T17274-Cyclohexyl-1-phenylthiosemicarbazide

价 格：￥电议型 号：T1727产 地：中国大陆

T17267XL228

XL228 is an inhibitor of multi-targeted tyrosine kinase (IC50s: 5, 3.1, 1.6, 6.1, 2 nM for Bcr-Abl, Aurora A, IGF-1R, Src, and Lyn, respectively).

价 格：￥电议型 号：T17267产 地：中国大陆

T17265XimelagatranH 376-95；H-37695；H 376/95；EXANTA；H37695；H 37695；希美加群

Ximelagatran, a direct thrombin inhibitor, can be taken orally and acts solely by inhibiting the actions of thrombin. Ximelagatran is converted to the active agent melagatran in vivo.

价 格：￥电议型 号：T17265产 地：中国大陆

T17263XEN907

XEN907 is a novel spiro oxindole NaV1.7 blocker. XEN907 also inhibits hNaV1.7 (IC50: 3 nM).

价 格：￥电议型 号：T17263产 地：中国大陆

T17262XE 991 dihydrochloride

XE 991 dihydrochloride is a Kv7 (KCNQ) channel blocker. XE 991 dihydrochloride potently inhibits Kv7.1 (KCNQ1), Kv7.2 (KCNQ2), Kv7.2 + Kv7.3 (KCNQ3) channel, and M-current (IC50s: 0.75 μM, 0.71 μM, 0.6 μM, and 0.98 μM, respectively).

价 格：￥电议型 号：T17262产 地：中国大陆

T17260WWL70

WWL70 is a selective alpha/beta hydrolase domain 6 inhibitors (IC50: 70 nM).

价 格：￥电议型 号：T17260产 地：中国大陆

T1726SB-4315424-[4-(1,3-苯并二唑-5-基)-5-(2-吡啶基)-1H-咪唑-2-基]-苯酰胺水合物；SB 431542

SB-431542 is a potent and selective inhibitor of ALK5 (IC50: 94 nM) and is also an inhibitor of ALK4 (IC50: 140 nM) and ALK7.

价 格：￥电议型 号：T1726产 地：中国大陆

T17258WRG-28

WRG-28 is a potent and selective, allosteric discoidin domain receptor 2 (ddr2) inhibitor(IC50 : 230 nM)

价 格：￥电议型 号：T17258产 地：中国大陆

T17257LWR-99210WR99210 hydrochloride(47326-86-3 free base)；6,6-Dimethyl-1-[3-(2,4,5-trichlorophenoxy)propox

WR-99210 is a potent inhibitor of Plasmodium falciparum dihydrofolate reductase (pfDHFR), which is a major malarial drug target. It has subnanomolar potency for the wild type, double mutant and quadruple mutant dihydrofolate reductases.

价 格：￥电议型 号：T17257L产 地：中国大陆

T17256Wnt pathway activator 1

Wnt pathway activator 1 is a potent Wnt activator with an IC50 of 28-29 nM. Wnt pathway activator 1 is a potent Wnt activator for the treatment of androgenetic alopecia (AGA) extracted from patent WO2012024404A1.

价 格：￥电议型 号：T17256产 地：中国大陆

T17254Amifloxacin氨氟沙星；Win49375

Amifloxacin is a synthetic antibacterial compound and showed moderate activity against Staphylococcus aureus, with MICs of less than or equal to 2 micrograms/ml.

价 格：￥电议型 号：T17254产 地：中国大陆

T17250W-54011

W-54011 is a potent non-peptide C5a receptor antagonist. W-54011 inhibits the binding of 125I-labeled C5a to human neutrophils (Ki = 2.2 nM). W-54011 inhibits C5a-induced intracellular Ca2+ mobilization, chemotaxis, and generation of ROS in human neutroph

价 格：￥电议型 号：T17250产 地：中国大陆

T1725Y-27632 dihydrochloride反式-4-[(R)-1-氨基乙基]-N-(4-吡啶基)环己烷甲酰胺二盐酸盐；Y-27632 2HCl

Y-27632 is a selective inhibitor of ROCKs including p160ROCK (Ki: 140 nM) and ROCK2 (IC50: 800 nM).

价 格：￥电议型 号：T1725产 地：中国大陆

T17244VU0467154

VU0467154 is a positive allosteric modulator of the M4 muscarinic acetylcholine receptor.

价 格：￥电议型 号：T17244产 地：中国大陆

T17243VU0463271N-Cyclopropyl-N-(4-methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide

VU0463271 is a potent and selective antagonist of the neuronal-specific potassium-chloride cotransporter 2 (KCC2), with an IC50 of 61 nM and >100-fold selectivity versus the closely related Na-K-2Cl cotransporter 1 (NKCC1) and no activity in a larger pane

价 格：￥电议型 号：T17243产 地：中国大陆

T1724SCR7 pyrazineSCR7 吡嗪；SCR7

Enhances CRISPR-Cas9-mediated homology-directed repair (HDR) efficiency in vitro up to 19-fold. Inhibits nonhomologous end-joining (NHEJ).

价 格：￥电议型 号：T1724产 地：中国大陆

T17238VU0152100VU152100

VU0152100 is an effective and selective allosteric potentiator of M4 mAChR (EC50: 380 ± 93 nM).

价 格：￥电议型 号：T17238产 地：中国大陆

T17226VericiguatBAY1021189；维利西呱

Vericiguat is a potent and orally available guanylate cyclase stimulator.

价 格：￥电议型 号：T17226产 地：中国大陆

T17225Vercirnon维塞诺；GSK-1605786；Traficet-EN；CCX282-B

Vercirnon is a selective and potent antagonist of CCR9 (IC50: 10 nM). It is also used in the research of inflammatory bowel diseases.

价 格：￥电议型 号：T17225产 地：中国大陆

T17224VER-246608

VER-246608 is an effective and ATP-competitive inhibitor of pyruvate dehydrogenase kinase (IC50s: 35 nM, 40 nM, 84 nM, and 91 nM for PDK-1, PDK-3, PDK-2, and PDK-4, respectively).VER-246608 disrupts Warburg metabolism and induces context-dependent cytosta

价 格：￥电议型 号：T17224产 地：中国大陆