T6793BRD7552promoter,BRD-7552,islets,human,inhibit,epigenetic,ductal,changes,insulin,BRD 7552,BRD7552,pri

BRD7552 is an inducer of transcription factor PDX1, which increases insulin expression. BRD7552 increases PDX1 expression in mouse αTC cells but not βTC cells.

价 格：￥电议型 号：T6793产 地：中国大陆

TQ0155Miglustat hydrochlorideN-Butyldeoxynojirimycin,OGT-918,type I gaucher disease,Miglustat,Miglustat hy

Miglustat hydrochloride is an inhibitor of glucosylceramide synthase and can be used for studies about Type I Gaucher disease.

价 格：￥电议型 号：TQ0155产 地：中国大陆

T8345CarbutamideInhibitor,BZ-55,first-generation,orally,Anti-diabetic,inhibit,Carbutamide,BZ 55,hypoglyce

Carbutamide is a sulfonylurea antidiabetic agent with hypoglycemic activity.

价 格：￥电议型 号：T8345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

TN65525,7-Dimethoxyluteolin5,7-dimethylluteolin,5,7 Dimethoxyluteolin,Dopamine Transporter,SLC6A3,DAT,5,7-

5,7-Dimethoxyluteolin is a natural product from Hovenia acerba. 5,7-Dimethoxyluteolin is a dopamine transporter (DAT) activator with an EC50 of 3.417 μM.

价 格：￥电议型 号：TN6552产 地：中国大陆

TCS1554trans-BenzylideneacetonePhospholipase,gram-negative,Inhibitor,inhibit,entomopathogenic,transBenzylid

trans-4-Phenyl-3-buten-2-one is used in various synthetic preparations.

价 格：￥电议型 号：TCS1554产 地：中国大陆

T8985NSC45586pleckstrin homology domain and leucine-rich repeat protein phosphatase,NSC-45586,NSC45586,in

NSC45586 is a protein phosphatase PHLPP inhibitor, which is selective for PHLPP1 and PHLPP2.

价 格：￥电议型 号：T8985产 地：中国大陆

T8955PCNA-I1PCNA-I1,PCNA-I-1,DNA/RNA Synthesis,inhibit,PCNAI1,Inhibitor,PCNA I1

PCNA-I1 is an inhibitor targeting PCNA chromatin association in prostate cancer.

价 格：￥电议型 号：T8955产 地：中国大陆

T60554Schnurri-3 inhibitor-1

Schnurri-3 inhibitor-1 is a potent inhibitor of schnurri-3, an essential regulator of adult bone formation. Schnurri-3 inhibitor-1 can inhibit Shn3 with EF1alpha promoter in Shn3FFL (osteoblast cell line, AC50= 2.09 μM). Schnurri-3 inhibitor-1 has research value in osteoporosis.

价 格：￥电议型 号：T60554产 地：中国大陆

TP1876LCREBtide acetate(149155-45-3 free base)CREBtide acetate(149155 45 3 free base),CREBtide acetate(1491

CREBtide acetate is a synthetic substrate for PKA (Km=3.9 μM), which is based on the phosphorylation sequence in d-CREB (cAMP response element binding protein).

价 格：￥电议型 号：TP1876L产 地：中国大陆

Fr13755Compound Fr13755Compound Fr13755

价 格：￥电议型 号：Fr13755产 地：中国大陆

TP1554LHPV16 E7 (86-93) acetateHPV16 E7 (86 93) acetate,HPV16 E7 (8693) acetate

HPV16 E7 (86-93) acetate is a derived peptide of human leukocyte antigen A2.1 restricted HPV16 E7 with immunogenic property in cervical carcinomas.

价 格：￥电议型 号：TP1554L产 地：中国大陆

TN1455Bryodulcosigenininhibit,Bryodulcosigenin,Inhibitor

Bryodulcosigenin has anti-inflammatory effect, it shows potent inhibitory effects on EBV-EA induction.

价 格：￥电议型 号：TN1455产 地：中国大陆

T7553(+)-PD 128907 hydrochloride(+)-PD 128907,Dopamine Receptor,inhibit,(+) PD 128907 hydrochloride,Inhib

(+)-PD 128907 hydrochloride is an agonist of D3 dopamine receptor .

价 格：￥电议型 号：T7553产 地：中国大陆

TP1911LCALP3 acetate(261969-05-5 free base)CALP-3 acetate(261969-05-5 free base),CALP3 acetate(261969055 fr

CALP3 acetate is a potent Ca2+ channel blocker that activates EF hand motifs of Ca2+-binding proteins. CALP3 acetate can functionally mimic increased [Ca2+]i by modulating the activity of Calmodulin (CaM), Ca2+ channels and pumps.

价 格：￥电议型 号：TP1911L产 地：中国大陆

T13553Arimoclomolaggregation,Heat shock proteins,HSP,co-inducer,system,BRX220,motor,Arimoclomol,inhibit,ub

Arimoclomol is a co-inducer of heat shock proteins (HSP) and can be used in studies about the treatment of amyotrophic lateral sclerosis (ALS).

价 格：￥电议型 号：T13553产 地：中国大陆

T9855BR102910?FAP Inhibitor,BR102910,POP,inhibit,prolyl oligopeptidase,Inhibitor,BR-102910,BR 102910,Prol

4-Thiazolecarboxamide, N-[2-[(2S)-2-cyano-4,4-difluoro-1-pyrrolidinyl]-2-oxoethyl]-2-[(3,4-dichlorophenyl)methyl]-(BR102910) is a selective inhibitor of fibroblast activated protein (FAP).

价 格：￥电议型 号：T9855产 地：中国大陆

T9557TNIK-IN-2inhibit,Inhibitor,TNIKIN2,TNIK IN 2,TNIK

TNIK-IN-2 is an inhibitor Traf2- and Nck-interacting protein kinase (TNIK, IC50 = 1.33 μM)) which is a downstream signal protein of the Wnt/β-catenin pathway.

价 格：￥电议型 号：T9557产 地：中国大陆

T6557KU-0060648mTOR,inhibit,KU-0060648,Phosphoinositide 3-kinase,Inhibitor,Mammalian target of Rapamycin,

KU-0060648 is a dual inhibitor of DNA-PK and PI3Kα, PI3Kβ, PI3Kδ with IC50 of 8.6 nM and 4 nM, 0.5 nM, 0.1 nM respectively, less inhibition of PI3Kγ with IC50 of 0.59 μM.

价 格：￥电议型 号：T6557产 地：中国大陆

T14946Ch55

Ch55 is an effective inducer of the differentiation of HL60 cells (EC50 = 200 nM) and shows high affinity with RAR-α and RAR-β receptors. Ch55 can be used in studies about cancer.

价 格：￥电议型 号：T14946产 地：中国大陆