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产品数：86101
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T7484LWKYMVM 2TFA(187986-17-0(free base))WKYMVM 2TFA(187986170(free base)),WKYMVM 2TFA(187986 17 0(free ba
WKYMVM 2TFA is a N-formyl peptide receptor (FPR1) agonist.
价 格：￥电议型 号：T7484L产 地：中国大陆
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T7794ZuranoloneInhibitor,inhibit,γ-Aminobutyric acid Receptor,Gamma-aminobutyric acid Receptor,GABA Recep
Zuranolone is an agonist of GABAA receptor.
价 格：￥电议型 号：T7794产 地：中国大陆
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T0794Mepenzolate BromideHCAR2,PUMA-G,inhibit,Muscarinic acetylcholine receptor,Inhibitor,hM3R,gastrointes
Mepenzolate Bromide is a muscarinic antagonist used to treat gastrointestinal conditions.
价 格：￥电议型 号：T0794产 地：中国大陆
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T7799BMP signaling agonist sb4Inhibitor,SMAD,bmp,cell,inhibit,BMP signaling agonist sb4,BRE-luc,BMP signa
SB 4 is an agonist of benzoxazole bone morphogenetic protein (BMP) signaling (EC50 :74 nM)
价 格：￥电议型 号：T7799产 地：中国大陆
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T7900BAY-474BAY-474,BAY 474,BAY474,epigenetics,probe,inhibit,Inhibitor,c-Met,SGC,c-Met/HGFR
BAY-474 is an inhibitor of tyrosine-protein kinase c-Met. It acts as an epigenetics probe
价 格：￥电议型 号：T7900产 地：中国大陆
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T6798TretazicarTretazicar,NQO1,DNA Alkylator/Crosslinker,rat,bifunctional,Inhibitor,inhibit,agent,cross-l
CB1954(Tretazicar), an anticancer prodrug, is activated by NAD(P)H quinone oxidoreductase 2. It is converted in the presence of the enzyme NQO2 and co-substrate caricotamide ( EP-0152R) (EP) into a potent cytotoxic bifunctional alkylating agent.
价 格：￥电议型 号：T6798产 地：中国大陆
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TQ0038BrensocatibDipeptidyl Peptidase,DPP,AZD 7986,inhibit,INS-1007,AZD-7986,Brensocatib,INS1007,Inhibitor
AZD7986 is a Dipeptidyl peptidase 1 (DPP1) inhibitor (pIC50s: 6.85, 7.7, 7.6, 7.8, and 7.8 in human, rat, mouse, rabbit, and dog, respectively).
价 格：￥电议型 号：TQ0038产 地：中国大陆
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T8798MSA-2interferon-β,Inhibitor,TMEM173,ERIS,MPYS,immunity,secretion,tumor,Stimulator of Interferon Gene
MSA-2 is a potent and orally available non-nucleotide STING agonist.
价 格：￥电议型 号：T8798产 地：中国大陆
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T7944VPS34 inhibitor 1 (Compound 19, PIK-III analogue)inhibit,VPS34,oral,VPS-34 inhibitor 1 (Compound 19,
VPS34 inhibitor 1 (Compound 19, PIK-III analogue) is a potent and selective inhibitor of VPS34( IC50 : 15 nM)
价 格：￥电议型 号：T7944产 地：中国大陆
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T7616LA 779 TFA(159432-28-7 free base)A 779 TFA(159432 28 7 free base),A 779 TFA(159432287 free base)
A 779(3TFA) is a potent antagonist of angiotensin-(1-7) receptor
价 格：￥电议型 号：T7616L产 地：中国大陆
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T6712Tyrphostin AG 879tyrosine,EGFR,phosphorylation,Tyrphostin AG-879,antiproliferation,Tyrphostin AG879,
Tyrphostin AG 879 effectively inhibits HER2/ErbB2 (IC50: 1 μM), 100- and 500-fold higher selective to ErbB2 than EGFR and PDGFR.
价 格：￥电议型 号：T6712产 地：中国大陆
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TN1879Lucideric acid Ainhibit,Lucideric acid A,Inhibitor,MMP,Matrix metalloproteinases
Lucideric acid A is a modulator of JNK and p38 and enhances LPS-induced immune responses in monocytic THP-1 cells possibly via the modulation of p38 and JNK/MAPKs activation.
价 格：￥电议型 号：TN1879产 地：中国大陆
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T6796CB-5083Inhibitor,inhibit,multiple,p97,VCP,solid,tumors,myeloma,AAA,ATPase,Cdc48,CB-5083
CB-5083 is a potent, selective, and orally bioavailable p97 AAA ATPase inhibitor ( IC50=11 nM).
价 格：￥电议型 号：T6796产 地：中国大陆
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TN1079DeoxyelephantopinAkt,Inhibitor,β-catenin,Deoxyelephantopin,MAPK,Nuclear factor-κB,NF-κB,PI3K,Nuclear
Deoxyelephantopin has anti-inflammatory, hepatoprotective, and wound healing activities; it also has antitumor activity.Deoxyelephantopin inhibits NF-κB, MAPK, PI3K/Akt, and β-catenin signaling
价 格：￥电议型 号：TN1079产 地：中国大陆
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TP1792LKKI-5 acetate(97145-43-2 free base)KKI5 acetate(97145432 free base),KKI 5 acetate(97145 43 2 free ba
KKI-5 acetate is a serine protease inhibitor that inhibits kallikrein and plasmin. KKI 5 may exhibit anticancer chemotherapeutic benefit and may also be used as a treatment for angioedema.
价 格：￥电议型 号：TP1792L产 地：中国大陆
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T6379AMG 517AMG 517,Inhibitor,inhibit,Transient receptor potential channels,TRP Channel
AMG 517 is an effective and specific TRPV1 antagonist, antagonizes proton (IC50: 0.76 nM), capsaicin (IC50: 0.62 nM), and heat activation (IC50: 1.3 nM) of TRPV1.
价 格：￥电议型 号：T6379产 地：中国大陆
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T7960Coumarin 7Coumarin-7,inhibit,Inhibitor,Coumarin7,Coumarin 7
Coumarin 7 is a natural product.
价 格：￥电议型 号：T7960产 地：中国大陆
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T87901-Methylhistamine dihydrochlorideEndogenous Metabolite,1Methylhistamine dihydrochloride,inhibit,Inhi
1-Methylhistamine dihydrochloride is a major metabolite of histamine by histamine N-methyltransferase in the pathway of histidine metabolism. It has been used as a biomarker of histaminergic system activity in the brains of Alzheimer´s disease patients as well as those with hypersomnia and other neurological conditions.
价 格：￥电议型 号：T8790产 地：中国大陆
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T6849UprosertibGSK-2141795,GSK 2141795,Uprosertib,inhibit,Akt,Inhibitor,PKB,Protein kinase B
Uprosertib (GSK2141795) is a selective, ATP-competitive, and orally bioavailable Akt inhibitor with IC50 of 180 nM, 328 nM, and 38 nM for Akt 1, 2 and 3, respectively. Phase 2.
价 格：￥电议型 号：T6849产 地：中国大陆
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T9079Apostatin-1Apostatin 1,TRADD,Apostatin-1,Beclin1,RIPK,Autophagy,SH-SY5Y,Receptor-interacting protein
Apostatin-1 is a novel TRADD inhibitor. Apostatin-1 can bind to a pocket on the N-terminal TRAF2 binding domain of TRADD.
价 格：￥电议型 号：T9079产 地：中国大陆
