T11358gamma-secretase modulator 1

gamma-secretase modulator 1 is a modulator of γ secretase and can be used in studies about the treatment of Alzheimer´s disease.

价 格：￥电议型 号：T11358产 地：中国大陆

T7013VorapaxarProtease Activated Receptor (PAR),Inhibitor,SCH-530348,Vorapaxar,SCH530348,Thrombin recepto

Vorapaxar (SCH 530348) is an effective and orally active thrombin receptor (PAR-1) antagonist (Ki: 8.1 nM).

价 格：￥电议型 号：T7013产 地：中国大陆

T131725Compound TCFN92660

价 格：￥电议型 号：T131725产 地：中国大陆

T6S0139Neobavaisoflavoneflavonoid,corylifolia,Neobavaisoflavone,anti-oxidation,polymerase,Apoptosis,anti-ca

1. Neobavaisoflavone is isolated as a DNA polymerase inhibitor. 2. Neobavaisoflavone might be a potential anabolic agent to treat bone loss-associated diseases. 3. Neobavaisoflavone has anti-inflammatory activity, can significantly inhibit the production of reactive oxygen species (ROS), reactive nitrogen species (RNS) and cytokines: IL-1β, IL-6, IL-12p4, IL-12p7, TNF-α in LPS+IFN-γ- or PMA- stimulated RAW264.7 macrophages.

价 格：￥电议型 号：T6S0139产 地：中国大陆

Fr13199Compound Fr13199Compound Fr13199

价 格：￥电议型 号：Fr13199产 地：中国大陆

T13890SMARCA-BD ligand 1 for Protac dihydrochlorideSMARCABD ligand 1 for Protac dihydrochloride,SMARCA BD

SMARCA-BD ligand 1 for Protac dihydrochloride binds to the BAF ATPase subunits SMARCA2, and used for degrading SMARCA2, based on PROTAC.

价 格：￥电议型 号：T13890产 地：中国大陆

T27613inS3-54-A26inS3 54 A26,inS354A26,inS-3-54-A26

inS3-54-A26 is an inhibitor of the DNA-binding domain of STAT3. inS3-54-A26 suppresses tumor growth, metastasis and the gene expression of STAT3.

价 格：￥电议型 号：T27613产 地：中国大陆

T6813Cyclo(RGDyK) trifluoroacetateIntegrin,Cyclo(RGDyK) trifluoroacetate,inhibit,Inhibitor

Cyclo(RGDyK) is a potent and selective αVβ3 integrin inhibitor with IC50 of 20 nM.

价 格：￥电议型 号：T6813产 地：中国大陆

T79132-Bromobiphenyl2 Bromobiphenyl,2Bromobiphenyl

2-Bromobiphenyl is a chemical compound

价 格：￥电议型 号：T7913产 地：中国大陆

T7021ZM241385P1 receptor,Inhibitor,ZM241385,inhibit,ZM 241385,ZM-241385,Adenosine Receptor

ZM-241385 is a high-affinity antagonist ligand selective for the adenosine A2A receptor.

价 格：￥电议型 号：T7021产 地：中国大陆

T7779Nelfinavirproduction,Human immunodeficiency virus,protease,myeloma,inhibit,AG-1341,phosphorylation,c

Nelfinavir is an antiretroviral drug used in the treatment of the human immunodeficiency virus (HIV) (Ki=2 nM). Nelfinavir is a broad-spectrum, anticancer agent.

价 格：￥电议型 号：T7779产 地：中国大陆

T6S1367Procyanidin B2inhibit,Procyanidin B2,Proanthocyanidin B 2,Procyanidin B 2,Inhibitor,Proanthocyanidin

Procyanidin B2 has vascular protective, anti-diabetic nephropathy, anti-cancer, anti-inflammatory, and antioxidant activities. Procyanidin B2 inhibited NLRP3 inflammasome activation via suppression of AP-1 pathway.

价 格：￥电议型 号：T6S1367产 地：中国大陆

T13918Tecalcet Hydrochloride

Tecalcet Hydrochloride is an allosteric and positive modulator of the calcium-sensing receptor(CaSR). Tecalcet Hydrochloride increases the sensitivity to the activation of extracellular Ca2+.

价 格：￥电议型 号：T13918产 地：中国大陆

TP1548LSIYRY acetate(178561-37-0 free base)SIYRY acetate(178561 37 0 free base),SIYRY acetate(178561370 fre

SIYRY is a Kb-restricted epitope peptide.

价 格：￥电议型 号：TP1548L产 地：中国大陆

T6756AMG 925CDK,AMG 925,Cluster of differentiation antigen 135,FLT3,Cyclin dependent kinase,inhibit,CD135

AMG 925 is a potent and orally bioavailable dual FLT3/CDK4 inhibitor with IC50 of 1 nM and 3 nM, respectively.

价 格：￥电议型 号：T6756产 地：中国大陆

T8013(S)?-?(-?)?-?CitronellalEndogenous Metabolite,Inhibitor,(S)? ?( ?)? ?Citronellal,(S)??(?)??Citronell

(S)-(-)-3,7-Dimethyl-6-Octenal is a monoterpenoid compound

价 格：￥电议型 号：T8013产 地：中国大陆

TMA2613Cyclo(Pro-Leu)

Cyclo(Pro-Leu) is a marine-derived natural product with brine shrimp lethality.

价 格：￥电议型 号：TMA2613产 地：中国大陆

Fr13755Compound Fr13755Compound Fr13755

价 格：￥电议型 号：Fr13755产 地：中国大陆

T9075BDP-13176inhibit,BDP13176,BDP-13176,Inhibitor,BDP 13176

BDP-13176 is a potent?inhibitor of fascin 1(Kd?of 90 nM and an?IC50?of 240 nM). It has potential as an anti-metastatic agent

价 格：￥电议型 号：T9075产 地：中国大陆

T12513PNZ5PNZ5,PNZ-5

PNZ5 is a potent and isoxazole-based pan-BET inhibitor, with high selectivity and potency similar to the well-established (+)-JQ1, with a KD of 5.43 nM for BRD4(1).

价 格：￥电议型 号：T12513产 地：中国大陆