T8595Practololreceptor,inhibit,arrhythmias,β1-adrenergic,Practolol,Beta Receptor,Adrenergic Receptor,card

Practolol is a selective β-adrenoceptor blocker.

价 格：￥电议型 号：T8595产 地：中国大陆

T8796CAN508inhibit,CAN 508,ATP-competitive,Cyclin dependent kinase,esophageal,cells,CDK,CAN508,Inhibitor,

CAN508 is a potent, ATP-competitive CDK9/cyclin T1 inhibitor with an IC50 of 0.35 μM. It is also a competitive inhibitor of Cdk2-cyclin E with respect to ATP, with Ki and IC50 values of 13.3 and 20 μM, respectively.CAN508 exhibits a 38-fold selectivity for CDK9/cyclin T over other CDK/cyclin complexes. Antitumor activity.

价 格：￥电议型 号：T8796产 地：中国大陆

T7741DS-1001binhibit,DS 1001b,Inhibitor,Isocitrate Dehydrogenase (IDH),DS-1001b,DS1001b

DS-1001b is an inhibitor of mutant IDH-1 (Isocitrate Dehydrogenase-1)

价 格：￥电议型 号：T7741产 地：中国大陆

TQ0283RS102895CC chemokine receptor,CCR,Inhibitor,RS102895,inhibit,RS-102895,RS 102895

RS102895 is a potent CCR2 antagonist (IC50: 360 nM) and shows no effect on CCR1.

价 格：￥电议型 号：TQ0283产 地：中国大陆

T9041AES-350Histone deacetylases,AES 350,MV4-11,AES-350,Apoptosis,acute myeloid leukemia,AML,Inhibitor,in

AES-350 is a potent and orally active HDAC6 inhibitor(IC50 and a Ki of 0.0244 μM and 0.035 μM, respectively). It is also against HDAC-3, -8, and -11 in an enzymatic activity assay with IC50 values of 0.187 μM, 0.245 μM, and >1μM, respectively. AES-350 triggers apoptosis in AML cells through HDAC inhibition and can be used for acute myeloid leukemia (AML) research.

价 格：￥电议型 号：T9041产 地：中国大陆

T6908NSC 228155Epidermal growth factor receptor,Histone Acetyltransferase,EGFR,HER1,HATs,inhibit,Inhibito

NSC228155 is an activator of EGFR, binding to the sEGFR dimerization domain II and modulate EGFR tyrosine phosphorylation.

价 格：￥电议型 号：T6908产 地：中国大陆

T6924Riviciclib hydrochlorideinhibit,Inhibitor,Riviciclib,CDK,Riviciclib hydrochloride,Cyclin dependent k

P276-00 is a novel CDK1, CDK4 and CDK9 inhibitor with IC50 of 79 nM, 63 nM and 20 nM, respectively. Phase 2/3.

价 格：￥电议型 号：T6924产 地：中国大陆

T39389KDM2B-IN-2KDM2B IN 2,KDM-2B-IN-2,KDM2BIN2

KDM2B-IN-2 is a potent histone demethylase (kdm2b) inhibitor.

价 格：￥电议型 号：T39389产 地：中国大陆

T8084Dimethyl 4-hydroxyisophthalateDimethyl 4-hydroxyisophthalate,inhibit,Dimethyl 4 hydroxyisophthalate,

Dimetghyl 4-Hydroxyisophthalate is a methyl salicylate analogue, used as a building block in the chemical synthesis.

价 格：￥电议型 号：T8084产 地：中国大陆

T6767TCS7010Aurora Kinase,inhibit,TCS 7010,Apoptosis,TCS-7010,TCS7010,Inhibitor

Aurora A Inhibitor I is a novel, potent, and selective inhibitor of Aurora A with IC50 of 3.4 nM in a cell-free assay. It is 1000-fold more selective for Aurora A than Aurora B.

价 格：￥电议型 号：T6767产 地：中国大陆

T14526Bemesetron

Bemesetron is a selective antagonist of 5-HT3 (IC50 = 0.33 nM) with neuroprotective effects.

价 格：￥电议型 号：T14526产 地：中国大陆

T7815LAOD9604 acetate(221231-10-3 free base)AOD9604 acetate(221231103 free base),AOD-9604 acetate(221231-1

AOD9604 acetate is a potential anti-obesity peptide based on the human growth hormone.

价 格：￥电议型 号：T7815L产 地：中国大陆

Fr14055Compound Fr14055Compound Fr14055

价 格：￥电议型 号：Fr14055产 地：中国大陆

T75283,7-dimethylocta-2,6-dienyl 5,9,13-trimethyltetradeca-4,8,12-enoate3,7dimethylocta2,6dienyl 5,9,13tr

3,7-dimethylocta-2,6-dienyl 5,9,13-trimethyltetradeca-4,8,12-enoate is a chemical compound

价 格：￥电议型 号：T7528产 地：中国大陆

T6443Chloroprocaine hydrochlorideinhibit,Na,K-ATPase,Sodium potassium pump,Chloroprocaine,anesthetic,2-Ch

Chloroprocaine HCl is a local anesthetic during surgical procedures.

价 格：￥电议型 号：T6443产 地：中国大陆

T7596FirocoxibLPS,COX-2,fever,ML1785713,Cyclooxygenase,COX,inhibit,Firocoxib,Inhibitor,anti-inflammatory,

Firocoxib is a selective non-steroidal inhibitor of cycooxygenase-2 (COX-2) (IC50 of 0.13 μM), with anti-inflammatory for use in dogs and horses.

价 格：￥电议型 号：T7596产 地：中国大陆

TP1545L1FFAGLDD amine saltFFAGLDD amine salt

FFAGLDD amine salt is MMP9 selective cleavage peptides, which used for cytosolic delivery of Doxorubi-cin (DOX) and achieve temporally and spatially controlled slow drug delivery and release.

价 格：￥电议型 号：TP1545L1产 地：中国大陆

T40652Meclizine

Meclizine (Meclozine) shows antihistamine activity and reversibly inhibits the interaction of histamine at the H1 receptors . Meclizine is a member of the piperazine class of H1 antagonists. Meclizine is an effective anti-motion sickness agent. Meclizine crosses the blood–brain barrier. Meclizine is an agonist ligand for mouse constitutive androstane receptor (CAR) and an inverse agonist for Human CAR. Meclizine can be used for the research of polyQ toxicity disorders, such as Huntington´s

价 格：￥电议型 号：T40652产 地：中国大陆

T8222SelpercatinibFVB/NRj mice,RET (WT),inhibit,Inhibitor,RET (G810R),LOXO 292,LOXO292,RET (V804M),Selper

Selpercatinib is a tyrosine kinase inhibitor with antineoplastic properties(IC50 of 14.0 nM, 24.1 nM, and 530.7 nM for RET (WT), RET (V804M) , and RET (G810R), respectively)

价 格：￥电议型 号：T8222产 地：中国大陆

Fr13877Compound Fr13877Compound Fr13877

价 格：￥电议型 号：Fr13877产 地：中国大陆