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TQ0210Savolitinibinhibit,Savolitinib,AZD 6094,Inhibitor,c-Met/HGFR,AZD6094,HMPL504,HMPL 504
Savolitinib (AZD-6094) is an effective, selective, and orally bioavailable c-Met inhibitor (IC50s: 5 nM/3 nM for c-Met/p-Met).
价 格：￥电议型 号：TQ0210产 地：中国大陆
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T9173HM-30181 mesylate monohydrateHM30181 mesylate monohydrate,HM 30181 mesylate monohydrate
HM-30181 mesylate monohydrate is an oral P-glycoprotein (P-gp) inhibitor, used to enhance the oral bioavailability of P-gp substrate drugs.
价 格：￥电议型 号：T9173产 地：中国大陆
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TQ0108MK-6892HCAR2,PUMA-G,MK-6892,HM74A,HCA2,Inhibitor,GPR109A,MK6892,inhibit,MK 6892
MK-6892 is a selective and full agonist for the high-affinity nicotinic acid receptor GPR109A (Ki: 4 nM; GTPγS EC50: 16 nM).
价 格：￥电议型 号：TQ0108产 地：中国大陆
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T8668HM03shock,HM 03,inhibit,heat,tumor,cancer,cell,HM03,protein,Heat shock proteins,HSP,Inhibitor,HCT116
HM03 is a potent and selective inhibitor of HSPA5, and has anticancer activity.
价 格：￥电议型 号：T8668产 地：中国大陆
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T35530IHMT-PI3Kδ-372IHMTPI3Kδ372,IHMT-PI-3Kδ-372,IHMT PI3Kδ 372
IHMT-PI3Kδ-372 is a selective inhibitor of PI3Kδ with an IC50 of 14 nM and can be used in studies about chronic obstructive pulmonary disease.
价 格：￥电议型 号：T35530产 地：中国大陆
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T10804CHMFL-PI3KD-317CHMFL-PI-3KD-317,CHMFLPI3KD317,CHMFL PI3KD 317
CHMFL-PI3KD-317 is a highly potent, selective and orally active PI3Kδ inhibitor, with an IC50 of 6 nM, and exhibits over 10-1500 fold selectivity over other class I, II and III PIKK family isoforms, such as PI3Kα (IC50, 62.6 nM), PI3Kβ (IC50, 284 nM), PI3Kγ (IC50, 202.7 nM), PIK3C2A (IC50, >10000 nM), PIK3C2B (IC50, 882.3 nM), VPS34 (IC50, 1801.7 nM), PI4KIIIA (IC50, 574.1 nM) and PI4KIIIB (IC50, 300.2 nM). CHMFL-PI3KD-317 inhibits PI3Kδ-mediated Akt T308 phosphorylation in Raji cells, with an E
价 格：￥电议型 号：T10804产 地：中国大陆
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T60196IHMT-PI3Kδ-372 S-isomerIHMTPI3Kδ372Sisomer
IHMT-PI3Kδ-372 S-isomer is a potent and selective PI3Kδ inhibitor with an IC50 of 14 nM. IHMT-PI3Kδ-372 S-isomer shows high selectivity over other class I PI3Ks (56?83 fold) and other protein kinases. IHMT-PI3Kδ-372 can be uesd for chronic obstructive pulmonary disease (COPD) research.
价 格：￥电议型 号：T60196产 地：中国大陆
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T67764hMAO-B-IN-4hMAOBIN4
hMAO-B-IN-4 is a selective, reversible and blood–brain barrier (BBB) penetrable inhibitor of human monoamine oxidase-B (hMAO-B, IC50=0.067 μM, Ki= 0.03 μM, hMAO-A, IC50= 33.82 μM).
价 格：￥电议型 号：T67764产 地：中国大陆
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T62404SHMT-IN-2
SHMT-IN-2 is a stereo specific inhibitor of human SHMT1/2 with IC50 values of 13 nM and 66 nM for SHMT1 and SHMT2, respectively. SHMT-IN-2 can block the growth of many human cancer cells, and has sensitivity for B-cell lymphomas.
价 格：￥电议型 号：T62404产 地：中国大陆
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T6333MM-102MM102；MM 102；HMTase Inhibitor IX
MM-102 is a high-affinity peptidomimetic MLL1 inhibitor with IC50 of 0.4 μM.
价 格：￥电议型 号：T6333产 地：中国大陆
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T4550Ajmaline(+)-Ajmaline；Cardiorythmine；Tachmalin；Raugalline；阿义吗啉；阿义马林
Ajmaline is a class Ia anti-arrhythmic compound that is widely used for the diagnosis of Brugada syndrome and the acute treatment of atrial or ventricular tachycardia. Ajmaline inhibits cardiac Kv1.5 and Kv4.3 channels at therapeutic concentrations.
价 格：￥电议型 号：T4550产 地：中国大陆
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T4268CHMFL-BMX-078
CHMFL-BMX-078 is a highly potent and selective type II irreversible BMX kinase inhibitor with an IC50 of 11 nM.
价 格：￥电议型 号：T4268产 地：中国大陆
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T4025HMN-154HMN154；HMN 154
HMN-154 is a novel benzenesulfonamide anticancer compound.
价 格：￥电议型 号：T4025产 地：中国大陆
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T3788Rehmannioside A
Rehmannioside A is an iridoid glucoside extracted from traditional Chinese medicine Rehmannia.
价 格：￥电议型 号：T3788产 地：中国大陆
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T3643HMN-176HMN 176；HMN176
HMN-176 is a stilbene derivative which inhibits mitosis, interfering with polo-like kinase-1 (plk1).
价 格：￥电议型 号：T3643产 地：中国大陆
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T353635-Hydroxymethylcytosine5hmC；5-Hydroxymethylcytosine
5-Hydroxymethylcytosine is a naturally occurring component of mammalian genomic DNA and is thought to be the sixth base of DNA [1]. 5-Hydroxymethylcytosine is an intermediate metabolite for demethylation of active DNA [2]. 5-Hydroxymethylcytosine is an ep
价 格：￥电议型 号：T35363产 地：中国大陆
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T3044Teriflunomide特立氟胺；HMR-1726；Flucyamide；Aubagio；A77 1726
Teriflunomide, a orally-available Pyrimidine Synthesis Inhibitor, is used to treat relapsing multiple sclerosis.
价 格：￥电议型 号：T3044产 地：中国大陆
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T2758Madecassic acidL-Fucose；6-Deoxy-L-Galactose；L-fucopyranose；Brahmic acid；羟基积雪草酸
Madecassic acid is extracted from the whole herb of Centella asiatica.
价 格：￥电议型 号：T2758产 地：中国大陆
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T2656Fruquintinib呋喹替尼；HMPL-013
Fruquintinib is an orally available, small molecule inhibitor of vascular endothelial growth factor receptors (VEGFRs), with potential anti-angiogenic and antineoplastic activities.
价 格：￥电议型 号：T2656产 地：中国大陆
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T2630PoziotinibHM781-36B；NOV120101
Poziotinib(NOV120101; HM781-36B) is an irreversible HER1/2/4 inhibitor (IC50s: 3/5/23 nM).
价 格：￥电议型 号：T2630产 地：中国大陆
