T7297KG-501Epigenetic Reader Domain,inhibit,Inhibitor,KG 501,Naphthol AS-E,KG501,KG-501

KG-501 is a cAMP response element-binding protein (CREB) inhibitor(IC50 : 6.89 μM).

价 格：￥电议型 号：T7297产 地：中国大陆

T7846Aegelineαsyn,Aegeline,yeast,Inhibitor,protein,Sec22p,inhibit,toxicity,Fungal,SNARE

Aegeline is an alkaloidal-amide, isolated from the leaves of Aegle marmelos and have shown antihyperglycemic as well as antidyslipidemic activities in the validated animal models of type 2 diabetes mellitus.

价 格：￥电议型 号：T7846产 地：中国大陆

T8700TKIMTKIM

TKIM is a TWIK-related potassium channel 1 (TREK-1) inhibitor, binding to the pocket of the intermediate (IM) state of TREK-1.

价 格：￥电议型 号：T8700产 地：中国大陆

TWS2045Bruceine DParasite,Notch,Apoptosis,Bruceine D,Inhibitor,inhibit

1. Bruceine D from Brucea javanica, may have the potential to be used as a natural viricide, or a lead compound for new viricides. 2. Bruceine D inhibits the growth of three pancreatic cancer cell lines, i.e., PANC-1, SW199 and CAPAN-1; induces cytotoxicity in Capan-2 cells via the induction of cellular apoptosis involving the mitochondrial pathway.

价 格：￥电议型 号：TWS2045产 地：中国大陆

T8877BonaftonBonafton

Bonafton is an antiviral agent.

价 格：￥电议型 号：T8877产 地：中国大陆

T6940PHA-767491 hydrochloridePHA767491,PHA 767491,inhibit,CAY-10572,Cyclin dependent kinase,CDK,CAY 10572

PHA-767491 is an effective ATP-competitive dual Cdc7/CDK9 inhibitor (IC50: 10/34 nM). It has ~20-fold selectivity against GSK3-β and CDK1/2, 50-fold selectivity against CDK5 and MK2, 100-fold selectivity against CHK2 and PLK1.

价 格：￥电议型 号：T6940产 地：中国大陆

T31425Dibenz[a,h]anthracene

Dibenz[a,h]anthracene has induced DNA damage and gene mutations in bacteria and gene mutations and transformation in several types of mammalian cell cultures.

价 格：￥电议型 号：T31425产 地：中国大陆

TPL0023Compound 80875-98-5Compound 80875985,Compound 80875 98 5

价 格：￥电议型 号：TPL0023产 地：中国大陆

T8423ML417neuroprotection,dopaminergic,β-arrestin,ML417,ML-417,translocation,phosphorylation,neurons,ML 4

ML417 is a selective and brain penetrant agonist of D3 Dopamine (EC50 : 38 nM).

价 格：￥电议型 号：T8423产 地：中国大陆

T8419XP-59XP 59,XP59,inhibit,Inhibitor,SARS-CoV,XP-59,SARS coronavirus

XP-59 is a potent the SARS-CoV Mpro inhibitor(Ki : 0.1 μM).

价 格：￥电议型 号：T8419产 地：中国大陆

T7117Sapropterin dihydrochloride(6R)-BH4,Sapropterin,Inhibitor,inhibit,Sapropterin dihydrochloride

Sapropterin dihydrochloride is phenylalanine hydroxylase agonist that is approved for the treatment of BH4 responsive PKU.

价 格：￥电议型 号：T7117产 地：中国大陆

TN2260Taxifolin 7-O-rhamnosideInhibitor,Taxifolin 7Orhamnoside,Taxifolin 7 O rhamnoside,inhibit

Taxifolin 7-O-rhamnoside is a natural product from Hypericum japonicum.

价 格：￥电议型 号：TN2260产 地：中国大陆

T6S1572Sauchinoneantioxidant,LPS,Diastereomeric,TNF-α,iNOS,anti-inflammatory,lignan,COX-2,inhibit,Nuclear f

1. Sauchinone is a useful adjunctive treatment for bacterial infection. 2. Sauchinone, an active lignan found in Saururus chinensis, to regulate the activation of HSCs, to prevent liver fibrosis, and to inhibit oxidative stress in vivo and in vitro. 3. Sauchinone diminishes LPS-induced neutrophil activation and acute lung injury. 4. Sauchinone-induced HO-1 expression plays a key role in the vascular protective effects of Sauchinone in HUVEC. 5. Sauchinone protects skin keratinocytes through inhi

价 格：￥电议型 号：T6S1572产 地：中国大陆

T9295BLU-263BLU 263,BLU263

BLU-263 is an investigational, potent, and selective oral small molecule inhibitor of KIT with sub-nanomolar potency against D816V-mutant KIT.

价 格：￥电议型 号：T9295产 地：中国大陆

T8478SC-43antiproliferative,Inhibitor,SC-43,SHP-1,PTPN6,Phosphatase,Apoptosis,caspase-3,SC 43,anti-fibrot

SC-43 is a potent and orally active agonist of SHP-1 (PTPN6). SC-43 inhibits the phosphorylation of STAT3 and induces cell apoptosis, and with anti-fibrotic and anticancer effects.

价 格：￥电议型 号：T8478产 地：中国大陆

T80582-Methyl-4-pentenoic Acidinhibit,Inhibitor,2 Methyl 4 pentenoic Acid,2Methyl4pentenoic Acid

2-Methyl-4-pentenoic acid is a branched-chain fatty acid.

价 格：￥电议型 号：T8058产 地：中国大陆

TN2272Tigloylgomisin Hinhibit,Inhibitor,Tigloylgomisin H

Tigloylgomisin H significantly induces quinone reductase (QR) activity in Hepa1c1c7 mouse hepatocarcinoma cells. Tigloylgomisin H functions as a novel monofunctional inducer that specifically upregulates phase II enzymes through the Nrf2-ARE pathway and can be used in liver cancer prevention studies.

价 格：￥电议型 号：TN2272产 地：中国大陆

T2573MisoprostolMisoprostol

价 格：￥电议型 号：T2573产 地：中国大陆

T9584UNC6934Inhibitor,UNC6934,Histone Methyltransferase,inhibit,UNC 6934,UNC-6934

UNC6934 is a chemical probe targeting the N-terminal PWWP (PWWP1) domain of NSD2.

价 格：￥电议型 号：T9584产 地：中国大陆

T6S0078Oxypeucedanin hydrateInhibitor,inhibit,Oxypeucedanin,(+)-Oxypeucedanin,Oxypeucedanin hydrate,D. anet

1. Oxypeucedanin hydrate has antioxidant activity. 2. Oxypeucedanin hydrate is an antimutagenic agent. 3. Oxypeucedanin hydrate exhibits carbohydrate metabolizing enzymes inhibitory effect.

价 格：￥电议型 号：T6S0078产 地：中国大陆