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T16104ML-9；ML-9盐酸盐ML-9
ML-9 suppresses MLCK, PKA, and PKC activity with Ki values of 4, 32, and 54 μM, respectively. ML-9 is a selective and effective inhibitor of Akt kinase, inhibits myosin light-chain kinase (MLCK), and stromal interaction molecule 1 (STIM1) activity. ML-9 causes autophagy by stimulating autophagosome formation and inhibiting their degradation.
价 格：￥电议型 号：T16104产 地：中国大陆
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T16103ML-9 Free Base；化合物 T16103ML-9 Free Base
ML-9 (free base) suppresses MLCK, PKA, and PKC activity (Ki: 4, 32, and 54 μM, respectively). ML-9 (free base) is a selective and effective inhibitor of Akt kinase, inhibits myosin light-chain kinase (MLCK), and stromal interaction molecule 1 (STIM1) activity. ML-9 (free base) causes autophagy by stimulating autophagosome formation and inhibiting their degradation.
价 格：￥电议型 号：T16103产 地：中国大陆
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T16102ML-792；化合物ML792ML-792
ML-792 is a specific small ubiquitin-like modifier (SUMO)-activating enzyme (SAE) inhibitor. Compared with NAE/NEDD8 and UAE/ubiquitin (IC50s of 32 μM and >100 μM, respectively), ML-792 is an effective and selective inhibitor of SAE/SUMO1 and SAE/SUMO2 in enzymatic assays (IC50s of 3 and 11 nM, respectively).
价 格：￥电议型 号：T16102产 地：中国大陆
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T16101ML-290；化合物ML-290ML-290
ML-290 is an effective relaxin/insulin-like family peptide receptor (RXFP1) agonist and activator of anti-fibrotic genes. It shows an EC50 of 94 nM.
价 格：￥电议型 号：T16101产 地：中国大陆
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T16100Balamapimod；化合物 T16100MKI 833；MKI 833
Balamapimod is a reversible inhibitor of Ras/Raf/MEK. It also has a potential anti-tumor activity.
价 格：￥电议型 号：T16100产 地：中国大陆
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T1610Metaxalone；美他沙酮Skelaxin|||Methaxalonum|||Zorane|||NSC170959|||AHR438；Skelaxin|||Methaxalonum|||美他沙酮|
Metaxalone (Methaxalonum) (marketed by King Pharmaceuticals under the brand name Skelaxin ) is a muscle relaxant used to relax muscles and relieve pain caused by strains, sprains, and other musculoskeletal conditions.
价 格：￥电议型 号：T1610产 地：中国大陆
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T15204EHT 1610；化合物EHT 1610EHT 5372；EHT 5372
EHT 1610 (EHT 5372) is a potent inhibitor of DYRK, with an IC50 of 0.36 nM and 0.59 nM for DYRK1A and DYRK1B, respectively. EHT 1610 has an inhibitory effect on leukemia, regulating cell cycle and inducing cell apoptosis.
价 格：￥电议型 号：T15204产 地：中国大陆
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T131610Bebeerine；化合物 BebeerineBebeerine
Bebeerine is a useful organic compound for research related to life sciences and the catalog number is T131610.
价 格：￥电议型 号：T131610产 地：中国大陆
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T11610Idelalisib D5；化合物 T11610CAL-101 D5|||GS-1101 D5；CAL-101 D5|||GS-1101 D5
Idelalisib D5, a version of Idelalisib marked with deuterium, is an orally bioavailable and highly selective inhibitor of p110δ.
价 格：￥电议型 号：T11610产 地：中国大陆
