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T4684ML241 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：中国大陆
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T4664ML 297ML297
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：中国大陆
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T4641BranaplamLMI 070；NVS-SM1
LMI070 (NVS-SM1) is a highly potent, selective and orally active small molecule SMN2 splicing modulator.
价 格：￥电议型 号：T4641产 地：中国大陆
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T4619ML-098CID-7345532；ML 098；ML098
ML-098 is an activator of the GTP-binding protein Rab7 (EC50: 77.6 nM).
价 格：￥电议型 号：T4619产 地：中国大陆
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T4540ML-18ML 18
ML-18 is a non-peptide bombesin receptor subtype-3 (BRS-3) antagonist with an IC50 of 4.8 μM.
价 格：￥电议型 号：T4540产 地：中国大陆
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T4399ML239CID-49843203
ML239 is a potent and selective inhibitor of breast cancer stem cells, with an IC50 of 1.16 μM.
价 格：￥电议型 号：T4399产 地：中国大陆
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T4390ML221
ML221 is a potent apelin /APJ functional antagonist, inhibiting apelin-13-mediated activation of APJ, with IC50s of 0.70 μM in the cAMP assay, and 1.75 μM in the β-arrestin assay, and EC80 of 10 nM in both assays.
价 格：￥电议型 号：T4390产 地：中国大陆
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T4347ML355
ML355, a specific, effective 12-Lipoxygenase(12-LOX) inhibitors(IC50=0.34 μM), possess favorable ADME properties.
价 格：￥电议型 号：T4347产 地：中国大陆
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T4316ML365
ML365 is a novel selective small molecule inhibitor of TASK1(KCNK3).
价 格：￥电议型 号：T4316产 地：中国大陆
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T4284Levamlodipine besylate左旋氨氯地平；(S)-Amlodipine Besylate (103129-82-4(free base))
Levamlodipine, also known as S-amlodipine, is a pharmacologically active enantiomer of amlodipine, an antihypertensive and anti-anginal medication. Levamlodipine belongs to the dihydropyridine group of calcium channel blockers. The names S-amlodipine and
价 格：￥电议型 号：T4284产 地：中国大陆
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T4252ML327
ML327 is a blocker of MYC which can also de-repress E-cadherin transcription and reverse Epithelial-to-Mesenchymal Transition (EMT).
价 格：￥电议型 号：T4252产 地：中国大陆
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T4084SibofimlocAntibiotic-202；VRT-1353385；Antibiotic 202
Antibiotic-202, an antibiotic compound, is used in treating bacterial infections.
价 格：￥电议型 号：T4084产 地：中国大陆
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T40661ML-60218
ML-60218 is a broad-spectrum RNA pol III inhibitor, with IC 50 s of 32 and 27 μM for Saccharomyces cerevisiae and human. ML-60218 disrupts already assembled viroplasms and to hamper the formation of new ones without the need for de novo transcription of c
价 格：￥电议型 号：T40661产 地：中国大陆
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T4052KML29
KML29 is highly selective and effective monoacylglycerol lipase (MAGL) inhibitor. It has effective inhibition of human/mouse/rat MAGL (IC50: 5.9/15/43 nM). It has not inhibitory for FAAH (IC50 > 50 μM). It also effectively and selectively blocks hydrolysi
价 格：￥电议型 号：T4052产 地：中国大陆
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T4030ML213CID-3111211
ML213 is a selective activator of Kv7.2 (KCNQ2) and Kv7.4 (KCNQ4) channels, enhances Kv7.2 and Kv7.4 channels with EC50s of 230 and 510 nM, respectively.
价 格：￥电议型 号：T4030产 地：中国大陆
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T4028ML329
ML329 is a small molecule inhibitor of MITF, inhibiting TRPM-1 promoter activity.
价 格：￥电议型 号：T4028产 地：中国大陆
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T3961CYM-5541ML249；CYM 5541；CID-17253208
CYM-5541 is a selective and allosteric S1P3 receptor agonist.
价 格：￥电议型 号：T3961产 地：中国大陆
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T3629GamithromycinML-1709460；加米霉素
Gamithromycin is a macrolide compound with antibacterial activity.
价 格：￥电议型 号：T3629产 地：中国大陆
