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T72231SARS-CoV-2/MERS Mpro-IN-2；化合物 SARS-CoV-2/MERS Mpro-IN-2SARS-CoV-2/MERS Mpro-IN-2
SARS-CoV-2/MERS Mpro-IN-2 is a potent inhibitor of the main proteases of SARS-CoV-2 and MERS, demonstrating IC50 values of 0.21 and 0.07 ?M, respectively.
价 格：￥电议型 号：T72231产 地：中国大陆
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T72059S1R agonist 2；化合物S1R agonist 2S1R agonist 2
S1R agonist 2 is a selective S1R agonist with a Ki of 88 nM for S2R and 1.1 nM for S1R and is protective against ROS and NMDA-induced neurotoxicity.
价 格：￥电议型 号：T72059产 地：中国大陆
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T72043SCFSkp2-IN-2；化合物SCFSkp2-IN-2SCFSkp2-IN-2
SCFSkp2-IN-2, a Skp2 inhibitor, exhibits a dissociation constant (K_D) of 28.77 μM. It demonstrates antitumor activities by inducing apoptosis in non-small cell lung cancer (NSCLC) cells.
价 格：￥电议型 号：T72043产 地：中国大陆
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T71749SF-22；化合物 SF-22SF-22
SF-22 is a neuropeptide Y receptor (Y2R) antagonist that crosses the blood-brain barrier and has potential anti-inflammatory activity for the study of diseases associated with neurological disorders.
价 格：￥电议型 号：T71749产 地：中国大陆
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T71619ST72；化合物 ST72ST72
ST72 is a potent inhibitor of FP2. ST72 exhibited strong growth inhibition of chloroquine-sensitive (3D7; EC50 = 2.8 ?M) and chloroquine-resistant (RKL-9; EC50 = 6.7 ?M) strains of Plasmodium falciparum
价 格：￥电议型 号：T71619产 地：中国大陆
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T71544STA-2842；化合物 STA-2842STA-2842
STA-2842 is an inhibitor of heat shock protein 90 (HSP90).
价 格：￥电议型 号：T71544产 地：中国大陆
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T71406SA 2572；化合物 SA 2572SA 2572
SA 2572 is a newly synthesized Ca2+ antagonist having a inhibitory effect on the fast Na+ inward channel.
价 格：￥电议型 号：T71406产 地：中国大陆
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T71201SCH-900822；化合物 SCH-900822SCH-900822
SCH-900822 is a potent and selective glucagon receptor antagonist.
价 格：￥电议型 号：T71201产 地：中国大陆
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T70922SKF32802；化合物 SKF32802SKF32802
SKF32802 is a novel potent, selective hERG potassium channel (Kv11.1) activator that induces a leftward shift in the voltage dependence of activation.
价 格：￥电议型 号：T70922产 地：中国大陆
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T70652SAR-104772；化合物 SAR-104772SAR-104772
SAR-104772 is a novel inhibitor of TAFIa (activated thrombin-activatable fibrinolysis inhibitor).
价 格：￥电议型 号：T70652产 地：中国大陆
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T70579SX 3202；化合物 SX 3202SX 3202
SX 3202 is an aldose reductase inhibitor being developed for the treatment of diabetic neuropathy.
价 格：￥电议型 号：T70579产 地：中国大陆
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T70201S 16020-2；化合物 S 16020-2S 16020-2
S 16020-2 is an olivacine derivative, and DNA topoisomerase II inhibitor endowed with a remarkable antitumor activity against various experimental tumors.
价 格：￥电议型 号：T70201产 地：中国大陆
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T6996SU 5402；化合物SU5402SU5402；SU5402
SU 5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM, 30 nM, and 510 nM for VEGFR2, FGFR1, and PDGF-Rβ, respectively.
价 格：￥电议型 号：T6996产 地：中国大陆
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T69920SAS-0132；化合物 SAS-0132SAS-0132
SAS-0132 is a modulator/antagonist of sigma2R/TMEM97 and has potential for treating TBIs, Alzheimer´s disease, and neuropathic pain.
价 格：￥电议型 号：T69920产 地：中国大陆
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T69903SKOG102；化合物 SKOG102SKOG102
SKOG102, a potent OLIG2 inhibitor, directly interacts with OLIG2, thereby inhibiting its DNA-binding capability. This compound is utilized in glioblastoma (GBM) research.
价 格：￥电议型 号：T69903产 地：中国大陆
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T6984SirReal2；化合物SirReal2SirReal2
SirReal2 is a potent and selective Sirt2 inhibitor with IC50 of 140 nM.
价 格：￥电议型 号：T6984产 地：中国大陆
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T69586SPD 502；化合物 SPD 502SPD 502
SPD 502 is a potential selective AMPA antagonist for epilepsy.
价 格：￥电议型 号：T69586产 地：中国大陆
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T69531SRX3212；化合物 SRX3212SRX3212
SRX3212 is a Novel BRD4/PI3Kα inhibitor, displaying an IC50 of 3.7 nM toward BRD4BD1 and 32 nM toward BRD4BD2, and therefore was~65-fold more potent inhibitor of BRD4BD1 and~48-fold more potent inhibitor of BRD4BD2 than SF2523 (GLXC-10641), retaining its high inhibitory activity for PI3Kα (IC50: 22 nM).
价 格：￥电议型 号：T69531产 地：中国大陆
