T8640G6PDi-1G6PDi1,G6PDi 1,G-6PDi-1

G6PDi-1 is an effective G6PD inhibitor. It depletes NADPH and decreases inflammatory cytokine production.

价 格：￥电议型 号：T8640产 地：中国大陆

T7338LDHBPDHBP

DHBP is an WalKR TCS activator. It works via targeting walk and selectively promoting the lysostaphin-induced lysis activity of the Newman wild-type strain.

价 格：￥电议型 号：T7338L产 地：中国大陆

T40732TMPD dihydrochloridedonor,Cytochrome-c,TMPD dihydrochloride,redox,inhibit,electron,enzymatically,blu

TMPD dihydrochloride is an active substrate of enzymatically convert redox and an electron donor for the reduction of heme peroxidases.

价 格：￥电议型 号：T40732产 地：中国大陆

PDK0035Compound PDK0035Compound PDK0035

价 格：￥电议型 号：PDK0035产 地：中国大陆

T7350Nelotanserin5-HT Receptor,Inhibitor,APD 125,inhibit,APD-125,Nelotanserin,Serotonin Receptor,5-hydrox

Nelotanserin is a potent 5-HT2A inverse agonist(IC50 : 1.7 nM), a moderately potent 5-HT2C partial inverse agonist t(IC50 :79 nM )and a weak 5-HT2B inverse agonistt(IC50 : 791 nM).

价 格：￥电议型 号：T7350产 地：中国大陆

T9805BAY 2666605anticancer effect,inhibit,BAY 2666605,orally active,PDE3A-SLFN12 Complex,Phosphodiesteras

BAY 2666605 is an orally active inhibitor of PDE3A and PDE3B with IC50s of 87 nM and 50 nM, respectively. BAY 2666605 has anticancer effects.

价 格：￥电议型 号：T9805产 地：中国大陆

T16448PD173212PD173212,PD-173212

PD 173212 is a blocker that blocks N-type voltage sensitive calcium channel (Cav2.2). PD173212 (0.0017-1.7 μmol/kg, Intraperitoneal Injection.) dose-dependently reduced DNBS-induced visceral hypersensitivity in mice.

价 格：￥电议型 号：T16448产 地：中国大陆

T12395PDE9-IN-1PDE-9-IN-1,PDE9IN1,PDE9 IN 1

PDE9-IN-1 is a selective and orally bioavailable Inhibitor of PDE9A(IC50 of 8.7 nM).

价 格：￥电议型 号：T12395产 地：中国大陆

T6189MirdametinibPD0325901；PD325901

PD0325901 is a specific and non-ATP-competitive MEK inhibitor (IC50: 0.33 nM).

价 格：￥电议型 号：T6189产 地：中国大陆

T6152PD318088

PD318088 is a non-ATP competitive allosteric MEK1/2 inhibitor, binding simultaneously with ATP in a region of the MEK1 active site that is adjacent to the ATP-binding site.

价 格：￥电议型 号：T6152产 地：中国大陆

T6136CanertinibPD-183805；CI-1033；卡纽替尼

Canertinib is a pan-erbB tyrosine kinase inhibitor which work against esophageal squamous cell carcinoma in vitro and in vivo. Canertinib treatment significantly affects tumour metabolism, proliferation and hypoxia as determined by PET.

价 格：￥电议型 号：T6136产 地：中国大陆

T6067PD 123319(S)-(+)-PD 123319；PD123319

PD 123319 is a potent, selective AT2 angiotensin II receptor antagonist.

价 格：￥电议型 号：T6067产 地：中国大陆

T5541PDM111-[2-(4-Chloro-phenyl)-vinyl]-3,5-diMeth；PDM 11

PDM 11 is an antagonist of aryl hydrocarbon receptor (AhR)

价 格：￥电议型 号：T5541产 地：中国大陆

T5411PDE10-IN-1SEP-0372814

PDE10-IN-1 is PDE10-IN-1 inhibitor extracted from Patent WO 2013192273 A1, for treating CNS and metabolic disorders.

价 格：￥电议型 号：T5411产 地：中国大陆

T5410PD158780

PD 158780 reversibly inhibits auto and transphosphorylation of all four members of the ErbB receptor superfamily: EGFR, ErbB2, ErbB3, and ErbB4 (IC50s: 8μM, 49 nM, 52 nM, and 52 nM in cell assay).

价 格：￥电议型 号：T5410产 地：中国大陆

T5047PD-168077 maleate

PD-168077 maleate is a selective agonist of dopamine D4 receptor(Ki : 9 nM)

价 格：￥电议型 号：T5047产 地：中国大陆

T4696BMS202 hydrochloride (1675203-84-5(free base))PD-1/PD-L1 inhibitor 2 hydrochloride

PD-1/PD-L1 inhibitor 2 is a small-molecule PD-1/PD-L1 interaction inhibitor (IC50: 18 nM). Biophysical studies demonstrate that BMS202 binds directly to PD-L1. Binding of BMS202 promotes PD-L1 dimerisation and blocks the PD-L1/ PD1 interaction.

价 格：￥电议型 号：T4696产 地：中国大陆

T4635RalinepagAPD811

Ralinepag is a potent, orally bioavailable and non-prostanoid prostacyclin (IP) receptor agonist, with EC50s of 8.5 nM, 530 nM and 850 nM for human and rat IP receptor and human DP1 receptor, respectively.

价 格：￥电议型 号：T4635产 地：中国大陆

T4608PDM2

PDM 2 is a potent and selective aryl hydrocarbon receptor (AhR) antagonist.

价 格：￥电议型 号：T4608产 地：中国大陆

T4431OlodanriganPD-126055；EMA401

EMA401, a highly selective AT2R antagonist, inhibition of augmented AngII/AT2R induced p38 and p42/p44 MAPK activation, and hence inhibition of DRG neuron hyperexcitability and sprouting of DRG neurons. EMA401 blocks p38, p42/p44 mitogen-activated protein

价 格：￥电议型 号：T4431产 地：中国大陆