TN1768IriflophenoneInhibitor,MCF-7,proliferation,Iriflophenone,cells,T-47D,inhibit

Iriflophenone?stimulates cells proliferation in?MCF-7 and T-47D human breast cancer.

价 格：￥电议型 号：TN1768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

T6683STF-62247renal,STF-62247,VHL,carcinoma,inhibit,cytotoxic,cell,RCC,Inhibitor,STF62247,intracytoplasmi

STF-62247 is TGN inhibitor with IC50 of 0.625 μM and 16 μM in RCC4 and RCC4/VHL cells, respectively.

价 格：￥电议型 号：T6683产 地：中国大陆

TN1417Azadirachtinpest,inhibit,cytoskeleton,cellular,transduction,signal,insecticides,Apoptosis,Azadiracht

Azadirachtin has antifungal activity, used as an insecticide.

价 格：￥电议型 号：TN1417产 地：中国大陆

T79823,6-Dihydroxyflavoneinhibit,Inhibitor,caspase cascade,cell viability,oxidative stress,3,6-DHF,Apopto

3,6-Dihydroxyflavone suppresses the epithelial-mesenchymal transition in breast cancer cells by inhibiting the Notch signaling pathway.

价 格：￥电议型 号：T7982产 地：中国大陆

T9753LEI110HepG2 cells,inhibit,thiol hydrolases,LEI110,Inhibitor,LEI-110,lipolysis,Phospholipase,LEI 110

LEI110 is a potent Phospholipase A2, group XVI (PLA2G16) inhibitor with an Ki value of 20 nM. LEI110 is a selective pan-inhibitor of the HRASLS family of thiol hydrolases (i.e., PLA2G16, HRASLS2, RARRES3 and iNAT).

价 格：￥电议型 号：T9753产 地：中国大陆

TN2069PicrocrocinInhibitor,Picrocrocin,antiproliferative,SKMEL-2,Apoptosis,malignant,melanoma,cells,human,

Picrocrocin is a natural product

价 格：￥电议型 号：TN2069产 地：中国大陆

TJS0328Nordalberginpromyelocytic,Inhibitor,coumarin,HL-60,cells,leukemia,differentiation,Nordalbergin,inhib

价 格：￥电议型 号：TJS0328产 地：中国大陆

T6668SGC-CBP30inhibit,IL-17A,HAT,HATs,BRD,Histone Acetyltransferase,ankylosing,SGCCBP30,cells,epigenetic,

SGC-CBP30 is an effective CREBBP/EP300 inhibitor (IC50: 21/38 nM).

价 格：￥电议型 号：T6668产 地：中国大陆

TN6737(25R)-Spirost-4-ene-3,12-dionenatural product,neutrophil,mast cells,histamine,Inhibitor,(25R)Spirost

(25R)-Spirost-4-ene-3,12-dione is a natural product.

价 格：￥电议型 号：TN6737产 地：中国大陆

T600175-Bromo-4-chloro-3-indoxyl-beta-D-cellobioside5 Bromo 4 chloro 3 indoxyl beta D cellobioside,5Bromo4

5-Bromo-4-chloro-3-indoxyl-beta-D-cellobioside is a chromogenic compound used to detect cellobiohydrolases.

价 格：￥电议型 号：T60017产 地：中国大陆

T6646Rosiglitazone hydrochloridemellitus,hepatocellular,PPAR,antihyperglycemic,Inhibitor,cancer,senescenc

Rosiglitazone HCl is a blood glucose-lowering drugs, stimulating insulin secretion by binding to the PPAR receptors in fat cells.

价 格：￥电议型 号：T6646产 地：中国大陆

T6866AUZ 454AUZ454,ACHN,Caki-1,cells,K 03861,K-03861,Cyclin dependent kinase,AUZ-454,AUZ 454,Inhibitor,in

K03861 is a type II CDK2 inhibitor with Kd of 50 nM, 18.6 nM, 15.4 nM, and 9.7 nM for CDK2(WT), CDK2(C118L), CDK2(A144C), and CDK2(C118L/A144C), respectlvely.

价 格：￥电议型 号：T6866产 地：中国大陆

T7200TAK-960Polo-like Kinase (PLK),cell,cancer,proliferation,Inhibitor,mitosis,TAK960,TAK 960,leukemia,in

TAK-960 is an orally bioavailable, selective inhibitor of Plks with IC50 values of 0.8, 16.9, and 50.2 nM for Plk1, Plk2, and Plk3, respectively.

价 格：￥电议型 号：T7200产 地：中国大陆

T9000PyrimorphPhytophthora capsici,Fungal,Cell wall,Cystospore germination,Pyrimorph,inhibit,Inhibitor,My

Pyrimorph is a fungicide with high activity against the plant pathogen Phytophthora capsici. Pyrimorph inhibited different stages in the life cycle of P. capsici including mycelial growth, sporangium production, zoospore release, and cystospore germination with EC(50) values of 1.84, 0.17, 4.92, and 0.09 microg mL(-1), respectively.

价 格：￥电议型 号：T9000产 地：中国大陆

T9810TNIK-IN-5inhibit,Colorectal cancer,TNIK,Wnt,Cell proliferation,Inhibitor,TNIKIN5,Wnt pathway,Migrati

TNIK-IN-5 is an potent TNIK inhibitor (IC50= 0.05 μM). TNIK-IN-5 potently inhibits Wnt signaling in intact cells. TNIK-IN-5 exhibits excellent in vitro anti-colorectal cancer activity.

价 格：￥电议型 号：T9810产 地：中国大陆

T2610BMS-599626AC 480,antitumor,BMS-599626,Epidermal growth factor receptor,Sal2,inhibit,cells,AC-480,Erb

BMS-599626 has been used in trials studying the treatment of Cancer, Metastases, and HER2 or EGFR Expressing Advanced Solid Malignancies.

价 格：￥电议型 号：T2610产 地：中国大陆

TP1015NFAT Inhibitorinhibit,NFAT Inhibitor 1,dephosphorylation,cell-permeable,NFAT-Luc,NFAT Inhibitor-1,In

NFAT inhibitor is a cell-permeable compound that selectively inhibits calcineurin-mediated dephosphorylation of NFAT.

价 格：￥电议型 号：TP1015产 地：中国大陆

T28036MI-2-2cell proliferation,inhibit,menin-MLL interaction,Epigenetic Reader Domain,Inhibitor,Hoxa9 expr

MI-2-2 is an inhibitor of bivalent protein-protein interaction between menin and MLL with an IC50 of 46 nM. MI-2-2 binds to menin with Kd of 22 nM.

价 格：￥电议型 号：T28036产 地：中国大陆

TN1153Polyporenic acid Ccell,Apoptosis,inhibit,Inhibitor,lung,cancer,NSCLC,Polyporenic acid C

Polyporenic acid C shows inhibitory activity against human collagenase.

价 格：￥电议型 号：TN1153产 地：中国大陆