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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
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T6S1587Notoginsenoside R2Notoginsenoside R2,inhibit,Notoginsenoside R-2,Notoginsenoside R 2,Inhibitor
Notoginsenoside R2 has neuroprotection against 6-OHDA-induced neurotoxicity, is associated with Notoginsenoside R2-mediated P90RSK and Nrf2 activation through MEK1/2-ERK1/2 pathways.
价 格：￥电议型 号：T6S1587产 地：中国大陆
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T15830M-110M 110,M110
M-110 is a highly selective, ATP-competitive inhibitor of PIM kinases with a preference for PIM-3 (IC50=47 nM). M-110 inhibits PIM-1 and PIM-2 with similar IC50s of 2.5 μM. M-110 inhibits the proliferation of prostate cancer cell lines with IC50s of 0.6 to 0.9 μM.
价 格：￥电议型 号：T15830产 地：中国大陆
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T11588Hydroxybupropion
Hydroxybupropion is the major active metabolite of Bupropion and an antagonist of nACh receptor. Hydroxybupropion inhibits norepinephrine uptake (IC50 = 1.7 μM).
价 格：￥电议型 号：T11588产 地：中国大陆
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TP1573LCLIP 86-100 acetate(648881-58-7 free base)CLIP 86100 acetate(648881587 free base),CLIP 86 100 acetat
This is amino acids 86 to 100 fragment of class II-associated invariant chain peptide called CLIP. The major histocompatibility complex class II molecule displays peptide fragments of foreign proteins to trigger a defensive reaction from the immune system. Before insertion of the foreign peptides into the binding groove, a place-holding peptide CLIP is removed. This is accomplished by the molecule DM, which is shown to increase the dissociation rate of a CLIP peptide from class II.
价 格：￥电议型 号：TP1573L产 地：中国大陆
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TN1589Dihydrowithaferin ADihydrowithaferin A,2,3-Dihydrowithaferin A,inhibit,Inhibitor,Cholinesterase (ChE
Dihydrowithaferin A is a withanolide isolated from Withania somnifera with activity against acetylcholinesterase (AChE). Dihydrowithaferin A in the diet may prevent or decrease the growth of tumors.
价 格：￥电议型 号：TN1589产 地：中国大陆
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TP1158Copper tripeptidehuman plasma,Copper tripeptide,inhibit,chemoattractant,fibroblast,endothelial,prote
Copper peptide GHK-Cu is a naturally occurring copper complex of the tripeptide glycyl-L-histidyl-L-lysine. The tripeptide has strong affinity for copper(II) and was first isolated from human plasma. It can be found also in saliva and urine.
价 格：￥电议型 号：TP1158产 地：中国大陆
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TQ0158AzaserineAntibiotic,Inhibitor,Bacterial,P165,CI 337,CI337,P 165,Azaserine,inhibit
Azaserine is a tumor-inhibiting antibiotic isolated from a species of Streptomyces and functions as an inhibitor of glutamine amidotransferase.
价 格：￥电议型 号：TQ0158产 地：中国大陆
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T22879JNJ 10191584 maleate
JNJ 10191584 maleate is an orally active and selective antagonist of H4 receptor (Ki = 26 nM). JNJ 10191584 maleate inhibits chemotaxis of eosinophils and mast cells (IC50 = 530 nM and 138 nM).
价 格：￥电议型 号：T22879产 地：中国大陆
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TN1586DihydrorotenoneApoptosis,inhibit,Dihydrorotenone,Inhibitor,Mitochondrial Metabolism
Dihydrorotenone is a potent mitochondrial inhibitor and probably induces Parkinsonian syndrome.
价 格：￥电议型 号：TN1586产 地：中国大陆
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T7370TalarozoleRetinoid X receptors,R 115866,Retinoic acid receptors,RAR/RXR,inhibit,Talarozole,Cytochrom
Talarozole is an oral systemic all-trans retinoic acid metabolism blocking agent (RAMBA). Talarozole inhibits both CYP26A1 and CYP26B1 with IC50s of 5.4 and 0.46 nM, respectively.Talarozole for the treatment of acne, psoriasis and other keratinization disorders.
价 格：￥电议型 号：T7370产 地：中国大陆
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T8158Tilianinantioxidant,Inhibitor,inflammatory,myocardial-protective,diabetic,hyperlipidemic,inhibit,Til
Tilianin is a flavonoid glycoside of Dragocephalum moldavicum L.
价 格：￥电议型 号：T8158产 地：中国大陆
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T15826Lometrexol
Lometrexol, an antipurine Antifolate, can inhibit the activity of glycinamide ribonucleotide formyltransferase (GARFT) but do not induce detectable levels of DNA strand breaks. Lometrexol can further inhibit de novo purine synthesis, causing abnormal cell proliferation and Apoptosis, even cell cycle arrest. Lometrexol has anticancer activity. Lometrexol also is a potent human Serine hydroxymethyltransferase1/2 (hSHMT1/2) inhibitor.
价 格：￥电议型 号：T15826产 地：中国大陆
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T11158EGFR-IN-11EGFRIN11,EGFR IN 11
EGFR-IN-11 is a selective inhibitor of EGFR-tyrosine kinase and induces cell apoptosis. EGFR-IN-11 inhibits triple mutant EGFRL858R/T790M/C797S with an IC50 of 18 nM and arrests cell cycle at G0/G1.
价 格：￥电议型 号：T11158产 地：中国大陆
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T15820Mibampator
Mibampator is an effective and selective AMPA receptor potentiator.
价 格：￥电议型 号：T15820产 地：中国大陆
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T21588OlomoucineOlomoucine,Inhibitor,cyclindependent kinases,cdc2,purines,cell cycle,non-small cell lung c
Olomoucine is an ATP competitive inhibitor of Cdk2/cyclin A, Cdc2/CyclinB, CDK2/CyclinE, CDK5/p35, and ERK1/p44 MAP kinase with IC50s of 7, 7, 7, 3 and 25 ?M, respectively. Olomoucine regulates cell cycle and exhibits anti-melanin tumor activities.
价 格：￥电议型 号：T21588产 地：中国大陆
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T7611ODM-203anti-tumor immunity,ODM-203,FGFR,HUVEC,H1581,Inhibitor,cancer,Vascular endothelial growth fac
ODM-203, a Selective Inhibitor of FGFR and VEGFR, Shows Strong Antitumor Activity, and Induces Antitumor Immunity
价 格：￥电议型 号：T7611产 地：中国大陆
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T60158PBRM1-BD2-IN-3PBRM1BD2IN3
PBRM1-BD2-IN-3 (compound 12) is a potent PBRM1-BD2 inhibitor with an IC50 value of 1.1 μM. PBRM1-BD2 Inhibitor can be used to research anticancer.
价 格：￥电议型 号：T60158产 地：中国大陆
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TN71582-(4-methoxyphenyl)-N-methyl-2-oxoacetamide
2-(4-methoxyphenyl)-N-methyl-2-oxoacetamide is a marine derived natural products found in Polycarpa aurata.
价 格：￥电议型 号：TN7158产 地：中国大陆
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T15815LY3295668
LY3295668 is a selective inhibitor of Aurora A with Kis of 0.8 nM and 1038 nM for Aurora A and B, respectively.
价 格：￥电议型 号：T15815产 地：中国大陆
