1/3.2 (GIRK1/2) channel activator (IC50 values are 160, 887 and 914 nM for GIRK1/2, GIRK1/4 and GIRK1/3 respectively). ML297 exhibits no effect on GIRK2, GIRK2/3, Kir2.1 and Kv7.4 channels, and has minimal effect on a panel of ot
价 格：￥电议型 号：T4664产 地：美洲
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T4684ML241 hydrochlorideML241 hydrochloride
ML241 is a potent and selective inhibitors of p97 ATPase.ML241 inhibits degradation of a p97-dependent but not a p97-independent proteasome substrate in a dual-reporter cell line. ML241 may be a novel agent for the chemotherapy of cancer, and provide a ra
价 格：￥电议型 号：T4684产 地：美洲
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T4736ML092ML092,Cruzain-IN-1,
Cruzain-IN-1 is a covalent and reversible Cruzain inhibitor (IC50: 10 nM).
价 格：￥电议型 号：T4736产 地：美洲
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T5160SR3335SR3335,ML 176,
SR 3335 is a selective inverse agonist of RORα, competitively inhibiting the binding of 25-hydroxycholesterol to the ligand binding domain (Ki: 220 nM).
价 格：￥电议型 号：T5160产 地：美洲
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T5413ML216ML216,CID-49852229,
ML-216 is a small molecule inhibitor of BLM helicase (IC50: 1.8 μM). It showed 28-fold selective against the related helicases RECQ1, RECQ5, and E. coli UvrD (IC50s > 50 μM).
价 格：￥电议型 号：T5413产 地：美洲
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T5425ML367ML367
ML367 is a potent inhibitor of ATPase family AAA domain-containing protein 5 (ATAD5) stabilization and acts as a probe molecule that has low micromolar inhibitory activity
价 格：￥电议型 号：T5425产 地：美洲
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T5496ML-030ML-030
ML-030 is a potent and selective inhibitor of PDE4(PDE4A, PDE4A1, PDE4B1, PDE4B2, PDE4C1,and PDE4D2 with IC50 of 6.7 nM, 12.9 nM, 48.2 nM, 37.2 nM, 452 nM and 49.2 nM, respectively)
价 格：￥电议型 号：T5496产 地：美洲
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T6146Dorsomorphin dihydrochlorideDorsomorphin dihydrochloride,Compound C dihydrochloride,BML-275 dihydroc
Dorsomorphin is a potent, selective and ATP-competitive AMPK inhibitor (Ki: 109 nM) and does not exhibit significant activity on structurally related kinases.
价 格：￥电议型 号：T6146产 地：美洲
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T6332PevonedistatPevonedistat,MLN4924,
MLN4924 is an effective and specific small molecule NEDD8-activating enzyme (NAE) inhibitor (IC50: 4.7 nM).
价 格：￥电议型 号：T6332产 地：美洲
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T8820BML-284 hydrochloride；化合物BML-284 HCLBML-284 HCL|||Wnt agonist 1 HCL；BML-284 HCL|||Wnt agonist 1 HCL
BML-284 hydrochloride (Wnt agonist 1 HCL) is a potent, selective Wnt canonical signaling activator and tubulin polymerization inhibitor.
价 格：￥电议型 号：T8820产 地：中国大陆
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T8694ML406；化合物ML406ML406
ML406 shows anti-tubercular activity via MtbbioA (DAPA synthase) enzyme inhibition(IC50 : 30 nM)
价 格：￥电议型 号：T8694产 地：中国大陆
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T8571ML-184；化合物ML-184CID2440433；CID2440433
ML-184 (CID2440433) is a potent synthetic agonist of GPR55 with EC50 of 0.26 μM.
价 格：￥电议型 号：T8571产 地：中国大陆
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T8538ML382；化合物ML382ML382
ML382 is a potent and selective MrgX1 positive allosteric modulator(EC50 : 190 nM).
价 格：￥电议型 号：T8538产 地：中国大陆
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T8533ML318；化合物ML318ML318
ML318 is a biaryl nitrile PvdQ acylase inhibitor (IC50 of 20 nM for binding in the acyl-binding site). ML318 inhibits P. aeruginosa (PAO1) with IC50 of 19 μM. ML318 prevents pyoverdine production and limits the growth of P. aeruginosa under iron-limiting conditions.
价 格：￥电议型 号：T8533产 地：中国大陆
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T8514LML134；化合物LML-134LML-134；LML-134
LML134 (LML-134) is an inverse agonist of Histamine 3 receptor (H3R)(hH3R cAMP and hH3R bdg with Kis of 0.3 nM and 12 nM).
价 格：￥电议型 号：T8514产 地：中国大陆
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T8473MLS000532223；化合物MLS000532223MLS000532223
MLS000532223 is a selectiveRho family GTPases inhibitor(EC50 : 16 μM to 120 μM).
价 格：￥电议型 号：T8473产 地：中国大陆
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T8423ML417；化合物ML417ML417
ML417 is a selective and brain penetrant agonist of D3 Dopamine (EC50 : 38 nM).
价 格：￥电议型 号：T8423产 地：中国大陆
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T8397Ixazomib citrate；枸橼酸艾沙佐米MLN9708；枸橼酸艾沙佐米|||MLN9708
Ixazomib citrate (MLN9708) is a prodrug of Ixazomib (MMLN-2238). MLN9708 is an orally bioavailable second generation proteasome inhibitor (IC50 of 3.4 nM ) with potential antineoplastic activity.
价 格：￥电议型 号：T8397产 地：中国大陆
