T7158OmbitasvirABT267,Hepatitis C virus,Inhibitor,inhibit,HCV,Ombitasvir,ABT 267

Ombitasvir is an orally bioavailable and potent inhibitor of the hepatitis C virus (HCV) non-structural protein 5A (NS5A).with EC50s of 0.82 to 19.3 pM against HCV genotypes 1 to 5, and 366 pM against genotype 6a

价 格：￥电议型 号：T7158产 地：中国大陆

T9221UNC926 hydrochlorideUNC926,methyl-lysine,L3MBTL3,Epigenetic Reader Domain,UNC-926 hydrochloride,UNC9

UNC926 hydrochloride is a methyl-lysine (Kme) reader domain inhibitor.

价 格：￥电议型 号：T9221产 地：中国大陆

T7395LanifibranorInhibitor,IVA 337,Lanifibranor,inhibit,PPAR,Peroxisome proliferator-activated receptors,

Lanifibranor is an agonist of peroxisome proliferator-activated receptors (PPARs) with EC50 values of 1,537, 866, and 206 nM for human recombinant PPARα, PPARβ, and PPARγ, respectively, for transactivation activity

价 格：￥电议型 号：T7395产 地：中国大陆

T8507MAC-545496Bacterial,S. aureus,Antivirulence,Inhibitor,MAC545496,mprF,nanomolar,GraR,MAC-545496,MRSA,

MAC-545496 is a glycopeptide-resistance-associated protein R (GraR) inhibitor, is an antivirulence agent.

价 格：￥电议型 号：T8507产 地：中国大陆

PDK0269Compound PDK0269Compound PDK0269

PBG (1-Phenylbiguanide HCl), as 5-HT3 receptor agonists(3–100 μM, pEC50 5.05±0.06), acutely increased XII (hypoglossal) burst frequency and regularity, and decreased bursts/episode . Phenylbiguanide produced a dose-related (10-500 microM) increase in the release of dopamine (280-2000%). When nomifensine (5 microM) was included in the Ringer solution, the effect of PBG on the release of dopamine was ameliorated or inhibited. Phenylbiguanide, infused intravenously for 15 min, elicited a sustained

价 格：￥电议型 号：PDK0269产 地：中国大陆

T6744Methylbenactyzium BromideInhibitor,Muscarinic acetylcholine receptor,Methylbenactyzium Bromide,inhib

Dimethadione is an anticonvulsant that is the active metabolite of trimethadione.

价 格：￥电议型 号：T6744产 地：中国大陆

T6667SF1670inhibit,Autophagy,SF1670,MMAC1,Inhibitor,SF 1670,SF-1670,Phosphatase and tensin homolog,Phosph

SF1670 is a specific PTEN inhibitor with IC50 of 2 μM.

价 格：￥电议型 号：T6667产 地：中国大陆

T6S1894LinderaneCYPs,Cytochrome P450,Linderane,inhibit,Inhibitor

1. Linderane was characterized as a mechanism-based inactivator of CYP2C9.

价 格：￥电议型 号：T6S1894产 地：中国大陆

PDK0236Compound PDK0236Compound PDK0236

价 格：￥电议型 号：PDK0236产 地：中国大陆

T7568LM22A-4LM-22A-4,Inhibitor,Trk Receptor,inhibit,LM22A4,LM22A-4,Tropomyosin related kinase receptor,LM

LM22A-4 is a brain-derived neurotrophic factor (BDNF) mimetic and agonist of the receptor tropomyosin-related kinase B (TrkB; IC50 : 47 nM in a fluorescence anisotropy assay)

价 格：￥电议型 号：T7568产 地：中国大陆

TP1790LTyr-Somatostatin-14 acetate(58100-03-1 free base)Tyr Somatostatin 14 acetate(58100 03 1 free base),T

Tyr-Somatostatin-14 acetate is a customized peptide that adds a Tyrosine amino acid to Somatostatin-14.

价 格：￥电议型 号：TP1790L产 地：中国大陆

TN6848Piperonylic acidformation,virus,natural,inactivator,Cytochrome P450,Piperonylic acid,quasi-irreversi

Piperonylic acid is a natural molecule bearing a methylenedioxy function that closely mimics the structure of trans-cinnamic acid. Piperonylic acid selectively inactivate the CYP73A P450 subpopulation.

价 格：￥电议型 号：TN6848产 地：中国大陆

T600175-Bromo-4-chloro-3-indoxyl-beta-D-cellobioside5 Bromo 4 chloro 3 indoxyl beta D cellobioside,5Bromo4

5-Bromo-4-chloro-3-indoxyl-beta-D-cellobioside is a chromogenic compound used to detect cellobiohydrolases.

价 格：￥电议型 号：T60017产 地：中国大陆

Fr14273Compound Fr14273Compound Fr14273

价 格：￥电议型 号：Fr14273产 地：中国大陆

T3696polygalaxanthone IIICYPs,Inhibitor,Cytochrome P450,inhibit,polygalaxanthone III

Polygalaxanthone III can significantly inhibit chlorzoxazone 6-hydroxylation catalyzed by CYP2E1.

价 格：￥电议型 号：T3696产 地：中国大陆

TN1037GroenlandicineTopoisomerase,Groenlandicine,inhibit,Inhibitor

Groenlandicine is a protoberberine alkaloid from Coptidis Rhizoma. Groenlandicine exhibits moderate inhibitory effect with IC50 value of 154.2 μM for human recombinant aldose reductase (HRAR). Groenlandicine selectively induces topoisomerase I-mediated DNA cleavage;Groenlandicine may be a promising anti-Alzheimer´s disease agent due to its potent inhibitory activity of both ChEs and beta-amyloids formation, as well as marked ONOO(-) scavenging and good ROS inhibitory capacities.

价 格：￥电议型 号：TN1037产 地：中国大陆

T7016VR23Apoptosis,VR-23,VR23,Proteasome,inhibit,Inhibitor,VR 23

VR23 is a potent proteasome inhibitor. Data shows IC50 =1 nM for trypsin-like proteasomes, IC50=50-100 nM for chymotrypsin-like proteasomes, and IC50=3 μM for caspase-like proteasomes.

价 格：￥电议型 号：T7016产 地：中国大陆

T9123DS-1205TRKA,c-Met/HGFR,migration,Axl,Tyro3,Trk Receptor,MET,DS 1205,Mer,Tropomyosin related kinase r

DS-1205 is a potent and selective inhibitor of AXL kinase, with an IC50 of 1.3 nM. DS-1205 also inhibits MER, MET, and TRKA, with IC50s of 63, 104, and 407 nM, respectively. DS-1205 can inhibit cell migration in vitro and tumor growth in vivo[1].

价 格：￥电议型 号：T9123产 地：中国大陆

T6800CCF642calcium,Inhibitor,PDI,CCF642,apoptosis,isomerases,disulfide,myeloma,CCF-642,protein,multiple,r

CCF642 is a novel PDI-inhibiting compound with antimyeloma activity.

价 格：￥电议型 号：T6800产 地：中国大陆

Fr16627Compound Fr16627Compound Fr16627

价 格：￥电议型 号：Fr16627产 地：中国大陆