T8177GalactinolGalactinol

Galactinol Hydrate belongs to the class of organic compounds known as O-glycosyl compounds.

价 格：￥电议型 号：T8177产 地：中国大陆

Fr13375Compound Fr13375Compound Fr13375

价 格：￥电议型 号：Fr13375产 地：中国大陆

TN71462,6-Dibromo-4-(hydroxymethyl)phenol

2,6-Dibromo-4-(hydroxymethyl)phenol is a marine derived natural products found in Thelepus setosus.

价 格：￥电议型 号：TN7146产 地：中国大陆

T643224-(9H-fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester

4-(9H-fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester is a bioactive substances.

价 格：￥电议型 号：T64322产 地：中国大陆

T9053Lats-IN-1inhibit,LatsIN1,YAP,Yes-associated protein,Lats IN 1,Inhibitor

Lats-IN-1 is a potent and ATP-competitive Lats1 and Lats2 kinases inhibitor. It promotes Yap-dependent proliferation in postmitotic mammalian tissues.

价 格：￥电议型 号：T9053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

Fr13623Compound Fr13623Compound Fr13623

价 格：￥电议型 号：Fr13623产 地：中国大陆

TN122625-O-Methylalisol A25OMethylalisol A,25 O Methylalisol A,Inhibitor,inhibit

25-O-Methylalisol A is a natural product

价 格：￥电议型 号：TN1226产 地：中国大陆

T8831Elamipretide 2TFAElamipretide 2TFA

Elamipretide is a novel mitochondrion-targeted antioxidant.

价 格：￥电议型 号：T8831产 地：中国大陆

T17195UC-112UC 112,UC112

UC-112 is a novel potent IAP inhibitor and potently inhibits cell growth in two human melanoma and two human prostate cancer cell lines (IC50=0.7-3.4 uM).

价 格：￥电议型 号：T17195产 地：中国大陆

TP1924L1ZIP acetate(863987-12-6 free base)ZIP acetate(863987126 free base),ZIP acetate(863987 12 6 free base

ZIP acetate is a novel, cell-permeable inhibitor of protein kinase Mζ (PKMζ), a constitutively active, atypical PKC isozyme involved in LTP maintenance. Selectively blocks PKMζ-induced synaptic potentiation in hippocampal slices in vitro. Reverses late-phase LTP (IC50 = 1 - 2.5 μM) and produces persistent loss of 1-day-old spatial memory following central administration in vivo.

价 格：￥电议型 号：TP1924L1产 地：中国大陆

TP1927L1d[Leu4,Lys8]-VP acetated[Leu4,Lys8]VP acetate,d[Leu4,Lys8] VP acetate

d[Leu4,Lys8]-VP acetate is a selective vasopressin V1b receptor agonist. The Kis for rat, human and mouse V1b receptors are 0.16 nM, 0.52 nM and 0.1.38 nM, respectively. d[Leu4,Lys8]-VP acetate exhibits weak antidiuretic, vasopressor and oxytocic activiti

价 格：￥电议型 号：TP1927L1产 地：中国大陆

T8690Brexpiprazole HClantipsychotic,OPC34712,OPC-34712,Serotonin Receptor,5-hydroxytryptamine Receptor,Br

Brexpiprazole is a new antipsychotic drug.

价 格：￥电议型 号：T8690产 地：中国大陆

T6431Levoleucovorin CalciumCL-307782,Antifolate,inhibit,anticancer,CL 307782,Levoleucovorin Calcium,5-Flu

Calcium Levofolinate, a calcium salt of the folinic acid, is used in cancer chemotherapy as an adjuvant.

价 格：￥电议型 号：T6431产 地：中国大陆

T6584MG 149HAT,Inhibitor,MG 149,Epigenetic Reader Domain,Apoptosis,HATs,inhibit,Histone Acetyltransferase

MG149 is a selective and potent Tip60 inhibitor with IC50 of 74 uM, similar potentcy for MOF(IC50= 47 uM).

价 格：￥电议型 号：T6584产 地：中国大陆

TQ0092NaquotinibEpidermal growth factor receptor,EGFR,ASP 8273,HER1,ErbB-1,ASP-8273,inhibit,Naquotinib,Inh

Naquotinib (ASP8273) is an orally available, mutant-selective and irreversible EGFR inhibitor; (IC50s: 8-33 nM and 230 nM toward EGFR mutants and EGFR.

价 格：￥电议型 号：TQ0092产 地：中国大陆

T8550NDMC101rheumatoid arthritis,inhibit,RAW 264.7,NSAID,Bone,Inhibitor,Nuclear factor-κB,NF-κB,DPP,NDMC1

NDMC101 is an inhibitor of dipeptidyl peptidase-IV activity in human T cells and exhibits immunomodulatory effects. It also acts as a novel inhibitor of NFATc1 and NF-κB activity.

价 格：￥电议型 号：T8550产 地：中国大陆

T9765TJ-M2010-5ischemia,MIRI,Anoxia,factor,MyD88,injury,reoxygenation,inhibit,reperfusion,differentiation

TJ-M2010-5 is a MyD88 inhibitor that binds to the TIR domain to interfere with its homodimerization and suppress MyD88 signaling. TJ-M2010-5 can be used in myocardial ischemia/reperfusion injury studies.

价 格：￥电议型 号：T9765产 地：中国大陆

Fr14428Compound Fr14428Compound Fr14428

价 格：￥电议型 号：Fr14428产 地：中国大陆

Fr13736Compound Fr13736Compound Fr13736

价 格：￥电议型 号：Fr13736产 地：中国大陆