T5831Selective PI3Kδ Inhibitor 1

Selective PI3Kδ Inhibitor 1 is a PI3Kδ Inhibitor( IC50 = 0.9 nM).

价 格：￥电议型 号：T5831产 地：中国大陆

T5830SKLB-23bb

SKLB-23bb is an orally bioavailable HDAC6-selective inhibitor and also has microtubule-disrupting ability.

价 格：￥电议型 号：T5830产 地：中国大陆

T5829H4 Receptor antagonist 1

H4 Receptor antagonist 1 is a potent and selective histamine H4 receptor inverse agonist, with an IC50 of 19 nM.

价 格：￥电议型 号：T5829产 地：中国大陆

T5828MS215705-(苄基硫代)-N-甲基-1,3,4-噻二唑-2-胺

MS21570 as a GPR171 antagonist based on its ability to block,with an IC50 of 220 Nm,that reduces anxiety-like behavior and fear conditioning in mice.

价 格：￥电议型 号：T5828产 地：中国大陆

T5827BI-6C9

BI-6C9 is an inhibitor of tBid (Kd = 20 μM).BI-6c9 prevented MOMP and mitochondrial fission, and protected the cells from cell death.

价 格：￥电议型 号：T5827产 地：中国大陆

T5826Eupalinolide A

Eupalinolide B is a natural product ,and demonstrates potent cytotoxicity against A-549, BGC-823, SMMC-7721, and HL-60 tumour cell lines.

价 格：￥电议型 号：T5826产 地：中国大陆

T5825Iadademstat dihydrochlorideORY-1001(trans)

ORY-1001, a Potent and Selective Covalent KDM1A/LSD1 Inhibitor, for the Treatment of Acute Leukemia.

价 格：￥电议型 号：T5825产 地：中国大陆

T5823D-Lin-MC3-DMA

D-Lin-MC3-DMA, an ionizable cationic lipid, is a potent siRNA delivery vehicle.

价 格：￥电议型 号：T5823产 地：中国大陆

T5822BTR-15-Benzylidene-3-ethyl rhodanine

5-Benzylidene-3-ethyl rhodanine(BTR-1) is an active anti-cancer agent. BTR-1 activates apoptosis and induces cell death.

价 格：￥电议型 号：T5822产 地：中国大陆

T5821BC-1215

BC-1215 is an inhibitor of F-box protein 3 (FBXO3, a ubiquitin E3 ligase component, IC50=0.9 μg/mL for IL-1β release).

价 格：￥电议型 号：T5821产 地：中国大陆

T5820Amsacrine hydrochloride盐酸胺苯吖啶；acridinyl anisidide hydrochloride；m-AMSA hydrochloride

Amsacrine hydrochloride is topoisomerase II inhibitor , is used in the treatment of acute myelogenous leukemia.

价 格：￥电议型 号：T5820产 地：中国大陆

T5819Rapastinel TrifluoroacetateThr-Pro-Pro-Thr-NH2 Trifluoroacetate；GLYX-13 Trifluoroacetate

Rapastinel Trifluoroacetate is an NMDA receptor modulator with glycine-site partial agonist properties.

价 格：￥电议型 号：T5819产 地：中国大陆

T5818Rigosertib sodiumRigosertib；ON-01910；Estybon

Rigosertib, a non-ATP-competitive inhibitor of PLK1(IC50=9 nM), exhibits 30-fold higher specificity activity over Plk2 and no effect on Plk3.

价 格：￥电议型 号：T5818产 地：中国大陆

T5817PKC-theta inhibitor hclPKC-theta inhibitor

PKC-theta inhibitor is a selective PKC-θinhibitor(IC50:12 nM).

价 格：￥电议型 号：T5817产 地：中国大陆

T5816Qstatin

QStatin, a Selective Inhibitor of Quorum Sensing in Vibrio Species( SmcR with an EC50 of 208.9 nM).

价 格：￥电议型 号：T5816产 地：中国大陆

T5815MJN110Cravatt Reagent

Cravatt Reagent is a potent and selective MAGL inhibitor. Cravatt Reagent inhibits MAGL (IC50 = 9.1 nM). MJN110 Produces Opioid-Sparing Effects in a Mouse Neuropathic Pain Model.

价 格：￥电议型 号：T5815产 地：中国大陆

T5814AurantiamideTMC-58B；橙黄胡椒酰胺

Aurantiamide has anti-cancer, anti-inflammatory and antinociceptive activities, it may suppress the growth of malignant gliomas by blocking autophagic flux.Aurantiamide has an anti-neuroinflammatory effect on LPS stimulation through its inhibition of the

价 格：￥电议型 号：T5814产 地：中国大陆

T5813BYAKANGELICIN

BYAKANGELICIN,a main furanocoumarin constituent isolated and characterized as an aldose reductase inhibitor,and is effective for the treatment of sugar cataracts and diabetic neuropathy and hence might be useful as a lead compound for the development of n

价 格：￥电议型 号：T5813产 地：中国大陆

T5812Zinc Phytate

价 格：￥电议型 号：T5812产 地：中国大陆

T5811Scopolamine hydrochloride莨菪碱；HYOSCINE HYDROCHLORIDE

HYOSCINE HYDROCHLORIDE versus placebo in preventing motion sickness has been shown to be effective.

价 格：￥电议型 号：T5811产 地：中国大陆